Orphanet Journal of Rare Diseases | |
Colchicine-free remission in familial Mediterranean fever: featuring a unique subset of the disease-a case control study | |
Avi Livneh1  Shaye Kivity3  Merav Lidar1  Olga Feld2  Tami Krichely-Vachdi2  Ilan Ben-Zvi3  | |
[1] Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel;Department of Medicine F and the Rheumatology unit, Sheba Medical Center, Tel-Hashomer, Israel;The Pinchas Borenstein Talpiot Medical Leadership Program 2012, Chaim Sheba, Medical Center, Tel-Hashomer, Israel | |
关键词: Colchicine; Severity; Demographics; Genetics; Remission; Familial Mediterranean fever; | |
Others : 863327 DOI : 10.1186/1750-1172-9-3 |
|
received in 2013-10-10, accepted in 2014-01-03, 发布年份 2014 | |
【 摘 要 】
Background
To demonstrate and clinically, genetically and demographically characterize familial Mediterranean fever (FMF) patients, maintaining remission despite colchicine abstinence.
Methods
FMF patients were screened for an endurance of prolonged remission (≥ 3 years), despite refraining from colchicine. Clinical, demographic and genetic parameters were collected. Data were compared with those of consecutive control FMF subjects, coming to the clinic for their periodic follow up examination.
Results
Of 1000 patients screened over 5 years, 33 manifested colchicine-free remission. The mean duration of the remission period was 12.6 ± 8.1 years. Patients in the remission group had milder severity of FMF, compared to the control group (22 vs. 11 patients with mild disease, respectively, p = 0.003) and a longer diagnosis delay (21 ± 15.7 vs. 13.4 ± 13.5 years, respectively, p = 0.04). Patients experiencing remission suffered mostly of abdominal attacks, low rate of attacks in other sites and low rate of chronic and non-attack manifestations. When the disease resumed activity, it responded well to colchicine, despite using a lower dose, as compared to the control subjects (p < 0.001). None of the patients in this group was homozygous for the M694V mutation (p = 0.0008).
Conclusions
Prolonged colchicine-free remission defines a rare and milder form of FMF with unique clinical, demographic, and molecular characteristics.
【 授权许可】
2014 Ben-Zvi et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20140725040934625.pdf | 300KB | download | |
56KB | Image | download |
【 图 表 】
【 参考文献 】
- [1]Ben-Zvi I, Livneh A: Chronic inflammation in FMF: markers, risk factors, outcomes and therapy. Nat Rev Rheumatol 2010, 2011:9.
- [2]A candidate gene for familial Mediterranean fever Nat Genet 1997, 17(1):25-31.
- [3]Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The international FMF consortium Cell 1997, 90(4):797-807.
- [4]Stojanov S, Kastner DL: Familial autoinflammatory diseases: genetics, pathogenesis and treatment. Curr Opin Rheumatol 2005, 17(5):586-599.
- [5]Touitou I, Lesage S, McDermott M, Cuisset L, Hoffman H, Dode C, et al.: Infevers: an evolving mutation database for auto-inflammatory syndromes. Hum Mutat 2004, 24(3):194-198.
- [6]Piram M, Frenkel J, Gattorno M, Ozen S, Lachmann HJ, Goldbach-Mansky R, et al.: A preliminary score for the assessment of disease activity in hereditary recurrent fevers: results from the AIDAI (auto-inflammatory diseases activity index) consensus conference. Ann Rheum Dis 2011, 70(2):309-314.
- [7]Mor A, Shinar Y, Zaks N, Langevitz P, Chetrit A, Shtrasburg S, et al.: Evaluation of disease severity in familial Mediterranean fever. Semin Arthritis Rheum 2005, 35(1):57-64.
- [8]Gershoni-Baruch R, Brik R, Zacks N, Shinawi M, Lidar M, Livneh A: The contribution of genotypes at the MEFV and SAA1 loci to amyloidosis and disease severity in patients with familial Mediterranean fever. Arthritis Rheum 2003, 48(4):1149-1155.
- [9]Livneh A, Langevitz P, Zemer D, Zaks N, Kees S, Lidar T, et al.: Criteria for the diagnosis of familial Mediterranean fever. Arthritis Rheum 1997, 40(10):1879-1885.
- [10]Kogan A, Shinar Y, Lidar M, Revivo A, Langevitz P, Padeh S, et al.: Common MEFV mutations among Jewish ethnic groups in Israel: high frequency of carrier and phenotype III states and absence of a perceptible biological advantage for the carrier state. Am J Med Genet 2001, 102(3):272-276.
- [11]Barakat MH, Karnik AM, Majeed HW, el-Sobki NI, Fenech FF: Familial Mediterranean fever (recurrent hereditary polyserositis) in Arabs--a study of 175 patients and review of the literature. Q J Med 1986, 60(233):837-847.
- [12]Schwabe AD, Peters RS: Familial Mediterranean fever in Armenians. Analysis of 100 cases. Med (Baltimore) 1974, 53(6):453-462.
- [13]Sohar E, Gafni J, Pras M, Heller H: Familial Mediterranean fever. A survey of 470 cases and review of the literature. Am J Med 1967, 43(2):227-253.
- [14]Mimouni A, Magal N, Stoffman N, Shohat T, Minasian A, Krasnov M, et al.: Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosis. Pediatrics 2000, 105(5):E70.
- [15]Pras E, Livneh A, Balow JE Jr, Kastner DL, Pras M, Langevitz P: Clinical differences between North African and Iraqi Jews with familial Mediterranean fever. Am J Med Genet 1998, 75(2):216-219.
- [16]Shohat M, Magal N, Shohat T, Chen X, Dagan T, Mimouni A, et al.: Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis. Eur J Hum Genet 1999, 7(3):287-292.
- [17]Ben-Chetrit E, Ben-Chetrit A: Familial Mediterranean fever and menstruation. BJOG 2001, 108(4):403-407.
- [18]Stoffman N, Magal N, Shohat T, Lotan R, Koman S, Oron A, et al.: Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups. Eur J Hum Genet 2000, 8(4):307-310.
- [19]Livneh A, Langevitz P, Shinar Y, Zaks N, Kastner DL, Pras M, et al.: MEFV mutation analysis in patients suffering from amyloidosis of familial Mediterranean fever. Amyloid 1999, 6(1):1-6.
- [20]Tamir N, Langevitz P, Zemer D, Pras E, Shinar Y, Padeh S, et al.: Late-onset familial Mediterranean fever (FMF): a subset with distinct clinical, demographic, and molecular genetic characteristics. Am J Med Genet 1999, 87(1):30-35.