Skip to main content
Erschienen in: Clinical Rheumatology 4/2011

01.04.2011 | Original Article

Mediterranean fever (MEFV) gene mutation frequency is not increased in adults with rheumatic heart disease

verfasst von: Ismail Simsek, Cem Koz, Nurcan Basar, Ismail Sari, Hakan Erdem, Salih Pay, Bunyamin Kisacik, Muhterem Bahce, Ayhan Dinc

Erschienen in: Clinical Rheumatology | Ausgabe 4/2011

Einloggen, um Zugang zu erhalten

Abstract

It is well established that there are people with higher risk of developing acute rheumatic fever (ARF) and rheumatic heart disease (RHD). Mediterranean fever (MEFV) gene mutations might be one of the genetic predisposition factors in the development of ARF/RHD since defect in familial Mediterranean fever (FMF) patients is proposed to be heightened inflammatory response to certain stimuli. Previous clinical observations suggested a relationship between FMF and ARF/RHD. The aim of this study was to investigate the role of the MEFV gene mutations in the susceptibility to RHD in Turkish patients. A total of 100 patients with RHD and 100 healthy controls were included in the study. Diagnosis of RHD was based on echocardiographic findings in which a predominant mitral stenosis was used as an inclusion criterion. Genetic analysis was carried out by sequence analysis investigating two hot spots (exons 2 and 10) for MEFV mutations. Mutation analysis showed that 22 RHD patients (22%) and 24 healthy controls (24%) carried at least one mutated allele. MEFV mutations were identified in 22 of 200 (11%) chromosomes in RHD patients while 26 of the 200 (13%) chromosomes of healthy controls were found to carry a mutated allele. No difference was found in allele frequencies and their distribution between the patients and healthy controls (p = 0.54). MEFV mutations are not associated with a predisposition to develop RHD in adult Turkish patients.
Literatur
1.
Zurück zum Zitat Guilherme L, Ramasawmy R, Kalil J (2007) Rheumatic fever and rheumatic heart disease: genetics and pathogenesis. Scand J Immunol 66(2–3):199–207PubMedCrossRef Guilherme L, Ramasawmy R, Kalil J (2007) Rheumatic fever and rheumatic heart disease: genetics and pathogenesis. Scand J Immunol 66(2–3):199–207PubMedCrossRef
2.
Zurück zum Zitat Gibofsky A, Kerwar S, Zabriskie JB (1998) Rheumatic fever. The relationships between host, microbe, and genetics. Rheum Dis Clin North Am 24(2):237–259PubMedCrossRef Gibofsky A, Kerwar S, Zabriskie JB (1998) Rheumatic fever. The relationships between host, microbe, and genetics. Rheum Dis Clin North Am 24(2):237–259PubMedCrossRef
3.
Zurück zum Zitat Spagnuolo M, Taranta A (1968) Rheumatic fever in siblings. Similarity of its clinical manifestations. N Engl J Med 278(4):183–188PubMedCrossRef Spagnuolo M, Taranta A (1968) Rheumatic fever in siblings. Similarity of its clinical manifestations. N Engl J Med 278(4):183–188PubMedCrossRef
4.
Zurück zum Zitat Tunca M, Akar S, Onen F, Ozdogan H, Kasapcopur O, Yalcinkaya F et al (2005) Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study. Medicine (Baltimore) 84(1):1–11CrossRef Tunca M, Akar S, Onen F, Ozdogan H, Kasapcopur O, Yalcinkaya F et al (2005) Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study. Medicine (Baltimore) 84(1):1–11CrossRef
5.
Zurück zum Zitat Tekin M, Yalcinkaya F, Tumer N, Cakar N, Kocak H (1999) Familial Mediterranean fever and acute rheumatic fever: a pathogenetic relationship? Clin Rheumatol 18(6):446–449PubMedCrossRef Tekin M, Yalcinkaya F, Tumer N, Cakar N, Kocak H (1999) Familial Mediterranean fever and acute rheumatic fever: a pathogenetic relationship? Clin Rheumatol 18(6):446–449PubMedCrossRef
6.
Zurück zum Zitat Shapiro TR, Ehrenfeld EN (1962) Recurrent polyserositis ("periodic disease," "familial Mediterranean fever") in children. Pediatrics 30:443–449PubMed Shapiro TR, Ehrenfeld EN (1962) Recurrent polyserositis ("periodic disease," "familial Mediterranean fever") in children. Pediatrics 30:443–449PubMed
