Common genetic variants associated with cognitive performance identified using the proxy-phenotype method.

Proc Natl Acad Sci U S A
Authors
Keywords
Abstract

We identify common genetic variants associated with cognitive performance using a two-stage approach, which we call the proxy-phenotype method. First, we conduct a genome-wide association study of educational attainment in a large sample (n = 106,736), which produces a set of 69 education-associated SNPs. Second, using independent samples (n = 24,189), we measure the association of these education-associated SNPs with cognitive performance. Three SNPs (rs1487441, rs7923609, and rs2721173) are significantly associated with cognitive performance after correction for multiple hypothesis testing. In an independent sample of older Americans (n = 8,652), we also show that a polygenic score derived from the education-associated SNPs is associated with memory and absence of dementia. Convergent evidence from a set of bioinformatics analyses implicates four specific genes (KNCMA1, NRXN1, POU2F3, and SCRT). All of these genes are associated with a particular neurotransmitter pathway involved in synaptic plasticity, the main cellular mechanism for learning and memory.

Year of Publication
2014
Journal
Proc Natl Acad Sci U S A
Volume
111
Issue
38
Pages
13790-4
Date Published
2014 Sep 23
ISSN
1091-6490
URL
DOI
10.1073/pnas.1404623111
PubMed ID
25201988
PubMed Central ID
PMC4183313
Links
Grant list
ETM/55 / Chief Scientist Office / United Kingdom
CZB/4/505 / Chief Scientist Office / United Kingdom
R01 AA009367 / AA / NIAAA NIH HHS / United States
MC_UU_12013/3 / Medical Research Council / United Kingdom
P30AG012810 / AG / NIA NIH HHS / United States
R01 AA011886 / AA / NIAAA NIH HHS / United States
MR/K026992/1 / Medical Research Council / United Kingdom
G0901245 / Medical Research Council / United Kingdom
102215 / Wellcome Trust / United Kingdom
MC_PC_15018 / Medical Research Council / United Kingdom
R01 DA024417 / DA / NIDA NIH HHS / United States
MC_UU_12013/1 / Medical Research Council / United Kingdom
R01 MH066140 / MH / NIMH NIH HHS / United States
CZD/16/6/4 / Chief Scientist Office / United Kingdom
MC_PC_U127561128 / Medical Research Council / United Kingdom
T32 MH016880 / MH / NIMH NIH HHS / United States
P01AG005842 / AG / NIA NIH HHS / United States
G0500079 / Medical Research Council / United Kingdom
T32AG000186-23 / AG / NIA NIH HHS / United States
F31 DA029377 / DA / NIDA NIH HHS / United States
BB/F019394/1 / Biotechnology and Biological Sciences Research Council / United Kingdom
P01 AG005842 / AG / NIA NIH HHS / United States
R37 DA005147 / DA / NIDA NIH HHS / United States
P30 AG012810 / AG / NIA NIH HHS / United States
T32 AG000186 / AG / NIA NIH HHS / United States
P01AG005842-20S2 / AG / NIA NIH HHS / United States
G9815508 / Medical Research Council / United Kingdom
R01 DA013240 / DA / NIDA NIH HHS / United States