Plasma p-tau231 and p-tau217 as state markers of amyloid-β pathology in preclinical Alzheimer’s disease

1Blood biomarkers that accurately indicate Alzheimer’s disease (AD) pathophysiology now offer a realistic, cost-effective and noninvasive assessment that will aid the diagnostic process in primary and secondary care. Plasma measures of phosphorylated tau at Thr181 (p-tau181), Thr217 (p-tau217) and Thr231 (p-tau231) have high diagnostic accuracy in differentiating AD from other neurodegenerative disorders in clinical studies–, which are validated by postmortem neuropathological studies,,. In some instances, the performance of plasma p-tau biomarkers is comparable or only marginally inferior to established cerebrospinal fluid (CSF) or PET examinations of Aβ and tau pathologies, but with the advantage of greater availability and tolerability for both clinicians and patients.

2There is often discordance between the clinical diagnosis of AD and neuropathological findings. Thus, a noninvasive indicator that can improve the confidence in such a decision during life is paramount. This biological indication is also critically important in the preclinical stage of the AD continuum (hereafter, preclinical AD), where cerebral Aβ pathology is accumulating but individuals are cognitively unimpaired (CU). However, it is not yet clear how blood biomarkers will inform on the preclinical evaluation of AD. As anti-Aβ therapeutic trials move toward the assessments in the preclinical phase, a cost-effective tool is needed to reduce the number of lumbar punctures and PET scans in the recruitment process. Moreover, a blood biomarker would reduce recruitment time and increase the level of participation from more diverse populations that better represent the global aging population. Indeed, blood measures of p-tau181, p-tau217, p-tau231, glial fibrillary acid protein (GFAP), neurofilament light (NfL) and Aβ42/40 have been shown to change in preclinical AD and can discriminate this state from CU individuals with non-AD pathological changes,,–. Yet, our previous results in CSF and, more recently, plasma suggest that the earliest change in the AD continuum may be better characterized by p-tau231. CSF p-tau231 showed the earliest change in association with Aβ pathology in the AD brain,. Subsequently, the first blood analysis of p-tau231 (ref. ) demonstrated earlier increases than plasma p-tau181 in a small set of participants.

3Amid these promising results, a direct comparison of the main plasma biomarkers in a large number of individuals with preclinical AD is still needed. This will also determine the threshold of Aβ burden at which these biomarkers change in blood. Therefore, the main aim of our study is to investigate the main p-tau blood biomarkers for AD (p-tau181, p-tau217, p-tau231) together with the other relevant AD-related blood biomarkers (GFAP, NfL, Aβ42/40) in preclinical AD and compare their capacity to indicate Aβ pathology in CU individuals. For these purposes, we leverage the unique characteristics of the ALFA+ cohort,, which is composed of 397 CU middle-aged individuals (61.1 ± 4.67 years), 135 (34.0%) of whom are Aβ positive as defined by CSF Aβ42/40, a state marker reflecting the balance between production and clearance of Aβ, and hence fall into preclinical AD (Supplementary Table 1). In addition, we used Aβ PET as a stage marker using two cut-offs. An early cut-off of Centiloids ≥12 (53 (15.6%) participants) is used to detect early Aβ aggregation in CU individuals, when Aβ pathology may be emerging,, and a later cut-off of Centiloids ≥30 (26 (7.7%) participants), reflecting more established Aβ plaque pathology–.

