Variation in Reported Human Head Tissue Electrical Conductivity Values

1Understanding electrical activity propagation throughout the head is essential in neurophysiology. In particular, forward and inverse solutions for source reconstruction in electroencephalography [EEG (Beltrachini,, )], magnetoencephalography [MEG (Haueisen et al.; Vorwerk et al. )], transcranial magnetic stimulation [TMS; (Opitz et al.; Salinas et al. ] and deep brain stimulation [DBS; (Butson et al.; Dabek et al.; McIntyre et al. )] are governed by such phenomenon. Accurate values of head tissue electrical conductivity are vital to model and localise primary current generators within the brain based on both invasive and non-invasive recordings. Misspecification of tissue conductivities can consequently contribute to significant errors in magnetic field strength and electric surface potential estimations (Cohen and Cuffin; Haueisen et al.; Okada et al. ), which may additionally introduce systemic errors in the EEG and MEG forward problems (Goncalves et al.,, ) and result in inaccurate source localisation (Akhtari et al.; Haueisen et al.; Pohlmeier et al.; Vatta et al. ). Anwander and colleagues 2002, for example, revealed mean EEG source localisation errors of 5.1 mm and 8.88 mm for radially- and tangentially-oriented sources, respectively, if white matter (WM) anisotropy was neglected in conductivity models. Whilst Hallez et al. reported average errors of 11.21 mm, increasing to 13.73 mm if skull anisotropy in addition to WM anisotropy was not considered. Even accounting for skull anisotropy has yielded maximum localisation errors of 6 mm (Dannhauer et al. ). Miscalculations can further lead to incorrect and inappropriate conclusions made regarding brain function, pathology and disease treatments inferred from E/MEG data (Wendel et al. ). Most notably regarding implications in epilepsy treatment (Akhtari et al.; Fabrizi et al. ), brain stimulation (De Lucia et al.; Sadleir et al.; Suh et al. ) and insights into psychiatric and neurological disorders (Frantseva et al.; Park et al.; Schlosser et al. ).

2Currently, head tissue conductivity values are often assumed from the literature to create a volume conductor model. Despite extensive research and subsequent review papers (Faes et al.; Gabriel et al.; Geddes and Baker ), considerable differences in conductivity are evident between and within reports. Head tissue segmentation is known to be of substantial importance when assigning conductivity values (Akhtari et al. ), however there remains discrepancies between such segmentation, for example, consideration of the various layers of the skull (Akhtari et al. ), the importance of the dura layer (Ramon et al. ) and the influence of blood vessels on high resolution EEG head modelling (Fiederer et al. ). Additionally, accounts are inconsistent for the influence of anisotropy on conductivity values (Güllmar et al.; Nicholson, ) and the brain-to-skull conductivity ratio [BSCR; (Gutierrez et al.; Wolters et al. )]. Furthermore, existing reports of conductivity vary depending on participant demographics, such as age and pathology, as well as measurement condition (i.e. in vivo, ex vivo or in vitro), applied frequency, tissue temperature and employed methodology.

3Unsurprisingly, utilising different methodologies, such as directly applied current (DAC), electrical impedance tomography (EIT), E/MEG, Magnetic Resonance EIT (MREIT) and Diffusion Tensor Imaging (DTI), yield diverse conductivity values. The relative strengths and limitations of these methods is essential to accurately characterise discrepancies and inform future research. With DAC we refer to any invasive method where current is directly applied to tissue, either via multiple implanted electrodes or onto excised tissue, and electrical conductivity is determined from the resulting potential difference between a pair of electrodes. DAC methods have the advantage of not requiring a computational head model, which often introduces simplified assumptions regarding the neurobiology and dynamics of the human head, as well as being cost effective with a low acquisition time, easily portable and useable and has the potential to analyse conductivity of all tissue types. DAC methods however, are invasive, requiring post-mortem samples or excised tissues that are not under biophysically natural conditions. Tissues obtained post-mortem, for example, are subject to biochemical processes initiated by death, such as changes in ion mobility and cell membrane polarisation, which consequently affect conductivity (Opitz et al. ). Opitz and colleagues importantly demonstrated, despite controlling for confounding variables (i.e. temperature), that live and post-mortem intracranial electrical fields significantly differed. Similarly, excised tissues undergo various extracting, preservation and holding procedures (i.e. saline soaked, time since excision, etc.) which can change the electrolyte concentration (Akhtari et al. ) and hence influence conductivity. On the other hand, EIT, E/MEG, MREIT and DTI methods are non-invasive and occur in vivo, having the advantage of remaining under natural conditions. Additionally, EIT and E/MEG are both portable and cost effective with low acquisition times, compared to MREIT and DTI methods which are non- portable, more expensive and with high acquisition times, but EIT and E/MEG have lower spatial resolution than MREIT and DTI and require the use of a computational head model. Both MREIT and DTI however, employ magnetic resonance (MR) imaging, making skull conductivity non-accessible due to weak MR signal towards bone layers. A further advantage of DTI is the ability to classify anisotropic and heterogenous conductivity values of soft tissues (Johansen-Berg and Behrens ). A summary of the strengths and weaknesses of the described methods are provided in Table 1.

4Considering the vast disparity in data, assuming conductivity from previous literature is insufficient when accurate and precise values are required. Significant and important factors affecting this variation, however, are currently unknown. Knowledge of influential variables, such as tissue segmentation, methodology employed, sample temperature or participant pathology can provide insights into the stability of tissue conductivity values and methodology, as well as suggest areas for future research. The current study aimed to systematically and extensively investigate all published reports of human head tissue electrical conductivity to (i) evidence any significant variations in conductivity values of different head tissue types; (ii) determine any significant factors contributing to variation; and (iii) analyse the impact these factors may have on source reconstruction in E/MEG. A systematic review, restricted to human head tissue, was carried out to identify relevant papers, and a meta-analysis was completed to reveal significant factor variables via a multiple regression. It was hypothesised that head tissue conductivity would vary between and within tissues. It was expected the meta-analysis would further reveal significant influential factors and their impact.

5Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) statement guidelines (Moher et al. ) were followed and a PRISMA checklist and flow diagram were completed (Appendix 1) An extensive literature search, spanning three databases (PubMed, Scopus and Web of Knowledge), was conducted to retrieve published and peer-reviewed studies exploring electrical conductivity (or equivalent) of the human head (or equivalent). The keywords utilised for the systematic literature search are provided in Appendix 2. Article titles were systematically searched using relevant and/or equivalent keywords, unrestricted by year of publication, language or design. Reference lists of included papers were hand-searched to identify additional papers. Duplicates following the initial literature search were removed.

6Papers met the inclusion criteria if they (i) provided at least one conductivity measure (or equivalent from which conductivity could be calculated), of the (ii) human (iii) head, where (iv) employed methodology and (v) tissue type were available. Reviews were only included as an information source to the original reference, where data was thus extracted. Exclusions were made if any of the five inclusion criteria were absent or ambiguous, or if an English version was unavailable after extensive search. In addition to conductivity value, methodology and tissue type, reports were collected on measurement condition (i.e. in vivo, ex vivo, or in vitro), applied frequency to determine the conductivity, tissue temperature, as well as participant’s age, gender and pathology. Missing information for one or more of these variables did not result in exclusion. Studies applying frequencies above 1 kHz were excluded from analysis on the grounds this frequency is besides the scope of typical brain activity recorded in E/MEG.

