miRNAs in patients with alcoholic liver disease: a systematic review and meta-analysis.

IF 3.8 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Tengyue Hu, Chang Hai Liu, Yurong Zheng, Jialin Ji, Yantong Zheng, Si-Ke He, Dongbo Wu, Wei Jiang, Qingmin Zeng, Nannan Zhang, Hong Tang
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引用次数: 0

Abstract

Introduction: Alcoholic liver disease (ALD) encompasses a spectrum of liver conditions, including liver steatosis, alcoholic hepatitis (AH), fibrosis, cirrhosis, and hepatocellular carcinoma (HCC). microRNAs (miRNAs) have garnered significant interest as potential biomarkers for ALD.

Methods: We searched PubMed, Embase, Web of Science and Cochrane Central Register of Controlled Trials (CENTRAL) systemically from inception to June 2024. All extracted data was stratified according to the stages of ALD. The vote-counting strategy performed a meta-analysis on miRNA expression profiles.

Results: We included 40 studies. In serum of individuals with alcohol-use vs. no alcohol-use, miRNA-122 and miRNA-155 were upregulated, and miRNA-146a was downregulated. In patients with ALD vs. healthy controls, miRNA-122 and miRNA-155 were also upregulated, and miRNA-146a was downregulated. However, in patients with AH vs. healthy individuals, only the serum miRNA-122 level was upregulated. Due to insufficient data on diagnostic accuracy, we failed to conclude the ability of miRNAs to distinguish between different stages of ALD-related liver fibrosis. The results for ALD-related HCC were also insufficient and controversial.

Conclusions: Circulating miRNA-122 was the most promising biomarker to manage individuals with ALD. More studies were needed for the diagnostic accuracy of miRNAs in ALD.

Registration: This protocol was registered on the International Prospective Register of Systematic Reviews (PROSPERO) (www.crd.york.ac.uk/prospero/) with registration number CRD42023391931.

酒精性肝病患者体内的 miRNA:系统综述与荟萃分析。
导言:酒精性肝病(ALD)包括一系列肝脏疾病,包括肝脂肪变性、酒精性肝炎(AH)、肝纤维化、肝硬化和肝细胞癌(HCC)。microRNAs(miRNAs)作为ALD的潜在生物标志物引起了人们的极大兴趣:我们对 PubMed、Embase、Web of Science 和 Cochrane Central Register of Controlled Trials (CENTRAL) 进行了从开始到 2024 年 6 月的系统检索。所有提取的数据均根据 ALD 的分期进行了分层。计票策略对 miRNA 表达谱进行了荟萃分析:我们纳入了 40 项研究。在酗酒者与未酗酒者的血清中,miRNA-122和miRNA-155上调,miRNA-146a下调。在 ALD 患者与健康对照组中,miRNA-122 和 miRNA-155 也上调,miRNA-146a 下调。然而,与健康人相比,AH 患者只有血清 miRNA-122 水平上调。由于诊断准确性方面的数据不足,我们未能就 miRNA 区分 ALD 相关肝纤维化不同阶段的能力得出结论。ALD相关性肝癌的研究结果也不充分,且存在争议:结论:循环 miRNA-122 是管理 ALD 患者最有希望的生物标志物。结论:循环 miRNA-122 是管理 ALD 患者最有希望的生物标志物,还需要更多研究来确定 miRNA 在 ALD 中的诊断准确性:本研究方案已在国际系统综述前瞻性注册中心(PROSPERO)(www.crd.york.ac.uk/prospero/)注册,注册号为CRD42023391931。
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来源期刊
Expert Review of Gastroenterology & Hepatology
Expert Review of Gastroenterology & Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.80
自引率
2.60%
发文量
86
审稿时长
6-12 weeks
期刊介绍: The enormous health and economic burden of gastrointestinal disease worldwide warrants a sharp focus on the etiology, epidemiology, prevention, diagnosis, treatment and development of new therapies. By the end of the last century we had seen enormous advances, both in technologies to visualize disease and in curative therapies in areas such as gastric ulcer, with the advent first of the H2-antagonists and then the proton pump inhibitors - clear examples of how advances in medicine can massively benefit the patient. Nevertheless, specialists face ongoing challenges from a wide array of diseases of diverse etiology.
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