Evidence map›Paper›PMID 42410805›Full record

ArticleMedicine2026

Association of high-sensitivity troponin with advanced fibrosis in metabolic dysfunction-associated steatotic liver disease and the potential mediating role of inflammation: A cross-sectional study of NHANES, 1999 to 2004.

Chun Yu Li, Yun Xiu Wu, Qing Zhang, Kai Wang

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Article in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Chun Yu LiDepartment of Gastroenterology, Guangdong Provincial People's Hospital, Zhuhai Hospital (Jinwan Central Hospital of Zhuhai), Zhuhai, Guangdong, China.
Yun Xiu WuDepartment of Endocrinology, Guangdong Provincial People's Hospital, Zhuhai Hospital (Jinwan Central Hospital of Zhuhai), Zhuhai, Guangdong, China.
Qing ZhangDepartment of Geriatrics, The Affiliated Taizhou People's Hospital of Nanjing Medical University, Taizhou, Jiangsu, China.
Kai WangDepartment of Gastroenterology, The Affiliated Taizhou People's Hospital of Nanjing Medical University, Taizhou, Jiangsu, China.ORCID 0009-0002-0122-6995

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given the high prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD) and its severe adverse hepatic outcomes, risk stratification for patients with MASLD is crucial. Notably, cardiovascular disease (CVD) represents the leading cause of mortality in this population. High-sensitivity troponin (hs-troponin) is a well-established biomarker of subclinical myocardial injury and predicts cardiovascular outcomes. However, its specific relationship with advanced liver fibrosis (ALF) in MASLD remains unexplored. Therefore, we investigated this association in individuals with MASLD without CVD. We analyzed data from 4684 adults aged ≥18 years in the 1999 to 2004 National Health and Nutrition Examination Survey. Multivariable logistic regression examined associations between hs-troponin and ALF. Diagnostic utility was assessed using receiver operating characteristic curve analysis. Moreover, we conducted a mediation analysis to explore the role of inflammation, as represented by the monocyte-to-lymphocyte ratio, in the aforementioned association. Among 4684 patients without CVD, 169 had ALF. After controlling for confounding factors, hs-troponin T showed a significant positive association with ALF (adjusted odds ratio: 1.02, 95% confidence interval: 1.01-1.03, P = .020). Additionally, receiver operating characteristic analysis indicated that at a cutoff of 7.28 ng/L, hs-troponin T predicted ALF with an area under the curve of 0.85 (95% confidence interval: 0.82-0.88). Further mediation analysis revealed that inflammation partially mediated the association between hs-troponin T and ALF. Our findings indicate that elevated hs-troponin T is independently associated with a higher risk of ALF, which can assist clinicians in risk stratification for this population. These findings suggest that hs-troponin T, a marker of subclinical cardiovascular stress, may also serve as a practical tool for hepatic risk stratification.

Indexed as

Fatty LiverInflammationLiver CirrhosisTroponinTroponin TAdultAgedBiomarkersCross-Sectional StudiesFemaleHumansMaleMiddle AgedNutrition SurveysROC CurveUnited StatesBiomarkersTroponinTroponin Tadvanced liver fibrosishs-troponin Tinflammation markermetabolic dysfunction-associated steatotic liver diseaseNHANES

Identifiers

PMID42410805
PMCPMC13337054

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.