临床荟萃 ›› 2024, Vol. 39 ›› Issue (7): 581-592.doi: 10.3969/j.issn.1004-583X.2024.07.001
• 循证研究 • 下一篇
岳江红1, 王恒2, 蔡钢3a, 张选明3a, 彭曦3b()
收稿日期:
2024-01-08
出版日期:
2024-07-20
发布日期:
2024-08-02
通讯作者:
彭曦
E-mail:pxshz@163.com
基金资助:
Yue Jianghong1, Wang Heng2, Cai Gang3a, Zhang Xuanming3a, Peng Xi3b()
Received:
2024-01-08
Online:
2024-07-20
Published:
2024-08-02
Contact:
Peng Xi
E-mail:pxshz@163.com
摘要:
目的 分析评估索格列净治疗2型糖尿病患者的疗效和安全性。方法 检索 PubMed、Embase、Web of Science、Medline、Cochrane Library、美国临床试验注册平台、CNKI、万方、维普、SinoMed等数据库,检索时间为建库起至2023年10月31日,收集有关索格列净与安慰剂(或其他口服降糖药)对照治疗2型糖尿病的随机对照试验(RCT),提取文献有效数据及质量评价后,应用RevMan 5.3软件进行meta分析。结果 共纳入14篇RCT,共计16959例患者。Meta分析结果显示:疗效方面,与对照组相比,索格列净能显著降低糖尿病患者糖化血红蛋白[MD=-0.45,95%CI(-0.58,-0.33),P<0.01]、空腹血糖[MD=-0.66,95%CI(-1.01,-0.31),P=0.0002] 和餐后2 h血糖[MD=-1.01,95%CI(-1.58,-0.44),P=0.0005]、提高糖化血红蛋白<7%达标率[RR=1.88,95%CI(1.64,2.15),P<0.01];与对照组相比索格列净可降低收缩压[MD=-2.13,95%CI(-2.81,-1.45),P<0.01]和体质量[MD=-1.40,95%CI(-1.63,-1.17),P<0.01];但在降低舒张压方面差异无统计学意义。安全性方面,索格列净组与对照组低血糖事件发生率相似[RR=1.00,95%CI(0.92,1.09),P=0.97];但索格列净组不良反应发生率更低[RR=0.92,95%CI(0.88,0.96),P<0.01]。按照索格列净使用剂量不同进行亚组分析显示,与对照组相比,索格列净200 mg和400 mg组均可显著降低患者的糖化血红蛋白、空腹血糖水平,提高糖化血红蛋白<7%达标率,降低收缩压、体质量等指标(P<0.05);且均未增加低血糖事件风险(P>0.05)。结论 索格列净可显著降低2型糖尿病患者的糖化血红蛋白、空腹血糖、餐后2 h血糖、收缩压和体质量,同时不增加低血糖风险以及不良反应发生率。
中图分类号:
岳江红, 王恒, 蔡钢, 张选明, 彭曦. 索格列净治疗2型糖尿病疗效和安全性的meta分析[J]. 临床荟萃, 2024, 39(7): 581-592.
Yue Jianghong, Wang Heng, Cai Gang, Zhang Xuanming, Peng Xi. Efficacy and safety of sotagliflozin in the treatment of type 2 diabetes mellitus: A meta-analysis[J]. Clinical Focus, 2024, 39(7): 581-592.
