College of Pharmacy, Taibah University, Medina, Al-Madinah Munawarah, Saudi Arabia.
Pharmacotherapy Research Group, Islamabad, Pakistan.
Cardiovasc Diabetol. 2017 Aug 14;16(1):103. doi: 10.1186/s12933-017-0584-9.
We aimed to investigate the efficacy of ascorbic acid and acetylsalicylic acid among type II diabetes mellitus patients using metformin (only) for diabetes management therapy.
A 12-month single blinded multicenter randomized control trial was designed to investigate the measured variables [Glycated Hemoglobin (HbA1c), Renal function, Albumin Creatinine Ratio (ACR) etc.]. The trial was randomized into 2 experimental parallel arms (ascorbic acid vs acetylsalicylic acid) were blinded with study supplements in combination with metformin and findings were compared to control arm with metformin alone and blinded with placebo. Withdrawal criteria was defined to maintain the equity and balance in the participants in the whole trial.
Patients with metformin and ascorbic acid (parallel arm I) was twice more likely to reduce HbA1c than metformin alone (control arm) in a year (OR 2.31 (95% CI 1.87-4.42) p < 0.001). Also Parallel arm I was ten times more likely to reduced risk factors contributing to long-term diabetes complications than participants of arm II in a year (OR 10.38 (95% CI 6.91-15.77) p < 0.001). In contrast, parallel arm II patients were seven times more effective to reduce the risk of expected CVD development in 10 years than arm I (OR 7.54 (95% CI 3.76-10.32) p < 0.001).
The trial concluded that ascorbic acid with metformin is more effective against reducing risks for diabetes related long-term complications (including ACR). TRIAL details Registration No: NTR-6100, Registry Name: Netherlands Trial Registry, URL: http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=6100 , Date of Registration: 20th October, 2016, Date of first Enrollment: 1 November, 2015.
本研究旨在探讨在二甲双胍基础上加用维生素 C 和乙酰水杨酸治疗 2 型糖尿病的疗效。
采用 12 个月的单盲、多中心随机对照试验设计,对糖化血红蛋白(HbA1c)、肾功能、白蛋白/肌酐比值(ACR)等指标进行检测。试验随机分为 2 个实验平行组(维生素 C 组和乙酰水杨酸组),采用联合研究补充剂和与单独使用二甲双胍并使用安慰剂进行双盲治疗,并与单独使用二甲双胍的对照组进行比较。定义退出标准是为了在整个试验中保持参与者的公平性和平衡。
与单独使用二甲双胍的对照组相比,加用维生素 C 的患者在 1 年内降低 HbA1c 的可能性是前者的两倍(OR 2.31(95% CI 1.87-4.42),p<0.001)。此外,在 1 年内,加用维生素 C 的患者降低长期糖尿病并发症风险因素的可能性是加用乙酰水杨酸的患者的 10 倍(OR 10.38(95% CI 6.91-15.77),p<0.001)。相比之下,在 10 年内,加用乙酰水杨酸的患者降低预期 CVD 风险的效果是加用维生素 C 的患者的 7 倍(OR 7.54(95% CI 3.76-10.32),p<0.001)。
该试验表明,与单独使用二甲双胍相比,二甲双胍联合维生素 C 治疗更能有效降低糖尿病相关的长期并发症风险(包括 ACR)。
试验详情 注册号:NTR-6100,注册名称:荷兰临床试验注册中心,网址:http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=6100,注册日期:2016 年 10 月 20 日,首次入组日期:2015 年 11 月 1 日。