Amyloidosis induced, end stage renal disease in patients with familial Mediterranean fever is highly associated with point mutations in the MEFV gene
- PMID: 11156548
- PMCID: PMC1753463
- DOI: 10.1136/ard.60.2.146
Amyloidosis induced, end stage renal disease in patients with familial Mediterranean fever is highly associated with point mutations in the MEFV gene
Abstract
Background: Familial Mediterranean fever (FMF) is an autosomal recessive disease characterised by recurrent attacks of fever and serositis. Amyloidosis is the most significant complication of FMF, leading to end stage renal disease (ESRD). Recently the gene (MEFV) causing this disease was cloned and more than 18 mutations have been identified. The hypothesis that the development of amyloidosis is associated with one of these mutations was tested.
Methods: 23 patients with FMF and ESRD were analysed for their MEFV mutations and correlated with their corresponding rectal and renal biopsies. As case controls 23 patients with FMF free of renal disease, but with similar origin, sex, age, and age at onset of FMF, were chosen.
Results: All the patients with ESRD induced by amyloidosis were homozygous for the M694V or M694I mutations. This finding was significantly different from that seen in the control group.
Conclusions: Amyloidosis is highly associated with the 694 substitution in the MEFV gene causing FMF. It seems that genetic predisposition plays a part in the development of this complication of FMF.
Similar articles
-
[Familial Mediterranean Fever (FMF): from diagnosis to treatment].Sante. 2004 Oct-Dec;14(4):261-6. Sante. 2004. PMID: 15745878 Review. French.
-
The M694I/M694I genotype: A genetic risk factor of AA-amyloidosis in a group of Algerian patients with familial Mediterranean fever.Eur J Med Genet. 2017 Mar;60(3):149-153. doi: 10.1016/j.ejmg.2016.12.003. Epub 2016 Dec 10. Eur J Med Genet. 2017. PMID: 27956278
-
Association of FMF-related (MEFV) point mutations with secondary and FMF amyloidosis.Nephron Clin Pract. 2004;96(4):c131-5. doi: 10.1159/000077375. Nephron Clin Pract. 2004. PMID: 15122067
-
Long-term outcome of renal transplantation in patients with familial Mediterranean fever amyloidosis: a single-center experience.Transplant Proc. 2013;45(10):3502-4. doi: 10.1016/j.transproceed.2013.09.021. Transplant Proc. 2013. PMID: 24314942
-
Familial Mediterranean fever at the millennium. Clinical spectrum, ancient mutations, and a survey of 100 American referrals to the National Institutes of Health.Medicine (Baltimore). 1998 Jul;77(4):268-97. doi: 10.1097/00005792-199807000-00005. Medicine (Baltimore). 1998. PMID: 9715731 Review.
Cited by
-
Perspectives for TNF-alpha-targeting therapies.Arthritis Res. 2002;4 Suppl 3(Suppl 3):S17-24. doi: 10.1186/ar564. Epub 2002 May 9. Arthritis Res. 2002. PMID: 12110119 Free PMC article. Review.
-
Prevalence and significance of the MEFV gene mutations in childhood Henoch-Schönlein purpura without FMF symptoms.Rheumatol Int. 2013 Feb;33(2):377-80. doi: 10.1007/s00296-012-2400-x. Epub 2012 Mar 27. Rheumatol Int. 2013. PMID: 22451026
-
The association of inflammatory bowel disease and Mediterranean fever gene (MEFV) mutations in Turkish children.Dig Dis Sci. 2010 Dec;55(12):3488-94. doi: 10.1007/s10620-010-1178-5. Epub 2010 Mar 21. Dig Dis Sci. 2010. PMID: 20306331
-
Adherence to best practice consensus guidelines for familial Mediterranean fever: a modified Delphi study among paediatric rheumatologists in Turkey.Rheumatol Int. 2022 Jan;42(1):87-94. doi: 10.1007/s00296-020-04776-1. Epub 2021 Jan 16. Rheumatol Int. 2022. PMID: 33454820 Free PMC article.
-
As a new inflammatory marker for familial Mediterranean fever: neutrophil-to-lymphocyte ratio.Inflammation. 2013 Dec;36(6):1357-62. doi: 10.1007/s10753-013-9675-2. Inflammation. 2013. PMID: 23794006
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Research Materials