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结节病遗传学的进展。

Advances in the genetics of sarcoidosis.

作者信息

Smith G, Brownell I, Sanchez M, Prystowsky S

机构信息

Department of Medicine, Beth Israel Medical Center, Albert Einstein College of Medicine, New York, NY, USA.

出版信息

Clin Genet. 2008 May;73(5):401-12. doi: 10.1111/j.1399-0004.2008.00970.x. Epub 2008 Feb 26.

Abstract

Sarcoidosis is an uncommon disease of granulomatous inflammation. Genetic predisposition to sarcoidosis is indicated by observations of familial clustering, increased concordance in monozygotic twins over other siblings, and variations in susceptibility and disease presentation among different ethnic groups. Published studies on sarcoidosis have investigated a variety of genetic associations. These studies used techniques ranging from classic human lymphocyte antigen genotype correlations to genome-wide linkage scans. Results have both supported and refuted disease associations with a number of genes potentially involved in the pathogenesis of sarcoidosis. Here, we review representative studies concerning the genetics of sarcoidosis. While investigations to date have failed to identify a unifying genetic signature associated with sarcoidosis, numerous studies have identified genetic associations with disease subtypes or within specific populations. These studies suggest that genetic susceptibility to sarcoidosis is complex and polygenic in nature. Future studies will help clarify the genetics of sarcoidosis and allow for the development of diagnostic, prognostic and therapeutic technologies.

摘要

结节病是一种罕见的肉芽肿性炎症疾病。家族聚集现象、同卵双胞胎相较于其他兄弟姐妹更高的一致性,以及不同种族群体在易感性和疾病表现上的差异,都表明结节病存在遗传易感性。已发表的关于结节病的研究调查了多种基因关联。这些研究使用的技术范围从经典的人类淋巴细胞抗原基因型相关性分析到全基因组连锁扫描。研究结果既支持也反驳了与一些可能参与结节病发病机制的基因的疾病关联。在此,我们回顾有关结节病遗传学的代表性研究。尽管迄今为止的调查未能确定与结节病相关的统一基因特征,但众多研究已确定了与疾病亚型或特定人群相关的基因关联。这些研究表明,结节病的遗传易感性本质上是复杂的且具有多基因性。未来的研究将有助于阐明结节病的遗传学,并推动诊断、预后和治疗技术的发展。

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