Angiotensin-I Converting Enzyme Insertion/deletion Polymorphism and Its Association with Diabetic Nephropathy: a Meta-analysis of Studies Reported Between 1994 and 2004 and Comprising 14,727 Subjects
Overview
Affiliations
Aims/hypothesis: The ACE insertion/deletion polymorphism has been examined for association with diabetic nephropathy over the past decade with conflicting results. To clarify this situation, we conducted a comprehensive meta-analysis encompassing all relevant studies that were published between 1994 and 2004 and investigated this potential genetic association.
Methods: A total of 14,727 subjects from 47 studies was included in this meta-analysis. Cases (n=8,663) were type 1 or 2 diabetic subjects with incipient (microalbuminuria) or advanced diabetic nephropathy (proteinuria, chronic renal failure, end-stage renal disease). Control subjects (n=6,064) were predominantly normoalbuminuric.
Results: No obvious publication bias was detected. Using a minimal-case definition based on incipient diabetic nephropathy, subjects with the II genotype had a 22% lower risk of diabetic nephropathy than carriers of the D allele (pooled odds ratio [OR]=0.78, 95% CI=0.69-0.88). While there was a reduced risk of diabetic nephropathy associated with the II genotype among Caucasians with either type 1 or type 2 diabetes, the association was most marked among type 2 diabetic Asians (Chinese, Japanese, Koreans) (OR=0.65, 95% CI=0. 51-0.83). This OR is significantly different from the OR of 0.90 (95% CI= 0.78-1.04) that was obtained for type 2 diabetic Caucasians (p=0.019). Using a stricter case definition based on advanced diabetic nephropathy, a comparable risk reduction of 24-32% was observed among the three subgroups, although statistical significance was reached only among Asians.
Conclusions/interpretation: The results of our meta-analysis support a genetic association of the ACE Ins/Del polymorphism with diabetic nephropathy. These findings may have implications for the management of diabetic nephropathy using ACE inhibitors especially among type 2 diabetic Asians.
Mohammedi K, Marre M, Alhenc-Gelas F Cardiovasc Diabetol. 2024; 23(1):453.
PMID: 39709470 PMC: 11662484. DOI: 10.1186/s12933-024-02544-0.
Kovacevic S, Zdravkovic V, Blagojevic J, Djordjevic S, Miolski J, Gasic V PLoS One. 2024; 19(10):e0312489.
PMID: 39446857 PMC: 11500908. DOI: 10.1371/journal.pone.0312489.
New insights on genetic background of major diabetic vascular complications.
Tariq Z, Abusnana S, Mussa B, Zakaria H Diabetol Metab Syndr. 2024; 16(1):243.
PMID: 39375805 PMC: 11457557. DOI: 10.1186/s13098-024-01473-y.
Kiconco R, Kalyesubula R, Kiwanuka G Diabetes Metab Syndr Obes. 2024; 17:2211-2220.
PMID: 38854447 PMC: 11162639. DOI: 10.2147/DMSO.S462740.
Ahmad H, Khan H, Haque S, Ahmad S, Srivastava N, Khan A J Renin Angiotensin Aldosterone Syst. 2023; 2023:7890188.
PMID: 37389408 PMC: 10307051. DOI: 10.1155/2023/7890188.