Department of Psychology, Northumbria University, Newcastle, UK.
Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
Mol Psychiatry. 2018 Mar;23(3):609-620. doi: 10.1038/mp.2017.5. Epub 2017 Feb 14.
Self-reported tiredness and low energy, often called fatigue, are associated with poorer physical and mental health. Twin studies have indicated that this has a heritability between 6 and 50%. In the UK Biobank sample (N=108 976), we carried out a genome-wide association study (GWAS) of responses to the question, 'Over the last two weeks, how often have you felt tired or had little energy?' Univariate GCTA-GREML found that the proportion of variance explained by all common single-nucleotide polymorphisms for this tiredness question was 8.4% (s.e.=0.6%). GWAS identified one genome-wide significant hit (Affymetrix id 1:64178756_C_T; P=1.36 × 10). Linkage disequilibrium score regression and polygenic profile score analyses were used to test for shared genetic aetiology between tiredness and up to 29 physical and mental health traits from GWAS consortia. Significant genetic correlations were identified between tiredness and body mass index (BMI), C-reactive protein, high-density lipoprotein (HDL) cholesterol, forced expiratory volume, grip strength, HbA1c, longevity, obesity, self-rated health, smoking status, triglycerides, type 2 diabetes, waist-hip ratio, attention deficit hyperactivity disorder, bipolar disorder, major depressive disorder, neuroticism, schizophrenia and verbal-numerical reasoning (absolute r effect sizes between 0.02 and 0.78). Significant associations were identified between tiredness phenotypic scores and polygenic profile scores for BMI, HDL cholesterol, low-density lipoprotein cholesterol, coronary artery disease, C-reactive protein, HbA1c, height, obesity, smoking status, triglycerides, type 2 diabetes, waist-hip ratio, childhood cognitive ability, neuroticism, bipolar disorder, major depressive disorder and schizophrenia (standardised β's had absolute values<0.03). These results suggest that tiredness is a partly heritable, heterogeneous and complex phenomenon that is phenotypically and genetically associated with affective, cognitive, personality and physiological processes.
自我报告的疲倦和乏力,通常称为疲劳,与较差的身心健康有关。双胞胎研究表明,这种情况的遗传性在 6%到 50%之间。在英国生物库样本(N=108976)中,我们对“在过去两周内,您感到疲倦或乏力的频率是多少?”这个问题的回答进行了全基因组关联研究(GWAS)。单变量 GCTA-GREML 发现,这个疲倦问题的所有常见单核苷酸多态性所解释的方差比例为 8.4%(标准误=0.6%)。GWAS 确定了一个全基因组显著命中(Affymetrix id 1:64178756_C_T;P=1.36×10)。连锁不平衡评分回归和多基因评分分析用于测试疲倦与来自 GWAS 联盟的 29 种身体和心理健康特征之间的共同遗传病因。在疲倦和身体质量指数(BMI)、C 反应蛋白、高密度脂蛋白(HDL)胆固醇、用力呼气量、握力、HbA1c、长寿、肥胖、自我评估健康、吸烟状况、甘油三酯、2 型糖尿病、腰臀比、注意力缺陷多动障碍、双相情感障碍、重度抑郁症、神经质、精神分裂症和言语数字推理之间,发现了显著的遗传相关性(绝对 r 效应大小在 0.02 到 0.78 之间)。在疲倦表型评分和 BMI、HDL 胆固醇、低密度脂蛋白胆固醇、冠心病、C 反应蛋白、HbA1c、身高、肥胖、吸烟状况、甘油三酯、2 型糖尿病、腰臀比、儿童认知能力、神经质、双相情感障碍、重度抑郁症和精神分裂症的多基因评分之间,也发现了显著的关联(标准化β的绝对值<0.03)。这些结果表明,疲倦是一种部分可遗传的、异质的和复杂的现象,在表型和遗传上与情感、认知、人格和生理过程有关。