Journals / Turkish archives of pediatrics (Online) / 2022 / Cilt: 57 - Sayı: 4

The Characteristics of Pediatric Patients with Familial Mediterranean Fever Treated with Anti-Interleukin-1 Treatment

Pages
448–452
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In pediatric familial Mediterranean fever patients who are resistant to colchicine, interleukin-1 inhibitors seem to be highly effective agents.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objective: Interleukin-1 inhibitors are effective agents used in colchicine resistance or intolerance during the treatment of familial Mediterranean fever.
📊
Key Findings & Data:This study aims to review the characteristics of patients treated with interleukin-1 inhibitors and their long-term follow-up in a large pediatric cohort of familial Mediterranean fever patients.
💡
Conclusion & Impact:In pediatric familial Mediterranean fever patients who are resistant to colchicine, interleukin-1 inhibitors seem to be highly effective agents.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Objective: Interleukin-1 inhibitors are effective agents used in colchicine resistance or intolerance during the treatment of familial Mediterranean fever. This study aims to review the characteristics of patients treated with interleukin-1 inhibitors and their long-term follow-up in a large pediatric cohort of familial Mediterranean fever patients. Materials and Methods: The study was conducted in a pediatric rheumatology reference center. The patients treated with interleukin-1 inhibitors for at least 6 months were included and compared to other patients with familial Mediterranean fever. Clinical and laboratory characteristics of the cohort were recorded. Results: Among 542 patients with familial Mediterranean fever, 6.1% (n = 33) were treated with interleukin-1 inhibitors. Colchicine resistance was the reason in 82.8% and renal amyloidosis in 17.2% of the patients. Patients with interleukin-1 inhibitors had earlier disease onset and higher frequencies of acute arthritis, chest pain, and erysipelas-like erythema with pathogenic exon 10 mutations of the MEFV gene (all P < .04). All patients diagnosed with renal amyloidosis also received interleukin-1 inhibitors. Six patients were switched from anakinra to canakinumab or vice versa to control ongoing disease activity. Attack frequency was reduced in all patients. Conclusion: Interleukin-1 inhibitors are used in a relatively small number of pediatric patients with familial Mediterranean fever. Patients presenting with earlier disease onset, acute arthritis, chest pain, and erysipelas-like erythema and carrying pathogenic exon 10 mutations of the MEFV gene may show a higher need for interleukin-1 inhibitors. In pediatric familial Mediterranean fever patients who are resistant to colchicine, interleukin-1 inhibitors seem to be highly effective agents.

🔖

Cite This Article

AYDIN, P. Ö. A., ÖZÇAKAR, Z. B., AYDIN, F., KARAKAŞ, H. D., YALÇINKAYA, F. (2022). The Characteristics of Pediatric Patients with Familial Mediterranean Fever Treated with Anti-Interleukin-1 Treatment. Turkish archives of pediatrics (Online), Cilt: 57 - Sayı: 4, 448–452. https://ajindex.com/articles/417333

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Ben-Chetrit E, Levy M. Familial Mediterranean fever. Lancet. 1998
  2. 351(9103):659-664. [CrossRef] 2. Leung YY, Yao Hui LL, Kraus VB. Colchicine-Update on mechanisms of action and therapeutic uses. Semin Arthritis Rheum. 2015
  3. 45(3):341-350. [CrossRef] 3. Özçakar ZB, Özdel S, Yılmaz S, Kurt-Şükür ED, Ekim M, Yalçınkaya F. Anti-IL-1 treatment in familial Mediterranean fever and related amyloidosis. Clin Rheumatol. 2016
  4. 35(2):441-446. [CrossRef] 4. Jamilloux Y, Lefeuvre L, Magnotti F, et al. Familial Mediterranean fever mutations are hypermorphic mutations that specifically decrease the activation threshold of the pyrin inflammasome. Rheumatology (Oxford). 2018
  5. 57(1):100-111. [CrossRef] 5. Chae JJ, Cho YH, Lee GS, et al. Gain-of-function pyrin mutations induce NLRP3 protein-independent interleukin-1β activation and severe autoinflammation in mice. Immunity. 2011
  6. 34(5):755-768. [CrossRef] 6. Mortensen SB, Hansen AE, Mogensen TH, et al. Pyrin inflammasome activation abrogates interleukin-1 receptor antagonist, suggesting a new mechanism underlying familial Mediterranean fever pathogenesis. Arthritis Rheumatol. 2021
  7. 73(11):2116-2126. [CrossRef] 7. Ugurlu S, Ergezen B, Egeli BH, Selvi O, Ozdogan H. Anakinra treatment in patients with familial Mediterranean fever: a single-centre experience. Rheumatology (Oxford). 2021
  8. 60(5):2327-2332. [CrossRef] 8. Hentgen V, Vinit C, Fayand A, Georgin-Lavialle S. The use of interleukine- 1 inhibitors in familial Mediterranean fever patients: a narrative review. Front Immunol. 2020
  9. [CrossRef] 9. Yalçınkaya F, Özen S, Özçakar ZB, et al. A new set of criteria for the diagnosis of familial Mediterranean fever in childhood. Rheumatology (Oxford). 2009
  10. 48(4):395-398. [CrossRef] 10. Tunca M, Kirkali G, Soytürk M, Akar S, Pepys MB, Hawkins PN. Acute phase response and evolution of familial Mediterranean fever. Lancet. 1999
  11. 353(9162):1415. [CrossRef] 11. Korkmaz C, Özdogan H, Kasapçopur O, Yazici H. Acute phase response in familial Mediterranean fever. Ann Rheum Dis. 2002
  12. 61(1):79-81. [CrossRef] 12. Özen S, Sag E, Ben-Chetrit E, et al. Defining colchicine resis tance /into leran ce in patients with familial Mediterranean fever: a modified-Delphi consensus approach. Rheumatology (Oxford). 2021
  13. 60(8):3799-3808. [CrossRef] 13. Gül A. Dynamics of inflammatory response in autoinflammatory disorders: autonomous and hyperinflammatory states. Front Immunol. 2018
  14. 9(2422):2422. [CrossRef] 14. Gül A. Approach to the patients with inadequate