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Cohort Profile Update: The HUNT Study, Norway
Bjørn Olav Åsvold, Arnulf Langhammer, Tommy Aune Rehn and 18 more
International Journal of Epidemiology · 2022 · CC BY
Abstract
In the HUNT Study, all residents aged ≥20 years in the Nord-Trøndelag region, Norway have been invited to repeated surveys since 1984-86. The study data may be linked to local and national health registries. The HUNT4 survey in 2017-19 included 56 042 participants in Nord-Trøndelag and 107 711 participants in the neighboring Sør-Trøndelag region. The HUNT4 data enable more long-term follow-up, studies of life-course health trajectories, and within-family studies. New measures include body composition analysis using bioelectrical impedance; a one-week accelerometer recording; physical and cognitive testing in older adults; measurements of hemoglobin and blood cell counts, HbA1c and phosphatidylethanol; and genotyping. Researchers can apply for HUNT data access from HUNT Research Centre if they have obtained project approval from the Regional Committee for Medical and Health Research Ethics, see www.ntnu.edu/hunt/data .
Full text
From PubMed Central, U.S. National Library of Medicine, as current on Oct 17, 2026. Paragraph numbers are ours, so an answer can point at one.
In the HUNT Study, all residents aged ≥20 years in the Nord-Trøndelag region, Norway, have been invited to repeated surveys since 1984-86. The study data may be linked to local and national health registries.The HUNT4 survey in 2017-19 included 56 042 participants in Nord-Trøndelag and 107 711 participants in the neighbouring Sør-Trøndelag region.The HUNT4 data enable more long-term follow-up, studies of life course health trajectories and within-family studies.New measures include body composition analysis using bioelectrical impedance; a 1-week accelerometer recording; physical and cognitive testing in older adults; measurements of haemoglobin and blood cell counts, HbA1c and phosphatidylethanol; and genotyping.Researchers can apply for HUNT data access from HUNT Research Centre if they have obtained project approval from the Regional Committee for Medical and Health Research Ethics, see [www.ntnu.edu/hunt/data].
In the HUNT Study, all residents aged ≥20 years in the Nord-Trøndelag region, Norway, have been invited to repeated surveys since 1984-86. The study data may be linked to local and national health registries.
The HUNT4 survey in 2017-19 included 56 042 participants in Nord-Trøndelag and 107 711 participants in the neighbouring Sør-Trøndelag region.
The HUNT4 data enable more long-term follow-up, studies of life course health trajectories and within-family studies.
New measures include body composition analysis using bioelectrical impedance; a 1-week accelerometer recording; physical and cognitive testing in older adults; measurements of haemoglobin and blood cell counts, HbA1c and phosphatidylethanol; and genotyping.
Researchers can apply for HUNT data access from HUNT Research Centre if they have obtained project approval from the Regional Committee for Medical and Health Research Ethics, see [www.ntnu.edu/hunt/data].
The original cohort
The Trøndelag Health Study (the HUNT Study) is a population-based cohort study of the adult population in Trøndelag County, Norway. It was previously called the Nord-Trøndelag Health Study, until the study in 2019 expanded to cover both regions of Trøndelag County, Nord-Trøndelag and Sør-Trøndelag. The study has been running in Nord-Trøndelag since 1984 and is designed to cover a broad range of health-related topics through repeated surveys with questionnaires, interviews, clinical examinations, laboratory measurements and storage of biological samples. Nord-Trøndelag is fairly representative of Norway except for the lack of large cities and immigrant populations, and the region is suitable for longitudinal studies due to low migration. The HUNT Study data can be linked to a wide range of local and national health registries by means of the unique identification number allocated to all Norwegian residents. All current residents ≥20 years of age in Nord-Trøndelag have been invited to each survey wave: the HUNT1 (1984–86, 77 202 participants, 89.4% of invitees participated), HUNT2 (1995-97, 65 228 participants, 69.5%) and HUNT3 (2006-08, 50 800 participants, 54.1%) surveys (Figure 1). Since 1995-97, all adolescents (13-19 years of age) in Nord-Trøndelag have been invited to participate in the corresponding Young-HUNT Study.
What is the reason for the new data collection?
