Department of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada.
Department of Biomedical Sciences, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada.
Neuropsychopharmacology. 2024 Sep;49(10):1609-1618. doi: 10.1038/s41386-024-01870-x. Epub 2024 Jun 11.
Coffee is one of the most widely consumed beverages. We performed a genome-wide association study (GWAS) of coffee intake in US-based 23andMe participants (N = 130,153) and identified 7 significant loci, with many replicating in three multi-ancestral cohorts. We examined genetic correlations and performed a phenome-wide association study across hundreds of biomarkers, health, and lifestyle traits, then compared our results to the largest available GWAS of coffee intake from the UK Biobank (UKB; N = 334,659). We observed consistent positive genetic correlations with substance use and obesity in both cohorts. Other genetic correlations were discrepant, including positive genetic correlations between coffee intake and psychiatric illnesses, pain, and gastrointestinal traits in 23andMe that were absent or negative in the UKB, and genetic correlations with cognition that were negative in 23andMe but positive in the UKB. Phenome-wide association study using polygenic scores of coffee intake derived from 23andMe or UKB summary statistics also revealed consistent associations with increased odds of obesity- and red blood cell-related traits, but all other associations were cohort-specific. Our study shows that the genetics of coffee intake associate with substance use and obesity across cohorts, but also that GWAS performed in different populations could capture cultural differences in the relationship between behavior and genetics.
咖啡是全球范围内最受欢迎的饮品之一。我们对美国 23andMe 参与者(N=130153)的咖啡摄入量进行了全基因组关联研究(GWAS),鉴定出了 7 个显著的位点,其中许多位点在三个多祖裔队列中得到了复制。我们检查了遗传相关性,并对数百种生物标志物、健康和生活方式特征进行了全表型关联研究,然后将我们的结果与英国生物库(UKB;N=334659)中最大的咖啡摄入量 GWAS 进行了比较。我们观察到在两个队列中,咖啡摄入量与物质使用和肥胖存在一致的正遗传相关性。其他遗传相关性存在差异,包括在 23andMe 中,咖啡摄入量与精神疾病、疼痛和胃肠道特征之间存在正遗传相关性,而在 UKB 中则不存在或呈负相关,以及与认知相关的遗传相关性在 23andMe 中呈负相关,而在 UKB 中呈正相关。使用 23andMe 或 UKB 汇总统计数据的多基因评分进行的全表型关联研究也揭示了与肥胖和红细胞相关特征的几率增加一致的关联,但所有其他关联都是队列特异性的。我们的研究表明,咖啡摄入量的遗传与物质使用和肥胖在不同队列中存在关联,但在不同人群中进行的 GWAS 也可能捕捉到行为和遗传之间关系的文化差异。
Br J Dermatol. 2025-8-18
Complex Psychiatry. 2025-3-24
J Transl Med. 2024-10-22
Ann Neurol. 2022-6