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内皮型一氧化氮合酶基因G894T多态性、勃起功能障碍及相关危险因素之间的关联。

The associations among eNOS G894T gene polymorphism, erectile dysfunction and related risk factors.

作者信息

Lee Yung-Chin, Huang Chun-Hsiung, Wang Chii-Jye, Liu Chia-Chu, Wu Wen-Jeng, Chang Lin-Li, Lin Hui-Hui

机构信息

Departments of Urology, Kaohsiung Medical University Hospital, and Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung, Taiwan.

出版信息

BJU Int. 2007 Nov;100(5):1116-20. doi: 10.1111/j.1464-410X.2007.07110.x. Epub 2007 Sep 14.

Abstract

OBJECTIVE

To investigate the possible correlations among eNOS G894T polymorphism, erectile dysfunction (ED) and related risk factors in a Taiwanese population.

MATERIALS AND METHODS

In all, 151 patients with ED and 77 healthy controls were enrolled. All the men had a complete clinical history taken and laboratory data was collected. To assess erectile conditions the five-item version of the International Index of Erectile Function (IIEF-5) was used. The eNOS G894T polymorphisms were determined using the polymerase chain reaction-restriction fragment length polymorphism method.

RESULTS

In all, 228 men were enrolled with a mean (sd) age of 58.6 (9.7) years. In a univariate analysis, age, serum testosterone level, and the prevalence of diabetes mellitus (DM) and hypertension were significantly different between patients with ED and the healthy controls (P < 0.01). In the multiple logistic regression analysis, DM, age and hypogonadism were three independent risk factors for ED (P = 0.018, P = 0.046 and P = 0.016, respectively). The prevalence of ED in T allele carriers (GT/TT) was significantly greater than in G allele carriers (GG; 80.0% vs 63.3%, P = 0.04). Also the eNOS 894T allele carriers had significantly lower IIEF-5 scores than the eNOS 894G allele carriers, at 13.2 (5.3) vs 15.7 (6.1) (P = 0.01) and it was associated with increment of T allele number (11.0 (5.6) vs 13.6 (5.2) vs 15.7 (6.1); P = 0.03).

CONCLUSION

Our results indicate that DM, age and hypoganadism are three significant independent risk factors for ED. Also, in the Taiwanese population, the eNOS 894T allele carriers are at greater risk of ED, both in prevalence and severity, and this might be a factor of genetic susceptibility.

摘要

目的

探讨台湾人群中内皮型一氧化氮合酶(eNOS)G894T基因多态性、勃起功能障碍(ED)及相关危险因素之间的可能关联。

材料与方法

共纳入151例ED患者和77例健康对照者。所有男性均有完整的临床病史记录,并收集实验室数据。采用国际勃起功能指数(IIEF-5)五项版本评估勃起状况。使用聚合酶链反应-限制性片段长度多态性方法测定eNOS G894T基因多态性。

结果

共纳入228名男性,平均(标准差)年龄为58.6(9.7)岁。单因素分析显示,ED患者与健康对照者在年龄、血清睾酮水平、糖尿病(DM)患病率和高血压患病率方面存在显著差异(P<0.01)。多因素逻辑回归分析显示,DM、年龄和性腺功能减退是ED的三个独立危险因素(分别为P = 0.018、P = 0.046和P = 0.016)。T等位基因携带者(GT/TT)的ED患病率显著高于G等位基因携带者(GG;80.0%对63.3%,P = 0.04)。此外,eNOS 894T等位基因携带者的IIEF-5评分显著低于eNOS 894G等位基因携带者,分别为13.2(5.3)对15.7(6.1)(P = 0.01),且与T等位基因数量增加相关(11.0(5.6)对13.6(5.2)对15.7(6.1);P = 0.03)。

结论

我们的结果表明,DM、年龄和性腺功能减退是ED的三个重要独立危险因素。此外,在台湾人群中,eNOS 894T等位基因携带者患ED的风险在患病率和严重程度上均更高,这可能是遗传易感性的一个因素

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