In 2017–19, all adult residents of Trøndelag were invited to the HUNT4 survey. The reasons for this new survey were, first, to collect follow-up and extended information on previous participants, and new information on individuals having moved into the region or reached adult age. After completion of HUNT4, about 19 000 individuals have more than 30 years of follow-up spanning all four study cycles (Figure 1). The continued follow-up also allows for monitoring of secular trends in public health. Second, improved measurement methods have become available for several health and lifestyle characteristics important for public health, as described in the later sections. Third, the HUNT Study previously lacked data from a large city. In 2019, HUNT4 expanded to include a survey in Sør-Trøndelag, which includes the city of Trondheim with ∼202 000 inhabitants (2019). The extended study population from both Nord-Trøndelag and Sør-Trøndelag is generally representative of Norway (Supplementary Table S1, available as Supplementary data at IJE online). A fourth reason for new data collection is the expansion of genetic and molecular epidemiology, where 70 517 participants of the HUNT2 or HUNT3 surveys have been genotyped.
What will be the new areas of research?
Extended follow-up of HUNT participants and high attendance among older adults enable a stronger focus on disease incidence, progression and life course health trajectories. New generations of HUNT participants enable more within-family and intergenerational studies. More valid studies of physical activity and anthropometry are possible due to new data including accelerometer recordings and body composition analyses using bioelectrical impedance. Other new assessments include cognitive and physical testing in old age, fecal sampling for microbiome studies and metabolomics and proteomics analyses for deeper molecular phenotyping. With available genotype information, analyses are expanded to, for example, genome-wide association studies and Mendelian randomization.
Who is in the cohort?
In Nord-Trøndelag, all residents aged ≥20 years at the estimated time of survey participation were invited to HUNT4 between 29 August 2017 and 23 February 2019 (the HUNT4-N Survey). Out of 103 800 invitees, 56 042 (54.0%) participated, defined as returning the main questionnaire. Participation across the HUNT1-HUNT4 surveys is shown in Figure 1.
In Sør-Trøndelag, all residents aged ≥18 years were invited to the HUNT4-S Survey and 107 711 (42.6%) participated out of 252 991 invitees. HUNT4-S consisted of two parts: 1745 residents ≥70 years of age in districts of Trondheim municipality took part in an examination between 26 October 2018 and 12 June 2019, and the remainder took part in a questionnaire survey between 3 October 2019 and 19 November 2019.
With the completion of HUNT4-N, 123 004 residents in Nord-Trøndelag have participated in at least one HUNT survey, of whom 68 586 have participated in more than one survey and 5881 participated in the Young-HUNT Study as adolescents. With the completion of HUNT4-S, 230 617 individuals have participated in one or more of the HUNT surveys.
Characteristics of HUNT4 participants are given in Table 1. Participation in HUNT4 differed by age, being highest in the age groups 40-79 years, and also slightly differed by marital status and urban vs rural residency (Table 2). Attrition from HUNT3 to HUNT4 was highest in older adults and was also moderately higher among people with chronic diseases or poor self-rated health or who were smokers (Supplementary Table S2, available as Supplementary data at IJE online). Questionnaire surveys were performed among non-participants of HUNT4-N and previous HUNT participants who were not invited to HUNT4-N because they had emigrated from the study area (Table 3;Supplementary Table S3, available as Supplementary data at IJE online). Those who had emigrated reported lower body mass index (BMI), more physical activity, less smoking, better self-rated health and more frequent alcohol intake than both participants and non-participants. The non-participants had less healthy lifestyle, lower self-reported health and higher proportion of cardiovascular diseases, chronic obstructive pulmonary disease, diabetes and antihypertensive medication use.
What has been measured?
Similar to previous HUNT surveys, HUNT4-N consisted of questionnaires, a short interview, clinical examination and biological sampling, and was conducted by trained health professionals at examination stations in each of 23 municipalities in Nord-Trøndelag. HUNT4-S was mainly a web-based questionnaire survey (except for the examination of 1745 residents ≥70 years of age in Trondheim), but printed questionnaires were sent on request and to older adults. The HUNT4 questionnaires covered a broad range of topics including socioeconomic conditions, health-related behaviours, symptoms, conditions and diseases, as described in Table 3. Selected HUNT4-N participants were also asked to complete questionnaires related to specific health topics, and a 19% random sample aged 20-69 years was invited to complete a web-based food frequency questionnaire. To evaluate the quality of the self-report of conditions in HUNT4, we compared the self-reported information with diagnostic codes recorded in the local or regional hospitals and on general practitioners’ reimbursement forms. Compared with these diagnoses as a reference standard, the sensitivity, specificity and predictive values of the self-reported information varied across diagnoses in both HUNT4-N (Supplementary Table S4, available as Supplementary data at IJE online) and HUNT4-S (Supplementary Table S5, available as Supplementary data at IJE online). Of note, the diagnostic codes may be inaccurate and do not constitute a definite reference standard. For example, in absence of a more suitable diagnostic code, a disease diagnosis may likely be reported on the reimbursement form by a general practitioner if a patient comes for testing for that disease, even if the disease was not confirmed. In-depth validity studies have been conducted for self-reported headache and insomnia in HUNT4. Validity studies of self-report of, for example, diabetes, psoriasis and atrial fibrillation, have been performed after previous HUNT surveys.
