Academic Journal
Low levels of PCSK9 are associated with remission in patients with rheumatoid arthritis treated with anti-TNF-α: potential underlying mechanisms
العنوان: | Low levels of PCSK9 are associated with remission in patients with rheumatoid arthritis treated with anti-TNF-α: potential underlying mechanisms |
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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 |
DOI: | 10.1186/s13075-020-02386-7 |
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