Hill W David, Davies Gail, Liewald David C, McIntosh Andrew M, Deary Ian J
Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, United Kingdom; Departments of Psychology, University of Edinburgh, Edinburgh, United Kingdom.
Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, United Kingdom; Psychiatry, University of Edinburgh, Edinburgh, United Kingdom.
Biol Psychiatry. 2016 Aug 15;80(4):266-273. doi: 10.1016/j.biopsych.2015.08.033. Epub 2015 Sep 4.
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.
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.
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 (rg = .360, p = .0009) and for educational attainment (rg = .322, p = 1.37e-5) but not in older age. In schizophrenia, we found a negative genetic correlation between older age cognitive function (rg = -.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 (rg = -.341, p = .001), educational attainment (rg = -.324, p = 1.15e-5), and with older age cognitive function (rg = -.324, p = 1.78e-5).
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.
一般认知功能可预测一生中的精神疾病。本研究探讨了基因多效性在解释认知功能与精神障碍之间联系中的作用。
我们使用了两个关于认知功能的大型全基因组关联研究数据集——一个来自老年人,样本量为53949人,另一个来自儿童,样本量为12441人。我们还使用了关于受教育程度的全基因组关联研究数据,样本量为95427人,以检验其作为认知功能替代表型的有效性。使用一种新方法——连锁不平衡回归,我们得出了遗传相关性,避免了精神疾病和认知功能之间临床状态的混杂影响。
我们发现一生中一般认知功能的遗传相关性为0.711(p = 2.26×10⁻¹²)。我们还发现自闭症谱系障碍与儿童期认知功能(rg = 0.360,p = 0.0009)以及受教育程度(rg = 0.322,p = 1.37×10⁻⁵)之间存在正遗传相关性,但在老年期不存在。在精神分裂症方面,我们发现老年期认知功能与精神分裂症之间存在负遗传相关性(rg = -0.231,p = 3.81×10⁻¹²),但在儿童期或受教育程度方面不存在。对于阿尔茨海默病,我们发现其与儿童期认知功能(rg = -0.341,p = 0.001)、受教育程度(rg = -0.324,p = 1.15×10⁻⁵)以及老年期认知功能(rg = -0.324,p = 1.78×10⁻⁵)之间存在负遗传相关性。
认知功能与精神障碍之间表现出的基因多效性在生命过程中发生了变化。这些年龄依赖性关联可能解释了为什么负选择没有消除与自闭症谱系障碍或精神分裂症有因果关系的变异。