补充肌醇预防和治疗妊娠期糖尿病的疗效:一项荟萃分析。

IF 4.6 3区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Ru-Tong Wang, Ying-Qi Feng, Meng-Yao Wang, Yan-Hong Wei, Yu-Jun Huang, Yu-Jia Guo, Xuan Liu, Xiao-Can Lei, Kong-Wei Huang, Hua Huang
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引用次数: 0

摘要

背景:妊娠期糖尿病(GDM)对妊娠期健康构成重大风险。然而,肌醇(MI)在GDM预防和管理中的作用仍然存在争议,因为先前的研究证据相互矛盾,方法也存在局限性。目的:评价心肌梗死预防和治疗GDM的疗效,为临床实践提供循证指导。方法:对PubMed、Web of Science和Embase数据库从建立日期到2024年7月发表的研究进行系统回顾。采用固定效应和随机效应模型的meta分析纳入了12项研究,共9018例患者。异质性采用i2统计量和Cochrane Q检验进行量化,研究质量采用A测量工具评估系统评价2检查表进行评价。结果:心肌梗死显著降低GDM发病率[相对危险度(RR): 0.37;95%可信区间(CI): 0.32-0.42],空腹血糖[标准平均差(SMD): -1.31 mg/dL;95%CI: -1.83至-0.79],改善了1小时(SMD: -2.63 mg/dL; 95%CI: -3.87至-1.40)和2小时(SMD: -0.95 mg/dL; 95%CI: -1.56至-0.34)的葡萄糖耐量试验结果。它还降低了早产(RR: 0.37; 95%CI: 0.28-0.47)和妊娠高血压(RR: 0.34; 95%CI: 0.25-0.47)的风险。剖宫产率降低趋势不显著(RR: 0.82; 95%CI: 0.71-0.94)。心肌梗死降低了新生儿体重(SMD: -0.25 kg; 95%CI: -0.32至-0.17),但对新生儿低血糖(RR: 0.30; 95%CI: 0.08-1.21)或出生时胎龄(SMD: -0.13周;95%CI: -0.04至0.29)没有影响。结论:心肌梗死具有预防和管理GDM的治疗潜力,支持其作为高危妇女早孕预防性补充的潜力。尽管如此,它对诊断为GDM的女性的治疗效果需要进一步验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of inositol supplementation in the prevention and treatment of gestational diabetes mellitus: A meta-analysis.

Background: Gestational diabetes mellitus (GDM) poses a substantial health risk during pregnancy. However, the role of myo-inositol (MI) in GDM prevention and management remains controversial due to conflicting evidence and methodological limitations in previous studies.

Aim: To assess the efficacy of MI in preventing and treating GDM, providing evidence-based guidance for clinical practice.

Methods: A systematic review was conducted on studies published on the PubMed, Web of Science, and Embase databases from their inception date to July 2024. Twelve studies encompassing 9018 patients were included in the meta-analysis using fixed-effect and random-effects models. Heterogeneity was quantified with I 2 statistics and the Cochrane Q test, and study quality was appraised using the A Measurement Tool to Assess Systematic Reviews 2 checklist.

Results: MI significantly reduced GDM incidence [relative risk (RR): 0.37; 95% confidence interval (CI): 0.32-0.42], fasting blood glucose [standard mean differences (SMD): -1.31 mg/dL; 95%CI: -1.83 to -0.79], and improved glucose tolerance test outcomes at 1-hour (SMD: -2.63 mg/dL; 95%CI: -3.87 to -1.40) and 2-hour (SMD: -0.95 mg/dL; 95%CI: -1.56 to -0.34). It also decreased the risk of preterm birth (RR: 0.37; 95%CI: 0.28-0.47) and pregnancy-induced hypertension (RR: 0.34; 95%CI: 0.25-0.47). A non-significant trend towards reduced cesarean section rates was observed (RR: 0.82; 95%CI: 0.71-0.94). MI reduced birth weight (SMD: -0.25 kg; 95%CI: -0.32 to -0.17), but had no effect on neonatal hypoglycemia (RR: 0.30; 95%CI: 0.08-1.21) or gestational age at birth (SMD: -0.13 weeks; 95%CI: -0.04 to 0.29).

Conclusion: MI demonstrates therapeutic potential in GDM prevention and management, supporting its potential use as a preventive supplement in early pregnancy for high-risk women. Nonetheless, its therapeutic effects in women diagnosed with GDM require further validation.

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来源期刊
World Journal of Diabetes
World Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
自引率
2.40%
发文量
909
期刊介绍: The WJD is a high-quality, peer reviewed, open-access journal. The primary task of WJD is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of diabetes. In order to promote productive academic communication, the peer review process for the WJD is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJD are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in diabetes. Scope: Diabetes Complications, Experimental Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus, Diabetes, Gestational, Diabetic Angiopathies, Diabetic Cardiomyopathies, Diabetic Coma, Diabetic Ketoacidosis, Diabetic Nephropathies, Diabetic Neuropathies, Donohue Syndrome, Fetal Macrosomia, and Prediabetic State.
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