An overview of HUNT4 measurements, performed as part of the main HUNT4 examination or as ancillary data collections, is provided in Table 3. New aspects of the clinical examination in HUNT4-N compared with previous HUNT surveys included detailed body composition analysis using bioelectrical impedance (InBody 770, Cerritos, CA, USA), a 1-week accelerometer recording (AX3, Axivity, Newcastle, UK) and physical and cognitive testing [Short Physical Performance Battery (SPPB), grip strength and Montreal Cognitive Assessment, (MoCA); participants ≥70 years of age]. Blood pressure, pulse and peripheral capillary oxygen saturation were recorded three times at 1-min intervals using Dinamap CARESCAPE V100 (GE Healthcare, Chicago, IL, USA). Oral health clinical and radiographic examinations [Planmeca ProOne (orthopantomogram) and Planmeca Intra/Prostyle Intra with ProSensor HD (bitewing), Helsinki, Finland], hearing test (air-conduction pure-tone audiometry at 0.25-8 kHz according to ISO 8253-1 using Interacoustics audiometers type AD629 with TDH-39P supra-aural audiometric earphones) and spirometry (Jaeger Masterscope spirometers, JLAB version latest upgrade 2016, CareFusion, Würzburg, Germany) were performed in selected samples, and other tests have subsequently been performed in subgroups. All participants provided blood samples drawn in a non-fasting state between 9 am and 8 pm and time since last meal was recorded. Biological sampling at the field stations included blood, urine and saliva, and feces kits were returned in pre-paid envelopes. Biological material was handled at the field stations according to appropriate standards and transported to the biobank every evening in a cold chain. For all participants, two blood tubes were delivered at the laboratory of Levanger Hospital, Nord-Trøndelag Hospital Trust the next day for immediate analyses or transport to other laboratories. New analyses in blood included haemoglobin (Hb) and blood cell counts, HbA1c and phosphatidylethanol (PEth, an indicator of alcohol intake). Three blood tubes were aliquoted and stored in automated freezers in HUNT Biobank.
Since the publication of the original cohort profile in 2013, new analyses of biological material stored in HUNT Biobank include the genotyping of 70 517 participants of HUNT2 or HUNT3, genotyping of 18 098 additional participants of HUNT4-N, and SomaLogic’s SomaScan proteomics analyses and measurements of vitamin D and troponin I in subsamples.
The HUNT participants have consented to linkage to the many high-quality health and administrative registries in Norway, and to information from medical records. Such linkages can be reliably made using the national identification numbers allocated to all Norwegian residents, and means that prospectively recorded information on health outcomes can be obtained also for participants who do not attend subsequent HUNT surveys. An overview of Norwegian health registries is given by the Directorate for e-Health at Helsedata.no [https://helsedata.no/en/].
What has it found? Key findings and publications
In Table 1, we present descriptive characteristics of the HUNT4-N and HUNT4-S participants, including prevalence estimates of a range of chronic conditions and diseases. The longitudinal nature of HUNT enables analyses of long-term population changes in health-related factors. For example, comparison of HUNT4-N with previous HUNT surveys shows how the prevalence of smoking, high blood pressure and atherogenic lipid levels has declined from the 1980s until now, whereas the prevalence of obesity and diabetes has increased (Figure 2;Supplementary Table S6, available as Supplementary data at IJE online). Although the prevalence of diabetes has increased, HbA1c measurements in HUNT4 indicate that the current prevalence of undiagnosed diabetes is low. The prevalence of tension-type headache has increased, whereas migraine and medication overuse headache have become less common, as has hearing impairment. Information from HUNT4 has further enabled prevalence estimates of dementia, mild cognitive impairment, periodontitis and depression and anxiety symptoms, and estimation of the longitudinal decline in VO2peak. Analyses of HUNT4 have further shown that shift work is associated with higher levels of C-reactive protein and chronic musculoskeletal pain, and that cognitive impairment is associated with lower physical performance.