4We first found that all plasma biomarkers were significantly changed in CU individuals who were Aβ positive (A+, as defined by CSF Aβ42/40 <0.071) but still tau negative (T−, as defined by CSF Mid(M)-p-tau181 ≤24 pg ml−1) (Fig. 1a and Supplementary Fig. 1). Plasma p-tau231, p-tau217 and Aβ42/40 showed the highest degree of change in this group (P < 0.0001; Cohen’s d = 0.76 for plasma p-tau231 and d = 0.74 for plasma p-tau217 and Aβ42/40), and were followed by GFAP (P < 0.0001; Cohen’s d = 0.55), p-tau181 (P = 0.001; Cohen’s d = 0.45) and NfL (P = 0.031; Cohen’s d = 0.33). All plasma biomarkers were also changed in the group of individuals with a low burden of Aβ pathology, namely those individuals who had abnormal CSF Aβ42/40 levels (and hence changes in soluble Aβ have started) but an Aβ PET <30 Centiloids (hence, not yet established Aβ plaque pathology) (Fig. 1b and Extended Data Fig. 1). Plasma p-tau231 and Aβ42/40 showed the highest degree of change in this group (P < 0.0001; Cohen’s d = 0.73), followed by GFAP (P < 0.0001; Cohen’s d = 0.57), p-tau217 (P = 0.0004; Cohen’s d = 0.49), p-tau181 (P = 0.004; Cohen’s d = 0.40) and NfL (P = 0.044; Cohen’s d = 0.30). To confirm the early changes of plasma biomarkers in the AD continuum, we applied a robust local weighted regression method to model their trajectories across preclinical AD using Aβ PET (Fig. 1c) and CSF Aβ42/40 (Fig. 1d) as proxies for the disease progression. For Aβ PET, we observed that plasma p-tau231 was the first blood biomarker to surpass the two z-score levels (used here as a definition of abnormality; Fig. 1c) at a corresponding Aβ PET of 26.4 Centiloids, followed by plasma p-tau217 (35.4 Centiloids) and plasma GFAP (65.5 Centiloids). Plasma p-tau181, NfL and Aβ42/40 did not reach this abnormality threshold. Using CSF Aβ42/40 as a proxy of disease progression, plasma p-tau231 and plasma p-tau217 showed a parallel and steep increase and were the only plasma biomarkers to surpass the two z-score threshold (Fig. 1d). We also investigated the voxel-wise associations between Aβ PET and each of the plasma biomarkers (Fig. 1e), and found that plasma p-tau231 and p-tau217 were the plasma biomarkers that had the strongest association with Aβ PET in areas known to show early Aβ accumulation, namely the orbitofrontal areas, anterior and posterior cingulate gyri, insula and precuneus. In contrast, the other biomarkers had weaker and less widespread associations across the brain with, in particular, less involvement of the insula (Fig. 1e). Correlations between plasma and CSF biomarkers are shown in Supplementary Figs. 2 and 3.

5We next examined the accuracy of the different plasma biomarkers to detect Aβ pathology, as measured by Aβ PET or CSF Aβ42/40, in CU individuals. We performed receiver operating characteristic (ROC) analyses and the resulting areas under the curve (AUCs) for each plasma biomarker, and their combinations with risk factors (sex, age and APOE ε4 status) were compared with a base model including only AD risk factors using DeLong’s test. When it comes to the discrimination of early Aβ pathology (Aβ PET burden ≥12 Centiloids), none of the plasma biomarkers alone significantly improved the base risk factors model. Yet, the combination of plasma p-tau181, p-tau217, p-tau231 or Aβ42/40 with the base risk factors model outperformed the base risk factors model alone, but plasma p-tau181 and p-tau231 did not survive correction for multiple comparisons (Extended Data Fig. 2 and Supplementary Table 2). When it comes to established Aβ pathology (Aβ PET burden ≥30 Centiloids), the combination of the base risk factors model with plasma p-tau217, Aβ42/40 or p-tau231 outperformed the base risk factors model alone, but plasma p-tau231 did not survive multiple comparison correction (Extended Data Fig. 2 and Supplementary Table 2).

