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纸质出版日期:2018
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陈一君, 吴庆光, 刘颖, 等. 黄连解毒汤单独用药及联合用药对2型糖尿病治疗效果的Meta分析[J]. 中国实验方剂学杂志, 2018,24(10):212-220.
CHEN Yi-jun, WU Qing-guang, LIU Ying, et al. Efficacy of Single Administration of Huanglian Jiedu Tang and Combined Administration with Basic Medicine for Type 2 Diabetes of Meta-analysis[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(10): 212-220.
陈一君, 吴庆光, 刘颖, 等. 黄连解毒汤单独用药及联合用药对2型糖尿病治疗效果的Meta分析[J]. 中国实验方剂学杂志, 2018,24(10):212-220. DOI: 10.13422/j.cnki.syfjx.20181041.
CHEN Yi-jun, WU Qing-guang, LIU Ying, et al. Efficacy of Single Administration of Huanglian Jiedu Tang and Combined Administration with Basic Medicine for Type 2 Diabetes of Meta-analysis[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(10): 212-220. DOI: 10.13422/j.cnki.syfjx.20181041.
目的:系统评价黄连解毒汤单用及联合糖尿病基础药物两种用药方式治疗2型糖尿病的效果。方法:计算机检索中国知网,万方数据库,维普中文期刊全文数据库,VIP,Pubmed,Elseviser science Direct电子期刊,Cochrane图书馆,筛选出有关黄连解毒汤治疗糖尿病的随机对照试验(randomized controlled trials,RCT)。由两名评价员对文献进行筛选、评价和资料提取,并使用RevMan5.3软件以及Stata SE12.0进行Meta分析。结果:共纳入12个RCT共1 022例患者。Meta分析结果显示单独用药亚组能降低糖化血红蛋白(HbAlc)[MD=-0.04,95% CI(-0.60,-0.68)],空腹血糖(FPG)[MD=-0.21,95% CI(-0.81,0.38)],餐后2小时血糖(2hPG)[MD=-0.30,95% CI(-0.98,0.37)]水平的效果以及降糖的有效率(OR=1.22,95% CI(0.74,2.03)]与对照组相当;降糖有效率合并为84.8%。体质量指数(BMI)的降低[MD=-0.18,95% CI(-0.29,0.66)],减肥有效率(OR=1.04,95% CI(0.61,1.78)]与对照组相当;减肥有效率合并为74.8%。联合用药亚组能明显降低HbAlc[MD=0.53,95% CI(0.33,0.73)],2hPG[MD=1.86,95% CI(1.59,2.14)]水平的效果明显优于对照组,差异有统计学意义;降低FPG水平[MD=1.21,95% CI(-0.02,2.43)]的效果则对照组相当。降糖有效率[OR=3.89,95% CI(2.18,6.93)]优于对照组,差异有统计学意义;降糖有效率合并为90.8%。BMI的降低[MD=0.17,95% CI(-0.97,1.31)],减肥有效率[OR=2.50,95% CI(0.74,8.50)]与对照组相当;减肥有效率为83.3%。结论:黄连解毒汤单独使用治疗2型糖尿病效果与二甲双胍相当。在联合糖尿病基础药物治疗中加用黄连解毒汤能有效地降低2型糖尿病患者Hb1Ac和2hPG水平,提示可适用于早期HbAlc<7.3%的2型糖尿病。但是由于研究缺乏且方法学质量较低,这一系统评估的结果仍然需要更多的高质量大规模的RCT来进一步验证。
Objective: To evaluate the efficacy of single administration of Huanglian Jiedu Tang and combined administration withbasic medicine for type 2 diabetes (T2D). Method: All of randomized controlled trials (RCTs) about the efficacy of single administration and combined administration of Huanglian Jiedu Tang in treating T2D were collected through CNKI
Wanfang Data
two Chinese periodical full text databases (CJDF and VIP)
Pubmed
Elseviser science Direct electronic journal
and Cochrane library. The assessment of methodological quality and data extraction of the included studies were performed independently by two reviewers
and the Meta-analysis was conducted with RevMan 5.3 software and stata SE 12.0 software. Result: A total of 12 RCTs involving 1 022 patients were included. According to meta-analysis
subgroup with single administration of Huanglian Jiedu Tang showed the reduction of HbAlc[MD=-0.04
95%CI (-0.60
-0.68)]
FPG[MD=-0.21
95%CI (-0.81
0.38)]
2hPG[MD=-0.30
95%CI (-0.98
0.37)]
and the effective rate of reducing blood sugar[OR=1.22
95%CI (0.74
2.03)]
which reached 84.8%
were equivalent to the control group without significant difference. The reduction of BMI[MD=-0.18
95%CI (-0.29
0.66)] and effective rate of loosing weight[OR=1.04
95%CI (0.61
1.78)]
which reached 74.8%
were also equivalent to the control group without significant difference; subgroup of combined administration of Huanglian Jiedu Tang showed the reduction of HbAlc[MD=0.53
95%CI (0.33
0.73)]
2hPG[MD=1.86
95%CI (1.59
2.14)]
effective rate of reducing blood sugar[OR=3.89
95%CI (2.18
6.93)]
which reached 90.8%
were significantly higher than the control group
but the reduction of FPG[MD=1.21
95%CI (-0.02
2.43)] was equivalent to the control group without significant difference. The reduction of BMI[MD=0.17
95%CI (-0.97
1.31)] and effective rate of loosing weight[OR=2.50
95%CI (0.74
8.50)]
which reached 83.3%
were also equivalent to the control group without significant difference. Conclusion: The efficacy of single administration of Huanglian Jiedu Tang for T2D is equivalent to Metformin. The combined administration of Huanglian Jiedu Tang with basic medicine for diabetes could reduce Hb1Ac and 2hPG obviously
which suggests that The combined administration of Huanglian Jiedu Tang could be beneficial for early-stage T2D with HbAlc<7.3%. However
due to the insufficiency of the included studies and the low methodology quality
the results of the system evaluation still need to be further verified by more high-quality large RCTs.
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