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1型糖尿病患者肾病及相关心血管疾病的遗传易感性:血管紧张素转换酶(ACE)及其他因素的作用;一篇综述

Genetic predisposition to nephropathy and associated cardiovascular disease in people with type 1 diabetes: role of the angiotensinI-converting enzyme (ACE), and beyond; a narrative review.

作者信息

Mohammedi Kamel, Marre Michel, Alhenc-Gelas François

机构信息

INSERM U1034, Biology of Cardiovascular Diseases, Bordeaux University Hospital, 33000, Bordeaux, France.

Department of Endocrinology, Diabetes, and Nutrition, Hôpital Haut-Lévêque, Avenue de Magellan, 33604, Pessac Cedex, France.

出版信息

Cardiovasc Diabetol. 2024 Dec 21;23(1):453. doi: 10.1186/s12933-024-02544-0.

Abstract

Hypertension, cardiovascular disease and kidney failure are associated with persistent hyperglycaemia and the subsequent development of nephropathy in people with diabetes. Diabetic nephropathy is associated with widespread vascular disease affecting both the kidney and the heart from an early stage. However, the risk of diabetic nephropathy in people with type 1 diabetes is strongly genetically determined, as documented in familial transmission studies. The search for the underlying genes has been extensive, using specific hypotheses, sibling linkage studies and genome-wide association studies (GWAS). The role of the angiotensinI-converting enzyme/kininase II (ACE) gene and genetic variability in ACE levels as a susceptibility and prognostic factor for diabetic nephropathy has been well documented in people with type 1 diabetes. The ACE gene insertion/deletion polymorphism, which is associated with plasma and tissue ACE levels, has been the most studied genomic variant in diabetic nephropathy. Recently, this polymorphism has also been associated with longevity in people with type 1 diabetes. The ACE I/D polymorphism has also been associated with vascular, extra-renal complications including myocardial infarction and lower-limb amputation in this population. Other genes and loci have been identified in linkage studies and GWAS, such as the COL4A3 gene or a region on chromosome 3q with the adiponectin gene. Replication was not always attempted and was rarely achieved, even for GWAS. Overall, effect sizes remain modest and no major gene has been identified, despite the strength of the genetic effect in transmission studies. We searched bibliographic databases for studies reporting genomic variants associated with diabetic nephropathy and meta-analyses of such studies. We selected important relevant studies for further discussion in this narrative review. This brief review attempts to summarise the current knowledge on the genetics of diabetic nephropathy and associated cardiovascular disease in people with type 1 diabetes, and discusses some conceptual and methodological issues relevant to the interpretation of past studies and the design of future ones.

摘要

高血压、心血管疾病和肾衰竭与持续性高血糖以及糖尿病患者随后发生的肾病有关。糖尿病肾病与早期影响肾脏和心脏的广泛血管疾病有关。然而,正如家族性传播研究所记录的那样,1型糖尿病患者发生糖尿病肾病的风险在很大程度上由基因决定。人们已经广泛地寻找潜在基因,采用了特定假设、同胞连锁研究和全基因组关联研究(GWAS)。血管紧张素I转换酶/激肽酶II(ACE)基因的作用以及ACE水平的遗传变异性作为糖尿病肾病的易感性和预后因素,在1型糖尿病患者中已有充分记录。与血浆和组织ACE水平相关的ACE基因插入/缺失多态性,是糖尿病肾病中研究最多的基因组变异。最近,这种多态性也与1型糖尿病患者的长寿有关。在该人群中,ACE I/D多态性还与血管、肾外并发症有关,包括心肌梗死和下肢截肢。在连锁研究和GWAS中还发现了其他基因和基因座,如COL4A3基因或3号染色体q臂上与脂联素基因相关的区域。即使对于GWAS,也并非总是尝试进行重复研究,而且很少能实现重复。总体而言,尽管在传播研究中遗传效应很强,但效应大小仍然适中,尚未确定主要基因。我们在文献数据库中搜索了报告与糖尿病肾病相关的基因组变异的研究以及此类研究的荟萃分析。我们选择了重要的相关研究,以便在本叙述性综述中进行进一步讨论。这篇简短的综述试图总结目前关于1型糖尿病患者糖尿病肾病和相关心血管疾病遗传学的知识,并讨论一些与解释过去研究和设计未来研究相关的概念和方法问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c137/11662484/834fbbd942fd/12933_2024_2544_Figa_HTML.jpg

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