6When assessing Aβ status based on CSF Aβ42/40 (Table 1 and Extended Data Fig. 3), which assesses soluble Aβ and changes earlier than Aβ PET, the highest AUCs were reached by plasma Aβ42/40 (AUC = 0.750 (95% confidence interval (CI) = 0.702–0.798)) and p-tau231 (AUC = 0.740 (95% CI = 0.688–0.793)). DeLong’s test revealed that plasma biomarkers performed similarly well, with only plasma p-tau231 and Aβ42/40 being significantly better than plasma NfL. In line with Aβ PET results, the performance of plasma biomarkers did not improve that of the base risk factors model to indicate Aβ pathology as defined by decreased CSF Aβ42/40 (AUC = 0.729 (95% CI = 0.678–0.779)). However, the addition of any plasma biomarker, except for NfL, to the base risk factors model significantly increased its performance. In particular, the highest AUCs were for risk factors combined with plasma p-tau231 (AUC = 0.810 (95% CI = 0.766–0.854)), plasma Aβ42/40 (AUC = 0.798 (95% CI = 0.754–0.843)) and plasma p-tau217 (AUC = 0.797 (95% CI = 0.751–0.842)) (Table 1 and Extended Data Fig. 3). We next assessed whether the accuracy of the plasma biomarkers differs with age, because that may be relevant to better understand the plasma biomarker changes across the continuum and also to define inclusion criteria in prevention clinical trials. We performed the ROC analyses separately in a younger (≤65 years; n = 309) and an older (>65 years; n = 88) age group (Table 1 and Supplementary Table 3). In the younger age group, the combination of the base risk factors model with plasma p-tau181, p-tau217, p-tau231, GFAP or Aβ42/40 was significantly better than the base risk factors model (Table 1), whereas in the older group only plasma p-tau217 and p-tau231 (the latter at nominal level) were significantly better than the base risk factors model (Table 1). We repeated the analyses stratifying by the median age of the sample (61.8 years). In the CU individuals aged ≤61.8 years, the combination of the risk factors model with plasma p-tau231 (AUC = 0.847 (95% CI = 0.791–0.903)) or plasma Aβ42/40 (AUC = 0.828 (95% CI = 0.767–0.888)) was the only model that significantly outperformed the base risk factors model (Supplementary Table 4).

7We calculated cut-off points for the discrimination of Aβ status (as defined by CSF Aβ42/40) for each plasma biomarker using Youden’s index or setting sensitivity at 85% (Supplementary Table 5). After setting sensitivity at 85%, all combinations of plasma biomarkers with the base risk factors model, except for plasma NfL, reached a specificity >50%. In addition, we also performed these analyses with Aβ PET as a marker of Aβ burden (Supplementary Table 6).

8We investigated whether baseline plasma biomarkers were associated with cognitive changes after 3 years of follow-up in a subset of participants with available data (n = 214; Supplementary Table 7). In the whole group, plasma p-tau181 was significantly associated with cognitive decline (as measured by the preclinical Alzheimer cognitive composite (PACC); P = 0.020), whereas p-tau231 was the only plasma biomarker with a significant interaction with Aβ status (as defined by CSF Aβ42/40) at the nominal level (P = 0.027) (Supplementary Table 8 and Extended Data Fig. 4). After stratification by CSF Aβ status, plasma p-tau231 was associated with cognitive decline in the Aβ-positive group (P = 0.023). Finally, we assessed whether baseline plasma biomarkers were associated with Aβ PET Centiloid changes after 3 years of follow-up (n = 145; Supplementary Table 7). All plasma biomarkers were associated with an increase in Aβ PET Centiloids but only the interaction between plasma p-tau231 and Aβ status was nominally significant (P = 0.015) (Supplementary Table 9 and Supplementary Fig. 4). We performed sensitivity analysis in those participants with <30 Centiloids, and hence no established Aβ pathology at baseline, and only plasma p-tau231 and p-tau217 were significantly associated with Aβ PET Centiloid increases at follow-up (P = 0.041, both; Supplementary Table 10 and Extended Data Fig. 5).