7All identified titles resulting from the literature search, following removal of duplicates, were initially screened for applicability and/or immediate exclusion. Remaining abstracts were further assessed, and full texts of potentially relevant papers were obtained to determine if they consequently met the inclusion criteria.

8All conductivity, resistivity or impedance values were extracted from each paper and converted to S/m for standardisation. The sample mean and standard deviation were subsequently calculated for every differentiation in methodology within each paper and characterised according to the aforementioned variables.

9For the current review, tissues were separated into four major compartments, each comprised of sub-compartments: the scalp (skin, fat, muscle), the skull (spongiform, inner and outer compact bone and sutures), cerebrospinal fluid (CSF) and the brain [grey matter (GM), WM, the dura layer, blood, cerebellum, lesions, epileptogenic zone (EZ)]. Conductivity values were assigned according to tissue type as reported. Tissues were classified as whole-scalp, whole-skull or whole-brain when no conductivity values for their sub-compartments were reported, similarly whole-compact bone was assigned if no values for the inner and outer compact bone were provided. If given, WM was further segmented into WM oriented in parallel (WM_par) or perpendicular (WM_perp) to the applied current. See Fig. 1 for a detailed representation of all tissue compartments. Additionally, when available, the BSCR was reported as a nominal ratio without units.

10Conditions were separated into three main categories:

11In vivo—“within the living”; experiment conducted on or in whole living organisms/cells. Electrical conductivity values obtained within a living head were considered in vivo.

12Ex vivo—“out of the living”; experiment in or on tissue from an organism in an external environment, but with minimal alteration of natural conditions, e.g. cultured cells derived from biopsies. Experiments where tissue was excised but kept within conditions similar to the human head were characterised as ex vivo.

13In vitro—“within the glass”; experiment within a controlled artificial environment outside of a living organism, isolated from their usual biological surroundings e.g. in a test tube/dish. Measurements where tissue was excised and stored in environments unlike the human head were classified as in vitro.

14Data acquisition techniques were categorised into five groups:

15DAC—invasive method of determining electrical conductivity, where a current was directly applied to the tissue, either via implanted electrodes in the head, or onto excised samples. The resulting electric potential difference from the applied current is measured via additional (implanted or applied to excised tissue) electrodes to calculate the electrical conductivity. Studies where electrical current was directly and invasively applied to the head tissue were characterised as DAC.

16EIT—a non-invasive medical imaging technique where alternating current at single or multiple frequencies is applied to the skin through two or more conducting surface electrodes. The resulting potential difference between the remaining measuring electrodes is then recorded. From this the electrical conductivity, permittivity and impedance can be inferred to create a tomographic image (Barber and Brown; Henderson and Webster ). Papers indicating an applied current of less than 1 kHz, injected through any number of electrodes and the resulting voltage were classified as EIT.

17MREIT—measures the induced magnetic flux density resulting from an injected current (as in EIT) using a magnetic resonance imaging (MRI) scanner. The internal current density is then computed and combined with magnetic flux density measurements to perform conductivity map reconstruction, using various inverse solutions (Bodenstein et al. ). Studies specifying acquisition of MRI data during current injection (as in any EIT method) to reconstruct conductivity (using any inverse method) were categorised as MREIT.

18E/MEG—electromagnetic data recorded from E/MEG employed to iteratively estimate the equivalent electrical conductivity that best matches the computed source localisation given the obtained E/MEG data Baysal and Haueisen. Articles estimating conductivity by employing data from E/MEG (of any set up) were characterised as E/MEG.

19DTI—diffusion-weighted MR images of the brain are acquired to measure the diffusion tensor eigenvalues, from which the electrical conductivity tensor eigenvalues are directly calculated (Sekino et al.; Tuch et al.; Tuch et al., ). Texts using diffusion imaging (of any protocol) to explicitly estimate the electrical conductivity tensor map were considered as employing DTI methodology for the current review. This included any method for estimating conductivity from the diffusion tensor. DTI papers where conductivity was not explicitly reported were not included in the current review.

20Frequency of applied or injected current (if applicable). Frequency was not extracted from papers where this was not specified.

21Classified according to whether the tissue sample was measured at/near body temperature (37 °C) or room temperature (18–25 °C). Unknown values were not reported for analysis.

22When available, mean and standard deviation of participant’s age were calculated for each paper and recorded in Table 2. Age at time of death was recorded for deceased participants. If specific age was unavailable, age was characterised as adult (all participants were over the age of 18), paediatric (all participants were under the age of 18), or both (participants were a mixture of over and under the age of 18).

23Participants were characterised as healthy if they had no neurological, developmental or psychological deficits, as reported in the research paper. Pathology was categorised as epilepsy for studies recruiting patients that presented with any classification of epileptic seizure. Similarly, tumour was assigned to papers where patients displayed any type of tumour, and neuro to patients with any type of neurological disorder that was not otherwise classifiable. Further pathologies included Parkinson’s Disease, Alzheimer’s Disease and stroke. All conductivity values were assumed to originate from healthy tissue, within the classified pathology, unless otherwise stated. Pathology was reported as unknown if not available in the literature.

24Drawing robust conclusions from systematic reviews and meta-analyses requires consideration of the systematic and random errors introduced in each included study by “assessing the methodological quality” (Moher et al.; Verhagen et al. ) in order to estimate “risk of bias”. Various tools are available for assessing study quality and addressing the systematic errors in each study, however none specifically to assess the quality of studies measuring the electrical conductivity of the human head. The current meta-analysis therefore, made use of the Cochrane Collaboration recommended Quality Assessment of Diagnostic Accuracy Studies (QUADAS) checklist (Whiting et al. ), where each item was adjusted for relevance, and any additional relevant items were added. A scaled numerical value was further assigned according to the studies compliance with each item; any irrelevant items were ignored. The sum, divided by the number of relevant items, was subsequently calculated to provide a final Quality Assessment Score (QAS), with an absolute maximum value of one (the closer the score is to one, the more reliable the study was considered). To ensure reliability of the QAS’s, papers were chosen at random and QASs calculated by two researchers, any discrepancies were discussed and if not resolved the mean QAS was assigned. The employed Quality Assessment Protocol and three examples are provided in Appendix 3.

25In addition to accounting for systematic errors within each study, random errors produced from inherently unpredictable variation in methodology were accounted for. This was adapted from the guidelines provided by Rosenthal and Borenstein and colleagues for meta-analysis weighting. Confidence values for each measurement were calculated to indicate the confidence each value of conductivity was 100% accurate. Firstly, the relative error was calculated for each conductivity value, as the standard deviation percentage of a multitude of values for a single tissue type for each participant (if the method is 100% precise, each value for the same tissue should be the same) or the error attributed to the measurement protocol—both described as a decimal. If both the standard deviation and measurement error were provided, the standard deviation was used to calculate the relative error. The relative error was then subtracted from one (where one indicates complete confidence the conductivity value is 100% accurate) to obtain a final confidence value of which the maximum is one. For example, a reported conductivity value with an associated standard deviation percentage of 8% will receive a confidence value of 0.92. Alternatively, when the standard deviation was not provided, the experimental error was utilised instead; e.g. a study with a methodological error of 0.05 would receive a confidence value of 0.95.

