Association between Angiotensin I-Converting Enzyme Insertion/Deletion Polymorphism and Prognosis of Kidney Transplantation: A Meta-Analysis
Author(s) -
Zhengkai Huang,
Bian Wu,
Jun Tao,
Zhijian Han,
Xiao Yang,
Lei Zhang,
Xuzhong Liu,
Zijie Wang,
Ruoyun Tan,
Min Gu,
Changjun Yin
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0127320
Subject(s) - transplantation , odds ratio , medicine , genotype , meta analysis , kidney transplantation , creatinine , renal function , angiotensin converting enzyme , confidence interval , kidney disease , gastroenterology , polymorphism (computer science) , renin–angiotensin system , endocrinology , biology , genetics , gene , blood pressure
Purpose Angiotensin I-converting enzyme (ACE) is crucial in the renin–angiotensin–aldosterone system. ACE insertion/deletion (I/D) polymorphism is a common genetic variation of this gene and is associated with several disease phenotypes. However, the results of published studies on the influence of this polymorphism on renal transplantation are inconsistent. Therefore, a meta-analysis was performed to evaluate the association between ACE I/D polymorphism and prognosis of kidney transplantation. Methods A meta-analysis was performed based on 21 case–control studies from 12 publications (1497 cases and 2029 controls) and 10 studies with quantitative values from 5 publications (814 patients). Pooled odds ratios (ORs) and weighted mean differences (WMDs) with their corresponding 95% confidence intervals (CIs) were used to estimate associations. Results ACE I/D polymorphism was found to be associated with acute rejection (AR) in genotypes DD+ID versus II (OR = 1.62, 95% CI = 1.14–2.29) and with serum creatinine concentration after renal transplantation in genotypes DD versus ID (WMD = 13.12, 95% CI = 8.09–18.16). Stratified analysis revealed that recipients transplanted within a year had higher serum creatinine concentrations in the DD versus ID model. No significant association was found between hypertension and ACE I/D polymorphism. Conclusion ACE I/D polymorphism is associated with AR and allograft function after kidney transplantation.
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