Evidence map›Paper›PMID 40652433›Full record

ArticleInternational journal of hematology2025

Growth differentiation factor-15 as a non-invasive biomarker of liver fibrosis in sickle cell disease.

Konstantinos Manganas, Sophia Delicou, Emilia Hadziyannis, Stavroula Giannouli, John Koskinas

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Article in International journal of hematology, 2025. 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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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

5 authors.

Konstantinos ManganasThalassemia and Sickle Cell Unit, Hippokration General Hospital, 114 Vas. Sofias, 11527, Athens, Greece. kmagganas92@gmail.com.ORCID http://orcid.org/0000-0002-9844-2813
Sophia DelicouThalassemia and Sickle Cell Unit, Hippokration General Hospital, 114 Vas. Sofias, 11527, Athens, Greece.
Emilia HadziyannisSecond Department of Internal Medicine and Research Laboratory, Medical School, National and Kapodistrian University of Athens, Hippokration General Hospital, Athens, Greece.
Stavroula GiannouliSecond Department of Internal Medicine and Research Laboratory, Medical School, National and Kapodistrian University of Athens, Hippokration General Hospital, Athens, Greece.
John KoskinasSecond Department of Internal Medicine and Research Laboratory, Medical School, National and Kapodistrian University of Athens, Hippokration General Hospital, Athens, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to evaluate the relationship between growth differentiation factor-15 (GDF-15) levels and liver fibrosis in patients with sickle cell disease (SCD) and assess the diagnostic performance of GDF-15 as a non-invasive biomarker. Thirty patients with SCD were categorized into two groups based on fibrosis severity (≥ F2 vs. < F2) determined by Fibroscan, AST to Platelet Ratio Index (APRI) and FIB-4. GDF-15 levels were compared between groups, and independent predictors of GDF-15 were identified by multiple linear regression. Patients with significant liver fibrosis (≥ F2) had significantly higher GDF-15 levels. Multivariate linear regression revealed that GDF-15 concentration was independently associated with liver elastography values (β = 0.619, p = 0.002). The area under the curve for detecting significant fibrosis using GDF-15 as a diagnostic test was 0.835 (95% CI: 0.686-0.983, p = 0.002). A GDF-15 cut-off of 4200 pg/ml had a positive predictive value of 73.6%, a negative predictive value of 81.8%, sensitivity of 87.5% and specificity of 64.3%. In conclusion, GDF-15 is strongly associated with liver fibrosis in SCD and demonstrates high diagnostic accuracy as a non-invasive biomarker. Given its role in inflammation, oxidative stress, and iron metabolism, GDF-15 may serve as a valuable tool for early fibrosis detection and disease monitoring.

Indexed as

Anemia, Sickle CellGrowth Differentiation Factor 15Liver CirrhosisAdolescentAdultBiomarkersElasticity Imaging TechniquesFemaleHumansMaleMiddle AgedYoung AdultBiomarkersGDF15 protein, humanGrowth Differentiation Factor 15FibroscanGDF-15Liver fibrosisNon-invasive diagnosisSickle cell disease

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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.