Biomarkers of Hepatic Toxicity: An Overview

IF 1.6 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Current Therapeutic Research-clinical and Experimental Pub Date : 2024-01-01 DOI:10.1016/j.curtheres.2024.100737
Simran Thakur Pharm.D , Vishal Kumar Pharm.D , Rina Das PhD , Vishal Sharma M.Pharm , Dinesh Kumar Mehta PhD
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Abstract

Background

Hepatotoxicity is the foremost issue for clinicians and the primary reason for pharmaceutical product recalls. A biomarker is a measurable and quantifiable attribute used to evaluate the efficacy of a treatment or to diagnose a disease. There are various biomarkers which are used for the detection of liver disease and the intent of liver damage.

Objective

This review aims to investigate the current state of hepatotoxicity biomarkers and their utility in clinical settings. Using hepatic biomarkers, the presence of liver injury, its severity, prognosis, causative agent, and type of hepatotoxicity can all be determined.

Methods

Relevant published articles up to 2022 were systematically retrieved from MEDLINE/PubMed, SCOPUS, EMBASE, and WOS databases using keywords such as drug toxicity, hepatotoxicity biomarkers, biochemical parameters, and nonalcoholic fatty liver disease.

Results

In clinical trials and everyday practice, biomarkers of drug-induced liver injury are essential for spotting the most severe cases of hepatotoxicity. Hence, developing novel biomarker approaches to enhance hepatotoxicity diagnosis will increase specificity and/or identify the person at risk. Importantly, early clinical studies on patients with liver illness have proved that some biomarkers such as aminotransferase, bilirubin, albumin, and bile acids are even therapeutically beneficial.

Conclusions

By assessing the unique signs of liver injury, health care professionals can rapidly and accurately detect liver damage and evaluate its severity. These measures contribute to ensuring prompt and effective medical intervention, hence reducing the risk of long-term liver damage and other major health concerns.

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肝脏毒性的生物标志物:概述
背景肝毒性是临床医生面临的首要问题,也是药品召回的主要原因。生物标志物是一种可测量、可量化的属性,用于评估治疗效果或诊断疾病。本综述旨在研究肝毒性生物标志物的现状及其在临床中的应用。方法使用药物毒性、肝毒性生物标志物、生化指标和非酒精性脂肪肝等关键词,从 MEDLINE/PubMed、SCOPUS、EMBASE 和 WOS 数据库中系统检索了截至 2022 年发表的相关文章。结果在临床试验和日常实践中,药物诱导肝损伤的生物标志物对于发现最严重的肝毒性病例至关重要。因此,开发新的生物标志物方法来提高肝毒性诊断的特异性和/或识别高危人群。重要的是,对肝病患者进行的早期临床研究已经证明,转氨酶、胆红素、白蛋白和胆汁酸等一些生物标志物甚至对治疗有益。这些措施有助于确保及时有效的医疗干预,从而降低长期肝损伤和其他重大健康问题的风险。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
31
审稿时长
3 months
期刊介绍: We also encourage the submission of manuscripts presenting preclinical and very preliminary research that may stimulate further investigation of potentially relevant findings, as well as in-depth review articles on specific therapies or disease states, and applied health delivery or pharmacoeconomics. CTR encourages and supports the submission of manuscripts describing: • Interventions designed to understand or improve human health, disease treatment or disease prevention; • Studies that focus on problems that are uncommon in resource-rich countries; • Research that is "under-published" because of limited access to monetary resources such as English language support and Open Access fees (CTR offers deeply discounted English language editing); • Republication of articles previously published in non-English journals (eg, evidence-based guidelines) which could be useful if translated into English; • Preclinical and clinical product development studies that are not pursued for further investigation based upon early phase results.
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