Evidence map›Paper›PMID 41286678›Full record

ArticleBMC infectious diseases2025

Serum asprosin levels as a potential prognostic biomarker in COVID-19: insights for future respiratory viral pandemics.

Esra Erdoğan, Azize Yetişgen

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Article in BMC infectious diseases, 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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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Esra ErdoğanDepartment of Basic Sciences of Pharmacy, Faculty of Pharmacy, Harran University, Yenişehir Campus, Şanlıurfa, Türkiye. esraerdogan@harran.edu.tr.
Azize YetişgenInfectious Diseases Clinic, Malatya Training and Research Hospital, Malatya, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough the initial surge of the COVID-19 pandemic has passed, identifying prognostic biomarkers remains critical for managing severe cases and preparing for future respiratory viral outbreaks. Asprosin, a metabolic hormone involved in energy homeostasis and inflammation, has been linked to cardiometabolic disorders, but its relationship with COVID-19 severity has not been fully elucidated. This prospective study aimed to investigate the association between serum asprosin levels, disease severity, and clinical outcomes in COVID-19 patients.

methodsA total of 121 participants were enrolled, including 95 hospitalized patients with RT-PCR-confirmed COVID-19 and 26 PCR-negative controls. Patients were classified into mild, moderate, or severe pneumonia groups based on chest CT findings. Demographic, clinical, and laboratory parameters-including serum asprosin-were analyzed for differences between groups and correlations with disease severity.

resultsSerum asprosin levels were significantly higher in COVID-19 patients compared to controls (p < 0.001) and served as an independent predictor of COVID-19 positivity (OR = 2.13, p = 0.017). ROC analysis demonstrated strong diagnostic performance (AUC = 0.849, p < 0.001), with a cut-off of 4.71 ng/mL yielding 98.9% sensitivity and 69.2% specificity. COVID-19 patients also showed higher ferritin, CRP, and urea, and lower platelet and albumin levels (p < 0.001). Mortality was strongly associated with pneumonia severity (p < 0.001); low oxygen saturation and hypertension emerged as independent predictors of severity. Asprosin correlated positively with fibrinogen and negatively with comorbidity count. Patients with diabetes mellitus had significantly lower asprosin levels (p = 0.042), while no significant differences were observed according to mortality status.

conclusionsElevated serum asprosin in COVID-19 patients suggests involvement in metabolic and inflammatory responses. Although unrelated to disease severity, it may aid diagnosis and reflect systemic stress. Larger multicenter studies are needed to confirm its biomarker and therapeutic potential. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

COVID-19Fibrillin-1AdipokinesAdultAgedBiomarkersFemaleHumansMaleMiddle AgedPandemicsPrognosisProspective StudiesROC CurveSARS-CoV-2Severity of Illness IndexAdipokinesBiomarkersFBN1 protein, humanFibrillin-1AsprosinCOVID-19Disease severityInflammationSARS-CoV-2

Identifiers

PMID41286678
PMCPMC12751601

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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.