Evidence map›Paper›PMID 39991164›Full record

ArticleJournal of medical biochemistry2025

Influence of TMPRSS6 genotype on iron status parameters in stable COPD patients.

Marko Trtica, Ivana Novaković, Violeta Dopsaj, Branislava Milenković, Jelena Janković, Sanja Dimić-Janjić, Vesna Dopuđa-Pantić, Jelena Martinović, Snežana Jovičić

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Article in Journal of medical biochemistry, 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

9 authors.

Marko TrticaUniversity of Belgrade, Faculty of Pharmacy, Department of Medical Biochemistry, Belgrade.
Ivana NovakovićUniversity of Belgrade, Faculty of Medicine, Institute of Human Genetics, Belgrade.
Violeta DopsajUniversity of Belgrade, Faculty of Pharmacy, Department of Medical Biochemistry, Belgrade.
Branislava MilenkovićUniversity of Belgrade, Faculty of Medicine, Belgrade.
Jelena JankovićUniversity of Belgrade, Faculty of Medicine, Belgrade.
Sanja Dimić-JanjićUniversity of Belgrade, Faculty of Medicine, Belgrade.
Vesna Dopuđa-PantićZvezdara Clinical Hospital Center, Clinical Department of Pulmonology and Allergology with Immunology, Belgrade.
Jelena MartinovićSante Biohemija, Belgrade.
Snežana JovičićUniversity of Belgrade, Faculty of Pharmacy, Department of Medical Biochemistry, Belgrade.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The SNP rs855791 has been linked to increased hepcidin levels, variations in serum iron, transferrin saturation and red blood cell indices. Our goal was to determine the prevalence of this polymorphism among COPD patients and to assess its impact on iron status parameters in patients with stable COPD. Methods: We analysed iron status parameters and genetic data from 29 COPD patients with wild-type genotype (WT group) and 65 COPD patients with either homozygous or heterozygous genotype (HH group). Additionally, the prevalence of SNP rs855791 was assessed in 192 volunteers. Results: The frequency distribution of SNP rs855791 was comparable between the COPD patients and control subjects (p=0.791). Iron status parameters were within their respective reference values and showed neither statistically nor clinically significant difference between the WT and HH group of COPD patients. However, after excluding patients with (sub)clinical vitamin B12 deficiency and/or hypoxemia, WT group of patients exhibited significantly lower erythropoietin levels (p=0.015). The area under the curve for erythropoietin was 0.688 (95% CI: 0.545-0.830, p=0.015), with an optimal cut-off of 9.74, sensitivity of 61.2% (95% CI: 58.1-64.3) and specificity of 65.0% (95% CI: 61.8-68.3). Conclusions: Iron status parameters do not differ between WT and HH groups of stable COPD patients. Statistical but not clinical difference in EPO levels was observed in a subgroup of patients. In addition to promoting erythropoiesis, EPO may regulate hepcidin levels and thus influence the development of iron deficiency and/or anaemia. Also, EPO's direct effect on immune cells and down-regulation of inflammatory reactions should be considered in this context.

Indexed as

B12 deficiencyCOPDerythropoietinhepcidiniron status parametersTMPRSS6 gene polymorphism

Identifiers

PMID39991164
PMCPMC11846647

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