Marioni R E, Yang J, Dykiert D, Mõttus R, Campbell A, Davies G, Hayward C, Porteous D J, Visscher P M, Deary I J
Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
Medical Genetics Section, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Mol Psychiatry. 2016 Oct;21(10):1477-82. doi: 10.1038/mp.2015.205. Epub 2016 Feb 9.
Obesity and low cognitive function are associated with multiple adverse health outcomes across the life course. They have a small phenotypic correlation (r=-0.11; high body mass index (BMI)-low cognitive function), but whether they have a shared genetic aetiology is unknown. We investigated the phenotypic and genetic correlations between the traits using data from 6815 unrelated, genotyped members of Generation Scotland, an ethnically homogeneous cohort from five sites across Scotland. Genetic correlations were estimated using the following: same-sample bivariate genome-wide complex trait analysis (GCTA)-GREML; independent samples bivariate GCTA-GREML using Generation Scotland for cognitive data and four other samples (n=20 806) for BMI; and bivariate LDSC analysis using the largest genome-wide association study (GWAS) summary data on cognitive function (n=48 462) and BMI (n=339 224) to date. The GWAS summary data were also used to create polygenic scores for the two traits, with within- and cross-trait prediction taking place in the independent Generation Scotland cohort. A large genetic correlation of -0.51 (s.e. 0.15) was observed using the same-sample GCTA-GREML approach compared with -0.10 (s.e. 0.08) from the independent-samples GCTA-GREML approach and -0.22 (s.e. 0.03) from the bivariate LDSC analysis. A genetic profile score using cognition-specific genetic variants accounts for 0.08% (P=0.020) of the variance in BMI and a genetic profile score using BMI-specific variants accounts for 0.42% (P=1.9 × 10(-7)) of the variance in cognitive function. Seven common genetic variants are significantly associated with both traits at P<5 × 10(-5), which is significantly more than expected by chance (P=0.007). All these results suggest there are shared genetic contributions to BMI and cognitive function.
肥胖与认知功能低下在整个生命过程中都与多种不良健康结果相关。它们存在较小的表型相关性(r = -0.11;高体重指数(BMI)-低认知功能),但它们是否具有共同的遗传病因尚不清楚。我们使用来自“苏格兰一代”的6815名无亲属关系、已进行基因分型的成员的数据,研究了这些性状之间的表型和遗传相关性,该群体是一个来自苏格兰五个地点的种族同质队列。使用以下方法估计遗传相关性:同一样本双变量全基因组复杂性状分析(GCTA)-GREML;使用“苏格兰一代”的认知数据和其他四个样本(n = 20806)的BMI数据进行独立样本双变量GCTA-GREML分析;使用迄今为止关于认知功能(n = 48462)和BMI(n = 339224)的最大全基因组关联研究(GWAS)汇总数据进行双变量LDSC分析。GWAS汇总数据还用于为这两个性状创建多基因分数,并在独立的“苏格兰一代”队列中进行性状内和跨性状预测。使用同一样本GCTA-GREML方法观察到的遗传相关性为-0.51(标准误0.15),而独立样本GCTA-GREML方法为-0.10(标准误0.08),双变量LDSC分析为-0.22(标准误0.03)。使用认知特异性基因变异的遗传特征分数占BMI方差的0.08%(P = 0.020),使用BMI特异性变异的遗传特征分数占认知功能方差的0.42%(P = 1.9×10⁻⁷)。七个常见基因变异在P<5×10⁻⁵时与这两个性状均显著相关,这显著多于偶然预期(P = 0.007)。所有这些结果表明BMI和认知功能存在共同的遗传贡献。