학술논문

Genetically predicted body mass index and Alzheimer's disease–related phenotypes in three large samples: Mendelian randomization analyses
Document Type
article
Source
Alzheimer's & Dementia. 11(12)
Subject
Biomedical and Clinical Sciences
Biological Psychology
Clinical Sciences
Neurosciences
Psychology
Brain Disorders
Clinical Research
Alzheimer's Disease
Neurodegenerative
Dementia
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Genetics
Aging
Acquired Cognitive Impairment
2.1 Biological and endogenous factors
Aetiology
Neurological
Aged
Aged
80 and over
Alzheimer Disease
Body Mass Index
Female
Genotype
Humans
Linear Models
Male
Mendelian Randomization Analysis
Obesity
Phenotype
Polymorphism
Single Nucleotide
Risk Factors
Alzheimer's disease
Mendelian randomization
Adult Changes in Thought Study Investigators
Religious Orders Study/Memory and Aging Project Investigators
Alzheimer's Disease Genetics Consortium
Geriatrics
Clinical sciences
Biological psychology
Language
Abstract
Observational research shows that higher body mass index (BMI) increases Alzheimer's disease (AD) risk, but it is unclear whether this association is causal. We applied genetic variants that predict BMI in Mendelian randomization analyses, an approach that is not biased by reverse causation or confounding, to evaluate whether higher BMI increases AD risk. We evaluated individual-level data from the AD Genetics Consortium (ADGC: 10,079 AD cases and 9613 controls), the Health and Retirement Study (HRS: 8403 participants with algorithm-predicted dementia status), and published associations from the Genetic and Environmental Risk for AD consortium (GERAD1: 3177 AD cases and 7277 controls). No evidence from individual single-nucleotide polymorphisms or polygenic scores indicated BMI increased AD risk. Mendelian randomization effect estimates per BMI point (95% confidence intervals) were as follows: ADGC, odds ratio (OR) = 0.95 (0.90-1.01); HRS, OR = 1.00 (0.75-1.32); GERAD1, OR = 0.96 (0.87-1.07). One subscore (cellular processes not otherwise specified) unexpectedly predicted lower AD risk.