第一作者及 发表年限 | 组别 | 例数 | 年龄 (岁) | 女性比例 (%) | HbA1c(%) | 干预措施 | 研究 周期 | 结局指标 |
---|---|---|---|---|---|---|---|---|
NCT03315143 Bhatt 2021[ SCORED | 试验组 对照组 | 5292 5292 | 69(63~74) 69(63~74) | 44.3 45.5 | ≥7 | 索格列净400 mg qd 安慰剂 | 64 | ⑨ |
NCT03521934 Bhatt 2021[ SOLOIST-WHF | 试验组 对照组 | 608 614 | 69(63~76) 70(64~76) | 32.6 34.9 | 7.1(6.4~8.3) 7.2(6.4~8.2) | 索格列净400 mg qd 安慰剂 | 36 | ⑨ |
NCT03242018 Cherney 2021[ | 试验组 | 92 | 66.8±10.0 | 52.2 | 8.3±1.0 | 索格列净200 mg qd | ||
92 | 67.3±9.6 | 46.7 | 8.3±0.9 | 索格列净400 mg qd | 52 | ①、②、④、⑤、⑦、⑧、⑨ | ||
对照组 | 93 | 68.0±8.3 | 54.8 | 8.4±1.1 | 安慰剂 | |||
NCT03242252 Cherney 2023[ | 试验组 | 263 | 69.6±7.5 | 45.6 | 8.3±0.9 | 索格列净200 mg qd | ||
264 | 69.5±8.2 | 42.4 | 8.3±0.9 | 索格列净400 mg qd | 52 | ①、②、④、⑤、⑦、⑧、⑨ | ||
对照组 | 260 | 69.3±8.1 | 42.7 | 8.3±1.0 | 安慰剂 | |||
NCT03462069 Posch 2022[ | 试验组 对照组 | 20 21 | 61.0±8.4 64.8±8.53 | 20.0 81.0 | 6.5-11 | 索格列净400 mg qd 恩格列净200 mg qd | 8 | ⑧、⑨ |
NCT01555008 Zambrowicz 2015[ | 试验组 对照组 | 16 15 | 64.8±8.53 68.1±7.33 | 50.0 40.0 | 不清楚 不清楚 | 索格列净400 mg qd 安慰剂 | 1 | ⑤、⑥、⑧、⑨ |
NCT01376557 Rosenstock 2014[ | 试验组 | 59 | 56± 9.61 | 42.4 | 8.0±0.9 | 索格列净75 mg qd | ||
60 | 55.6±9.25 | 71.7 | 8.3±1.0 | 索格列净200 mg qd | ||||
60 | 56.1±9.51 | 51.7 | 8.1±1.0 | 索格列净400 mg qd | 12 | ①、②、④、⑤、⑥、⑦、⑨ | ||
60 | 56.4±8.76 | 51.7 | 8.4±0.9 | 索格列净200 mg bid | ||||
对照组 | 60 | 55.1±9.79 | 56.7 | 7.9±0.9 | 安慰剂 | |||
NCT02926937[ | 试验组 | 107 | 52.3±11.4 | 49.5 | 8.00±0.81 | 索格列净200 mg qd | ||
142 | 54.7±11.2 | 47.9 | 8.14±0.92 | 索格列净400 mg qd | 26 | ①、②、③、④、⑤、⑦、⑧、⑨ | ||
对照组 | 150 | 55.3±11.2 | 48.0 | 8.11±0.88 | 安慰剂 | |||
NCT02926950[ | 试验组 对照组 | 259 259 | 60.0±10.1 59.9±9.4 | 45.2 43.6 | 8.20±0.78 8.20±0.78 | 索格列净400 mg qd 安慰剂 | 26 | ①、②、③、④、⑤、⑦、⑧、⑨ |
NCT03351478 SOTA-EMPA[ | 试验组 | 307 | 58.9±9.7 | 45.9 | 8.23±0.84 | 索格列净400 mg qd | ||
309 | 59.7±9.6 | 51.1 | 8.21±0.93 | 恩格列净25 mg qd | 26 | ①、②、③、④、⑤、⑦、⑨ | ||
对照组 | 154 | 59.8±9.6 | 48.7 | 8.21±0.93 | 安慰剂 | |||
NCT03285594 SOTA-INS[ | 试验组 | 141 | 62.1±10.2 | 46.1 | 8.76±0.83 | 索格列净200 mg qd | ||
286 | 62.7±9.1 | 46.2 | 8.69±0.80 | 索格列净400 mg qd | 52 | ①、②、⑤、⑦、⑧、⑨ | ||
对照组 | 144 | 62.2±8.9 | 40.3 | 8.76±0.79 | 安慰剂 | |||
