Journal
BIOLOGICAL PSYCHIATRY
Volume 80, Issue 4, Pages 266-273Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2015.08.033
Keywords
Aging; Autism; Cognitive function; Genetics; Pleiotropy; Schizophrenia
Categories
Funding
- Biotechnology and Biological Sciences Research Council
- Medical Research Council
- University of Edinburgh
- Age UK (Disconnected Mind Project)
- Wellcome Trust [104036/Z/14/Z]
- BBSRC [BB/F019394/1] Funding Source: UKRI
- MRC [G0700704] Funding Source: UKRI
- Biotechnology and Biological Sciences Research Council [BB/F019394/1] Funding Source: researchfish
- Medical Research Council [G0700704, MR/K026992/1] Funding Source: researchfish
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BACKGROUND: General cognitive function predicts psychiatric illness across the life course. This study examines the role of pleiotropy in explaining the link between cognitive function and psychiatric disorder. METHODS: We used two large genome-wide association study data sets on cognitive function-one from older age, n = 53,949, and one from childhood, n = 12,441. We also used genome-wide association study data on educational attainment, n = 95,427, to examine the validity of its use as a proxy phenotype for cognitive function. Using a new method, linkage disequilibrium regression, we derived genetic correlations, free from the confounding of clinical state between psychiatric illness and cognitive function. RESULTS: We found a genetic correlation of .711 (p = 2.26e-12) across the life course for general cognitive function. We also showed a positive genetic correlation between autism spectrum disorder and cognitive function in childhood (r(g) = .360, p = .0009) and for educational attainment (r(g) = .322, p = 1.37e-5) but not in older age. In schizophrenia, we found a negative genetic correlation between older age cognitive function (r(g) = -2.231, p = 3.81e-12) but not in childhood or for educational attainment. For Alzheimer's disease, we found negative genetic correlations with childhood cognitive function (r(g) = -.341, p = .001), educational attainment (r(g) = -.324, p = 1.15e-5), and with older age cognitive function (r(g) = -.324, p = 1.78e-5). CONCLUSIONS: The pleiotropy exhibited between cognitive function and psychiatric disorders changed across the life course. These age-dependent associations might explain why negative selection has not removed variants causally associated with autism spectrum disorder or schizophrenia.
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