26To incorporate both the systematic and random errors associated with each study, the Quality Assessment Score of each study and the confidence values of each conductivity value were combined to provide a “weight”. This weight was calculated by multiplying the QAS by the confidence value (both with a maximum of one). The maximum associated weight each value has towards the analysis is therefore one. Values assigned weights closer to one were therefore regarded as being more accurate.

27Data was pooled and grouped according to tissue type, in order to determine (i) the variation in conductivity for each tissue, (ii) which significant variables account for differences in conductivity, (iii) whether mean conductivity values for each tissue type are statistically different depending on employed methodology and participant demographics, and (iv) reveal any statistical relationship between conductivity and reported variables.

28Boxplot diagrams, presenting the range, median and mean of conductivity measurements for each tissue type were created to demonstrate variation in conductivity within different tissues. For each tissue with more than three results in at least two variables, a weighted multiple regression was carried out using SPSS (Corp ). The dependent variable (conductivity) was regressed against every independent variable (IV; measurement condition, method, frequency, temperature, age and pathology) collectively, to determine the proportion of variance accounted for by all factors, and individually to discover significant factors predicting variation in conductivity. Weights for each conductivity value were assigned according to the Quality Analysis described above (Sect. 2.5). A two-tailed t test (when comparing two independent variables) or a one-way Analysis of Variance (ANOVA; when comparing more than two independent variables) was conducted to reveal differences in conductivity for each tissue, according to categorical IV’s previously revealed to account for a significant proportion of variance. A Pearson correlation analysis was alternatively conducted for continuous IV’s accounting for significant variation to reveal any statistical relationships.

29Following removal of duplicates, 3121 studies were identified through the literature and reference list search, of which 382 abstracts were screened for relevance and 211 full text articles were obtained and assessed for eligibility. A total of 155 papers were excluded (see Appendix 1, Figure A. 1: PRISMA flow diagram).

30A total of 56 studies (407 participants) were included in the quantitative synthesis (Table 2). Seventeen different tissue types were identified, using five methodologies and three measurement conditions. Conductivity was measured in vivo in 42, in vitro in seven and ex vivo in eight research papers. Measurements were obtained using DAC in 14 studies, using EIT in 10, E/MEG in 7, MREIT in 15 and DTI in 9 papers. Conductivity was acquired at frequencies varying between 0 and 1005 Hz, and tissue temperatures between 18.5 and 37.5 °C. Of the 23 articles that specified, total participant age ranged from 4 months to 87 years old, whilst the remainder classified subjects into adults or children. Forty papers reported on healthy participants, participants from ten studies were diagnosed with epilepsy, patients with tumours were included in three studies, stroke patients were employed in two papers, whilst separate papers included patients with various neurological disorders and Parkinson’s Disease. Descriptive statistics for each tissue type are provided (Table 3), in addition to a boxplot displaying variation in conductivity values for different tissue types (Fig. 2). The average mean was calculated for each tissue type, where all conductivity values contributed equally to the mean. A weighted average mean was additionally calculated to take into consideration the quality of each study and provide a recommended value that was obtained under suitable and realistic conditions. The weighted average mean and standard deviation (in S/m) for the main tissue types were: scalp = 0.41 ± 0.18, whole skull = 0.02 ± 0.02, spongiform skull layer = 0.048 ± 0.07, whole compact skull layer = 0.005 ± 0.002, outer compact = 0.005 ± 0.003, inner compact = 0.007 ± 0.004, CSF = 1.71 ± 0.3, GM = 0.47 ± 0.24, WM = 0.22 ± 0.17, BSCR = 50.4 ± 39. A boxplot evidencing the average weights assigned to each study according to the employed methodology is further demonstrated (Fig. 3). Average study weights were revealed to be significantly different depending on methodology [F (4, 56) = 3.121, p =.022)].

31Following visual inspection, it can be seen conductivity values vary considerably within and between tissue types. Insufficient data was available to calculate regression statistics for muscle, fat, blood, the epileptogenic zone, the dura layer and the cerebellum.

32A weighted multiple regression revealed scalp conductivity variation was insignificantly predicted by the IV’s collectively (p >.05). Although insignificantly different, a comparison between employed method (as shown in Fig. 4) was made to graphically display any elevated values and further demonstrate variation despite statistical insignificance. Figure 4 further reveals less deviation within values for EIT than for E/MEG. Huang and colleagues yielded conductivity measurements significantly above the inter-quartile range. Additionally, Baysal and Haueisen revealed highly elevated conductivity values beyond the axis range displayed in Fig. 4, with standard deviation > 5000% (see Sect. 4.1 for further explanation of outliers).

33A weighted multiple regression revealed deviation in whole-skull conductivity could be significantly predicted by the methodology, condition, temperature, frequency, pathology and age collectively [R2(6, 36) =.827, p <.001]. A one-way ANOVA revealed conductivity of the whole skull varied significantly according to employed methodology [Fig. 5; F(2, 96) = 4.088, p =.020]. Differences in conductivity values for the whole-skull were statistically different according to method, where values obtained using EIT were significantly lower than those obtained with DAC and E/MEG.

34A weighted multiple regression revealed variation in conductivity values of the spongiform bone layer of the skull was significantly predicted by condition, temperature, frequency, pathology and age [R2(5, 6) =.832, p =.026]. Spongiform conductivity measurements were significantly different according to condition [Fig. 6; F(2, 15) = 11.357, p =.001] and temperature [t(16) = 2.449, p =.001).

35None of the IV’s significantly predicted variation in conductivity values of the whole compact layer, the inner compact bone layer or the outer compact bone layer according to the weighted multiple regression analysis. Despite insignificant results, a graphical representation of conductivity for the different compact bone layers revealed clear diversions within and between each of the layers (Fig. 7).

36Significant differences [t(36) = 2.695, p =.006] in measurements obtained at body (~ 1.79 S/m) and room (~ 1.45 S/m) temperature as revealed from Baumann and colleagues, hence values at room temperature were revealed prior to regression and comparison of means analysis. Variability in CSF conductivity was discovered to be insignificantly explained by the weighted multiple regression model. Despite insignificant results, the boxplot in Fig. 8 allowed for a graphical representation of the large spread of values obtained using MREIT.

37Differences in whole-brain conductivity values were not significantly predicted by the independent variables according to the weighted multiple regression analysis. Figure 9 reveals the large variation in data obtained for conductivity values of the whole-brain for each methodology, suggesting no one method generates a stable result for conductivity of the brain as a whole compartment.

38Variation in GM conductivity was not significantly explained by the weighted multiple regression model. However, a one-way ANOVA determined significant differences in GM conductivity according to method [Fig. 10; F(3, 62) = 17.896, p <.001], where results obtained with MREIT were significantly higher than DTI which were in turn significantly higher than EIT. Pathology further yielded significantly different conductivity results for GM [Fig. 11; F(4, 61) = 2.968, p =.026].

