Evidence map›Paper›PMID 42779140›Full record

ArticleJournal of clinical laboratory analysis2026

Association of IFN-γ +874 T/A Polymorphism With COVID-19 Susceptibility, Severity, and Inflammatory Response: A Case-Control Study From Southern Iran.

Nasir Arefinia, Bahman Aghcheli, Seyed Mohammad Ali Hashemi, Zohreh-Al-Sadat Ghoreshi, Emad Behboudi

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Article in Journal of clinical laboratory analysis, 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Nasir ArefiniaBio Environmental Health Hazards Research Center, Jiroft University of Medical Sciences, Jiroft, Iran.ORCID https://orcid.org/0000-0002-7282-3538
Bahman AghcheliInfectious Disease Research Center, Gonabad University of Medical Sciences, Gonabad, Iran.ORCID https://orcid.org/0000-0001-9444-7337
Seyed Mohammad Ali HashemiDepartment of Bacteriology & Virology, Shiraz University of Medical Sciences, Shiraz, Iran.
Zohreh-Al-Sadat GhoreshiFaculty of Medicine, Jiroft University of Medical Sciences, Jiroft, Iran.
Emad BehboudiDepartment of Basic Medical Sciences, Khoy University of Medical Sciences, Khoy, Iran.ORCID https://orcid.org/0000-0002-8971-0775

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSignificant interpatient variability in Coronavirus Disease 2019 (COVID-19) manifestations highlights the influence of host genetic factors on disease outcomes. This study examines its association with COVID-19 susceptibility, severity, and inflammatory markers in an Iranian population.

methodsA retrospective case-control analysis was performed on 210 COVID-19 patients and 210 age- and sex-matched control subjects to evaluate whether the Interferon-gamma (IFN-γ) gene polymorphism (+874 T/A) is associated with disease severity.

resultsPatients had more comorbidities (e.g., diabetes 26.2% vs. 14.3%; hypertension 29.5% vs. 16.7%) and pronounced paraclinical abnormalities, including elevated Neutrophil-to-Lymphocyte Ratio (NLR) (8.1 vs. 1.9), C-reactive protein (CRP) (45.5 vs. 3.2 mg/L), and lymphopenia (1.1 vs. 2.1 × 10

conclusionThe IFN-γ +874 TA genotype was independently associated with severe COVID-19. The TA genotype appears to confer increased risk of severe disease, whereas the AA genotype may be linked to a milder clinical presentation despite elevated inflammatory markers. Integration of genetic and hematological parameters may enhance risk stratification; however, further validation in larger and diverse populations is warranted.

Indexed as

clinical outcomeCOVID‐19disease severityhost geneticsIFN‐γinterleukin‐6

Identifiers

PMID42779140
PMCPMC13601768

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