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Erschienen in: Inflammation Research 5/2018

06.02.2018 | Original Research Paper

HIF-1A gene polymorphisms and its protein level in patients with rheumatoid arthritis: a case–control study

verfasst von: Agnieszka Paradowska-Gorycka, Barbara Stypinska, Andrzej Pawlik, Ewa Haladyj, Katarzyna Romanowska-Próchnicka, Marzena Olesinska

Erschienen in: Inflammation Research | Ausgabe 5/2018

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Abstract

Objectives

The aim of the study was to identify HIF-1A genetic variants and their possible association with HIF-1α, VEGF, KDR, RORc and Foxp3 protein levels, and susceptibility to and severity of RA.

Methods

The HIF-1A gene polymorphisms were genotyped for 587 RA patients and 341 healthy individuals. The HIF-1α, VEGF, KDR, RORc and Foxp3serum levels were evaluated.

Results

Under the codominant model, the frequency of the rs12434438 GG genotype was lower in RA patients than in controls (P = 0.02). Under the recessive model (AA + AG vs GG), the association was also significant (OR 3.32; CI 1.19–9.24; P = 0.02). Overall, rs12434438 A/G and rs1951795 A/C are in almost completed linkage disequilibrium with D′ = 0.96 and r2 = 0.85. The HIF-1A rs1951795 A allele was associated with rheumatoid factor (P = 0.02) and mean value of erythrocyte sedimentation rate (ESR) (P = 0.05). In RA patients with HIF-1A rs12434439 GG genotype, the parameters of disease activity such as DAS-28, VAS score, Larsen score or HAQ score were lower compared to RA patients with the HIF-1A rs12434439 AA genotype. Moreover, we also observed that Foxp3 serum levels were higher, and RORc2 serum levels were lower in RA patients with rs12434439 GG.

Conclusion

The polymorphic HIF-1A rs12434439 GG genotype may play a protective role for RA development.
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Metadaten
Titel
HIF-1A gene polymorphisms and its protein level in patients with rheumatoid arthritis: a case–control study
verfasst von
Agnieszka Paradowska-Gorycka
Barbara Stypinska
Andrzej Pawlik
Ewa Haladyj
Katarzyna Romanowska-Próchnicka
Marzena Olesinska
Publikationsdatum
06.02.2018
Verlag
Springer International Publishing
Erschienen in
Inflammation Research / Ausgabe 5/2018
Print ISSN: 1023-3830
Elektronische ISSN: 1420-908X
DOI
https://doi.org/10.1007/s00011-018-1134-y

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