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斯洛文尼亚患者中血管紧张素转换酶/DD基因型与结节病易感性的关联。

Association of angiotensin-converting enzyme/DD genotype with sarcoidosis susceptibility in Slovenian patients.

作者信息

Salobir Barbara, Medica Igor, Tercelj Marjeta, Kastrin Andrej, Sabovic Miso, Peterlin Borut

机构信息

Department of Pulmonary Diseases and Allergy, University Medical Center, Ljubljana, Slovenia.

出版信息

Med Sci Monit. 2007 Dec;13(12):CR538-42.

Abstract

BACKGROUND

Sarcoidosis is a multisystemic chronic inflammatory disorder of unknown etiology with multifactorial genetic predisposition. An elevated ACE serum level is considered to be the activity marker of the disease. The involvement of the ACE I/D polymorphism in sarcoidosis susceptibility has been investigated in different populations, but results have been inconclusive. The purpose of this study was to evaluate the possible association of angiotensin-converting enzyme (ACE) gene insertion (I)/deletion (D) polymorphism with sarcoidosis in the Slovene population.

MATERIAL/METHODS: In 105 sarcoidosis patients (69 female, 36 male, mean age: 41+/-1 years) and in 80 sex- and age-matched control subjects, genotyping for the ACE gene I/D polymorphism was performed by PCR and restriction enzyme digestion.

RESULTS

An increased frequency of DD homozygotes vs. II homozygotes + ID heterozygotes was found in the group of sarcoidosis patients compared with the control group (OR: 2.19, 95%CI: 1.12-4.26, p=0.02). No differences in genotype frequencies were found in the group of sarcoidosis patients when considering the clinical course or presentation of the disease.

CONCLUSIONS

These results indicate that the ACE gene I/D polymorphism might be a risk factor for sarcoidosis susceptibility in the Slovene population and imply the possible role of population origin in the modulation of the influence of ACE gene variability in the pathophysiology of sarcoidosis.

摘要

背景

结节病是一种病因不明的多系统慢性炎症性疾病,具有多因素遗传易感性。血清血管紧张素转换酶(ACE)水平升高被认为是该疾病的活动标志物。不同人群中已对ACE I/D多态性与结节病易感性的关系进行了研究,但结果尚无定论。本研究的目的是评估斯洛文尼亚人群中血管紧张素转换酶(ACE)基因插入(I)/缺失(D)多态性与结节病之间可能存在的关联。

材料/方法:对105例结节病患者(69例女性,36例男性,平均年龄:41±1岁)和80例性别及年龄匹配的对照者,采用聚合酶链反应(PCR)和限制性内切酶消化法进行ACE基因I/D多态性基因分型。

结果

与对照组相比,结节病患者组中DD纯合子的频率相对于II纯合子+ID杂合子有所增加(比值比:2.19,95%置信区间:1.12 - 4.26,p = 0.02)。在考虑结节病患者组的临床病程或表现时,未发现基因型频率存在差异。

结论

这些结果表明,ACE基因I/D多态性可能是斯洛文尼亚人群中结节病易感性的一个危险因素,并暗示人群来源在调节ACE基因变异性对结节病病理生理学影响方面可能发挥的作用。

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