Barcelona Institute for Global Health (ISGlobal), Barcelona 08003, Spain; IMIM (Hospital del Mar Research Institute), Barcelona 08003, Spain; Centro de Investigación Biomédica en Red en Epidemiologia y Salud Pública (CIBERESP), Barcelona 08003, Spain; Department of Mathematics, Universitat Autònoma de Barcelona (UAB), Barcelona 08193, Spain.
Barcelona Institute for Global Health (ISGlobal), Barcelona 08003, Spain; IMIM (Hospital del Mar Research Institute), Barcelona 08003, Spain.
Am J Hum Genet. 2020 Jun 4;106(6):846-858. doi: 10.1016/j.ajhg.2020.04.017. Epub 2020 May 28.
The burden of several common diseases including obesity, diabetes, hypertension, asthma, and depression is increasing in most world populations. However, the mechanisms underlying the numerous epidemiological and genetic correlations among these disorders remain largely unknown. We investigated whether common polymorphic inversions underlie the shared genetic influence of these disorders. We performed an inversion association analysis including 21 inversions and 25 obesity-related traits on a total of 408,898 Europeans and validated the results in 67,299 independent individuals. Seven inversions were associated with multiple diseases while inversions at 8p23.1, 16p11.2, and 11q13.2 were strongly associated with the co-occurrence of obesity with other common diseases. Transcriptome analysis across numerous tissues revealed strong candidate genes for obesity-related traits. Analyses in human pancreatic islets indicated the potential mechanism of inversions in the susceptibility of diabetes by disrupting the cis-regulatory effect of SNPs from their target genes. Our data underscore the role of inversions as major genetic contributors to the joint susceptibility to common complex diseases.
包括肥胖症、糖尿病、高血压、哮喘和抑郁症在内的几种常见疾病的负担在大多数世界人群中都在增加。然而,这些疾病之间存在大量流行病学和遗传相关性的潜在机制在很大程度上仍然未知。我们研究了常见的多态性倒位是否是这些疾病的共同遗传影响的基础。我们对总共 408898 名欧洲人进行了包含 21 个倒位和 25 个肥胖相关特征的倒位关联分析,并在 67299 名独立个体中验证了结果。七个倒位与多种疾病相关,而 8p23.1、16p11.2 和 11q13.2 上的倒位与肥胖与其他常见疾病同时发生的强烈相关。对多个组织的转录组分析揭示了与肥胖相关特征的强候选基因。在人类胰岛中的分析表明,倒位通过破坏 SNP 与其靶基因的顺式调控作用,从而导致糖尿病易感性的潜在机制。我们的数据强调了倒位作为常见复杂疾病共同易感性的主要遗传贡献者的作用。