A 16-week study to compare the effect of vildagliptin versus gliclazide on postprandial lipoprotein concentrations and oxidative stress in patients with type 2 diabetes inadequately controlled with metformin monotherapy

被引:7
作者
Nasser Hissa, Marcelo R. [1 ]
Albuquerque Cavalcante, Lilian Loureiro [1 ]
Guimaraes, Sergio Botelho [2 ]
Hissa, Miguel Nasser [3 ]
机构
[1] Univ Fed Ceara, Dept Surg, Postgrad Program, Fortaleza, Ceara, Brazil
[2] Univ Fed Ceara, Dept Surg, LABCEX, Fortaleza, Ceara, Brazil
[3] Univ Fed Ceara, Dept Med, Diabet & Endocrine Metab Unit Res, Fortaleza, Ceara, Brazil
关键词
ACUTE GLUCOSE FLUCTUATIONS; PEPTIDASE-IV INHIBITOR; CORONARY-HEART-DISEASE; DRUG-NAIVE PATIENTS; NONFASTING TRIGLYCERIDES; RISK; MELLITUS; INSULIN; SITAGLIPTIN; EFFICACY;
D O I
10.1186/s13098-015-0058-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Diabetes is closely linked with coronary artery disease, either by means of direct effects of hyperglycemia, or indirectly by its frequent association with dyslipidemia. Any treatment for diabetes that has beyond the capacity of reduce glycated hemoglobin, the propensity to improve lipid profile and reduce weight will bring many benefits to patients. Method: We compare the effects of vildagliptin with the gliclazide on lipid profile before and after a standardized meal test, on glycemic control and oxidative stress in diabetic patients using metformin without adequate glycemic control. This is a prospective study of 16 weeks with diabetic patients using metformin without adequate glycemic control. Patients were randomized to receive gliclazide 30-120 mg/day or vildagliptin 100 mg/day. Results: 36 patients were randomized, with no loss of follow up. Regarding the lipid profile the difference observed at the end of the study was a higher HDL level in the vildagliptin group compared with gliclazide fasting (62.3 vs. 51.3 mg/dL, p = 0.021) and postprandial (62.9 vs. 51.1 mg/dL, p = 0.015). We also observed a variation of negative weight (decrease the end compared to the beginning) of the vildagliptin and a positive (increase) in the gliclazide (-0.3 vs. + 1.4 Kg, p = 0.048). The decrease in A1c was lower in the vildagliptin group compared to gliclazide (-1.7 vs.-2.3 %, P = 0.031), however there was no difference in the number of patients reaching target glycated hemoglobin < 7 % (50 vs. 61.1 %, p = 0.738). Only the group of vildagliptin presented at the end of the study compared to the beginning, decreased insulin values (599.6 vs. 705, 59 pg/ml, p = 0.021), glucagon (46.6 vs. 65, 2 pg/ml, p = 0.004) and the marker of oxidative stress TBARS (8.0 vs. 9.0 nmol MDA/ml, p = 0.035). Conclusion: Vildagliptin showed some advantages in addition to metformin in relation to addition of gliclazide. Patients treated with vildagliptin had a higher HDL at the end of the study, less variance in weight, reduced insulin and glucagon as well as reduction of oxidative stress.
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页数:7
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