Chemokines in Gestational Diabetes Mellitus

被引:23
作者
Liu, Hongying [1 ]
Liu, Aizhong [1 ,2 ]
Kaminga, Atipatsa C. [1 ,3 ]
McDonald, Judy [4 ]
Wen, Shi Wu [5 ,6 ,7 ]
Pan, Xiongfeng [1 ]
机构
[1] Cent South Univ, Xiangya Sch Publ Hlth, Dept Epidmiol & Hlth Stat, Changsha, Peoples R China
[2] Cent South Univ, Xiangya Sch Publ Hlth, Hunan Prov Key Lab Clin Epidmiol, Changsha, Peoples R China
[3] Mzuzu Univ, Dept Math & Stat, Mzuzu, Malawi
[4] Univ Ottawa, Fac Med, McLaughlin Ctr Populat Hlth Risk Assessment, Ottawa, ON, Canada
[5] Ottawa Hosp, OMNI Res Grp, Res Inst, Ottawa, ON, Canada
[6] Univ Ottawa, Fac Med, Dept Obstet & Gynaecol, Ottawa, ON, Canada
[7] Univ Ottawa, Fac Med, Sch Epidemiol & Publ Hlth, Ottawa, ON, Canada
关键词
chemokines; gestational diabetes mellitus; inflammatory; immune microenvironment; meta-analysis; INSULIN-RESISTANCE; ADIPOSE-TISSUE; TNF-ALPHA; INFLAMMATION; EXPRESSION; PLASMA; PREGNANCY; PLACENTA; WOMEN; POLYMORPHISMS;
D O I
10.3389/fimmu.2022.705852
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundStudies investigating chemokines in gestational diabetes mellitus (GDM) have yielded mixed results. The purpose of this meta-analysis was to explore whether concentrations of chemokines in patients with GDM differed from that of the controls. MethodsFollowing Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, we systematically searched Web of Science, Embase, Cochrane Library, and PubMed databases for articles, published in any language, on chemokines and GDM through August 1st, 2021. The difference in concentrations of chemokines between patients with GDM and controls was determined by a standardized mean difference (SMD) with a 95% confidence interval (CI), calculated in the meta-analysis of the eligible studies using a random-effects model with restricted maximum-likelihood estimator. ResultsSeventeen studies met the inclusion criteria for the meta-analysis. Altogether, they included nine different chemokines comparisons involving 5,158 participants (1,934 GDM patients and 3,224 controls). Results showed a significant increase of these chemokines (CCL2, CXCL1, CXCL8, CXCL9, and CXCL12) in the GDM patients compared with the controls. However, there was a significant decrease of the chemokines, CCL4, CCL11 and CXCL10, in the GDM patients compared with the controls. Moreover, subgroup analysis revealed a potential role of chemokines as biomarkers in relation to laboratory detection (different sample type and assay methods) and clinical characteristics of GDM patients (ethnicity and body mass index). ConclusionGDM is associated with several chemokines (CCL2, CCL4, CCL11, CXCL1, CXCL8, CXCL9, CXCL10 and CXCL12). Therefore, consideration of these chemokines as potential targets or biomarkers in the pathophysiology of GDM development is necessary. Notably, the information of subgroup analysis underscores the importance of exploring putative mechanisms underlying this association, in order to develop new individualized clinical and therapeutic strategies.
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页数:13
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