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Circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis
BACKGROUND: Chemerin is a novel adipokine which is associated with metabolic syndrome and type 2 diabetes mellitus. However, recent investigations regarding circulating chemerin levels in gestational diabetes mellitus (GDM) are conflicting. This meta-analysis is to evaluate and determine their assoc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058359/ https://www.ncbi.nlm.nih.gov/pubmed/30041634 http://dx.doi.org/10.1186/s12944-018-0826-1 |
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author | Zhou, Zhongwei Chen, Hongmei Ju, Huixiang Sun, Mingzhong |
author_facet | Zhou, Zhongwei Chen, Hongmei Ju, Huixiang Sun, Mingzhong |
author_sort | Zhou, Zhongwei |
collection | PubMed |
description | BACKGROUND: Chemerin is a novel adipokine which is associated with metabolic syndrome and type 2 diabetes mellitus. However, recent investigations regarding circulating chemerin levels in gestational diabetes mellitus (GDM) are conflicting. This meta-analysis is to evaluate and determine their associations. METHODS: A systematic literature search was performed in PubMed, EMBASE and Web of Science up to 13 December 2017. Pooled standardized mean differences (SMD) and 95% confidence interval (CI) were calculated using a random-effect model. RESULTS: Eleven studies comprising 742 GDM patients and 840 normal pregnant women were included. Circulating chemerin levels were increased in GDM patients compared with healthy pregnant women (SMD: 1.16; 95% CI: 0.29, 2.04; P = 0.009). Subgroup analyses revealed such difference was especially available in the groups of the second trimester (SMD: 1.47; 95% CI: 0.28, 2.67) and mean age < 30 years (SMD: 2.30; 95% CI: 0.69, 3.91) of GDM patients. There was significant heterogeneity among studies (I(2) = 98.0%, P < 0.001); however, heterogeneity disappeared or markedly decreased in the subgroups of European populations (I(2) = 0.0%, P = 0.531), age ≥ 30 years (I(2) = 28.2%, P = 0.223) and WHO diagnostic criteria (I(2) = 0.0%, P = 0.490) when stratifying by study location, trimester of chemerin measurement and the diagnostic criteria of GDM. CONCLUSIONS: The elevated levels of circulating chemerin were associated with GDM, which suggests it might play an important role in the pathogenetic mechanism of GDM. |
format | Online Article Text |
id | pubmed-6058359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60583592018-07-30 Circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis Zhou, Zhongwei Chen, Hongmei Ju, Huixiang Sun, Mingzhong Lipids Health Dis Review BACKGROUND: Chemerin is a novel adipokine which is associated with metabolic syndrome and type 2 diabetes mellitus. However, recent investigations regarding circulating chemerin levels in gestational diabetes mellitus (GDM) are conflicting. This meta-analysis is to evaluate and determine their associations. METHODS: A systematic literature search was performed in PubMed, EMBASE and Web of Science up to 13 December 2017. Pooled standardized mean differences (SMD) and 95% confidence interval (CI) were calculated using a random-effect model. RESULTS: Eleven studies comprising 742 GDM patients and 840 normal pregnant women were included. Circulating chemerin levels were increased in GDM patients compared with healthy pregnant women (SMD: 1.16; 95% CI: 0.29, 2.04; P = 0.009). Subgroup analyses revealed such difference was especially available in the groups of the second trimester (SMD: 1.47; 95% CI: 0.28, 2.67) and mean age < 30 years (SMD: 2.30; 95% CI: 0.69, 3.91) of GDM patients. There was significant heterogeneity among studies (I(2) = 98.0%, P < 0.001); however, heterogeneity disappeared or markedly decreased in the subgroups of European populations (I(2) = 0.0%, P = 0.531), age ≥ 30 years (I(2) = 28.2%, P = 0.223) and WHO diagnostic criteria (I(2) = 0.0%, P = 0.490) when stratifying by study location, trimester of chemerin measurement and the diagnostic criteria of GDM. CONCLUSIONS: The elevated levels of circulating chemerin were associated with GDM, which suggests it might play an important role in the pathogenetic mechanism of GDM. BioMed Central 2018-07-24 /pmc/articles/PMC6058359/ /pubmed/30041634 http://dx.doi.org/10.1186/s12944-018-0826-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Zhou, Zhongwei Chen, Hongmei Ju, Huixiang Sun, Mingzhong Circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis |
title | Circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis |
title_full | Circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis |
title_fullStr | Circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis |
title_full_unstemmed | Circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis |
title_short | Circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis |
title_sort | circulating chemerin levels and gestational diabetes mellitus: a systematic review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058359/ https://www.ncbi.nlm.nih.gov/pubmed/30041634 http://dx.doi.org/10.1186/s12944-018-0826-1 |
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