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银屑病关节炎患者的血管紧张素转换酶基因多态性

Angiotensin-converting enzyme gene polymorphism in patients with psoriatic arthritis.

作者信息

Al-Awadhi Adel M, Hasan Eman A, Sharma Prem N, Haider M Zafaryab, Al-Saeid Khaled

机构信息

Department of Medicine, Faculty of Medicine, Kuwait University, P.O. Box: 24923, Al-Safat, 13110, Kuwait.

出版信息

Rheumatol Int. 2007 Oct;27(12):1119-23. doi: 10.1007/s00296-007-0349-y. Epub 2007 Apr 14.

Abstract

To investigate the frequency of angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism genotypes in adults with psoriatic arthritis (PsA), a heterogeneous chronic disease with autoimmune pathology. ACE gene I/D polymorphism influences the plasma and tissue levels of ACE and has an involvement in inflammatory mechanism. The frequency of ACE gene I/D polymorphism genotypes was determined in 51 adults with PsA from Kuwait, and compared to that in 100 ethnically matched healthy controls using polymerase chain reaction. The distribution of ACE I/D polymorphism and allele frequencies in PsA patients were not significantly different from controls (P > 0.05). Further analyses of PsA patients showed that ACE I/D gene polymorphism was not associated with family history, clinical manifestations, and disease severity. However, the frequency of II genotype was significantly higher in patients with late disease onset than in those with early onset (25 vs. 3%; P = 0.04). No difference was found between the distribution of the ACE genotype in PsA patients and the general population in Kuwait. However, the presence of II genotype may confer susceptibility to the development of late onset PsA.

摘要

为了研究血管紧张素转换酶(ACE)基因插入/缺失(I/D)多态性基因型在银屑病关节炎(PsA)成年患者中的频率,银屑病关节炎是一种具有自身免疫病理的异质性慢性疾病。ACE基因I/D多态性影响ACE的血浆和组织水平,并参与炎症机制。采用聚合酶链反应测定了51例科威特成年PsA患者的ACE基因I/D多态性基因型频率,并与100例种族匹配的健康对照者进行比较。PsA患者中ACE I/D多态性和等位基因频率的分布与对照组无显著差异(P>0.05)。对PsA患者的进一步分析表明,ACE I/D基因多态性与家族史、临床表现和疾病严重程度无关。然而,疾病发病较晚的患者中II基因型的频率显著高于发病较早的患者(25%对3%;P=0.04)。PsA患者的ACE基因型分布与科威特普通人群之间未发现差异。然而,II基因型的存在可能使患者易患晚发型PsA。

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