9In summary, we demonstrate that plasma biomarkers change in the preclinical stage of the AD continuum but with differences among them. Several pieces of evidence consistently support plasma p-tau231 and p-tau217 being biomarkers indicating very early Aβ changes. First, plasma p-tau231 reaches abnormal levels at only 26.4 Centiloids and plasma p-tau217 at 35.4 Centiloids. Second, both plasma p-tau231 and p-tau217 had the strongest association with Aβ PET uptake in brain areas with known early Aβ deposition. Third, we show that, in individuals who have not yet established Aβ pathology at baseline (Aβ PET <30 Centiloids), plasma p-tau231 and p-tau217 are associated with longitudinal increases in Aβ PET uptake. Of note, plasma p-tau231 was associated with cognitive decline in Aβ-positive CU individuals. Moreover, plasma p-tau231, together with plasma Aβ42/40, has the largest change in the group with a low Aβ burden, and they both, in combination with age, sex and APOE ε4 status, also show the higher AUC to indicate Aβ pathology in the younger CU individuals, when Aβ pathology presumably starts. Conversely, plasma p-tau217, p-tau231, GFAP and Aβ42/40 are all adequate to detect established Aβ pathology (as measured by Aβ PET, a stage biomarker).

10Some study limitations should be noted. First, different platforms have been used to measure the plasma biomarkers and the contribution of assay platform in regard to diagnostic accuracy remains unclear. Second, ALFA+ includes participants with a higher risk for AD by design (high prevalence of APOE ε4 carriership and Aβ positivity) and, therefore, it does not represent normal aging in the general population.

11Amid the recent developments in anti-Aβ therapies and the increasing awareness of treating AD as early as possible, the use of plasma biomarkers—particularly p-tau231 and p-tau217—will facilitate the recruitment of participants in clinical trials at this early stage of the disease, but the choice of the plasma biomarker may differ depending on its goal. Plasma p-tau231 may be more suited to trials in middle-aged individuals with changes in soluble Aβ but subthreshold levels of Aβ pathology in PET, whereas other plasma biomarkers also have a satisfactory performance in older individuals and/or in the presence of established Aβ PET pathology.

12The present study was performed in the ALFA+ cohort, a nested longitudinal study from the ALFA (for ALzheimer’s and FAmilies) study. The ALFA study includes 2,743 middle-aged, CU individuals, with a high proportion of AD patients’ offspring (47.4%) and APOE ε4 carriers (34.7%).

13The ALFA+ study includes 450 participants who were invited to participate based on their specific AD risk profile, determined by an algorithm in which participants’ AD parental history and APOE status, verbal episodic memory score and CAIDE score were taken into consideration. A detailed phenotyping was performed in ALFA+ participants, including a lumbar puncture for the measurement of CSF biomarkers and imaging (magnetic resonance imaging (MRI) and positron emission tomography (PET)) biomarker acquisition. ALFA+ inclusion criteria were: (1) individuals who had previously participated in the ALFA study; (2) age between 45 and 65 years at the moment of inclusion in ALFA; and (3) long-term commitment to the study: inclusion and follow-up visits and agreement to undergo all tests and study procedures (MRI, PET and lumbar puncture). ALFA+ exclusion criteria were: (1) cognitive impairment (Clinical Dementia Rating (CDR) >0, Mini-Mental State Examination (MMSE) <27 or semantic fluency <12); (2) any systemic illness or unstable medical condition that could lead to difficulty complying with the protocol; (3) any contraindication to any test or procedure; and (4) a family history of monogenic AD. In the present study, we included 397 individuals with available baseline CSF and plasma biomarker measurements, of whom 339 also had available baseline Aβ PET. A subset of participants had longitudinal cognitive (n = 214) and Aβ PET (n = 145) data (follow-up of 3 years).

