Evidence map›Paper›PMID 41896785›Full record

ArticleBMC pediatrics2026

Fibroblast growth factor 21 and growth differentiation factor 15 as biomarkers for oxidative stress in children with methylmalonic acidemia.

Maha A Abd Elbaky, Mohamed Shehata, Khalil Abdelkhalek, Marian Y Girgis, Mohamed A Elmonem

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Article in BMC pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers 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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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Maha A Abd ElbakyDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Mohamed ShehataDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Khalil AbdelkhalekDepartment of Pediatrics, Faculty of Medicine, Cairo University, Cairo, Egypt.
Marian Y GirgisDepartment of Pediatrics, Faculty of Medicine, Cairo University, Cairo, Egypt.
Mohamed A ElmonemDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt. mohamed.abdelmonem@kasralainy.edu.eg.ORCID 0000-0002-3154-1948

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMethylmalonic acidemia (MMA) is a rare autosomal recessive inborn error of metabolism commonly presenting in infancy with episodes of metabolic acidosis that can lead to considerable morbidity and early mortality. Oxidative stress is a major aspect in the pathogenesis of MMA. We aimed to evaluate the clinical utility of fibroblast growth factor 21 (FGF21) and growth differentiation factor 15 (GDF15) and correlate their levels with established biomarkers of oxidative stress, such as reduced glutathione (GSH) and reduced/oxidized (GSH/GSSG) glutathione ratio in MMA children in a clinical setting.

methodsNineteen MMA pediatric patients (median 5.7; IOR 2.9–7.3 years) were recruited. Thirty age and sex matched healthy children were further recruited as a comparator group. Total glutathione, reduced glutathione, FGF21 and GDF15 were assayed for both cohorts.

resultsTotal and reduced glutathione were significantly reduced in MMA patients compared to controls (P < 0.001 for both), while FGF21 and GDF15 were significantly elevated (P = 0.037 and < 0.001, respectively). Both FGF21 and GDF15 had a significant negative correlation with GSH/GSSG ratio (r=–0.256; P = 0.038 and r=–0.367; P = 0.005, respectively); however, only GDF15 had a negative correlation with both total and reduced glutathione (r=–0.443; P < 0.001 and r=–0.459; P < 0.001, respectively). GDF15 had a better performance in the ROC curve analysis; AUC = 0.805 vs. 0.668 for FGF21, while FGF21 was a significant predictor of eGFR in the linear regression analysis.

conclusionsFGF21 and GDF15 were both significantly increased in the studied MMA pediatric patients and had strong correlations with established oxidative stress biomarkers. Since both are more stable during storage and easier to assay than glutathione based indicators, their use as candidate biomarkers for oxidative stress in MMA children can be considered.

Indexed as

Amino Acid Metabolism, Inborn ErrorsFibroblast Growth FactorsGrowth Differentiation Factor 15Oxidative StressBiomarkersCase-Control StudiesChildChild, PreschoolFemaleGlutathioneHumansMaleROC CurveBiomarkersFGF21 protein, humanfibroblast growth factor 21Fibroblast Growth FactorsGDF15 protein, humanGlutathioneGrowth Differentiation Factor 15FGF21GDF15GlutathioneOrganic acidemiaOxidative stress

Identifiers

PMID41896785
PMCPMC13063588

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