4.7 Article

Causal Associations Between Modifiable Risk Factors and the Alzheimer's Phenome

Journal

ANNALS OF NEUROLOGY
Volume 89, Issue 1, Pages 54-65

Publisher

WILEY
DOI: 10.1002/ana.25918

Keywords

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Funding

  1. JPB Foundation
  2. National Institutes of Health [U01AG052411, U01AG058635]
  3. UK Medical Research Council [MR/N015746/1]
  4. National Institute of Health [R01MH122866]
  5. National Institute on Aging (NIA) [U01AG032984, RC2AG036528]
  6. NCRAD: Samples from the National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD) [U24 AG21886]
  7. NIA/NIH [U01 AG016976]
  8. NIA

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This study comprehensively examined the genetic evidence for causal relationships between previously reported risk factors in Alzheimer's disease using polygenic risk scores and Mendelian randomization. The results suggest that education level, blood pressure, cholesterol levels, smoking, and diabetes are causally associated with the Alzheimer's disease phenome.
Objective The purpose of this study was to infer causal relationships between 22 previously reported risk factors for Alzheimer's disease (AD) and the AD phenome: AD, AD age of onset (AAOS), hippocampal volume, cortical surface area and thickness, cerebrospinal fluid (CSF) levels of amyloid-beta (A beta(42)), tau, and ptau(181), and the neuropathological burden of neuritic plaques, neurofibrillary tangles (NFTs), and vascular brain injury (VBI). Methods Polygenic risk scores (PRS) for the 22 risk factors were computed in 26,431 AD cases/controls and the association with AD was evaluated using logistic regression. Two-sample Mendelian randomization (MR) was used to infer the causal effect of risk factors on the AD phenome. Results PRS for increased education and diastolic blood pressure were associated with reduced risk for AD. MR indicated that only education was causally associated with reduced risk of AD, delayed AAOS, and increased cortical surface area and thickness. Total- and LDL-cholesterol levels were causally associated with increased neuritic plaque burden, although the effects were driven by single nucleotide polymorphisms (SNPs) within theAPOElocus. Diastolic blood pressure and pulse pressure are causally associated with increased risk of VBI. Furthermore, total cholesterol was associated with decreased hippocampal volume; smoking initiation with decreased cortical thickness; type 2 diabetes with an earlier AAOS; and sleep duration with increased cortical thickness. Interpretation Our comprehensive examination of the genetic evidence for the causal relationships between previously reported risk factors in AD using PRS and MR supports a causal role for education, blood pressure, cholesterol levels, smoking, and diabetes with the AD phenome. ANN NEUROL 2020

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