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Connective Tissue Diseases and Related Disorders

Do all colchicine preparations have the same effectiveness in patients with familial Mediterranean fever?

ORCID Icon, ORCID Icon & ORCID Icon
Pages 481-484 | Received 20 May 2020, Accepted 18 Jun 2020, Published online: 20 Jul 2020
 

Abstract

Aim

Colchicine is the primary treatment for familial Mediterranean fever (FMF). Several colchicine preparations are currently using available globally. This study aimed to describe the demographic, clinical, and genetic features of FMF patients treated with multiple colchicine preparations.

Materials and methods

The records of patients diagnosed as FMF and followed-up by our pediatric rheumatology department were retrospectively evaluated. Patients that were treated with multiple colchicine preparations were included. Patient demographic, clinical, and laboratory data were obtained from the patient files and the hospital patient database. The daily colchicine dose and FMF attack frequency before and after switching from domestically produced (DP)-coated colchicine tablets to foreign produced (FP)-compressed colchicine tablets were compared.

Results

The study included 35 pediatric FMF patients (22 males and 13 females) with a mean age of 12.85 ± 4.62 years. Mean age at disease onset was 3.66 ± 2.11 years, versus 5.57 ± 4.28 years at diagnosis. The mean attack frequency before and after treatment with FP-compressed colchicine tablets was 9.50 ± 4.46 and 1.85 ± 1.41/year, respectively (p < .001). The mean attack duration significantly decreased in all the patients treated with FP-compressed colchicine tablets (p < .001). The difference in acute phase reactants during the attack-free periods before and after FP-compressed colchicine tablet treatment was significant (p < .001).

Conclusion

The present findings show that pediatric FMF patients with ongoing attacks and elevated acute phase reactants during attack-free periods while treated with DP-coated colchicine tablets might benefit from switching to FP-compressed colchicine tablets before initiating biologic treatment. Long-term controlled studies are warranted, so as to obtain better evidence of the benefits of multiple colchicine preparations in pediatric FMF patients.

Author contributions

EB and SO contributed to the study design, case recruitment, acquisition and interpretation of data, statistical analysis, writing the manuscript and multiple revisions, final approval of the manuscript. EB, SO and MB contributed to data acquisition, manuscript revision, and final approval of the manuscript. MB contributed to interpretation of data, statistical analysis, multiple revisions of the manuscript, and final approval of the manuscript. All authors read and approved the final manuscript.

Conflict of interest

None.

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