Circulating glycated albumin levels and gestational diabetes mellitus.

IF 4.2 3区 医学 Q1 ENDOCRINOLOGY & METABOLISM World Journal of Diabetes Pub Date : 2024-08-15 DOI:10.4239/wjd.v15.i8.1802
Wei Xiong, Zhao-Hui Zeng, Yuan Xu, Hui Li, Hui Lin
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Abstract

Background: Gestational diabetes mellitus (GDM) is characterized by glucose intolerance that is first diagnosed during pregnancy, making it the most common complication associated with this period. Early detection and targeted treatment of GDM can minimize foetal exposure to maternal hyperglycaemia and subsequently reduce the associated adverse pregnancy outcomes. Previous studies have inconsistently suggested that the level of glycated albumin (GA) might predict GDM.

Aim: To review and synthesize existing evidence to evaluate the relationship between GA levels and the development of GDM.

Methods: We sought to compare GA levels between GDM and control groups in this meta-analysis by systematically searching the Web of Science, PubMed, Cochrane Library, and Embase databases for articles published up to June 2023. The analysis utilized the weighted mean difference (WMD) as the primary metric. The data were meticulously extracted, and the quality of the included studies was assessed. Additionally, we conducted a subgroup analysis based on study region and sample size. We assessed heterogeneity using I 2 statistics and evaluated publication bias through funnel plots. Additionally, trim-and-fill analysis was employed to detect and address any potential publication bias.

Results: The meta-analysis included a total of 11 studies involving 5477 participants, comprising 1900 patients with GDM and 3577 control individuals. The synthesized results revealed a notable correlation between elevated GA levels and increased susceptibility to GDM. The calculated WMD was 0.42, with a 95% confidence interval (95%CI) ranging from 0.11 to 0.74, yielding a P value less than 0.001. Concerning specific GA levels, the mean GA level in the GDM group was 12.6, while for the control group, it was lower, at 11.6. This discrepancy underscores the potential of GA as a biomarker for assessing GDM risk. Moreover, we explored the levels of glycated haemoglobin (HbA1c) in both cohorts. The WMD for HbA1c was 0.19, with a 95%CI ranging from 0.15 to 0.22 and a P value less than 0.001. This observation suggested that both GA and HbA1c levels were elevated in individuals in the GDM group compared to those in the control group.

Conclusion: Our meta-analysis revealed a substantial correlation between elevated GA levels and increased GDM risk. Furthermore, our findings revealed elevated levels of HbA1c in GDM patients, emphasizing the significance of monitoring both GA and HbA1c levels for early GDM detection and effective management.

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循环糖化白蛋白水平与妊娠糖尿病。
背景:妊娠期糖尿病(GDM)的特点是在妊娠期间首次诊断出葡萄糖不耐受,这也是妊娠期最常见的并发症。早期发现并有针对性地治疗 GDM 可最大限度地减少胎儿受母体高血糖影响的机会,从而减少相关的不良妊娠结局。目的:回顾并综合现有证据,评估糖化白蛋白(GA)水平与 GDM 发生之间的关系:我们通过系统搜索 Web of Science、PubMed、Cochrane Library 和 Embase 数据库中截至 2023 年 6 月发表的文章,试图在这项荟萃分析中比较 GDM 组和对照组之间的 GA 水平。分析采用加权平均差(WMD)作为主要指标。我们对数据进行了细致的提取,并对纳入研究的质量进行了评估。此外,我们还根据研究地区和样本大小进行了亚组分析。我们使用I 2统计量评估了异质性,并通过漏斗图评估了发表偏倚。此外,我们还采用了修剪填充分析来检测和解决任何潜在的发表偏倚:荟萃分析共纳入了 11 项研究,涉及 5477 名参与者,其中包括 1900 名 GDM 患者和 3577 名对照者。综合结果显示,GA 水平升高与 GDM 易感性增加之间存在显著相关性。计算得出的 WMD 为 0.42,95% 置信区间 (95%CI) 为 0.11 至 0.74,P 值小于 0.001。关于具体的 GA 水平,GDM 组的平均 GA 水平为 12.6,而对照组则较低,为 11.6。这一差异凸显了 GA 作为评估 GDM 风险的生物标志物的潜力。此外,我们还研究了两组人群的糖化血红蛋白(HbA1c)水平。HbA1c 的 WMD 为 0.19,95%CI 为 0.15 至 0.22,P 值小于 0.001。这一观察结果表明,与对照组相比,GDM 组的 GA 和 HbA1c 水平均有所升高:我们的荟萃分析表明,GA 水平升高与 GDM 风险增加之间存在密切联系。此外,我们的研究结果还显示,GDM 患者的 HbA1c 水平也有所升高,这强调了监测 GA 和 HbA1c 水平对于早期发现 GDM 并进行有效管理的重要性。
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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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