血管紧张素转化酶插入/缺失多态性与中国人银屑病易感性的关系。
Angiotensin-converting enzyme insertion/deletion polymorphism and susceptibility to psoriasis in a Chinese population.
机构信息
1Department of Pathology, College of Basic Medical Sciences, Central South University, China.
出版信息
J Renin Angiotensin Aldosterone Syst. 2014 Mar;15(1):39-43. doi: 10.1177/1470320313494433. Epub 2013 Jul 11.
INTRODUCTION
The relationship between the angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism and psoriasis has previously been studied mainly in Caucasians and only once in Asians. The aim of this study is to evaluate the association between the ACE I/D polymorphism and the risk of psoriasis in a Chinese population.
MATERIALS AND METHODS
The study population consisted of 668 psoriasis patients and 668 matched control subjects. The ACE I/D gene polymorphism was analyzed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).
RESULTS
The frequency of the ACE II genotype (odds ratio (OR) = 1.32, 95% confidence interval (CI) = 1.06, 1.63; P = 0.01) and I allele (OR = 1.25, 95% CI = 1.06, 1.48; P = 0.01) in patients with psoriasis was significantly higher than that in the control group. And the D allele frequency in patients with psoriasis was significantly lower (OR = 0.80, 95% CI = 0.68, 0.95; P = 0.01) than that in the control group. When stratified by family history, the frequency of the DD genotype was marginally significantly lower in patients with a positive family history of psoriasis (familial psoriasis) than in those with negative (sporadic psoriasis) (OR = 0.47, 95% CI = 0.23, 0.97; P = 0.04). When stratified by onset of the disease, type of psoriasis and the severity of psoriasis, no statistically significant result was observed.
CONCLUSION
Our study suggested that the ACE II genotype and I allele might confer susceptibility to psoriasis in a Chinese population.
简介
血管紧张素转换酶(ACE)插入/缺失(I/D)多态性与银屑病之间的关系此前主要在白种人群中进行了研究,而在亚洲人群中仅研究过一次。本研究旨在评估 ACE I/D 多态性与中国人群银屑病发病风险之间的相关性。
材料与方法
研究人群包括 668 例银屑病患者和 668 名匹配的对照者。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析 ACE I/D 基因多态性。
结果
银屑病患者 ACE II 基因型(比值比(OR)=1.32,95%置信区间(CI)=1.06,1.63;P=0.01)和 I 等位基因(OR=1.25,95%CI=1.06,1.48;P=0.01)的频率明显高于对照组。银屑病患者 D 等位基因的频率明显较低(OR=0.80,95%CI=0.68,0.95;P=0.01)。按家族史分层时,阳性家族史(家族性银屑病)患者的 DD 基因型频率明显低于阴性家族史(散发型银屑病)患者(OR=0.47,95%CI=0.23,0.97;P=0.04)。按发病年龄、银屑病类型和疾病严重程度分层时,未观察到统计学显著结果。
结论
本研究提示 ACE II 基因型和 I 等位基因可能使中国人易患银屑病。