Evidence map›Paper›PMID 41721256›Full record

ArticleBMC gastroenterology2026

Leptin, vitamin D, and APRI values during the six months post-liver transplantation.

Yasmine A Algobashy, A S Shehatta, Mabdel Wahab, Magdy M Youssef

Abstract read
In one paragraph

Article in BMC gastroenterology, 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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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

4 authors.

Yasmine A AlgobashyDepartment of Biochemistry, Faculty of Science, Mansoura University, Mansoura, Egypt. yasmeenalganiny@mans.edu.eg.
A S ShehattaGastrointestinal Surgery Center, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Mabdel WahabDepartment of Surgery, Faculty of Medicine, Gastrointestinal Surgery Center, Mansoura University, Mansoura, Egypt.
Magdy M YoussefDepartment of Biochemistry, Faculty of Science, Mansoura University, Mansoura, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLiver fibrosis is a common outcome of chronic liver disease, characterized by accumulating extracellular matrix proteins. Aims: While the gold standard in the assessment of liver fibrosis remains liver biopsy, non-invasive methods have been increasingly used for estimating liver fibrosis. This study aims at contributing to our understanding of the role of leptin,vitamin D, APRI, and FIB-4 in the progression of liver disease. For this purpose, we evaluate the clinical significance of leptin, vitamin D, APRI, and FIB-4 in cirrhotic patients with different ratios of steatosis and in cirrhotic pateints with different grades of hepatocellular carcinoma. We compare the performance of simple biochemical scores (FIB-4 and APRI) with leptin and vitamin D. Also, We identified the proteins in the serum of liver fibrosis and showed the role of these proteins in the pathogenesis of liver fibrosis. Also, we identified the relationship between leptin and vitamin D with extracellular matrix proteins using bioinformatics analysis.

methodsThe current study included 50 liver fibrosis patients who underwent liver transplantation. We measured the levels of serum vitamin D and leptin in these patients at pre-LT and three- and six-months post-LT using enzyme-linked immunosorbent assay. We performed qualitative proteomic analysis to identify the proteins in the sera from patients with liver fibrosis. Among these proteins, there are extracellular matrix proteins. One-way ANOVA test was used.

resultsWe found that serum leptin levels and APRI values were significantly higher in liver fibrosis patients than in controls, after three- and six-months following LT serum leptin levels and APRI values significantly decreased. While serum vitamin D levels were significantly lower in liver fibrosis patients than in controls, after three- and six-months following LT, serum vitamin D levels significantly increased. ROC curves analysis showed that the area under the curve (AUC) of vitamin D and leptin was 1 and 0.997, respectively. Gene ontology analysis demonstrated that the proteins participate in a diverse array of biological processes, emphasizing the systemic effects of liver fibrosis disease. From the STRING database, the proteins are at least partially biologically connected, as a group with leptin and vitamin D explaining the promiscuous nature of leptin and vitamin D. This emphasized the role of leptin and vitamin D in accumulation and increased synthesis of extracellular matrix proteins that incorporated in the pathogenesis of liver fibrosis, and showed that the leptin and vitamin D are involved in the pathogenesis process where the total proteins are involved.

conclusionsIn summary, serum vitamin D and leptin could serve as a valuable supplemental biomarker for predicting the liver fibrosis.

Indexed as

Aspartate AminotransferasesLeptinLiver CirrhosisLiver TransplantationVitamin DAdultBiomarkersCarcinoma, HepatocellularDisease ProgressionExtracellular Matrix ProteinsFatty LiverFemaleHumansLiver NeoplasmsMaleMiddle AgedAspartate AminotransferasesBiomarkersExtracellular Matrix ProteinsLeptinVitamin DAPRIFIB-4LeptinLiver fibrosisVitamin D

Identifiers

PMID41721256
PMCPMC12930583

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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.