Kumar Subodh, Pathak Anuj Kumar, Saikia Dibyajyoti, Kumar Amish
Assistant Professor, Department of Pharmacology, SRMSIMS , Bareilly, UP, India .
Senior Resident, Department of Pharmacology, IGIMS , Patna, India .
J Clin Diagn Res. 2015 Dec;9(12):FC07-10. doi: 10.7860/JCDR/2015/17027.6888. Epub 2015 Dec 1.
Metformin is a preferred drug for starting treatment in type 2 diabetes mellitus. But, eventually most of the patients need additional drug to control blood sugar level. The choice of drug depends upon several factors including patient specific criteria, economical factors and treatment satisfaction.
The aim of the present study is to investigate the effects of adding sitagliptin or glimepiride on efficacy, safety and treatment satisfaction in patients with type 2 diabetes mellitus.
It was a retrospective observational study on 50 patients each in sitagliptin and glimepiride group, who are receiving treatment for at least 12 weeks and are stable on respective treatment regimen. Glycated haemoglobin (HBA1c) was the primary measure of efficacy. Safety was assessed by checking weight gain/loss, hypoglycaemia episodes and other laboratory investigations. Patient satisfaction was assessed by Diabetes Treatment Satisfaction Questionnaire.
The HbA1c level after 12-24 weeks of treatment was not found to be significant compared to each other or from baseline. Compared to baseline fasting plasma glucose & postprandial plasma glucose were lower in glimepiride group. Sitagliptin was associated with less episodes of hypoglycaemia. Weight gain was associated with glimepiride but it was non-significant (p=0.08). Overall treatment satisfaction score were better for sitagliptin but were not statistically significant.
The efficacy of sitagliptin was comparable. Sitagliptin had superior adverse effect profile with less chances of hypoglycaemia and weight gain. Questionnaire scores were higher for sitagliptin indicating better treatment satisfaction compared to glimepiride.
二甲双胍是2型糖尿病起始治疗的首选药物。但最终,大多数患者需要加用其他药物来控制血糖水平。药物的选择取决于多个因素,包括患者的具体情况、经济因素和治疗满意度。
本研究旨在探讨加用西格列汀或格列美脲对2型糖尿病患者疗效、安全性及治疗满意度的影响。
这是一项回顾性观察研究,西格列汀组和格列美脲组各50例患者,他们接受治疗至少12周且各自治疗方案稳定。糖化血红蛋白(HbA1c)是疗效的主要衡量指标。通过检查体重增加/减轻、低血糖发作及其他实验室检查来评估安全性。通过糖尿病治疗满意度问卷评估患者满意度。
治疗12 - 24周后,两组间及与基线相比,HbA1c水平无显著差异。与基线相比,格列美脲组空腹血糖和餐后血糖较低。西格列汀与低血糖发作次数较少相关。体重增加与格列美脲有关,但无统计学意义(p = 0.08)。西格列汀的总体治疗满意度评分更好,但无统计学意义。
西格列汀的疗效相当。西格列汀具有更优的不良反应谱,低血糖和体重增加的几率更低。西格列汀的问卷评分更高,表明与格列美脲相比治疗满意度更高。