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Genetic contributions to self-reported tiredness

机译:遗传导致自我报告的疲倦

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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~(?11)). 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 _(g) 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.
机译:自我报告的疲倦和低能量(通常称为疲劳)与较差的身心健康有关。双胞胎研究表明,其遗传力在6%至50%之间。在英国生物库样本(N = 108?976)中,我们针对以下问题进行了全基因组关联研究(GWAS):“在过去的两周中,您多久感到疲倦或很少感到疲劳单变量GCTA-GREML发现,对于该疲劳问题,所有常见单核苷酸多态性所解释的方差比例为8.4%(se = 0.6%)。 GWAS鉴定出一个全基因组显着的命中基因(Affymetrix id 1:64178756_C_T; P = 1.36×10〜(?11))。连锁不平衡得分回归和多基因谱得分分析被用于检验疲劳和GWAS联盟多达29种身心健康特征之间的共有遗传病因。疲劳和体重指数(BMI),C反应蛋白,高密度脂蛋白(HDL)胆固醇,强迫呼气量,抓地力,HbA1c,寿命,肥胖,自我评估的健康状况,吸烟状况,甘油三酸酯,2型糖尿病,腰臀比,注意缺陷多动障碍,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(绝对r_(g)效应大小在0.02至0.78之间)。在BMI,HDL胆固醇,低密度脂蛋白胆固醇,冠状动脉疾病,C反应蛋白,HbA1c,身高,肥胖,吸烟状况,甘油三酯,2型糖尿病,腰围–的疲劳表型得分与多基因谱得分之间存在显着相关性髋部比率,儿童认知能力,神经质,躁郁症,重度抑郁症和精神分裂症(标准化的β的绝对值<0.03)。这些结果表明,疲劳是部分可遗传的,异质的和复杂的现象,在表型和遗传上与情感,认知,个性和生理过程有关。

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