39A weighted multiple regression analysis revealed variation in isotropic WM conductivity was significantly explained by methodology, condition, frequency, pathology and age collectively [R2(5, 36) =.696, p <.001], where values varied significantly according to method [Fig. 12; F(4,99) = 34.659, p <.001], condition [F(2, 101] = 30.089, p <.001], pathology [F(2, 101) = 34.437, p <.001), temperature [t(102) = 3.877, p <.001] and frequency [(r(104) = −.362, p =.001]. Furthermore, pathology and age collectively explained a significant proportion of variation in WM conductivity measured perpendicularly [R2(2, 14) =.459, p =.014] and in parallel [R2(2, 14) =.677, p <.001]. Where perpendicular WM values varied according to condition [F(2, 38) = 36.828, p <.001], temperature [t(39) = 1.105, p =.031] and participant age [r(41) =.638, p =.006], whilst parallel WM measurements differed with condition [F(2, 38) = 9.78, p <.001] and age [r(41) =.520, p =.032].

40Variation in BSCR calculations was significantly predicted by methodology, frequency, pathology and age collectively, in the weighted regression analysis [R2(4, 26) =.302, p =.046]. Figure 13 displays the variation of BSCR according to method, although a comparison of means revealed no significant differences between employed technique. Additionally, BSCR values correlated positively with participant age [Fig. 14; r(51) =.376, p =.014].

41The current study systematically investigated variation in conductivity of 17 different head tissues as reported in 56 research papers, identified through a literature search of three relevant databases. The mean, standard deviation, minimum and maximum were calculated for each tissue type (Table 3). In addition, we computed the weighted average mean, which provided an optimum (and therefore suggested) value when conductivity is unable to be obtained on an individual basis. The weighted average mean and standard deviation (in S/m) for each tissue type were: scalp = 0.41 ± 0.18, whole skull = 0.02 ± 0.02, spongiform skull layer = 0.048 ± 0.07, whole compact skull layer = 0.005 ± 0.002, outer compact = 0.005 ± 0.003, inner compact = 0.007 ± 0.004, CSF = 1.71 ± 0.3, GM = 0.47 ± 0.24, WM = 0.22 ± 0.17, WM perpendicular = 0.12 ± 0.05,WM parallel = 0.12 ± 0.09, Blood = 0.57 ± 0.11 and BSCR = 50.4 ± 39. The differences between values for each tissue were statistically tested against methodological and participant demographical variables to reveal significant predictors. Inadequate data was available for muscle, fat, blood, the epileptogenic zone, the dura layer, the cerebellum and brain lesions to carry out a multiple regression. Collectively, the independent variables (related to both methodology and demographics) insignificantly explained variation in the scalp, the compact layers of the skull, cerebrospinal fluid, the whole-brain and grey matter. In contrast, variation in whole-skull conductivity could significantly be explained by all the IV’s collectively, where values were revealed to specifically differ significantly depending on method. Variation in the conductivity of the spongiform bone layer of the skull was significantly predicted by condition, frequency, pathology and age, where values were significantly different according to condition and temperature. Despite insignificant results for regression analysis, GM significantly differed depending on method and pathology. Variation in isotropic WM electrical conductivity was significantly predicted by methodology, condition, frequency, pathology and age collectively in the regression model, where values significantly diverged according to method, condition, pathology, temperature and frequency. A significant proportion of variation in WM conductivity measured perpendicularly and in parallel was further explained by pathology and age collectively. Specifically, perpendicular WM values differed with condition, temperature and age, whilst parallel WM measurements fluctuated with condition and age. Lastly, the meta-regression revealed the BSCR could be significantly attributed to variation in methodology, frequency, pathology and age collectively, revealing a positive correlation between the ratio and participant’s age.

42Explanations for the presence of outliers and reasons for any data exclusion in the current meta-analysis are further discussed. Firstly, data acquired at frequencies higher than 1000 Hz were removed, as these conditions were deemed unnatural, considering the bandwidth of most neuronal signals is 1 Hz–1 kHz, with resonant frequencies of < 100 Hz for the brain (Groppe et al. ) and < 1000 Hz for the skull (Håkansson et al. ). Conductivity results obtained from Baysal and Haueisen employing a conventional least-squares estimator (LSEE) on E/MEG data were further revealed from the weighting algorithm, as stated by the authors as being “unrealistic [negative resistivities] and unstable” Baysal and Haueisen. These unstable results were evident from the large standard deviation percentage (> 5000% for the scalp, > 200% for the skull and > 240% for the brain). The authors suggested such inaccuracies occurred from the use of LSEE linearization in a highly non-linear problem, and hence were omitted from their own analysis. Furthermore, skull conductivity values reported by (Hoekema et al. ) were elevated approximately 10-fold, suggested to be “as expected [due to measurements] in non-physiological circumstances” (namely, saline-coated cadaver), however were not excluded from the current analysis as methodology was in line with previous cadaver studies and therefore should yield similar results. Huang and colleagues yielded significant outliers for the scalp, skull, whole-brain, GM and WM, where median optimal conductivity obtained by fitting model outputs (from literature) to recordings. These deviations may be explained by the use of an optimisation EIT approach where “best-fit” values were free to compensate for all inaccurate/simplified sources, tissue segmentation errors, changes in electrode location, etc., and therefore cannot reflect “true” conductivity values. Outliers were additionally revealed for the spongiform (but not compact) skull layer by Fernández-Corazza and colleagues, which employed boundary EIT (bEIT) for reconstructing the electrical conductivity for a subset of the regional tissue parameters. The authors acknowledged low sensitivity of bEIT to spongiform variations, due to the relatively small proportion of spongiform to head volume and concluded such approximations may be difficult for unbiased bEIT estimators but remain valid for compact bone estimates. Substantial outliers were further exposed for CSF, GM and WM (as well as subsequent EMA whole-brain calculations) in Ropella and Noll’s paper, which employed MREIT and revealed standard deviations of 80.2–518.8%. The validity and reliability of MREIT as a method is later discussed. The Quality Analysis in the current paper attributing a confidence weighting to each value, is deemed acceptable to consider the large standard deviations leading to outliers. All outliers were therefore included in order to fully account for and explore reasons for variation in values.

43Additional deviations, although not classified as outliers, were revealed from (Gutierrez et al. ) for the scalp, where maximum likelihood estimation (MLE) was used to estimate the electrical conductivity from E/MEG measurements. Such results may be due, in part, to the necessity of accurate source location and head geometry knowledge to avoid estimation bias. The authors suggest the use of a Bayesian approach, which permits incorporating a priori information on conductivity distribution to reduce bias. Realistic measurements (excluding outliers and deviations, as discussed) of scalp conductivity, for example, ranged between 0.25 and 0.435 S/m, which could not be attributed to any of the IV’s. Such variation can be relevant in source localisation based on E/MEG. In particular, dipole sources close to measurement electrodes are sensitive to scalp conductivity (Gençer and Acar; Goncalves et al.,, ). These results coupled with those of the current meta-analysis indicate that assuming scalp conductivity from the literature is not only inaccurate but can lead to E/MEG source mislocalisation. These errors do not appear to be explainable by anything other than individual variability and hence personalised models of scalp conductivity should be considered to improve E/MEG activity localisation.