14We classified ALFA+ participants as Aβ positive (A+) if CSF Aβ42/40 <0.071 and tau positive (T+) if CSF Mid(M)-p-tau181 >24 pg ml−1 (ref. ) We further classified participants according to their CSF/PET Aβ status. The group with a low burden of Aβ pathology was defined as CSF Aβ42/40 <0.071 and Aβ PET Centiloids <30 and was compared with CSF/PET Aβ negative (CSF Aβ42/40 ≥0.071 and Aβ PET Centiloids <30) and CSF/PET Aβ positive (CSF Aβ42/40 <0.071 and Aβ PET Centiloids ≥30).

15In addition, we used Aβ PET as a stage biomarker with two cut-points, an early cut-off (12 Centiloids), where pathology may be emerging, and a later cut-point (30 Centiloids), reflecting established Aβ pathology. The 12-Centiloid threshold is the optimal cut-off validated in neuropathology to detect CERAD moderate-to-frequent, neuritic plaque scores, early detection of Aβ abnormalities by PET and agreement against CSF AD biomarkers. Our choice of 30 Centiloids as a later cut-off was based on our previous findings that it has the best agreement with the CSF t-tau/Aβ42 ratio in pooled data of ALFA+ and AD neuroimaging (ADNI) cohort biomarkers. This is also in line with the findings that showed that 26 Centiloids is an optimal cut-off in agreement with visual reads, which has been validated against CERAD pathology, and with the 35.7 Centiloid cut-off for established Aβ abnormalities in PET described by Bullic et al.. Moreover, the range from 12 Centiloids to 30 Centiloids has been proposed to reflect the ‘gray zone’ of Aβ deposition.

16The ALFA+ study (ALFA-FPM-0311) was approved by the independent ethics committee ‘Parc de Salut Mar’, Barcelona, and registered at Clinicaltrials.gov (identifier: NCT02485730). All participating subjects signed the study’s informed consent form which had also been approved by the independent ethics committee ‘Parc de Salut Mar’, Barcelona.

17The CSF sample collection and processing followed standard procedures and have been described previously. In short, participants fasted for at least 8 h and a lumbar puncture was performed at the intervertebral space L3–L4, L4–L5 or L5–S1 using a standard needle. CSF was collected into a 15-ml sterile polypropylene sterile tube (Sarstedt, catalog no. 62.554.502), aliquoted in volumes of 0.5 ml into sterile poly(propylene) tubes (0.5-ml Screw Cap Micro Tube Conical Bottom, catalog no. 72.730.005) and immediately frozen at −80 °C.

18The blood sample collection and processing procedure have been described previously. Blood samples were obtained on the same day as the lumbar puncture in fasting conditions. Whole blood was drawn with a 20G or 21G needle gauge into a 10-ml EDTA tube (BD Hemogard, 10 ml, K2EDTA, catalog no. 367525). Tubes were gently inverted 5–10 times and centrifuged at 2,000g for 10 min at 4 °C. The supernatant was aliquoted in volumes of 0.5 ml into sterile poly(propylene) tubes (Sarstedt Screw Cap Micro Tube, 0.5 ml, PP, ref. no. 72.730.105) and immediately frozen at −80 °C. The samples were processed at room temperature. The time between collection and freezing of both CSF and plasma samples was <30 min.

19All CSF and plasma biomarkers, except for CSF and plasma p-tau217, were analyzed at the Clinical Neurochemistry Laboratory at the University of Gothenburg, Sweden. Measurements of CSF p-tau181 and GFAP (Simoa platform) and CSF p-tau231 (ELISA) have been described previously,. CSF Aβ40, Aβ42 and NfL were measured with the exploratory NTK robust immunoassays (Roche Diagnostic International Ltd) on a cobas e 411 analyzer or cobas e 601 module. CSF M-p-tau181 and M-t-tau (both corresponding to the mid-region (M) domain of tau protein) were measured using the electrochemiluminescence Elecsys Phospho-Tau (181P) CSF and total-tau CSF immunoassays, respectively, on a fully automated cobas e 601 module (Roche Diagnostics International Ltd).

