The heritability of blood‐based biomarkers related to risk of Alzheimer's disease in a population‐based sample of early old‐age men

Author:

Gillespie Nathan A.12,Elman Jeremy A.34,McKenzie Ruth E.56,Tu Xin M.47,Xian Hong89,Reynolds Chandra A.10,Panizzon Matthew S.34,Lyons Michael J.11,Eglit Graham M. L.312,Neale Michael C.1,Rissman Robert A.34,Franz Carol34,Kremen William S.3413

Affiliation:

1. Virginia Institute for Psychiatric and Behaviour Genetics Department of Psychiatry Virginia Commonwealth University Richmond Virginia USA

2. QIMR Berghofer Medical Research Institute Brisbane Queensland Australia

3. Department of Psychiatry University of California, San Diego La Jolla California USA

4. Center for Behavior Genetics of Aging University of California, San Diego La Jolla California USA

5. Department of Psychology Boston University Boston Massachusetts USA

6. School of Education and Social Policy Merrimack College North Andover Massachusetts USA

7. Department of Family Medicine and Public Health University of California, San Diego La Jolla California USA

8. Department of Epidemiology and Biostatistics Saint. Louis University St. Louis Missouri USA

9. Research Service, VA St. Louis Healthcare System St. Louis Missouri USA

10. Department of Psychology University of California Riverside California USA

11. Department of Psychological and Brain Sciences Boston University Boston Massachusetts USA

12. Sam and Rose Stein Institute for Research on Aging University of California San Diego La Jolla California USA

13. Department of Neurosciences University of California, San Diego La Jolla California USA

Abstract

AbstractINTRODUCTIONDespite their increased application, the heritability of Alzheimer's disease (AD)–related blood‐based biomarkers remains unexplored.METHODSPlasma amyloid beta 40 (Aβ40), Aβ42, the Aβ42/40 ratio, total tau (t‐tau), and neurofilament light (NfL) data came from 1035 men 60 to 73 years of age (μ = 67.0, SD = 2.6). Twin models were used to calculate heritability and the genetic and environmental correlations between them.RESULTSAdditive genetics explained 44% to 52% of Aβ42, Aβ40, t‐tau, and NfL. The Aβ42/40 ratio was not heritable. Aβ40 and Aβ42 were genetically near identical (rg = 0.94). Both Aβ40 and Aβ42 were genetically correlated with NfL (rg = 0.35 to 0.38), but genetically unrelated to t‐tau.DISCUSSIONExcept for Aβ42/40, plasma biomarkers are heritable. Aβ40 and Aβ42 share mostly the same genetic influences, whereas genetic influences on plasma t‐tau and NfL are largely unique in early old‐age men. The absence of genetic associations between the Aβs and t‐tau is not consistent with the amyloid cascade hypothesis.

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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