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Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
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Acta Endocrinologica (Buc)
Saremi L, Lotfipanah S, Feizy F, Ghaffari ME, Babaniamansour S, Saltanatpour Z
Association between PRO12ALa Polymorphism of PAR?2 Gene and Coronary Artery Disease in Iranian Population with Type Two Diabetes Mellitus
Acta Endo (Buc) 2022, 18 (2): 139-144doi: 10.4183/aeb.2022.139
Context. Coronary artery disease (CAD) is one
of the common diseases in patients with type two diabetes
mellitus (T2DM). The nuclear hormone receptor peroxisome
proliferator-activated receptor-gamma (PPARγ) plays a vital
role in dyslipidemia, and oxidative stress is involved in
atherogenesis.
Objective. The study aimed to determine the
association between Pro12Ala polymorphism of the PPARγ2
gene(rs1801282) and CAD risk in T2DM patients in the
Iranian population.
Design. A group of 145 T2DM patients with a
history of CAD were enrolled, together with 145 sex and
gender-matched individuals who had neither CAD nor
history of T2DM who were enrolled in a case-control study.
Subjects and Methods. Polymerase chain reactionrestriction
fragment length polymorphism technique was
applied to genotype the PPARγ2 gene polymorphisms.
Statistical analysis was done using SPSS version 22.
Results. CC and GC genotypes of Pro12Ala had a
higher frequency in the control and case groups, respectively.
The GC genotype was associated with a significantly
increased CAD risk compared to the CC genotype
(adjusted OR= 2.66, 95% CI = 1.5-29.5, p<0.01). The mean
triglycerides and total cholesterol level were significantly
higher in the CC genotype than the GC genotype in both
case and control groups (p<0.05). The mean level of fasting
blood glucose was significantly higher in the CC genotype
compared to GC genotype in the case group (p<0.05). The
mean of creatinine, lipid profiles, microalbuminuria, and
hemoglobin A1c had no significant difference between CC
and GC genotypes in both groups (p>0.05).
Conclusion. PPARγ2 Pro12Ala polymorphism
could be an essential indicator for the increased risk of CAD
in the Iranian people with T2DM.
Keywords: Coronary Artery Disease, Diabetes Mellitus, Diabetes Complications, Polymorphism, Genetic
Correspondence: Zohreh Saltanatpour, PhD, Tehran University of Medical Sciences, Pediatric Cell and Gene Therapy Research Center/
Stem Cell and Regenerative Medicine Center of Excellence, Tehran, Iran, E-mail: zohre_saltanatpour@yahoo.com