NCT03066830[ | 试验组 对照组 | 253 254 | 63.3±8.8 63.0±9.9 | 41.1 48.8 | 8.20±0.83 8.18±0.83 | 索格列净400 mg qd 安慰剂 | 26 | ①、②、④、⑤、⑦、⑧、⑨ |
NCT03332771 SOTA-GLIM[ | 试验组 | 160 | 58.6±9.9 | 46.9 | 8.11±0.86 | 索格列净200 mg qd | ||
317 | 59.7±10.4 | 49.5 | 8.09±0.78 | 索格列净400 mg qd | 52 | ①、④、⑦、⑧、⑨ | ||
对照组 | 159 | 58.8±11.2 | 48.4 | 8.12±0.73 | 安慰剂 | |||
NCT03386344 SOTA-BONE[ | 试验组 | 125 | 66.1±6.7 | 44.8 | 8.32±0.96 | 索格列净200 mg qd | ||
125 | 66.5±6.9 | 44.0 | 8.32±0.95 | 索格列净400 mg qd | 26 | ①、②、④、⑤、⑦、⑧、⑨ | ||
对照组 | 126 | 66.3±5.7 | 44.4 | 8.38±0.91 | 安慰剂 |
表1 纳入研究的基线特征
Tab.1 Baseline characteristics of the included studies
第一作者及 发表年限 | 组别 | 例数 | 年龄 (岁) | 女性比例 (%) | HbA1c(%) | 干预措施 | 研究 周期 | 结局指标 |
---|---|---|---|---|---|---|---|---|
NCT03315143 Bhatt 2021[ SCORED | 试验组 对照组 | 5292 5292 | 69(63~74) 69(63~74) | 44.3 45.5 | ≥7 | 索格列净400 mg qd 安慰剂 | 64 | ⑨ |
NCT03521934 Bhatt 2021[ SOLOIST-WHF | 试验组 对照组 | 608 614 | 69(63~76) 70(64~76) | 32.6 34.9 | 7.1(6.4~8.3) 7.2(6.4~8.2) | 索格列净400 mg qd 安慰剂 | 36 | ⑨ |
NCT03242018 Cherney 2021[ | 试验组 | 92 | 66.8±10.0 | 52.2 | 8.3±1.0 | 索格列净200 mg qd | ||
92 | 67.3±9.6 | 46.7 | 8.3±0.9 | 索格列净400 mg qd | 52 | ①、②、④、⑤、⑦、⑧、⑨ | ||
对照组 | 93 | 68.0±8.3 | 54.8 | 8.4±1.1 | 安慰剂 | |||
NCT03242252 Cherney 2023[ | 试验组 | 263 | 69.6±7.5 | 45.6 | 8.3±0.9 | 索格列净200 mg qd | ||
264 | 69.5±8.2 | 42.4 | 8.3±0.9 | 索格列净400 mg qd | 52 | ①、②、④、⑤、⑦、⑧、⑨ | ||
对照组 | 260 | 69.3±8.1 | 42.7 | 8.3±1.0 | 安慰剂 | |||
NCT03462069 Posch 2022[ | 试验组 对照组 | 20 21 | 61.0±8.4 64.8±8.53 | 20.0 81.0 | 6.5-11 | 索格列净400 mg qd 恩格列净200 mg qd | 8 | ⑧、⑨ |
NCT01555008 Zambrowicz 2015[ | 试验组 对照组 | 16 15 | 64.8±8.53 68.1±7.33 | 50.0 40.0 | 不清楚 不清楚 | 索格列净400 mg qd 安慰剂 | 1 | ⑤、⑥、⑧、⑨ |
NCT01376557 Rosenstock 2014[ | 试验组 | 59 | 56± 9.61 | 42.4 | 8.0±0.9 | 索格列净75 mg qd | ||
60 | 55.6±9.25 | 71.7 | 8.3±1.0 | 索格列净200 mg qd | ||||
60 | 56.1±9.51 | 51.7 | 8.1±1.0 | 索格列净400 mg qd | 12 | ①、②、④、⑤、⑥、⑦、⑨ | ||
60 | 56.4±8.76 | 51.7 | 8.4±0.9 | 索格列净200 mg bid | ||||
对照组 | 60 | 55.1±9.79 | 56.7 | 7.9±0.9 | 安慰剂 | |||
NCT02926937[ | 试验组 | 107 | 52.3±11.4 | 49.5 | 8.00±0.81 | 索格列净200 mg qd | ||
142 | 54.7±11.2 | 47.9 | 8.14±0.92 | 索格列净400 mg qd | 26 | ①、②、③、④、⑤、⑦、⑧、⑨ | ||