7.
Zurück zum Zitat Livneh A, Langevitz P (2000) Diagnostic and treatment concerns in familial Mediterranean fever. Baillières Best Pract Res Clin Rheumatol 14(3):477–498PubMedCrossRef Livneh A, Langevitz P (2000) Diagnostic and treatment concerns in familial Mediterranean fever. Baillières Best Pract Res Clin Rheumatol 14(3):477–498PubMedCrossRef
8.
Zurück zum Zitat Ozer FL, Kaplaman E, Zileli S (1971) Familial Mediterranean fever in Turkey. A report of twenty cases. Am J Med 50(3):336–339PubMedCrossRef Ozer FL, Kaplaman E, Zileli S (1971) Familial Mediterranean fever in Turkey. A report of twenty cases. Am J Med 50(3):336–339PubMedCrossRef
9.
Zurück zum Zitat Siegal S (1964) Familial paroxysmal polyserositis. Analysis of fifty cases. Am J Med 36:893–918PubMedCrossRef Siegal S (1964) Familial paroxysmal polyserositis. Analysis of fifty cases. Am J Med 36:893–918PubMedCrossRef
10.
Zurück zum Zitat The International FMF Consortium (1997) Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell 90(4):797–807CrossRef The International FMF Consortium (1997) Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell 90(4):797–807CrossRef
11.
Zurück zum Zitat The French FMF Consortium (1996) Localization of the familial Mediterranean fever gene (FMF) to a 250-kb interval in non-Ashkenazi Jewish founder haplotypes. Am J Hum Genet 59(3):603–612 The French FMF Consortium (1996) Localization of the familial Mediterranean fever gene (FMF) to a 250-kb interval in non-Ashkenazi Jewish founder haplotypes. Am J Hum Genet 59(3):603–612
12.
Zurück zum Zitat Ozen S (2003) Familial mediterranean fever: revisiting an ancient disease. Eur J Pediatr 162(7–8):449–454PubMedCrossRef Ozen S (2003) Familial mediterranean fever: revisiting an ancient disease. Eur J Pediatr 162(7–8):449–454PubMedCrossRef
13.
Zurück zum Zitat Yalcinkaya F, Ince E, Ucar T, Ozkaya N, Tekin M, Elhan AH et al (2002) Antistreptococcal response is exaggerated in children with familial Mediterranean fever. Clin Rheumatol 21(5):378–381PubMedCrossRef Yalcinkaya F, Ince E, Ucar T, Ozkaya N, Tekin M, Elhan AH et al (2002) Antistreptococcal response is exaggerated in children with familial Mediterranean fever. Clin Rheumatol 21(5):378–381PubMedCrossRef
14.
Zurück zum Zitat Special Writing Group of the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in the Young of the American Heart Association (1992) Guidelines for the diagnosis of rheumatic fever. Jones Criteria, 1992 update. JAMA 268(15):2069–2073CrossRef Special Writing Group of the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in the Young of the American Heart Association (1992) Guidelines for the diagnosis of rheumatic fever. Jones Criteria, 1992 update. JAMA 268(15):2069–2073CrossRef
15.
Zurück zum Zitat Kelsey JL, Thompson WA, Evans AS, Thompson WD (1996) Methods of sampling and estimation of sample size. In: Kelsey JL (ed) Methods in observational epidemiology. Oxford University Press, New York, pp 332–334 Kelsey JL, Thompson WA, Evans AS, Thompson WD (1996) Methods of sampling and estimation of sample size. In: Kelsey JL (ed) Methods in observational epidemiology. Oxford University Press, New York, pp 332–334
16.
Zurück zum Zitat Livneh A, Langevitz P, Zemer D, Zaks N, Kees S, Lidar T et al (1997) Criteria for the diagnosis of familial Mediterranean fever. Arthritis Rheum 40(10):1879–1885PubMedCrossRef Livneh A, Langevitz P, Zemer D, Zaks N, Kees S, Lidar T et al (1997) Criteria for the diagnosis of familial Mediterranean fever. Arthritis Rheum 40(10):1879–1885PubMedCrossRef
17.
Zurück zum Zitat Gershoni-Baruch R, Broza Y, Brik R (2003) Prevalence and significance of mutations in the familial Mediterranean fever gene in Henoch-Schonlein purpura. J Pediatr 143(5):658–661PubMedCrossRef Gershoni-Baruch R, Broza Y, Brik R (2003) Prevalence and significance of mutations in the familial Mediterranean fever gene in Henoch-Schonlein purpura. J Pediatr 143(5):658–661PubMedCrossRef
18.