44According to the meta-regression, variation in whole-skull conductivity can be accounted for by differences in all of the independent variables (methodology, condition, temperature, frequency, pathology and age), with specific differences between methodology and condition. Such significant results, however, may be due to overfitting of the data and meta-regression parameters employed. Future research could utilise machine learning techniques in order to refine the regression analysis and determine the most influential variables. This analysis was beyond the scope of the current paper and ideally would require more data which is not presently available.

45Values obtained from excised tissue in non-physiological circumstances after undergoing various processing, may change the electrolyte concentration and therefore skull conductivity (Akhtari et al. ). Considering the contrast between a saline-soaked processed cadaver and live skulls that remain in natural conditions between the scalp and meninges, differences in conductivity values post-mortem should be expected. Early research determined conductivity of rat femurs to decrease by a factor of 2.5–3 from live-to-50 h post-mortem (Kosterich et al., ). This was further corroborated in the human skull, indicating a scaling factor of 2.5–4 from live-to-post-mortem (Wendel et al. ). These results are validated by Rush and Driscoll’s mathematical model stating the skull conductivities dependency on the fluid (i.e. saline vs naturally positioned between meninges, surrounded by blood/CSF, etc.) permeating it (Rush and Driscoll ), suggesting, a live skull to have higher conductivity than a saline-soaked (with conductivity 1 S/m) cadaver skull. It is consequently unsurprising in vitro values of skull conductivity differ from in vivo values—predicting increased conductivity in vivo (Akhtari et al.; Law ). The results from the previous literature coupled with the current meta-analysis, therefore indicate skull conductivity should be measured in in vivo (i.e. at body temperature, within the live head, etc.) in order to avoid bias and increase reliability.

46Within in vivo reports, despite all under similar conditions, skull conductivity values obtained using E/MEG appeared to be elevated compared to those employing EIT. These results may be explained by the use of statistically constrained estimating algorithms for E/MEG measurements, for which conductivity is optimally estimated from E/MEG arrays acquired during electrical nerve stimulation. Furthermore, whole-skull conductivity was found to vary as a function of frequency, although the nature of the relationship was unclear. Previous literature has examined skull conductivity in wider frequencies, revealing a positive relationship, especially at frequencies higher than 10 kHz (Gabriel et al.; Tang et al. ), and suggest skull conductivity may exponentially increase at high frequencies. Within the relevant range for brain activity, skull conductivity increased by ~ 6.7% from 11 to 127 Hz (Dabek et al. ) and ~ 13% from 10 to 90 Hz (Akhtari et al. ), of which the authors developed a non-linear model for frequency dependence of different skull layers (Akhtari et al. ). Variation as a function of frequency may be expected due to interactions between mobile electrolytes (i.e. sodium and chloride) and relatively immobile molecules (i.e. proteins and blood components) which affect the relaxation rate of conductivity dependent on the currents frequency (Akhtari et al.; Latif et al.. Importantly, this frequency dependence has been implicated in causing the volume conductor to act as a low pass filter, which potentially contributes to E/MEG forward solutions errors and may therefore reduce accuracy in E/MEG source localisation.

47Furthermore, results exploring differences according to age in the BSCR (see Fig. 14) have implications for skull conductivity variation. Research has indicated skull, rather than brain, conductivity plays a larger role in BSCR values (Goncalves et al.,, ), consequently suggesting skull conductivity varies with age. These results are discussed further in Sect. 4.3.1 (layered skull conductivity) and 4.6 (BSCR).

48The majority of previous studies simplify the skull as a homogeneous layer, not accounting for differences in conductivity between the compact (upper, lower) and spongiform layers of the skull. Distinct conductivities for the three layers of the skull has been previously indicated (Akhtari et al.; Akhtari et al.; Fernández-Corazza et al.; Tang et al. ), as supported by the current meta-analysis (see Fig. 2). This is unsurprising considering the higher prevalence of fluid filled pores and cavities in spongiform (and hence higher conductivity) compared to compact bone. Importantly, neglecting inhomogeneous estimations for a tri-layer skull has yielded significant errors in source localisation irrespective of model parameters (Dannhauer et al.; Haueisen et al.; Haueisen et al.; Ollikainen et al.; Pohlmeier et al. ). These authors have thus concluded realistic modelling of the skull layers to be necessary for accurate E/MEG source localisation. The current meta-analysis, however, revealed that variations exist between individuals even whilst considering a tri-layer skull. Variation in the electrical conductivity of the spongiform skull layer was revealed to be significant and attributed to deviations in condition, temperature, frequency, pathology and age. Suggesting true values for conductivity of the spongiform layer will not only depend on methodological parameters but also individual demographics. Likewise, although the compact layers of the skull were insignificantly predicted by any of the parameters, large variation was still evident. This further elucidates the hypothesis that conductivity values fluctuate between individuals and support the suggestion for personalised models of skull conductivity.

49Interestingly, a relationship with age was to be expected, regardless of homogeneity, considering the presence of the fontanels and open sutures (un-ossified bone filled with cartilage, chondroid and vascular tissue) which may remain unfused for several years (Hansman ). Firstly, bone formation (remodelling) from direct laying down or cartilage, known as ossification, remains approximately 50% complete at birth, not reaching 100% until age 20. This indicates a higher proportion of cartilage and “soft” (trabecular) bone, consisting of higher water and less lipid content (Silau et al. ), in the neonatal skull, which linearly decreases until fully ossified (Christie ). Furthermore, neonatal brain growth occurs at a rate higher than bone ossification, resulting in four fontanelles between the skull plates. The fontanelles, although relatively small at birth, become larger within the first few months (up to 3 cm) until closing at approximately 18 months old (Hansman ). As well as inter-subject variability, the size and width of fontanelles significantly vary in children with central nervous system pathology. Moreover, unclosed sutures in an infant skull, although present in an adult skull, are wider near the fontanelles, and may not close for several years in healthy children (Erasmie and Ringertz ). In addition to the fontanelles, the sutures close at various times of development. The frontal suture, for example, normally fuses between 3 and 9 months old (Vu et al. ), whereas the sphenofrontal suture (lying between the sphenoid bone and posterior horizontal orbital plates) and sagittal suture (connecting the two parietal bones) typically close by age 15 and 22 years, respectively. Moreover, the squamosal sutures (connecting the temporal squama and parietal bone), do not fully close until 60 years of age (Vijay Kumar et al. ). Lastly, the skull thickness increases with age, from 2–3 mm at birth to 3–6 mm during early adulthood (Despotovic et al.; Hansman ). This increase however is non-linear, slowing down towards 3 years of age, and is non-uniformly distributed throughout the skull, with higher thickness in occipital than frontal and parietal regions (Li et al. ).

