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024 7 |a 10.1016/j.clim.2025.110541  |2 doi 
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041 |a eng 
100 1 |a Nobre, Christiane Aguiar  |e verfasserin  |4 aut 
245 1 0 |a ProBNP, cytokines, and the Nrf2/HO-1 signaling pathway  |b A cross-sectional study on cardiovascular risk in rheumatoid arthritis 
264 1 |c 2025 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 16.07.2025 
500 |a Date Revised 16.07.2025 
500 |a published: Print-Electronic 
500 |a Citation Status MEDLINE 
520 |a Copyright © 2025 Elsevier Inc. All rights reserved. 
520 |a We evaluated associations between clinical/laboratory findings and serum cytokines, Nrf2/HO-1 pathway expression and cardiovascular risk in both RA patients and controls. Sixty RA patients and 60 controls were included in the study. Serum cytokine and proBNP levels were assessed by ELISA, while serum Nrf2 and HO-1 mRNA levels were quantified by qRT-PCR. The RA group (91.7 % women) and the control group (90 % women) were aged 52 ± 12 and 52 ± 13 years, respectively. ProBNP levels were higher in the RA group than in controls (p = 0.009). Nrf2 mRNA levels were higher (p < 0.001) and HO-1 mRNA levels were lower (p = 0.030) in the RA group than in controls. CDAI scores were significantly associated with serum IL-6 levels (p = 0.033). This study found a significant dysregulation in Nrf2/HO-1 pathway activity in RA patients, although without association with cardiovascular risk, RA-related clinical and laboratory variables. Moderate/high disease activity was positively associated with IL-6 levels 
650 4 |a Journal Article 
650 4 |a Cardiovascular risk factors 
650 4 |a Cytokines 
650 4 |a Nrf2/HO-1 signaling pathway 
650 4 |a Oxidative stress 
650 4 |a ProBNP 
650 4 |a Rheumatoid arthritis 
650 7 |a NF-E2-Related Factor 2  |2 NLM 
650 7 |a NFE2L2 protein, human  |2 NLM 
650 7 |a Heme Oxygenase-1  |2 NLM 
650 7 |a EC 1.14.14.18  |2 NLM 
650 7 |a Cytokines  |2 NLM 
650 7 |a Interleukin-6  |2 NLM 
650 7 |a HMOX1 protein, human  |2 NLM 
650 7 |a EC 1.14.14.18  |2 NLM 
650 7 |a RNA, Messenger  |2 NLM 
700 1 |a Rodrigues, Carlos Ewerton Maia  |e verfasserin  |4 aut 
700 1 |a Cavalcante, Natacha Xavier  |e verfasserin  |4 aut 
700 1 |a Nascimento, Thácilla Siqueira Eugênio  |e verfasserin  |4 aut 
700 1 |a Brayner, João Gabriel Marques  |e verfasserin  |4 aut 
700 1 |a Sousa, Giovanna Azevedo  |e verfasserin  |4 aut 
700 1 |a de Sousa, Nayara Alves  |e verfasserin  |4 aut 
700 1 |a Ribeiro, Regislane Pinto  |e verfasserin  |4 aut 
700 1 |a de Fiqueirêdo, Vanessa Maria Eufrásio  |e verfasserin  |4 aut 
700 1 |a Paiva, Giulia Albuquerque  |e verfasserin  |4 aut 
700 1 |a do Nascimento Costa, José Jackson  |e verfasserin  |4 aut 
700 1 |a Goes, Paula  |e verfasserin  |4 aut 
700 1 |a Chaves, Hellíada Vasconcelos  |e verfasserin  |4 aut 
700 1 |a Mont'Alverne Parente Feijão, Ticiana  |e verfasserin  |4 aut 
700 1 |a Bezerra, Mirna Marques  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Clinical immunology (Orlando, Fla.)  |d 1999  |g 278(2025) vom: 03. Juli, Seite 110541  |w (DE-627)NLM098196855  |x 1521-7035  |7 nnas 
773 1 8 |g volume:278  |g year:2025  |g day:03  |g month:07  |g pages:110541 
856 4 0 |u http://dx.doi.org/10.1016/j.clim.2025.110541  |3 Volltext 
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952 |d 278  |j 2025  |b 03  |c 07  |h 110541