20Plasma GFAP and NfL were quantified with GFAP Discovery (no. 102336) and NF-light Advantage (no. 103186) commercial kits, respectively. Plasma Aβ42/40 was measured with the commercial Neurology 4-Plex E Advantage Kit (no. 103670). New plasma p-tau181 was measured using an in-house Simoa assay developed at the University of Gothenburg, as previously described. All Simoa assays were performed on the Simoa HD-X (Quanterix).

21The new plasma p-tau231 Simoa assay has been previously described and validated. Briefly, monoclonal mouse antibodies were generated using a synthetic peptide (K224KVAVVR(pT)PPKSPSSAK240C) as a KLH-coupled antigen, numbered according to full-length tau-441 phosphorylated on Thr231. Candidate hybridomas were selected on brain extracts of AD and control brain tissue. The final cloned and purified monoclonal antibody (ADx253) was characterized on synthetic peptides, spanning amino acids Thr217 to Ser241 of full-length tau, for its affinity, its phospho-specificity, using both phosphorylated and nonphosphorylated peptides, and its preferred selectivity in which position 232 was replaced by a Pip, to simulate cis-selectivity of ADx253. A biotin-conjugated, amino-terminal, anti-tau mouse monoclonal antibody was used for detection (MAB2241, no. 806502, BioLegend). Full-length recombinant tau-441 phosphorylated in vitro by glycogen synthase kinase 3β was used as the calibrator.

22Eli Lilly and Company provided the measurements of the previously published in-house assay for CSF and plasma p-tau217 (ref. ) using the Meso Scale Discovery platform (MSD). This assay uses a streptavidin small spot plate (MSD, L45SA) and customized p-tau217-specific biotinylated monoclonal capture and sulfo-tagged N-terminal tau detection antibodies. The lower limit of quantification of the assay is defined as 0.04 pg ml−1 using a customized, synthetic tau dipeptide, standard phosphorylated specifically at Thr217 of the full-length (2N4R) tau protein (synthesized by CPC Scientific). The dipeptide standard contains the epitope of the capture antibody, a poly(ethylene glycol) polymer linker, and the epitope of the detector antibody. The standard was verified to be >95% pure by high-performance liquid chromatography and identity was confirmed by mass spectrometry.

23Participants underwent [18F]flutemetamol (amyloid) PET scans after a cranial computed tomography scan for attenuation correction on a Biograph mCT scanner (Siemens Healthcare) at Hospital Clinic, Barcelona. Participants received an intravenous bolus dose of 185 MBq (range 104.25–218.3 MBq, mean ± s.d.: 191.75 ± 14.04) and, 90 min post-injection, PET data were acquired for 20 min (4 frames of 5 min each, mean ± s.d.: 90.15 ± 7.36 min). PET images were reconstructed in 4 frames × 5 min using the three-dimensional Ordered Subset Expectation Maximization algorithm by incorporating time of flight and point spread function modeling.

24Amyloid PET processing was performed after a validated Centiloid pipeline using SPM12 (ref. ). Centiloid values were calculated from the mean values of the standard Centiloid target region (http://www.gaain.org/centiloid-project) and the whole cerebellum as the reference region using the transformation previously calibrated.

25Before using the linear transformation to obtain Centiloid values, standardized uptake value ratio images were obtained from the previous images in the MNI space. These images were included in a voxel-wise linear model as a dependent variable to assess their association with the plasma biomarkers (independent variables) in univariate independent models. In all models, age and sex were included as covariates. These analyses were performed with the SPM12 toolbox. The statistical threshold was set at P < 0.001 with a cluster size of k > 100.

26CSF and plasma biomarkers were tested for normality using visual inspection of histograms. None of the biomarkers, except the CSF and plasma Aβ42/Aβ40 ratio, followed a normal distribution and were therefore log10-transformed.

