POLYMORPHISM OF THE ANGIOTENSIN-CONVERTING ENZYME (ACE) GENE IN INDIVIDUALS WITH TYPE 2 DIABETES AND CHRONIC KIDNEY DISEASE
Y.A. Saienko1,2, D.S. Krasnenkov1, K.K. Midlovets1, V.V. Korcheva1, Y.E. Rebrova1,3, D.D. Yepishyna1, B.M. Mankovsky1
- State Institution “D.F. Chebotarev Institute of Gerontology, National Academy of Medical Sciences of Ukraine”, Kyiv, Ukraine
- State Institution “Center for Cardiology and Cardiac Surgery of the Ministry of Health of Ukraine”, Kyiv, Ukraine
- P.L. Shupyk National University of Health Care of Ukraine, Kyiv, Ukraine
DOI: https://doi.org/10.15407/fz71.03.037

Abstract
Chronic kidney disease (CKD) is one of the most common
complications of type 2 diabetes mellitus (T2DM), signifi-
cantly increasing the risk of cardiovascular events and mortal-
ity. One of the key mechanisms in the pathogenesis of CKD
is the activation of the renin-angiotensin-aldosterone system,
in which the angiotensin-converting enzyme (ACE) plays a
central role. Genetic variations in the ACE1 gene, particu-
larly the insertion/deletion (I/D) polymorphism (rs4646994),
may influence ACE activity and thus affect susceptibility to
diabetes-related complications. The aim of this study was to
investigate the association between the ACE1 I/D polymor-
phism and the presence of CKD in patients with T2DM, as well
as to assess the potential protective effect of specific alleles.
A total of 174 individuals were examined: 134 patients with
T2DM (78 with CKD and 56 without CKD) and 40 healthy
controls. Genotyping of the ACE1 I/D polymorphism was
performed using real-time polymerase chain reaction (PCR)
with melting curve analysis. Genotype and allele frequencies
were analyzed, Hardy–Weinberg equilibrium was assessed,
odds ratios (ORs) were calculated, and the Cochran–Armitage
test for trend was applied. No statistically significant differ -
ences in genotype or allele frequencies were found between
T2DM patients (with or without CKD) and the control group.
However, a trend toward a higher frequency of the D allele
in the control group was observed. The calculated OR sug-
gested a potentially protective effect of the D allele against the
development of T2DM (OR = 0.458). Thus, within the scope
of this study, no significant association was found between the
ACE1 polymorphism and the presence of CKD in patients with
T2DM. The observed trend toward a protective role of the D
allele against T2DM warrants further investigation in larger
population-based samples.
Keywords:
type 2 diabetes mellitus; chronic kidney disease; angiotensin-converting enzyme; ACE1; I/D polymorphism; genetic association
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