Zurück zum Zitat Imirzalioglu N, Dursun A, Tastan B, Soysal Y, Yakicier MC (2005) MEFV gene is a probable susceptibility gene for Behcet's disease. Scand J Rheumatol 34(1):56–58PubMedCrossRef Imirzalioglu N, Dursun A, Tastan B, Soysal Y, Yakicier MC (2005) MEFV gene is a probable susceptibility gene for Behcet's disease. Scand J Rheumatol 34(1):56–58PubMedCrossRef
19.
Zurück zum Zitat Atagunduz P, Ergun T, Direskeneli H (2003) MEFV mutations are increased in Behcet's disease (BD) and are associated with vascular involvement. Clin Exp Rheumatol 21(4 Suppl 30):S35–S37PubMed Atagunduz P, Ergun T, Direskeneli H (2003) MEFV mutations are increased in Behcet's disease (BD) and are associated with vascular involvement. Clin Exp Rheumatol 21(4 Suppl 30):S35–S37PubMed
20.
Zurück zum Zitat Rabinovich E, Shinar Y, Leiba M, Ehrenfeld M, Langevitz P, Livneh A (2007) Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis. Scand J Rheumatol 36(1):48–52PubMedCrossRef Rabinovich E, Shinar Y, Leiba M, Ehrenfeld M, Langevitz P, Livneh A (2007) Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis. Scand J Rheumatol 36(1):48–52PubMedCrossRef
21.
Zurück zum Zitat Ayaz NA, Ozen S, Bilginer Y, Erguven M, Taskiran E, Yilmaz E et al (2009) MEFV mutations in systemic onset juvenile idiopathic arthritis. Rheumatology (Oxford) 48(1):23–25CrossRef Ayaz NA, Ozen S, Bilginer Y, Erguven M, Taskiran E, Yilmaz E et al (2009) MEFV mutations in systemic onset juvenile idiopathic arthritis. Rheumatology (Oxford) 48(1):23–25CrossRef
22.
Zurück zum Zitat Tutar E, Akar N, Atalay S, Yilmaz E, Akar E, Yalcinkaya F (2002) Familial Mediterranean fever gene (MEFV) mutations in patients with rheumatic heart disease. Heart 87(6):568–569PubMedCrossRef Tutar E, Akar N, Atalay S, Yilmaz E, Akar E, Yalcinkaya F (2002) Familial Mediterranean fever gene (MEFV) mutations in patients with rheumatic heart disease. Heart 87(6):568–569PubMedCrossRef
23.
Zurück zum Zitat Olson LJ, Subramanian R, Ackermann DM, Orszulak TA, Edwards WD (1987) Surgical pathology of the mitral valve: a study of 712 cases spanning 21 years. Mayo Clin Proc 62(1):22–34PubMed Olson LJ, Subramanian R, Ackermann DM, Orszulak TA, Edwards WD (1987) Surgical pathology of the mitral valve: a study of 712 cases spanning 21 years. Mayo Clin Proc 62(1):22–34PubMed
24.
Zurück zum Zitat Ben-Chetrit E, Lerer I, Malamud E, Domingo C, Abeliovich D (2000) The E148Q mutation in the MEFV gene: is it a disease-causing mutation or a sequence variant? Hum Mutat 15(4):385–386PubMedCrossRef Ben-Chetrit E, Lerer I, Malamud E, Domingo C, Abeliovich D (2000) The E148Q mutation in the MEFV gene: is it a disease-causing mutation or a sequence variant? Hum Mutat 15(4):385–386PubMedCrossRef
25.
Zurück zum Zitat Booth DR, Lachmann HJ, Gillmore JD, Booth SE, Hawkins PN (2001) Prevalence and significance of the familial Mediterranean fever gene mutation encoding pyrin Q148. QJM 94(10):527–531PubMedCrossRef Booth DR, Lachmann HJ, Gillmore JD, Booth SE, Hawkins PN (2001) Prevalence and significance of the familial Mediterranean fever gene mutation encoding pyrin Q148. QJM 94(10):527–531PubMedCrossRef
26.
Zurück zum Zitat Topaloglu R, Ozaltin F, Yilmaz E, Ozen S, Balci B, Besbas N et al (2005) E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever. Ann Rheum Dis 64(5):750–752PubMedCrossRef Topaloglu R, Ozaltin F, Yilmaz E, Ozen S, Balci B, Besbas N et al (2005) E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever. Ann Rheum Dis 64(5):750–752PubMedCrossRef
Metadaten
Titel
Mediterranean fever (MEFV) gene mutation frequency is not increased in adults with rheumatic heart disease
verfasst von
Ismail Simsek
Cem Koz
Nurcan Basar
Ismail Sari
Hakan Erdem
Salih Pay
Bunyamin Kisacik
Muhterem Bahce
Ayhan Dinc
Publikationsdatum
01.04.2011
Verlag
Springer-Verlag
Erschienen in
Clinical Rheumatology / Ausgabe 4/2011
Print ISSN: 0770-3198
Elektronische ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-010-1537-9

