IJPDS International Journal of Population Data Science IJPDS 2399-4908 Swansea University 10.23889/ijpds.v10i3.3203 10:3:169 Generation Scotland – Linking all the records we can Campbell Archie 1 Buchanan David 1 Milbourn Hannah 1 Whalley Heather 1 Sudlow Cathie 1 University of Edinburgh, Edinburgh, United Kingdom 01 06 2025 2025 8 4 3203 This work is licenced under a Creative Commons Attribution 4.0 International License. This article is available from the IJPDS website at: https://ijpds.org/article/view/3203 Objectives

We started a family-based genetic epidemiology study in 2006-11 which recruited 24,000 adult volunteers from 7000 families across Scotland with consent for follow-up through medical record linkage and re-contact. In 2022-25 we are recruiting another 20,000, with consent extended to administrative records, and age range now 12+.

 Method

Original volunteers completed demographic, health and lifestyle questionnaires, provided biological samples, and underwent detailed clinical assessment. The samples, phenotype and genotype data form a resource for research on the genetics of conditions of public health importance. This has become a longitudinal dataset by linkage to routine NHS records: hospital, maternity, lab test, prescriptions, dentistry, mortality, imaging, cancer screening, GP data, Covid-19 testing and vaccinations, as well as follow-up questionnaires. The new wave of recruitment is all online and can be done on a smartphone, with DNA from saliva collected by post. Teenagers aged 12-15 can join with parental consent.

 Results

Genotyping has been done on quantitative traits and biomarkers, with DNA methylation data and proteomics available for most of the cohort. Our “CovidLife” surveys collected data on effects of the pandemic.

Researchers can find prevalent and incident disease cases and controls to test research hypotheses on a stratified population. They can also do targeted recruitment of participants to new studies, including recall by genotype. We have established and validated E-HR linkage with the NHS Scotland CHI Register, overcoming technical and governance issues in the process. We contribute to major international consortia, with collaborators from institutions worldwide, both academic and commercial. Recruits also give consent to linkage to other administrative data, and reuse of samples from routine NHS tests for medical research.

 Conclusion

We plan to extend the linkage process to include other administrative data from national datasets as and when approvals are obtained. New types of data can also be collected by online questionnaires. The Research Tissue Bank resources are available to academic and commercial researchers through a managed access process.