Zhang Qin, Zhou Siyuan, Liu Lijun
Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 100053, China.
South Hospital Area of the Fifth Medical Center of the PLA General Hospital, Beijing, 100053, China.
Diabetol Metab Syndr. 2023 Jun 7;15(1):118. doi: 10.1186/s13098-023-01092-z.
The clinical efficacy and safety of SGLT2i in treating patients with type 2 diabetes mellitus and hypertension lack immense data support.
To systematically evaluate the clinical efficacy and safety of SGLT2i in patients with type 2 diabetes mellitus and hypertension by collecting the previously published randomized controlled trials on SGLT2i to provide data support for SGLT2i as an adjuvant in the first-line antihypertensive regimen in patients with type 2 diabetes mellitus and hypertension.
Randomized controlled trials comparing SGLT2i with a placebo in treating type 2 diabetes with hypertension were screened strictly according to inclusion and exclusion criteria. The primary efficacy endpoints included 24H systolic blood pressure, 24H diastolic blood pressure, office systolic blood pressure, and office diastolic blood pressure. The secondary efficacy endpoints included HbA1c. The safety indicators were hypoglycemia, urinary tract infection, genital infection, and renal impairment.MD was the combined effect size for continuous variables, and RR was the combined effect size for dichotomous variables.
10 RCTs with 9913 participants (6293 in the SGLT2i group and 3620 in the control group) were included for analysis.SGLT2i is effective in reducing blood pressure compared with placebo in patients with type 2 diabetes and hypertension, 24HSBP (- 5.06 mmHg, 95% CI [- 7.10, - 3.01], t = - 6.19, P < 0.05), 24HDBP (- 2.39 mmHg, 95% CI [- 4.11, - 0.67], t = - 4.15, P = 0.004), Office SBP (- 4.53 mmHg, 95% CI [- 5.66, - 3.40], t = - 9.50, P < 0.05), Office DBP (- 2.12 mmHg, 95% CI [- 3.42, - 0.82], t = - 4.88, P = 0.001). HbA1c decreased significantly (- 0.57%, 95% CI [- 0.60, - 0.54], z = 37.02, p < 0.01). SGLT2i did not increase hypoglycemia compared to placebo (RR = 1.22, 95% CI [0.916, 1.621], z = 1.36 p = 0.174), urinary tract infection (RR = 1.56, 95% CI [0.96, 2.52], z = 1.79 p = 0.073), risk of renal injury (RR = 0.78, 95% CI [0.54, 1.13], Z = 1.31, P = 0.19), but the risk of genital tract infection increased by 2.32 times (RR = 2.32, 95% CI [1.57, 3.42], Z = 4.23, P = 0.00).
SGLT2i can effectively control blood pressure and blood glucose and generally has high safety. For patients with type 2 diabetes mellitus and hypertension with a low risk of genital infection, SGLT2i should be considered as an adjuvant drug for a first-line antihypertensive regimen.
钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)治疗2型糖尿病合并高血压患者的临床疗效和安全性缺乏大量数据支持。
通过收集既往发表的关于SGLT2i的随机对照试验,系统评价SGLT2i治疗2型糖尿病合并高血压患者的临床疗效和安全性,为SGLT2i作为2型糖尿病合并高血压患者一线降压方案的辅助用药提供数据支持。
严格按照纳入和排除标准筛选比较SGLT2i与安慰剂治疗2型糖尿病伴高血压的随机对照试验。主要疗效终点包括24小时收缩压、24小时舒张压、诊室收缩压和诊室舒张压。次要疗效终点包括糖化血红蛋白(HbA1c)。安全指标为低血糖、尿路感染、生殖器感染和肾功能损害。均数差(MD)为连续变量的合并效应量,相对危险度(RR)为二分变量的合并效应量。
纳入10项随机对照试验,共9913例参与者(SGLT2i组6293例,对照组3620例)进行分析。与安慰剂相比,SGLT2i可有效降低2型糖尿病合并高血压患者的血压,24小时收缩压(-5.06 mmHg,95%置信区间[-7.10,-3.01],t=-6.19,P<0.05),24小时舒张压(-2.39 mmHg,95%置信区间[-4.11,-0.67],t=-4.15,P=0.004),诊室收缩压(-4.53 mmHg,95%置信区间[-5.66,-3.40],t=-9.50,P<0.05),诊室舒张压(-2.12 mmHg,95%置信区间[-3.42,-0.82],t=-4.88,P=0.001)。HbA1c显著降低(-0.57%,95%置信区间[-0.60,-0.54],z=37.02,P<0.01)。与安慰剂相比,SGLT2i未增加低血糖风险(RR=1.22,95%置信区间[0.916,1.621],z=1.36,P=0.174)、尿路感染风险(RR=1.56,95%置信区间[0.96,2.52],z=1.79,P=0.073)、肾损伤风险(RR=0.78,95%置信区间[0.54,1.13],Z=1.31,P=0.19),但生殖器感染风险增加2.32倍(RR=2.32,95%置信区间[1.57,3.42],Z=4.23,P=0.00)。
SGLT2i可有效控制血压和血糖,总体安全性较高。对于生殖器感染风险较低的2型糖尿病合并高血压患者,SGLT2i可考虑作为一线降压方案的辅助用药。