The new focus on genetic and molecular epidemiology has resulted in, for example, genome-wide association studies (GWAS) identifying new genetic variants associated with atrial fibrillation, serum lipids, thyroid stimulating hormone (TSH) and bone mineral density. Mendelian randomization studies have examined the causal associations between serum lipids and kidney function and provided support for the causal role of smoking heaviness on mortality, of higher body mass on psoriasis and bloodstream infections and of PCSK9 on serum cholesterol and coronary heart disease. Anthropometric measures spanning 6 decades have demonstrated how body mass index (BMI) increases more strongly in genetically predisposed individuals during transition to a more obesogenic environment., The predictive value of circulating proteins in secondary cardiovascular events has been examined using proteomics analyses. The large number of relatives participating in HUNT has enabled within-family studies. Parent-offspring analyses have suggested that maternal intrauterine environment, as proxied by maternal single nucleotide polymorphisms (SNPs) that influence offspring birthweight, is unlikely to be a major determinant of adverse cardiometabolic outcomes in population-based samples of offspring. Within-family Mendelian randomization analyses have enabled correction for familial biases in, for example, studies of the effects of height and body mass on educational attainment.Supplementary Table S7 (available as Supplementary data at IJE online) provides examples of studies showing how HUNT data have been used across a range of health topics since the original cohort profile was published in 2013.
What are the main strengths and weaknesses?
HUNT is suitable for longitudinal studies due to the long-term follow-up with repeated measurements since the 1980s, low migration, possibilities for registry linkages, and available valid information on migration and deaths from the National Population Register. The HUNT surveys cover a broad range of health-related topics, and many questionnaire items have been kept unchanged across the surveys to enable longitudinal comparisons. Quality-controlled HUNT data are stored at the HUNT Databank and biological material is stored in the state-of-the-art HUNT Biobank at the HUNT Research Centre, Levanger.
As the HUNT Study has invited the entire population in the area over decades, the study population includes many family members, both siblings and across generations, and is therefore suitable for within-family studies. A particular asset compared with many other studies is available offspring information in adult age. The study population has cryptic relatedness that may have to be considered in the analytical approach of, for example, GWAS, but is quite outbred with a mean inbreeding coefficient of 0.0024 (calculated using KING software).
The relatively high participation indicates a generally lower concern for selection bias. Nevertheless, attrition from HUNT3 to HUNT4 was somewhat higher among participants with chronic diseases or other indices of ill health, and lifestyle differed among non-participants and migrants compared with participants of HUNT4. To inform about selective participation by ill health among all HUNT4 invitees, we also examined primary health care diagnostic codes across a range of diseases, as well as primary health care use, for HUNT4 invitees and participants recorded during the calendar year 2017 (for HUNT4-N) or 2019 (for HUNT4-S). The proportion being assigned each diagnostic code generally did not differ substantially between participants and invitees, but results vary between diagnoses as detailed in Supplementary Table S8 (available as Supplementary data at IJE online). For example, a dementia diagnosis was less often recorded among participants than among invitees. General practice visits were more frequent among participants than non-participants at ages >80 years. In contrast, home nursing and nursing home residency were more common among non-participants (Supplementary Figure S1, available as Supplementary data at IJE online). The ethnically homogeneous population limits the generalizability to people of non-European ancestry.
Can I get hold of the data? Where can I find out more?
Researchers affiliated to a Norwegian research institution can apply for HUNT data access from HUNT Research Centre [www.ntnu.edu/hunt] if they have obtained project approval from the Regional Committee for Medical and Health Research Ethics (REC). Researchers not affiliated to a Norwegian research institution should collaborate with and apply through a Norwegian principal investigator. Information on the application and conditions for data access is available at [www.ntnu.edu/hunt/data]. The HUNT Databank website provides a detailed overview of the available variables in HUNT [www.ntnu.edu/hunt/databank]. Certain data from ancillary HUNT projects may be subject to a time-limited exclusivity provided to the researchers who have financed and conducted the data collection. Biological material is available for analyses, and information on procedures is found at the HUNT Biobank website [https://www.ntnu.edu/hunt/hunt-biobank]. Data from the health registries are not kept by HUNT; instead, linkages between HUNT and registry data have to be made for each research project and require that the principal investigator has obtained project-specific approval for such linkage by REC and each registry owner.
Ethics approval
The work presented in this Cohort Profile Update was approved by the Mid-Norway Regional Committee for Medical and Health Research Ethics (REK midt 67445).
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