Domínguez-Pérez Mayra, Jacobo-Albavera Leonor, Canizales-Quinteros Samuel, Villarreal-Molina Ma Teresa
Laboratorio de Genómica de Enfermedades Cardiovasculares, Instituto Nacional de Medicina Genómica.
Unidad de Genómica de Poblaciones Aplicada a la Salud, Departamento de Biología, Facultad de Química, Universidad Nacional Autónoma de México e Instituto Nacional de Medicina Genómica. Mexico City, Mexico.
Gac Med Mex. 2025;161(1):66-74. doi: 10.24875/GMM.24000415.
Understanding the genetic architecture of complex disease has helped identify at risk individuals, new pathways involved in pathophysiology, and potential pharmacological targets for prevention and/or treatment. Thus, the identification of susceptibility variants of Native American or Mexican origin can potentially benefit any patient, regardless of ethnic origin. The purpose of this review is to provide an overview of the most relevant contributions of Mexican researchers to knowledge on genomics of cardiometabolic disease in the Mexican population, including ethnic-specific variants and population genomics studies, stressing the importance of evolutionary approaches in understanding complex disease. Collaborative efforts and large long-term cohort studies including genomic, multi-omic, fine phenotyping and environmental exposure data are necessary to identify the clinical relevance of these variants and how they interact with the environment, in order to apply this knowledge to personalized medicine.
了解复杂疾病的遗传结构有助于识别高危个体、参与病理生理学的新途径以及预防和/或治疗的潜在药理学靶点。因此,识别具有美洲原住民或墨西哥血统的易感性变异可能会使任何患者受益,无论其种族出身如何。本综述的目的是概述墨西哥研究人员对墨西哥人群心脏代谢疾病基因组学知识的最相关贡献,包括种族特异性变异和群体基因组学研究,强调进化方法在理解复杂疾病中的重要性。为了将这些知识应用于个性化医疗,需要开展合作研究以及大型长期队列研究,包括基因组、多组学、精细表型分析和环境暴露数据,以确定这些变异的临床相关性以及它们如何与环境相互作用。