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糖尿病中缺血修饰白蛋白的系统评价与荟萃分析。

A systematic review and meta-analysis of ischemia-modified albumin in diabetes mellitus.

作者信息

Zinellu Angelo, Mangoni Arduino A

机构信息

Department of Biomedical Sciences, University of Sassari, Sassari, Italy.

Discipline of Clinical Pharmacology, College of Medicine and Public Health, Flinders University, Adelaide, Australia.

出版信息

Heliyon. 2024 Aug 10;10(16):e35953. doi: 10.1016/j.heliyon.2024.e35953. eCollection 2024 Aug 30.

Abstract

AIM

There is an ongoing search for novel biomarkers of diabetes. We conducted a systematic review and meta-analysis of the serum concentrations of ischemia-modified albumin (IMA), a candidate biomarker of oxidative stress, acidosis, and ischemia, in patients with pre-diabetes, different types of diabetes mellitus (type 1, T1DM, type 2, T2DM, and gestational, GDM), and healthy controls.

METHODS

We searched for case-control studies published in PubMed, Web of Science, and Scopus from inception to December 31, 2023. The risk of bias and the certainty of evidence were assessed using the Joanna Briggs Institute Critical Appraisal Checklist and GRADE, respectively.

RESULTS

In 29 studies, T2DM patients had significantly higher IMA concentrations when compared to controls (standard mean difference, SMD = 1.83, 95 % CI 1.46 to 2.21, p˂0.001; I = 95.7 %, p < 0.001; low certainty of evidence). Significant associations were observed between the SMD and glycated hemoglobin (p = 0.007), creatinine (p = 0.003), triglycerides (p = 0.029), and the presence of diabetes complications (p = 0.003). Similar trends, albeit in a smaller number of studies, were observed in T1DM (two studies; SMD = 1.59, 95 % CI -0.09 to 3.26, p˂0.063; I = 95.8 %, p < 0.001), GDM (three studies; SMD = 3.41, 95 % CI 1.14 to 5.67, p = 0.003; I = 97.0 %, p < 0.001) and pre-diabetes (three studies; SMD = 15.25, 95 % CI 9.86 to 20.65, p˂0.001; I = 99.3 %, p < 0.001).

CONCLUSION

Our study suggests that IMA is a promising biomarker for determining the presence of oxidative stress, acidosis, and ischemia in pre-diabetes and T1DM, T2DM, and GDM. However, the utility of measuring circulating IMA warrants confirmation in prospective studies investigating clinical endpoints in pre-diabetes and in different types of diabetes (PROSPERO registration number: CRD42024504690).

摘要

目的

一直在寻找新型糖尿病生物标志物。我们对糖尿病前期、不同类型糖尿病(1型糖尿病,T1DM;2型糖尿病,T2DM;妊娠糖尿病,GDM)患者及健康对照者血清中缺血修饰白蛋白(IMA)的浓度进行了系统评价和荟萃分析,IMA是氧化应激、酸中毒和缺血的候选生物标志物。

方法

检索了PubMed、Web of Science和Scopus数据库中从建库至2023年12月31日发表的病例对照研究。分别使用乔安娜·布里格斯研究所批判性评价清单和GRADE评估偏倚风险和证据确定性。

结果

在29项研究中,与对照组相比,T2DM患者的IMA浓度显著更高(标准均数差,SMD = 1.83,95%可信区间1.46至2.21,p < 0.001;I = 95.7%,p < 0.001;证据确定性低)。观察到SMD与糖化血红蛋白(p = 0.007)、肌酐(p = 0.003)、甘油三酯(p = 0.029)以及糖尿病并发症的存在(p = 0.003)之间存在显著关联。在T1DM(两项研究;SMD = 1.59,95%可信区间 -0.09至3.26,p < 0.063;I = 95.8%,p < 0.001)、GDM(三项研究;SMD = 3.41,95%可信区间1.14至5.67,p = 0.003;I = 97.0%,p < 0.001)和糖尿病前期(三项研究;SMD = 15.25,95%可信区间9.86至20.65,p < 0.001;I = 99.3%,p < 0.001)中也观察到了类似趋势,尽管研究数量较少。

结论

我们的研究表明,IMA是用于确定糖尿病前期、T1DM、T2DM和GDM中氧化应激、酸中毒和缺血存在情况的有前景的生物标志物。然而,测量循环IMA的效用有待在前瞻性研究中得到证实,这些研究调查糖尿病前期和不同类型糖尿病的临床终点(PROSPERO注册号:CRD(2024)504690)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6978/11366936/86719806d1e9/gr1.jpg

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