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The effect of metformin on low birth weight girls with precocious puberty: A protocol for systematic review and meta-analysis

In recent years, the role of metformin in girls with precocious puberty (PP) has been increasingly frequently studied. The objective of this present study is to assess the effect of metformin on low birth weight girls with precocious puberty (LBW-PP girls). METHODS: We search the confirmed studies a...

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Autores principales: Lin, Zhiheng, Sui, Xiaohui, Li, Lijuan, Wang, Ying, Zhao, Junde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239663/
https://www.ncbi.nlm.nih.gov/pubmed/35776991
http://dx.doi.org/10.1097/MD.0000000000029765
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author Lin, Zhiheng
Sui, Xiaohui
Li, Lijuan
Wang, Ying
Zhao, Junde
author_facet Lin, Zhiheng
Sui, Xiaohui
Li, Lijuan
Wang, Ying
Zhao, Junde
author_sort Lin, Zhiheng
collection PubMed
description In recent years, the role of metformin in girls with precocious puberty (PP) has been increasingly frequently studied. The objective of this present study is to assess the effect of metformin on low birth weight girls with precocious puberty (LBW-PP girls). METHODS: We search the confirmed studies about circulating metformin and PP from the databases of EMBASE, PubMed, and Web of Science. Data were reported as weighted mean difference (WMD) and associated 95% confidence intervals (CIs). Analysis was performed by Review Manager 5.3 and Stata version 12.0. RESULTS: A total of 205 cases (metformin group n = 102, untreated group n = 103) were included in this study. The meta-analysis of randomized controlled trials (RCTs) suggested that metformin had statistically significant effects on testosterone (P = .001), androstenedione (P = .022), bone mineral density (BMD; P = .151), triglycerides (P ≤ .001), body mass index Z score (BMI Z score; P ≤ .001), dehydroepiandrosterone-sulfate (DHEAS; P = .053), sex hormone-binding globulin (SHBG; P = .049), high-density lipoprotein (HDL) cholesterol (P ≤ .001), low-density lipoprotein (LDL) cholesterol (P = .021), fat mass (P ≤ .001), lean mass (P = .025), and fasting insulin (P = .002). CONCLUSION: This meta-analysis provided evidence of the efficacy of metformin in girls with LBW-PP girls, which proved that metformin could improve metabolism and reduce weight. Metformin had a positive effect on preventing LBW-PP girls from developing into obesity and polycystic ovarian syndrome. In addition, this meta-analysis provided important reference opinions and directions for the treatment of LBW-PP girls.
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spelling pubmed-92396632022-06-30 The effect of metformin on low birth weight girls with precocious puberty: A protocol for systematic review and meta-analysis Lin, Zhiheng Sui, Xiaohui Li, Lijuan Wang, Ying Zhao, Junde Medicine (Baltimore) Research Article In recent years, the role of metformin in girls with precocious puberty (PP) has been increasingly frequently studied. The objective of this present study is to assess the effect of metformin on low birth weight girls with precocious puberty (LBW-PP girls). METHODS: We search the confirmed studies about circulating metformin and PP from the databases of EMBASE, PubMed, and Web of Science. Data were reported as weighted mean difference (WMD) and associated 95% confidence intervals (CIs). Analysis was performed by Review Manager 5.3 and Stata version 12.0. RESULTS: A total of 205 cases (metformin group n = 102, untreated group n = 103) were included in this study. The meta-analysis of randomized controlled trials (RCTs) suggested that metformin had statistically significant effects on testosterone (P = .001), androstenedione (P = .022), bone mineral density (BMD; P = .151), triglycerides (P ≤ .001), body mass index Z score (BMI Z score; P ≤ .001), dehydroepiandrosterone-sulfate (DHEAS; P = .053), sex hormone-binding globulin (SHBG; P = .049), high-density lipoprotein (HDL) cholesterol (P ≤ .001), low-density lipoprotein (LDL) cholesterol (P = .021), fat mass (P ≤ .001), lean mass (P = .025), and fasting insulin (P = .002). CONCLUSION: This meta-analysis provided evidence of the efficacy of metformin in girls with LBW-PP girls, which proved that metformin could improve metabolism and reduce weight. Metformin had a positive effect on preventing LBW-PP girls from developing into obesity and polycystic ovarian syndrome. In addition, this meta-analysis provided important reference opinions and directions for the treatment of LBW-PP girls. Lippincott Williams & Wilkins 2022-06-30 /pmc/articles/PMC9239663/ /pubmed/35776991 http://dx.doi.org/10.1097/MD.0000000000029765 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lin, Zhiheng
Sui, Xiaohui
Li, Lijuan
Wang, Ying
Zhao, Junde
The effect of metformin on low birth weight girls with precocious puberty: A protocol for systematic review and meta-analysis
title The effect of metformin on low birth weight girls with precocious puberty: A protocol for systematic review and meta-analysis
title_full The effect of metformin on low birth weight girls with precocious puberty: A protocol for systematic review and meta-analysis
title_fullStr The effect of metformin on low birth weight girls with precocious puberty: A protocol for systematic review and meta-analysis
title_full_unstemmed The effect of metformin on low birth weight girls with precocious puberty: A protocol for systematic review and meta-analysis
title_short The effect of metformin on low birth weight girls with precocious puberty: A protocol for systematic review and meta-analysis
title_sort effect of metformin on low birth weight girls with precocious puberty: a protocol for systematic review and meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239663/
https://www.ncbi.nlm.nih.gov/pubmed/35776991
http://dx.doi.org/10.1097/MD.0000000000029765
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