Risk of dementia in APOE ε4 carriers is mitigated by a polygenic risk score. Issue 1 (14th September 2021)

• Record Type: Journal Article
• Authors: Ebenau, Jarith L.; van der Lee, Sven J.; Hulsman, Marc; Tesi, Niccolò; Jansen, Iris E.; Verberk, Inge M.W.; van Leeuwenstijn, Mardou; Teunissen, Charlotte E.; Barkhof, Frederik; Prins, Niels D.; Scheltens, Philip; Holstege, Henne; van Berckel, Bart N.M.; van der Flier, Wiesje M.
• Is Part Of: Alzheimer's & dementia. Volume 13:Issue 1(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-09-14
• Subjects: Alzheimer's disease -- APOE -- ATN classification -- biomarkers -- dementia -- polygenic risk score -- subjective cognitive decline; Alzheimer's disease -- Periodicals; Alzheimer's disease -- Diagnosis -- Periodicals; Dementia -- Periodicals; Dementia -- Diagnosis -- Periodicals; 616.831
• DOI: 10.1002/dad2.12229
• Languages: English
• ISSNs: 2352-8729

Abstract

Abstract: Introduction: We investigated relationships among genetic determinants of Alzheimer's disease (AD), amyloid/tau/neurodegenaration (ATN) biomarkers, and risk of dementia. Methods: We studied cognitively normal individuals with subjective cognitive decline (SCD) from the Amsterdam Dementia Cohort and SCIENCe project. We examined associations between genetic variants and ATN biomarkers, and evaluated their predictive value for incident dementia. A polygenic risk score (PRS) was calculated based on 39 genetic variants. The APOE gene was not included in the PRS and was analyzed separately. Results: The PRS and APOE ε4 were associated with amyloid‐positive ATN profiles, and APOE ε4 additionally with isolated increased tau (A–T+N–). A high PRS and APOE ε4 separately predicted AD dementia. Combined, a high PRS increased while a low PRS attenuated the risk associated with ε4 carriers. Discussion: Genetic variants beyond APOE are clinically relevant and contribute to the pathophysiology of AD. In the future, a PRS might be used in individualized risk profiling.