对照组 | 150 | 55.3±11.2 | 48.0 | 8.11±0.88 | 安慰剂 | |||
NCT02926950[ | 试验组 对照组 | 259 259 | 60.0±10.1 59.9±9.4 | 45.2 43.6 | 8.20±0.78 8.20±0.78 | 索格列净400 mg qd 安慰剂 | 26 | ①、②、③、④、⑤、⑦、⑧、⑨ |
NCT03351478 SOTA-EMPA[ | 试验组 | 307 | 58.9±9.7 | 45.9 | 8.23±0.84 | 索格列净400 mg qd | ||
309 | 59.7±9.6 | 51.1 | 8.21±0.93 | 恩格列净25 mg qd | 26 | ①、②、③、④、⑤、⑦、⑨ | ||
对照组 | 154 | 59.8±9.6 | 48.7 | 8.21±0.93 | 安慰剂 | |||
NCT03285594 SOTA-INS[ | 试验组 | 141 | 62.1±10.2 | 46.1 | 8.76±0.83 | 索格列净200 mg qd | ||
286 | 62.7±9.1 | 46.2 | 8.69±0.80 | 索格列净400 mg qd | 52 | ①、②、⑤、⑦、⑧、⑨ | ||
对照组 | 144 | 62.2±8.9 | 40.3 | 8.76±0.79 | 安慰剂 | |||
NCT03066830[ | 试验组 对照组 | 253 254 | 63.3±8.8 63.0±9.9 | 41.1 48.8 | 8.20±0.83 8.18±0.83 | 索格列净400 mg qd 安慰剂 | 26 | ①、②、④、⑤、⑦、⑧、⑨ |
NCT03332771 SOTA-GLIM[ | 试验组 | 160 | 58.6±9.9 | 46.9 | 8.11±0.86 | 索格列净200 mg qd | ||
317 | 59.7±10.4 | 49.5 | 8.09±0.78 | 索格列净400 mg qd | 52 | ①、④、⑦、⑧、⑨ | ||
对照组 | 159 | 58.8±11.2 | 48.4 | 8.12±0.73 | 安慰剂 | |||
NCT03386344 SOTA-BONE[ | 试验组 | 125 | 66.1±6.7 | 44.8 | 8.32±0.96 | 索格列净200 mg qd | ||
125 | 66.5±6.9 | 44.0 | 8.32±0.95 | 索格列净400 mg qd | 26 | ①、②、④、⑤、⑦、⑧、⑨ | ||
对照组 | 126 | 66.3±5.7 | 44.4 | 8.38±0.91 | 安慰剂 |
结局指标 | 随机效应模型 | 固定效应模型 | 去除权重大的研究 | 去除权重小的研究 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MD/RR(95%CI) | P值 | MD/RR(95%CI) | P值 | MD/RR(95%CI) | P值 | MD/RR(95%CI) | P值 | |||||||||
HbA1c水平 | -0.45[-0.58,-0.33] | <0.01 | -0.43[-0.44,-0.42] | <0.01 | -0.50[-0.60,-0.41] | <0.01 | -0.44[-0.56,-0.31] | <0.01 | ||||||||
低血糖事件发生率 | 1.00[0.92,1.08] | 0.94 | 1.00[0.92,1.09] | 0.97 | 1.00[0.90,1.11] | 0.98 | 1.00[0.92,1.10] | 0.93 |
表2 敏感性分析
Tab.2 Sensitivity analysis
结局指标 | 随机效应模型 | 固定效应模型 | 去除权重大的研究 | 去除权重小的研究 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MD/RR(95%CI) | P值 | MD/RR(95%CI) | P值 | MD/RR(95%CI) | P值 | MD/RR(95%CI) | P值 | |||||||||
HbA1c水平 | -0.45[-0.58,-0.33] | <0.01 | -0.43[-0.44,-0.42] | <0.01 | -0.50[-0.60,-0.41] | <0.01 | -0.44[-0.56,-0.31] | <0.01 | ||||||||
低血糖事件发生率 | 1.00[0.92,1.08] | 0.94 | 1.00[0.92,1.09] | 0.97 | 1.00[0.90,1.11] | 0.98 | 1.00[0.92,1.10] | 0.93 |
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