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结节病的流行病学:最新进展与未来展望

Epidemiology of sarcoidosis: recent advances and future prospects.

作者信息

Rybicki Benjamin A, Iannuzzi Michael C

机构信息

Department of Biostatistics and Research Epidemiology, Henry Ford Health System, Detroit, Michigan 48202, USA.

出版信息

Semin Respir Crit Care Med. 2007 Feb;28(1):22-35. doi: 10.1055/s-2007-970331.

Abstract

Sarcoidosis is by definition a disease of "unknown causes," but recent epidemiologic advances suggest that the long-standing definition of sarcoidosis may soon need to be amended. The recently completed ACCESS (A Case-Control Etiologic Study of Sarcoidosis) study was not able to definitively identify the "cause" of sarcoidosis, but yielded important findings regarding familial and environmental risks that have advanced our understanding of this disease. The HLA-DRB1 associations reported in ACCESS along with the results of two recently completed genome scans of sarcoidosis in German Caucasians and African-Americans, respectively, have further defined the genetics of sarcoidosis. These studies suggest genetic heterogeneity of sarcoidosis risk between Caucasians and African-Americans and multiple susceptibility genes that interact together and with environmental factors in the disease pathogenesis. Genes that influence sarcoidosis clinical phenotypes may also be largely separate from sarcoidosis susceptibility genes. Although genetic studies of sarcoidosis in African-American populations are confounded by Caucasian admixture, this same admixture may be useful in identifying sarcoidosis genes linked with African ancestry. Case-only methods may be useful in identifying recent acute exposures linked to disease, genetic variants of risk, and gene-environment interactions. In summary, the epidemiology of sarcoidosis has a promising future that should eventually provide the answers to the etiologic origins of this complex disease.

摘要

根据定义,结节病是一种“病因不明”的疾病,但最近的流行病学进展表明,结节病的长期定义可能很快需要修订。最近完成的ACCESS(结节病病例对照病因学研究)研究未能明确确定结节病的“病因”,但得出了有关家族和环境风险的重要发现,这些发现推进了我们对这种疾病的理解。ACCESS报告的HLA-DRB1关联以及最近分别在德国白种人和非裔美国人中完成的两项结节病基因组扫描结果,进一步明确了结节病的遗传学特征。这些研究表明,白种人和非裔美国人在结节病风险方面存在遗传异质性,并且存在多个易感基因,它们在疾病发病机制中相互作用并与环境因素相互作用。影响结节病临床表型的基因可能也在很大程度上与结节病易感基因不同。尽管非裔美国人人群中结节病的遗传研究因白种人基因混合而受到干扰,但这种相同的基因混合可能有助于识别与非洲血统相关的结节病基因。仅病例研究方法可能有助于识别与疾病相关的近期急性暴露、风险的基因变异以及基因-环境相互作用。总之,结节病的流行病学前景广阔,最终应该能够为这种复杂疾病的病因起源提供答案。

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