Hamid Ali-Bahar, Maysam Mard-Soltani, Yousef Paridar, Zahra Nasirbaghban, Z. Hashemi, Alireza Zakeri, S. Khalili
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引用次数: 0
摘要
背景:糖尿病视网膜病变(DR)是糖尿病(DM)的主要微血管并发症之一。研究表明,血管紧张素转换酶(ACE)基因多态性与DR进展相关。因此,阐明ACE基因多态性与DR发生风险之间的关系似乎非常重要。方法:将195例2型糖尿病(T2DM)患者分为有视网膜病变的病例组(99人)和无视网膜病变的对照组(96人)。眼科医生通过临床检查和荧光素血管造影筛查DR。不同的ACE基因型(II型、ID型和DD型)通过采集血样、提取DNA和使用特定引物进行PCR扩增进行鉴定。结果:病例组与对照组基因型频率分布差异有统计学意义(P = 0.009)。有趣的是,与DI和II基因型相比,拥有DD基因型的糖尿病患者患DR的可能性分别增加了约2.5倍(95% CI = 1.271 - 4.840, P = 0.007)和3.25倍(95% CI = 1.312 - 8.051, P = 0.01)。此外,拥有D等位基因的糖尿病人比拥有I等位基因的糖尿病人患DR的几率高1.75倍(95% CI = 1.167 - 2.623, P = 0.007)。结论:我们的研究结果支持了ACE基因DD基因型和D等位基因可能在DR发病机制中起作用的假设。
Distribution of DD Genotype of Angiotensin-Converting Enzyme Gene and Its Correlation with Diabetic Retinopathy
Background: One of the major microvascular complications of diabetes mellitus (DM) is diabetic retinopathy (DR). Studies have shown that angiotensin-converting enzyme (ACE) gene polymorphisms are correlated with DR progression. Accordingly, the elucidation of the association between ACE gene polymorphism and the risk of DR development seems to be highly crucial. Methods: In this study, 195 individuals with type 2 diabetes mellitus (T2DM) were classified as the case group with retinopathy (99 people) and control group without retinopathy (96 people). Screening for DR was performed by ophthalmologists using clinical examination and fluorescein angiography. Different ACE genotypes (II, ID, and DD) were identified by the collection of blood samples, extraction of DNA, and PCR amplification using specific primers. Results: The frequency distribution of genotypes was significantly different between the case and control groups (P = 0.009). Interestingly, possessing a DD genotype made diabetic patients approximately 2.5 folds (95% CI = 1.271 - 4.840, P = 0.007) and 3.25 folds (95% CI = 1.312 - 8.051, P = 0.01) more susceptible to DR when compared to having DI and II genotypes, respectively. Moreover, having a D allele made diabetic individuals nearly 1.75 folds (95% CI = 1.167 - 2.623, P = 0.007) more susceptible to DR than possessing an I allele. Conclusions: Our results potentiate the hypothesis that the DD genotype and D allele of the ACE gene might play a role in the pathogenesis of DR.