First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
National Clinical Research Center for Chinese Medicine Acupuncture and Moxibustion, Tianjin, China.
Medicine (Baltimore). 2024 Jun 14;103(24):e32095. doi: 10.1097/MD.0000000000032095.
Diabetes nephropathy (DN), as one of the common complications of diabetes, is characterized by persistent albuminuria, decreased glomerular filtration rate, and elevated arterial blood pressure. At present, Xuebijing injection is widely used in the treatment of DN. However, few systematic reviews and meta-analysis related to Xuebijing injection intervention in DN were published. In order to more systematically and objectively evaluate the clinical efficacy of Xuebijing injection intervention in DN, we conducted systematic reviews and meta-analysis to verify it.
The purpose of the research was to systematically evaluate the clinical efficacy of Xuebijing injection combined with alprostadil in the treatment of diabetic nephropathy.
We searched the China National Knowledge Infrastructure (CNKI), China Biomedical Database (SinoMed), Weipu Database (VIP), Wanfang Database, PubMed, The Cochrane Library, Embase, Web of Science and other databases by computer, and searched the randomized controlled trials of Xuebijing injection combined with alprostadil in the treatment of DN at home and abroad from the establishment of the database to 2022. The main outcome indicators included blood glucose, and the secondary outcome indicators included blood lipid, renal function, urinary protein, and safety. Two evaluators independently screened the literature, extracted the data and evaluated the risk of bias in the included studies. RevMan 5.3 software was used to analyze the data.
A total of 14 randomized controlled trials were included, including 1233 cases, 618 cases in the treatment group and 615 cases in the control group. The results of meta-analysis demonstrated that compared with the control group, the treatment group could effectively reduce fasting plasma glucose [mean difference [MD] = -1.90, 95% CI (-2.40, -1.40), P < .00001], glycosylated hemoglobin A1c [MD = -2.38, 95% CI (-2.51, -2.25), P < .00001], 2h postprandial blood glucose [MD = -2.92, 95% CI (-3.95, -1.89), P < .00001], triacylglycerol [MD = -1.08, 95% CI (-1.66, -0.50), P = .0003], total cholesterol [MD = -1.17, 95% CI (-1.39, -0.95), P < .00001], low-density lipoprotein cholesterol [MD = -1.19, 95% CI (-1.60, -0.78), P < .00001], high-density lipoprotein cholesterol [MD = 0.32, 95% CI (0.23, 0.42), P < .00001], serum creatinine [MD = -42.95, 95% CI (-57.46, -28.43), P < .00001], blood urea nitrogen [MD = -2.24, 95%CI (-2.62,-1.86), P < .00001], blood β2 microglobulin [SMD = -1.49, 95% CI (-1.70, -1.28), P < .00001], urine β2 microglobulin [SMD = -0.81, 95% CI (-1.04, -0.58), P < .00001], 24-hour urinary protein quantification [MD = -0.20, 95% CI (-0.26, -0.14), P < .00001], urinary albumin excretion rate [SMD = -1.15, 95% CI (-1.38, -0.93), P < .00001].
Xuebijing injection combined with alprostadil has more advantages in treating DN compared to routine Western medicine.
糖尿病肾病(DN)作为糖尿病常见的并发症之一,其特征为持续白蛋白尿、肾小球滤过率降低和动脉血压升高。目前,血必净注射液广泛用于 DN 的治疗。然而,很少有关于血必净注射液干预 DN 的系统评价和荟萃分析。为了更系统、客观地评价血必净注射液干预 DN 的临床疗效,我们进行了系统评价和荟萃分析来验证。
研究旨在系统评价血必净注射液联合前列地尔治疗糖尿病肾病的临床疗效。
我们通过计算机检索中国知网(CNKI)、中国生物医学文献数据库(SinoMed)、维普数据库(VIP)、万方数据库、PubMed、The Cochrane Library、Embase、Web of Science 等国内外数据库,从数据库建立到 2022 年,检索国内外关于血必净注射液联合前列地尔治疗 DN 的随机对照试验。主要结局指标包括血糖,次要结局指标包括血脂、肾功能、尿蛋白和安全性。由 2 位评价员独立筛选文献、提取数据并评价纳入研究的偏倚风险。采用 RevMan 5.3 软件进行数据分析。
共纳入 14 项随机对照试验,包括 1233 例患者,治疗组 618 例,对照组 615 例。Meta 分析结果表明,与对照组相比,治疗组可有效降低空腹血糖[均数差(MD)=-1.90,95%置信区间(CI)(-2.40,-1.40),P<0.00001]、糖化血红蛋白 A1c(MD=-2.38,95%CI(-2.51,-2.25),P<0.00001)、餐后 2 小时血糖[MD=-2.92,95%CI(-3.95,-1.89),P<0.00001]、三酰甘油(MD=-1.08,95%CI(-1.66,-0.50),P=0.0003)、总胆固醇(MD=-1.17,95%CI(-1.39,-0.95),P<0.00001)、低密度脂蛋白胆固醇(MD=-1.19,95%CI(-1.60,-0.78),P<0.00001)、高密度脂蛋白胆固醇(MD=0.32,95%CI(0.23,0.42),P<0.00001)、血清肌酐(MD=-42.95,95%CI(-57.46,-28.43),P<0.00001)、血尿素氮(MD=-2.24,95%CI(-2.62,-1.86),P<0.00001)、血β2 微球蛋白(SMD=-1.49,95%CI(-1.70,-1.28),P<0.00001)、尿β2 微球蛋白(SMD=-0.81,95%CI(-1.04,-0.58),P<0.00001)、24 小时尿蛋白定量(MD=-0.20,95%CI(-0.26,-0.14),P<0.00001)、尿白蛋白排泄率(SMD=-1.15,95%CI(-1.38,-0.93),P<0.00001)。
血必净注射液联合前列地尔治疗 DN 较常规西药具有更多优势。