Mendelian randomization highlights significant difference and genetic heterogeneity in clinically diagnosed Alzheimer’s disease GWAS and self-report proxy phenotype GWAX
Haijie Liu; Yang Hu; Yan Zhang; Haihua Zhang; Shan Gao; Longcai Wang; Tao Wang; Zhifa Han · 2022 · Alzheimer s Research & Therapy
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract
BACKGROUND: Until now, Mendelian randomization (MR) studies have investigated the causal association of risk factors with Alzheimer's disease (AD) using large-scale AD genome-wide association studies (GWAS), GWAS by proxy (GWAX), and meta-analyses of GWAS and GWAX (GWAS+GWAX) datasets. However, it currently remains unclear about the consistency of MR estimates across these GWAS, GWAX, and GWAS+GWAX datasets. METHODS: Here, we first selected 162 independent educational attainment genetic variants as the potential instrumental variables (N = 405,072). We then selected one AD GWAS dataset (N = 63
Abstract by Haijie Liu; Yang Hu; Yan Zhang; Haihua Zhang; Shan Gao; Longcai Wang; Tao Wang; Zhifa Han, Alzheimer s Research & Therapy (2022) — licensed CC BY 4.0.
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Metadata source: OpenAlex · DOI 10.1186/s13195-022-00963-3
