Evidence map›Paper›PMID 42230515›Full record

ArticleIrish journal of medical science2026

Circulating fibroblast growth factor-21 in coronary artery disease: a systematic review and meta-analysis.

Feryal Shawa, Fatma Izzeddin, Gulsah Koc

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Article in Irish journal of medical science, 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Feryal ShawaInstitute of Graduate Studies, Molecular Medicine Program, Istanbul Aydin University, Istanbul, Turkey.ORCID http://orcid.org/0009-0004-5586-5893
Fatma IzzeddinInstitute of Graduate Studies, Molecular Medicine Program, Istanbul Aydin University, Istanbul, Turkey.ORCID http://orcid.org/0009-0002-1113-7654
Gulsah KocDepartment of Medical Biology, Faculty of Medicine, Istanbul Aydin University, Istanbul, Turkey. gulsahkoc@aydin.edu.tr.ORCID http://orcid.org/0000-0002-9678-5652

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFibroblast growth factor-21 (FGF21) is a metabolic regulator involved in glucose and lipid homeostasis and has emerged as a potential biomarker in cardiometabolic diseases. The relationship between circulating FGF21 levels and coronary artery disease (CAD) remains unclear. We performed a systematic review and meta-analysis to clarify this association and assess its clinical relevance.

methodsPubMed, Web of Science, and Scopus were searched for observational studies reporting circulating FGF21 levels in adult CAD patients. Standardized mean differences (SMDs) with 95% confidence intervals were calculated using a random-effects model. Subgroup and meta-regression analyses were conducted to explore heterogeneity.

resultsFourteen studies including 2963 CAD patients were analyzed. Circulating FGF21 levels were significantly higher in CAD patients than in controls (SMD = 0.90; 95% CI: 0.26-1.54; p = 0.0056). In acute CAD, the increase was more pronounced (SMD = 1.70; 95% CI: 0.20-3.21). Elevated FGF21 persisted even when diabetes prevalence was low (SMD = 1.50; 95% CI: 0.15-2.84). Meta-regression identified BMI and HDL as independent contributors to inter-study variability. Sensitivity analyses confirmed robustness, and no strong evidence of publication bias was detected.

conclusionsCirculating FGF21 is elevated in CAD, primarily reflecting metabolic disturbances-particularly adiposity and dyslipidemia-rather than diabetes or CAD itself. Levels tend to be higher during acute events, suggesting that FGF21 may serve as a marker of metabolic stress and lipid abnormalities rather than a direct diagnostic biomarker.

Indexed as

Acute coronary syndromeBiomarkerCoronary artery diseaseFibroblast growth factor 21Meta-analysisMyocardial infarction

Identifiers

PMID42230515

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