ACE gene polymorphism and its association with serum erythropoietin and hemoglobin ‎in Iraqi hemodialysis patients.

The Application of Clinical Genetics Pub Date : 2019-07-01 eCollection Date: 2019-01-01 DOI:10.2147/TACG.S198992
Mohanad Yasir Al-Radeef, Hayder Adnan Fawzi, Ali Abdulmajid Allawi
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引用次数: 9

Abstract

Purpose: To evaluate the frequencies of angiotensin-converting enzyme gene ‎polymorphism in ‎Iraqi hemodialysis patients and to examine the association ‎between this polymorphism and ‎serum erythropoietin and hemoglobin levels.‎.

Methods: In this study, 70 chronic renal failure Iraqi patients on ‎maintenance ‎hemodialysis (patient group) and 20 healthy subjects (control ‎group) were genotyped for ‎angiotensin-converting enzyme gene polymorphism. The distribution of genotype and allele ‎frequencies of this polymorphism in ‎these subjects were also evaluated.‎.

Results: The distribution of angiotensin-converting enzyme genotypes between ‎groups was ‎similar, and the ID genotype was the most frequent, followed by DD and II ‎genotypes (‎50%‎, ‎37%‎, and ‎13%). The control group ‎had a nonsignificant difference in serum ‎erythropoietin levels among different angiotensin-converting enzyme genotypes, ‎while patients with ID and DD genotypes displayed significant ‎elevation in ‎serum erythropoietin with time. No significant differences in hemoglobin ‎levels ‎were observed in patient and control groups. A significant positive correlation ‎was ‎observed between serum erythropoietin and hemoglobin in the control group ‎with different ‎angiotensin-converting enzyme genotypes, while a nonsignificant ‎negative correlation was ‎observed in the patient group throughout the study. ‎.

Conclusions: Chronic kidney disease did not significantly alter angiotensin-converting enzyme ‎genotypes, and angiotensin-converting enzyme gene ‎polymorphism had a significant effect on ‎serum erythropoietin levels and a non‎significant effect on hemoglobin levels. ‎.

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伊拉克血液透析患者ACE基因多态性及其与血清促红细胞生成素和血红蛋白的关系
目的:评价伊拉克血液透析患者血管紧张素转换酶基因多态性的频率,并探讨这种多态性与血清促红细胞生成素和血红蛋白水平的关系。方法:对70例进行维持性血液透析的伊拉克慢性肾衰竭患者(患者组)和20例健康者(对照组)进行血管紧张素转换酶基因多态性分型。并对该多态性的基因型分布和等位基因频率进行了分析。结果:血管紧张素转换酶基因型在不同组间分布相似,以ID基因型最多,其次是DD和II基因型(分别占50%、37%和13%)。对照组不同血管紧张素转换酶基因型患者血清促红细胞生成素水平差异不显著,而ID和DD基因型患者血清促红细胞生成素水平随时间显著升高。患者与对照组血红蛋白水平无显著差异。不同血管紧张素转换酶基因型的对照组血清促红细胞生成素和血红蛋白呈显著正相关,而在整个研究过程中,患者组血清促红细胞生成素和血红蛋白呈不显著负相关。‎。结论:慢性肾病对血管紧张素转换酶基因型无显著影响,血管紧张素转换酶基因多态性对血清促红细胞生成素水平有显著影响,对血红蛋白水平无显著影响。‎。
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