The Predisposition for Type 2 Diabetes Mellitus and Metabolic Syndrome

被引:5
|
作者
Zenoaga-Barbarosie, C. [1 ]
Berca, L. [2 ]
Vassu-Dimov, T. [1 ]
Toma, M. [3 ]
Nica, M., I [4 ]
Alexiu-Toma, O. A. [1 ]
Ciornei, C. [5 ,6 ]
Albu, A. [6 ]
Nica, S. [6 ,7 ,11 ]
Nistor, C. [5 ,8 ]
Nica, R. [9 ,10 ]
机构
[1] Univ Bucharest, Dept Genet, Bucharest, Romania
[2] Natl Res & Dev Inst Food Bioresources IBA Buchares, Mol Biol Dept, Bucharest, Romania
[3] Cent Mil Emergency Hosp Dr Carol Davila, Emergency Dept, Bucharest, Romania
[4] Univ Med & Pharm Carol Davila, Bucharest, Romania
[5] Univ Med & Pharm Carol Davila, Preclin Dept, Bucharest, Romania
[6] Bucharest Emergency Univ Hosp, Emergency Dept, Bucharest, Romania
[7] Univ Med & Pharm Carol Davila, Clin Dept 4, Bucharest, Romania
[8] Cent Mil Emergency Hosp Dr Carol Davila, Thorac Surg, Bucharest, Romania
[9] Cent Mil Emergency Hosp Dr Carol Davila, Surg 2, Bucharest, Romania
[10] Univ Med & Pharm Carol Davila, Special Disciplines, Bucharest, Romania
[11] Bucharest Emergency Univ Hosp, Splaiul Independentei St,169, Bucharest 5, Romania
关键词
ACE ID; eNOS VNTR 4a; b; metabolic syndrome; OXTR (A > G); SOD1+35A; C; type 2 diabetes mellitus; ANGIOTENSIN-CONVERTING ENZYME; RECEPTOR GENE POLYMORPHISM; INSERTION/DELETION POLYMORPHISM; GENDER-DIFFERENCES; D-ALLELE; ACE-I/D; ASSOCIATION; OXYTOCIN; RISK; PATHOPHYSIOLOGY;
D O I
10.2478/bjmg-2023-0003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Type 2 diabetes mellitus (T2DM) and metabolic syndrome (MetS) are diseases caused by the interaction of genetic and non-genetic factors. Therefore, the aim of our study was to investigate the association between six common genetic polymorphisms and T2DM and MetS in males. A total of 120 T2DM, 75 MetS, and 120 healthy controls (HC) were included in the study. ACE ID, eNOS 4a/b, ATR1 A1166C, OXTR (A>G), SOD1 +35A/C, CAT-21A/T gene polymorphisms were genotyped by PCR or PCR-RFLP techniques. T2DM was diagnosed at an earlier age compared to MetS (54 vs 55 years old, p=0.0003) and the difference was greater in carriers of the OXTR G allele (54 vs 56 years old, p=0.0002) or both OXTR G and eNOS b alleles (54 vs 56, p=0.00016). The SOD1 AA genotype (O.R.=0.11, p=0.0006) and the presence of both ACE I and OXTR1 A (O.R.=0.39, p=0.0005) alleles revealed to be protective for T2DM. SOD1 AA and AC genotypes were protective factors for triglyceride (p=0.0002 and p=0.0005, respectively) and HDL cholesterol (p=0.0002 and p=0.0004, respectively) levels in T2DM patients. ACE DD was identified more frequently in hypertensive T2DM patients (O.R.=3.77, p=0.0005) and in those who reported drinking alcohol (p=0.0001) comparing to HC and T2DM patients who did not drink alcohol, respectively. We observed that T2DM patients who reported drinking alcohol had an increased frequency of ACE DD and eNOS bb (p<0.0001), or ACE DD and OXTR G (p<0.0001) compared to non-drinkers. No gene polymorphisms were associated with MetS.
引用
收藏
页码:21 / 26
页数:6
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