{"title":"Circulating Asprosin and Neuregulin-4 in metabolic dysfunction-associated steatotic liver disease (MASLD): A systematic review and meta-analysis","authors":"Roshan Kumar Mahat , Vedika Rathore","doi":"10.1016/j.cegh.2025.102041","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Adipokines, such as asprosin and neuregulin 4 (Nrg4), are implicated in the pathogenesis of metabolic dysfunction-associated steatotic liver disease (MASLD) and may function as potential diagnostic biomarkers and therapeutic targets. The objective of this meta-analysis is to compare the circulating levels of asprosin and Nrg4 between populations with MASLD and those without the condition.</div></div><div><h3>Methods</h3><div>A systematic review and meta-analysis were conducted in accordance with the PRISMA guidelines. Databases including PubMed, Scopus, and Europe PMC were systematically searched for observational studies published until October 7, 2024. Inclusion criteria consisted of studies that reported extractable data on circulating asprosin and Nrg4 in populations with and without MASLD. Random-effects models were employed to calculate standardized mean differences (SMDs) and mean differences (MDs) with 95 % confidence intervals (CIs). Heterogeneity among studies was assessed using Cochrane's Q test, as well as <em>I</em><sup><em>2</em></sup> and Tau<sup>2</sup> statistics. Furthermore, sensitivity analysis and publication bias were evaluated to ensure the robustness of the findings.</div></div><div><h3>Results</h3><div>Ten studies were included, with four analysing asprosin and six analysing Nrg4. Patients with MASLD exhibited significantly higher circulating asprosin levels (SMD = 0.82, 95 % CI: 0.49–1.15; <em>p</em> < 0.01; <em>I</em><sup><em>2</em></sup> = 65 %) and lower Nrg4 levels (SMD = −1.12, 95 % CI: 1.77 to −0.46; <em>p</em> < 0.01; <em>I</em><sup><em>2</em></sup> = 94 %) compared to non-MASLD individuals. Sensitivity analyses confirmed the robustness of these findings.</div></div><div><h3>Conclusions</h3><div>Elevated asprosin and reduced Nrg4 levels are associated with MASLD, highlighting their potential as biomarkers and therapeutic targets. Further studies are warranted to validate these findings.</div></div>","PeriodicalId":46404,"journal":{"name":"Clinical Epidemiology and Global Health","volume":"33 ","pages":"Article 102041"},"PeriodicalIF":1.7000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Epidemiology and Global Health","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213398425001307","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/23 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Adipokines, such as asprosin and neuregulin 4 (Nrg4), are implicated in the pathogenesis of metabolic dysfunction-associated steatotic liver disease (MASLD) and may function as potential diagnostic biomarkers and therapeutic targets. The objective of this meta-analysis is to compare the circulating levels of asprosin and Nrg4 between populations with MASLD and those without the condition.
Methods
A systematic review and meta-analysis were conducted in accordance with the PRISMA guidelines. Databases including PubMed, Scopus, and Europe PMC were systematically searched for observational studies published until October 7, 2024. Inclusion criteria consisted of studies that reported extractable data on circulating asprosin and Nrg4 in populations with and without MASLD. Random-effects models were employed to calculate standardized mean differences (SMDs) and mean differences (MDs) with 95 % confidence intervals (CIs). Heterogeneity among studies was assessed using Cochrane's Q test, as well as I2 and Tau2 statistics. Furthermore, sensitivity analysis and publication bias were evaluated to ensure the robustness of the findings.
Results
Ten studies were included, with four analysing asprosin and six analysing Nrg4. Patients with MASLD exhibited significantly higher circulating asprosin levels (SMD = 0.82, 95 % CI: 0.49–1.15; p < 0.01; I2 = 65 %) and lower Nrg4 levels (SMD = −1.12, 95 % CI: 1.77 to −0.46; p < 0.01; I2 = 94 %) compared to non-MASLD individuals. Sensitivity analyses confirmed the robustness of these findings.
Conclusions
Elevated asprosin and reduced Nrg4 levels are associated with MASLD, highlighting their potential as biomarkers and therapeutic targets. Further studies are warranted to validate these findings.
期刊介绍:
Clinical Epidemiology and Global Health (CEGH) is a multidisciplinary journal and it is published four times (March, June, September, December) a year. The mandate of CEGH is to promote articles on clinical epidemiology with focus on developing countries in the context of global health. We also accept articles from other countries. It publishes original research work across all disciplines of medicine and allied sciences, related to clinical epidemiology and global health. The journal publishes Original articles, Review articles, Evidence Summaries, Letters to the Editor. All articles published in CEGH are peer-reviewed and published online for immediate access and citation.