Why the study?
Does the concomitant presence of ACE D and eNOS T alleles increase the risk of macroalbuminuria in patients with type 2 diabetes mellitus?
Does the concomitant presence of ACE D and eNOS T alleles increase the risk of macroalbuminuria in patients with type 2 diabetes mellitus?
The concomitant presence of ACE D and eNOS T alleles is associated with an increased risk of macroalbuminuria in T2DM patients, suggesting a synergistic genetic predisposition to diabetic nephropathy.
No immediate clinical implications in T2DM; leaves open synergistic genetic effects on nephropathy progression.
AIM: The present study investigated the influence of insertion (I)/deletion (D) polymorphism of the angiotensin II-converting enzyme (ACE) gene in combination with endothelial nitric oxide (eNOS) G894T polymorphism on the predisposition to diabetic nephropathy (DN). METHODS: Using polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism (PCR-RFLP) method, the ACE and eNOS polymorphisms were genotyped in 72 microalbuminuric, 68 macroalbuminuric and 72 normoalbuinuric type 2 diabetes mellitus (T2DM) patients from Western Iran. RESULTS: The presence of eNOS T or ACE D allele was not associated with increased risk of macroalbuminuria (odds ratio (OR) = 1.36, P = 0.27 and OR = 1.6, P = 0.062, respectively). However, in the presence of both alleles there was a trend towards increased risk of macroalbuminuria (fivefold, P = 0.05). CONCLUSION: Our study indicates that the concomitant presence of both ACE D and eNOS T alleles tends to be associated with an elevation risk of macroalbuminuria compared with the presence of each polymorphism alone. This risk could be attributed to the increasing activity of ACE and angiotensin II level in the presence of D allele and decreasing NO production in the presence of T allele accelerating diabetic nephropathy.
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Rahimi et al. (2011) studied this question.
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