50Taken together, the structural differences between the neonatal and adult skull elucidate differences in skull conductivity to be expected. As such, previous studies have revealed higher skull conductivity for infants compared to adults, (Gibson et al.; Pant et al. ) and an inverse correlation between skull conductivity and thickness with increasing age (Gibson et al. ). The inner and outer compact layers are thought to become thicker, whilst the spongiform layer becomes thinner with age, hence decreasing whole-skull conductivity. Additionally, paediatric skull tissue ordinarily contains greater quantities of ions and water, compared to calcified cranial bones of adults, hence higher conductivity may be expected (Schönborn et al. ). Further support from animal studies have revealed skull conductivity to decrease with age, for example, in the rat (Peyman et al. ), pig (Peyman et al. ) and cow (Schmid and Überbacher ). Although this expectation was not confirmed in the current meta-analysis, for accurate source localisation, skull conductivity variations with age should be taken into consideration. For example, Lew and colleagues assessed the effect of sutures and fontanels on E/MEG source analysis, where omission produced a maximum position error of 3.6 mm and 0.6 mm for tangentially- and radially-oriented sources, respectively (Lew et al. ). Elevated EEG localisation errors with respect to MEG were further replicated in simulation studies (Flemming et al. ), suggesting an advantage in employing MEG for developmental studies. The literature however suggests both modalities require individualised, or in the least an infant-specific volume conductor model to accommodate for relevant developmental changes (Bystron et al.; Rakic; Song et al. ).

51Following from this, development of the human skull does not cease after infancy, but continues to undergo remodelling, microstructural, density and histological changes until death, further impacting conductivity. Firstly, total cranial thickness has been observed to increase with age (Todd ) notably related to increase in diploë thickness (Hatipoglu et al.; Sabancıoğulları et al. which in one study was accompanied with inner and outer compact thinning (Skrzat et al. ). An increase in diploë (and hence spongiform bone) thickness would suggest conductivity of the skull to increase with age, as revealed by (Tang et al. ). Recently, Antonakakis and colleagues revealed a trend between participant age and skull conductivity but noted the small sample size (n = 15) and large inter-subject variability rendered robust conclusions difficult and inadequate. Further results have also been inconsistent, finding no such relationship between skull thickness and age (Ishida and Dodo,; Lynnerup; Lynnerup et al.; Pensler and McCarthy; Sullivan and Smith, ). The presence of suture lines, not limited to infants, was furthermore shown to increase conductivity of the skull sample, by providing a path of high conductance (Law; Tang et al. ). Additionally, the percentage of spongiform bone within the skull was positively correlated with skull conductivity (Tang et al. ), whilst, skull thickness, which is non-uniform within and between individuals (Lynnerup; Lynnerup et al. ), was inversely correlated with scalp potentials (Chauveau et al. ). One paper, for example, revealed that a 20% and 40% decrease in skull thickness resulted in a 5–10% and 20–25% decrease in conductivity, respectively (Lai et al. ). Insufficient results were available to analyse the influence of sutures or skull thickness in the current review; however, the discussed structural deviations further illuminate the importance of employing individualised models of head conductivity.

52The influence of skull conductivity and segmentation inaccuracies has been explored extensively, revealing overwhelming source localisation errors for EEG (Lanfer et al.; Montes-Restrepo et al.; Wolters et al. ) and MEG (Cho et al.; Lau et al. ) of up to 2 cm. E/MEG source analysis can importantly be utilised during presurgical epilepsy diagnoses, together with MRI data. Aydin and colleagues recently developed a multimodal technique, of which they emphasised the importance of individualised high-resolution finite element head models with WM anisotropy modelled from DTI and individually calibrated skull conductivity, alongside combined E/MEG and MRI information. Importantly, they note creating such realistic head models may not always be feasible, and therefore recommend, at minimum, skull conductivity to be individually adjusted to improve combined E/MEG source analysis. Variations in skull conductivity have been found to impact transcranial electric stimulation focality and dose (Santos et al.; Schmidt et al.; Wenger et al. ), with one study revealing an error of 8% in dose (Fernández-Corazza et al. ). Such inaccuracies are clinically relevant, particularly regarding source estimation for refractory epilepsy (Brodbeck et al. ) and determining electrical current dose required for treatment of epilepsy (Berényi et al.; Liebetanz et al. ), depression (Kalu et al. ) and other psychiatric disorders (Brunoni et al. ). Of note, Dannhauer and colleagues investigated variations in layered skull structures for EEG forward modelling and revealed an inhomogenous but not isotropic modelling to be of most importance. For optimum skull modelling, they recommended assigning each skull voxel to a tissue type (compact or spongiform bone) with individually estimated or measured conductivity values. To optimise source localisation accuracy, we therefore recommend employing personalised models of skull conductivity to sufficiently consider individual variability.

53The results of the current meta-analysis are in line with previous report from Baumann and colleagues (1997), displaying significant variation in CSF conductivity dependent on temperature. They revealed 23% higher conductivity at body (37 °C), approximately 1.79 S/m, than room (25 °C) temperature, which corresponded to the temperature coefficient of 2% per 0.1 ml of potassium chloride (comparable to CSF conductivity and ion concentration (Fishman,; McGale et al.; Wu et al. ). The result from Baumann et al. study is frequently considered as a reference value for CSF conductivity. However, the current meta-analysis has revealed large variation in measurements, potentially suggesting instability in CSF conductivity between individuals. The majority of such variation stems from values obtained using MREIT. One such study, (Ropella and Noll ) reported values with standard deviations up to 518% of the mean, which indicates instability in the methodology. The combination of large standard deviations within and between studies potentially call into question the validity of MREIT for measuring conductivity of the human head—this is further discussed in the grey matter subsection (4.5.1). Further deviating from Baumann’s approximation (1.79 S/m), (Cohen and Cuffin ) reported a considerably lower conductivity for CSF (1.39 S/m). These results may be explained by their use of optimum estimation, rather than direct measurements; where conductivity was adjusted so the maximum potential in a theoretical EEG map matched the experimental equivalent. Considering the variation due to methodological error, CSF appears to be relatively stable between individuals, with an average conductivity converging around Baumann’s results. Despite this, Fig. 8 suggests CSF conductivity ranges between ~ 1.5 and 2 S/m, elucidating the need for individualised measurements. Deviation in CSF conductivity in that range however, may not significantly affect E/MEG forward and inverse modelling solutions. Future work could therefore employ a sensitivity analysis to explore the influence CSF conductivity has on electromagnetic source localisation and determine the necessity of individualised models.

54The meta-regression failed to explain variation in conductivity of the brain as a homogeneous layer, however values were revealed to significantly vary according to the employed method. Despite these significant results, variation between acquisition techniques are minimal, where large variations within each method remain evident. These variations further support the suggestion that individual values of conductivity should be obtained. However, assuming homogeneous conductivity over the whole brain is generally considered a vast oversimplification and highly inaccurate. Such an assumption fails to consider differences between GM and WM conductivity, as well as structural variation of GM/WM proportion in the brain. Early research determined GM to contain higher proportions of water than WM (Stewart-Wallace ), demonstrating expected higher electrical conductivity for GM compared to WM. Additionally, extensive literature has shown GM and WM volume to vary with development (Giorgio et al.; Groeschel et al.; Miller et al. ) and pathology; i.e. multiple sclerosis (Sastre-Garriga et al. ), Alzheimer’s Disease (Salat et al. ), schizophrenia (Douaud et al. ), attention deficit-hyperactivity disorder (McAlonan et al. ), among others. These observations further support the use of individualised models of head volume and conductivity profiles for the most accurate representation of the human head.

