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将基因组置于背景之中:2型糖尿病中的基因-环境相互作用

Putting the Genome in Context: Gene-Environment Interactions in Type 2 Diabetes.

作者信息

Franks Paul W, Paré Guillaume

机构信息

Genetic and Molecular Epidemiology Unit, Lund University Diabetes Center, Department of Clinical Sciences, Clinical Research Center, Skåne University Hospital Malmö, Lund University, Building 91, Level 10, Jan Waldenströms gata 35, 205 02, Malmö, Sweden.

Department of Public Health and Clinical Medicine, Umeå University, 90188, Umeå, Sweden.

出版信息

Curr Diab Rep. 2016 Jul;16(7):57. doi: 10.1007/s11892-016-0758-y.

Abstract

The genome is often the conduit through which environmental exposures convey their effects on health and disease. Whilst not all diseases act by directly perturbing the genome, the phenotypic responses are often genetically determined. Hence, whilst diseases are often defined has having differing degrees of genetic determination, genetic and environmental factors are, with few exceptions, inseparable features of most diseases, not least type 2 diabetes. It follows that to optimize diabetes, prevention and treatment will require that the etiological roles of genetic and environmental risk factors be jointly considered. As we discuss here, studies focused on quantifying gene-environment and gene-treatment interactions are gathering momentum and may eventually yield data that helps guide health-related choices and medical interventions for type 2 diabetes and other complex diseases.

摘要

基因组常常是环境暴露对健康和疾病产生影响的传导途径。虽然并非所有疾病都是通过直接干扰基因组起作用,但表型反应往往由基因决定。因此,尽管疾病通常被定义为具有不同程度的基因决定性,但除了少数例外情况,遗传和环境因素是大多数疾病,尤其是2型糖尿病不可分割的特征。由此可见,为了优化糖尿病的预防和治疗,需要共同考虑遗传和环境风险因素的病因学作用。正如我们在此所讨论的,专注于量化基因-环境和基因-治疗相互作用的研究正在兴起,最终可能会产生有助于指导2型糖尿病和其他复杂疾病的健康相关选择及医疗干预的数据。

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