Weitere Artikel der Ausgabe 4/2011

Clinical Rheumatology 4/2011 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Alphablocker schützt vor Miktionsproblemen nach der Biopsie

16.05.2024 alpha-1-Rezeptorantagonisten Nachrichten

Nach einer Prostatabiopsie treten häufig Probleme beim Wasserlassen auf. Ob sich das durch den periinterventionellen Einsatz von Alphablockern verhindern lässt, haben australische Mediziner im Zuge einer Metaanalyse untersucht.

Eingreifen von Umstehenden rettet vor Erstickungstod!

15.05.2024 Fremdkörperaspiration Nachrichten

Wer sich an einem Essensrest verschluckt und um Luft ringt, benötigt vor allem rasche Hilfe. Dass Umstehende nur in jedem zweiten Erstickungsnotfall bereit waren, diese zu leisten, ist das ernüchternde Ergebnis einer Beobachtungsstudie aus Japan. Doch es gibt auch eine gute Nachricht.

Neue S3-Leitlinie zur unkomplizierten Zystitis: Auf Antibiotika verzichten?

15.05.2024 Harnwegsinfektionen Nachrichten

Welche Antibiotika darf man bei unkomplizierter Zystitis verwenden und wovon sollte man die Finger lassen? Welche pflanzlichen Präparate können helfen? Was taugt der zugelassene Impfstoff? Antworten vom Koordinator der frisch überarbeiteten S3-Leitlinie, Prof. Florian Wagenlehner.

Schadet Ärger den Gefäßen?

14.05.2024 Arteriosklerose Nachrichten

In einer Studie aus New York wirkte sich Ärger kurzfristig deutlich negativ auf die Endothelfunktion gesunder Probanden aus. Möglicherweise hat dies Einfluss auf die kardiovaskuläre Gesundheit.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.