55The questionable validity of MREIT for estimating conductivity was further reinforced considering the number of outliers (Ropella and Noll ), coupled with elevated values (Voigt et al. ) for GM conductivity acquired with MREIT. Measurements utilising MREIT were over twice those from EIT and approximately one and a half times those of DTI values. Significant variation in GM conductivity may be further explained by increased DTI values relative to EIT. Firstly, the Tuch et al. model derived the conductivity tensor from the water diffusion tensor through differential effective medium approximation (EMA), which uses an electromagnetic depolarisation factor to consider the impact of cell geometry to overall conductivity. This depolarisation factor was originally developed for WM structure, consisting of myelinated pyramidal cells, and therefore may not be completely translational to GM. Tuch and colleagues’ later paper, however, utilised the EMA method to show there exists a strong linear relationship between the conductivity and diffusion tensors, regardless of tissue type. They generated a conductivity tensor image, where conductivity could be assigned to three groups: GM, WM parallel or WM perpendicular to the fibre tract. Their results indicate the EMA method is appropriate for GM conductivity estimation, despite having lower anisotropy than WM. The established linear relationship mapping the diffusion to electrical conductivity tensor employed (Tuch et al.; Tuch et al., ) has been further validated in a silk yarn phantom (Oh et al. ). However, (Rullmann et al. ) detected the use of Tuch’s scaling factor would have generated values 3.5 times greater than isotropic values (taken from (Ramon et al. )). For this reason, they chose to employ a volume constraint approach with scaling factor 0.21 (compared to 0.844) which minimised differences between isotropic and anisotropic EEG forward modelling in their study. Similarly, (Sekino et al. ) estimated the effective GM conductivity from only the fast diffusion component (attributed to extracellular fluid), rather than both the fast and slow (attributed to intracellular fluid) components. The produced conductivity maps were therefore not simply linearly scaled diffusion maps, and hence may explain their considerable low GM conductivity measurement (0.06 S/m). Importantly, the deviations in GM conductivity dependent on the chosen diffusion tensor method are acknowledged, emphasising the non-trivial nature of relating the diffusion and electrical conductivity tensors. Future studies should examine this relationship, in order to accurately determine a realistic scaling factor to improve conductivity tensor estimations.

56Additionally, Rullmann and colleagues results were limited to one paediatric participant with epilepsy, of which his age may have influenced the increased brain conductivity. Higher conductivities in paediatric brains are perhaps expected due to the general abundance of water in GM (Dobbing and Sands ). The current meta-analysis failed to find a significant correlation between GM conductivity and age, however, considering normal GM development and the frequently observed decrease in mean diffusivity of GM with age (Pal et al. ), further research may expose such a relationship.

57In line with this observation, participant pathology significantly affected GM conductivity, but was not a significant predictor in the regression model. Large variation can be seen within and between different participant pathologies (Fig. 11), but no clear conclusion could be made. This is perhaps due to the limited number of values available for each classified pathology, reducing the statistical power. In tumours, for example, firstly, all values may not have been made from healthy tissues (due to the diffusing nature of malignant tumours), but also an increased conductivity in “healthy” GM tissue may also be a consequence of tumour cysts increasing the water/CSF concentration in nearby tissues. Previous literature has indicated abnormalities in GM volume, structure, myelination and topography in Multiple Sclerosis, Parkinson’s Disease, Alzheimer’s Disease and other forms of dementia (Compta et al.; Frisoni et al.; Geurts and Barkhof ), as well as abnormalities in psychiatric and developmental disorders (Greimel et al.; Job et al.; Wise et al. ). It is therefore unsurprising that GM conductivity varied with participant pathology. Due to the unknown nature of this variation with disease and age, the use of individualised models of head conductivity that are inhomogeneous and anisotropic are especially essential for electromagnetic source imaging (Birot et al. ). Increasing the feasibility and accessibility of this could be explored with further research involving DTI parameters.

58The current meta-analysis failed to explain variation in anisotropic WM conductivity, however this may be due to the limited sample size available for analysis. The crucial consideration of anisotropic conductivities has been more recently determined, where neglecting WM anisotropy produced EEG-localisation errors of ~ 1.6–5.1 mm and 4.72–8.8 mm for radially- and tangentially-oriented sources, respectively (Anwander et al.; Güllmar et al. ), with one study reporting a maximum error of 26.3 mm (Hallez et al. ). Additionally, disregarding anisotropy had a large influence on the induced electric fields from TMS (De Lucia et al. ), whilst WM anisotropy influenced the electrical potential distribution following application of deep brain stimulation (Butson et al.; McIntyre et al. ). Uncertainty in WM conductivity also had a significantly large effect on tDCS stimulation amplitudes and current density estimations, which were especially pronounced in the auditory cortex, implying orientation to be a determining factor in tDCS applications (Schmidt et al. ).

59Isotropic WM conductivities however were found to vary dependent on method, measurement condition, pathology and age, additionally diverging with temperature and frequency. As previously observed, MREIT produced elevated WM conductivity values with larger variation between values compared to other methods, supporting the uncertainty and apparently low reliability of MREIT for estimating conductivity. Furthermore, DTI values produced similar, largely varying results. As previously discussed by Rullmann and colleagues (, elevated conductivity values from DTI may be a result of an overestimated scaling factor from the diffusion tensor to the conductivity tensor, proposed by the authors. In line with this, Akhtari and colleagues failed to verify this relationship and instead revealed an inverse linear relationship with a scaling factor of − 0.367, and considerable variability between values. For this reason, Güllmar et al. compensated for isotropic variation by normalising the conductivity tensors (by calculating the anisotropy ratio between eigenvalues) in one model and using fixed artificial anisotropy ratios to preserve diffusion tensor orientation, in another model (volume constraint model). By comparing both models with Tuch’s, they revealed that employing the latter significantly affected MEG and EEG forward computations differently by changing the mean scalar representation of isotropic tensors. This study, alongside previous investigations, emphasised the importance of modelling anisotropy, but has also insinuated further, more detailed research should explore the linear relationship between the diffusion and electrical conductivity tensors.

60Additionally, differences were revealed between perpendicularly- and parallelly-oriented WM conductivities that are due to the results being obtained from different papers. Of note, the minimum WM_par conductivity value (0.0543 S/m) is less than the minimum WM-perp value (0.0620 S/m), with only small differences reported between the means. These results are not indicative of WM conductivity themselves, but instead highlight the variation in values between studies. Moreover, this may reflect the differences between the methods employed for approximating the conductivity tensor from the diffusion tensor, due to the fact that WM is more anisotropic than these results indicate. A recent paper (Wu et al. ) reviewed the current anisotropic conductivity models of WM based on DTI. The linear relation model (i.e. Tuch’s model) was discussed as not directly considering the impact of geometrical brain tissue structure, whilst the Wang-constraint (Wang et al. ) and volume-constraint models, both of which assume diffusion and conductivity tensors share the same eigenvalues (similar to Tuch’s model), ignore brain tissue heterogeneity but can relate anisotropy and physiological structure. The equilibrium model (Sekino et al. ), which decomposes extracellular and intracellular diffusion, can be less accurate as extracellular diffusion may result difficult to quantify (Jones et al. ). Wu et al. determined that obtaining the conversion coefficient between the anisotropic conductivity tensor and the diffusion tensor eigenvalues to be of most importance. Further, they concluded the optimum model to be the electrochemical model, which calculates the conversion coefficient according to the concentration of charged particles in interstitial fluid and has the added benefit of being able to calculate a conversion coefficient for GM and avoids having to consider the effect WM structure has on water molecules and electrical charges. They noted however, that the models are not contradictory, but instead complement each other to inform the relationship between conductivity and diffusion tensors. This emphasises the need for more research to elucidate the prime conversion coefficient before robust conclusions can be made. Exploration and evaluation of different diffusion-to-conductivity methods are beyond the scope of the current meta-analysis, however, considering the variable results in combination with Wu et al. analysis, caution should be taken when applying conversion algorithms between conductivity and diffusion tensors.

