Academic Journal

Low levels of PCSK9 are associated with remission in patients with rheumatoid arthritis treated with anti-TNF-α: potential underlying mechanisms

التفاصيل البيبلوغرافية
العنوان: Low levels of PCSK9 are associated with remission in patients with rheumatoid arthritis treated with anti-TNF-α: potential underlying mechanisms
المؤلفون: Frostegård, Johan, Ahmed, Sabbir, Hafström, Ingiäld, Ajeganova, Sofia, Rahman, Mizanur
المساهمون: Amgen Foundation, Reumatikerförbundet
المصدر: Arthritis Research & Therapy ; volume 23, issue 1 ; ISSN 1478-6362
بيانات النشر: Springer Science and Business Media LLC
سنة النشر: 2021
الوصف: Background Proprotein convertase subtilisin kexin 9 (PCSK9) targets the LDL-receptor (LDLR) which raises LDL-levels. In addition, PCSK9 has proinflammatory immunological effects. Here, we investigate the role of PCSK9 in relation to the inflammatory activity in patients with rheumatoid arthritis (RA). Methods PCSK9-levels were determined at baseline by ELISA in 160 patients with RA not previously treated with biologics. The patients started anti-TNF-α (adalimumab, infliximab, or etanercept) treatment and were followed-up for 1 year. Disease activity was determined by DAS28. Effects of PCSK9 on cytokine production from macrophages of healthy individuals and synoviocytes from RA patients and inhibition by anti-PCSK9 antibodies were studied in supernatants by ELISA. Results A significantly lower level of PCSK9 at baseline, p = 0.035, was observed in patients who reached remission within 1 year, defined as DAS28 < 2.6, compared to those not in remission. At 12 months of TNF-α antagonist treatment, the mean DAS28 was reduced but was significantly greater in patients with highest quartile PCSK9 (Q4) compared to those at lowest PCSK9 (Q1) in both crude ( p = 0.01) and adjusted analysis ( p = 0.004). In vitro, PCSK9 induced TNF-alpha and IL-1beta in macrophages and monocyte chemoattractant protein-1 (MCP1) in synoviocytes. These effects were inhibited by anti-PCSK9 antibodies. Conclusions Low levels of PCSK9 at baseline are associated with being DAS28-responder to anti-TNF-α treatment in RA. An underlying cause could be that PCSK9 stimulates the production of proinflammatory cytokines from macrophages and synoviocytes, effects inhibited by anti-PCSK9 antibodies. PCSK9 could thus play an immunological role in RA.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1186/s13075-020-02386-7
DOI: 10.1186/s13075-020-02386-7.pdf
DOI: 10.1186/s13075-020-02386-7/fulltext.html
الاتاحة: http://dx.doi.org/10.1186/s13075-020-02386-7
http://link.springer.com/content/pdf/10.1186/s13075-020-02386-7.pdf
http://link.springer.com/article/10.1186/s13075-020-02386-7/fulltext.html
Rights: http://creativecommons.org/licenses/by/4.0/ ; http://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.B62918B2
قاعدة البيانات: BASE
الوصف
DOI:10.1186/s13075-020-02386-7