27Differences in age, education and cognitive performance (MMSE) between Aβ-positive and Aβ-negative groups were assessed using a Student’s t-test, whereas group differences in sex and APOE ε4 status frequencies were tested using Pearson’s χ2 test. Centiloid values, CSF and plasma biomarker levels were compared with a one-way analysis of covariance (ANCOVA), adjusted for age and sex. Similarly, we compared the levels of plasma biomarkers among AT or CSF/PET Aβ groups with an ANCOVA adjusting for age and sex, followed by Tukey’s corrected, post-hoc, pairwise comparisons. The effect size of group differences was estimated by calculating Cohen’s d, in which the dependent variable was the residual of log10-transformed plasma biomarkers regressed on age and sex.

28We modeled the trajectories of plasma biomarkers as a function of Aβ PET (Centiloids) or CSF Aβ42/40, as proxies of progression throughout the preclinical stage of the AD continuum. To do so, we corrected each plasma biomarker value by age and sex and computed the mean and s.d. of each biomarker in a group of participants with CSF Aβ42/40 >0.1, used here as a reference group, and converted biomarker values to z-scores. Next, we applied a robust local weighted regression method (rlowess; ‘smooth’ function in Matlab and a span of 300) in 1,000 bootstrap subsamples of the original sample (‘bootstrp’ function in Matlab). The final model was built as the mean z-score for all values of the proxy measurements.

29Next, we performed ROC analyses to obtain the AUC for Aβ PET (Aβ PET Centiloids ≥12, early cut-off, or Centiloid ≥30, late cut-off) or CSF-defined (CSF Aβ42/40 <0.071) Aβ burden. DeLong’s test was used to compare AUCs for the different plasma biomarkers. Values for sensitivity and specificity were obtained by using Youden’s index cut-off points or setting a sensitivity of 85%. In addition, we performed ROC analyses categorizing participants by age groups using age 65 years or cohorts’ median age (61.8 years) as a cut-off point to define the two age groups.

30Finally, we tested whether plasma biomarkers were associated with longitudinal changes in cognitive performance or in Aβ deposition measured with Aβ PET Centiloids. Cognitive performance was assessed with the PACC, which was calculated in the ALFA study was based on the one proposed by Donohue et al. and the later proposals by Papp et al. and Jonaitis et al.. According to these previous works, we included categorical fluency measures, and we dropped the MMSE because of its lack of sensitivity. The PACC was calculated averaging the z-scores of the Free and Cued Selective Reminding Test (immediate total recall), the WMS-IV Logical Memory test (delayed recall), the WAIS-IV Coding subtest and the Semantic Fluency test (animals in 1 min). The means and s.d. used to create the z-scores of the whole sample were calculated from the subsample of individuals with negative AD biomarkers in CSF (A−T−). PACC scores at visit 2 were also created using the means and s.d. from baseline. Annualized change in the PACC and Centiloids was computed as the subtraction of PACC scores or Centiloid values at visit 2 minus those at visit 1, divided by the time between the two visits in years (mean time PACC: 3.26 (0.31) years; mean time Centiloids: 3.37 (0.44) years). The association between baseline levels of plasma biomarkers and longitudinal change in cognition or Aβ PET was assessed in a linear regression with the annualized change in PACC scores or Centiloid values as the dependent variable, adjusting for age and sex. Years of education were also included as a covariate in the models with annualized change in PACC scores as the dependent variable.

31All tests were two tailed, with a significance level of α = 0.05, and we corrected for multiple comparisons applying the false discovery rate (FDR) approach, if not otherwise specified. Statistical analyses were performed in SPSS IBM v.20.0, statistical software and the open-source statistical software R v.4.1.2. Figures were built using R and Matlab (v.2018b).

32Further information on research design is available in the Nature Research Reporting Summary linked to this article.

33Any methods, additional references, Nature Research reporting summaries, extended data, supplementary information, acknowledgements, peer review information; details of author contributions and competing interests; and statements of data and code availability are available at 10.1038/s41591-022-01925-w.