61Furthermore, as formerly discussed, measurements obtained in vitro or ex vivo, as well as at room temperature, are likely to differ from in vivo results due to the non-physiological conditions. It is therefore recommended investigations should be completed at body temperature, in vivo and at frequencies in line with resonant frequencies of the brain (< 100 Hz). Subsequently, a significant correlation between WM conductivity and applied frequency may have only be revealed due to values obtained at 500 Hz. A large pool of conductivity values were obtained at 500 Hz, whilst the remainder of values were measured at frequencies < 150 Hz, hence, the higher conductivity values at a considerably higher frequency than all other results may have skewed the data to reveal a positive relationship, which may not otherwise be there. Additional conductivity values measured with frequencies between 150 and 500 Hz are needed to further elucidate the presence or not of a significant relationship.

62WM conductivity values were additionally revealed to vary with pathological condition, however insufficient results were available to extract clear conclusions. Such variation with pathology is nevertheless, expected, for example intracranial pathology from epilepsy patients potentially alters cytoarchitecture of affected and non-affected areas, such as cortical neuronal disorganisation and surplus WM cells (Mathern et al. ). Akhtari and colleagues suggested pathological changes in myelin and diseased-active cells may disrupt cell geometry organisation, which, when coupled with histological demyelination and cell population alterations, may increase proton diffusion as it is no longer constrained by myelin walls or tight organisation. Interestingly, a significant relationship between fluctuations in DTI eigenvalues and histological alterations in temporal lobe epilepsy has been found (Kimiwada et al. ). Furthermore, extensive research has revealed marked differences in WM structure in numerous diseases and pathologies, such as Multiple Sclerosis, Alzheimer’s Disease, Schizophrenia and Parkinson’s Disease (Bozzali et al.; Burton et al.; Kubicki et al.; Kutzelnigg et al. ). Conductivity and anisotropy surrounding diseased tissues is subsequently likely to affect the generated electrical and magnetic fields from a source, compared to such distributions in healthy individuals (Park et al.; Youn et al. ).

63Although no significant correlation was revealed, WM conductivity as a function of age was revealed to contribute to the meta-regression model. This observation is unsurprising considering the well-researched nature of WM development with age, suggesting a decline in WM integrity, WM volume, myelination, diffusivity, etc. (Gunning‐Dixon et al.; Guttmann et al.; Salat et al.; Schmithorst et al. ). The degeneration of WM with age allows for higher CSF and liquid concentrations within the WM, therefore increasing conductivity of the tissue. Considering the large variation of WM with methodology, pathology and participant demographics, assuming conductivity of WM from the literature is clearly insufficient for accurate head conductivity profiles.

64Combining the current results for WM and GM conductivity values, a clear discrepancy exists between both tissues, indicating the heterogeneity of the brain. Assuming the brain to have homogeneous and isotropic conductivity, as in research considering the brain as a whole, is therefore insufficient for accurate conductivity profiles. Assuming the brain as a homogeneous conductor consequently results in considerable EEG and MEG source localisation errors (Acar et al.; Awada et al.; Cohen and Cuffin ).

65The ratio between brain and skull conductivity was significantly different for epilepsy compared to healthy participants, however, all BSCR values with epileptic pathology were obtained from paediatric samples. In accordance with this observation, BSCR was revealed to increase with age, suggesting paediatric samples, and hence epilepsy in the current review, to have lower conductivity ratios. In support of previous literature examining the influence of age on skull conductivity, such a relationship is expected, considering increased conductivity and decreased thickness of paediatric skulls. In contrast, paediatric brain tissue contains relatively higher water content and lower myelin deposition than adults (Knickmeyer et al.; Peterson et al. ), indicating higher conductivity. Together, higher conductivity of both the skull and the brain in paediatric samples would suggest the brain-to-skull ratio to remain relatively stable throughout age. However, this would require an equal rate of decline for both tissues, which is unlikely the case. The role of skull conductivity for BSCR calculations was elucidated by (Goncalves et al.,, ), who concluded their BSCR discrepancies to be a consequence of skull, as opposed to brain, conductivity variation. Their results indicated brain conductivity to be of less importance when calculating the brain-to-skull conductivity ratio, rendering decline in brain conductivity, whether equal or not to skull conductivity decline, irrelevant.

66In contrast, assuming isotropic and homogeneous properties of the skull may contribute to variations in brain-to-skull estimations. For example, current injection at different locations may result in differing impedance distribution within the skull, hence altering BSCR estimations when isotropic compared to anisotropic skull models are used (van den Broek et al. ). However, it is noted that more recent papers acknowledge the importance of segmenting the skull layers, hence the use of skull anisotropy to optimise estimates of layered skull conductivity may not be required. Additionally, the heterogeneity in the skull will evidently introduce conductivity variation when homogeneous models are used, hence contributing to variation in BSCR values. These observations similarly apply for brain homogeneity and anisotropy, which would consequently affect BSCR estimations and contribute to variation. Considering BSCR estimations are clearly dependent on accurate conductivity of the skull and brain, which are subject to large variability, it is suggested personalised models of whole-head conductivity are essential to accurately determine the brain-to-skull conductivity ratio.

67The current meta-analysis systematically investigated variation in reported human head electrical conductivity values for 17 different tissue types to evidence deviation within and between tissues, determine any influential factors and evaluate the impact on E/MEG source reconstruction. Adhering to the hypothesis, conductivity was revealed to significantly vary throughout the literature, specifically for the scalp, different layers of the skull, the whole-brain, grey matter, white matter and the brain-to-skull conductivity ratio. To decrease variation and increase stability of conductivity estimates, values should be obtained at body temperature, at frequencies < 100 Hz and in natural, in vivo conditions. Conductivity was significantly discovered to vary dependent on participant pathology, suggesting separate values should be acquired for different pathologies. However, further research was suggested to enhance the understanding of pathological effects on the electrical conductivity field. Additionally, electrical conductivity significantly correlated with participant’s age for the skull, WM and BSCR. Previous literature was presented indicating large EEG and MEG source localisation errors occurring as a result of inaccurate conductivity values, particularly when neglecting anisotropy and heterogeneity of the head. The impact of incorrect conductivity on E/MEG forward and inverse solutions, coupled with the high variability of conductivity for each tissue type, suggests that assuming conductivity from the literature is insufficient. In conclusion, to optimise source reconstruction in EEG and MEG, and reduce localisation errors, personalised models of head electrical conductivity should be obtained for each individual.