The relative contribution of environmental and genetic factors to phenotypic variation in familial Mediterranean fever (FMF)

被引:37
作者
Ben-Zvi, Ilan [2 ,3 ]
Brandt, Benny [2 ,3 ]
Berkun, Yackov [1 ]
Lidar, Merav [2 ,3 ]
Livneh, Avi [2 ,3 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Pediat A, IL-52621 Tel Hashomer, Israel
[2] Sheba Med Ctr, Dept Internal Med F, IL-52621 Ramat Gan, Israel
[3] Sheba Med Ctr, Natl FMF Ctr, IL-52621 Ramat Gan, Israel
关键词
Familial Mediterranean fever; Twins; Phenotype; Environment; Genetics; RENAL AMYLOIDOSIS; DISEASE SEVERITY; MEFV; POLYMORPHISMS; GENOTYPES; TWIN; SAA1; VASCULITIS; MUTATIONS; DIAGNOSIS;
D O I
10.1016/j.gene.2011.10.005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Introduction: Familial Mediterranean fever (FMF) is an autosomal recessive disease, caused by mutations in the FMF gene MEFV (MEditerranean FeVer). It has a large phenotypic diversity even in patients with similar genotypes. Despite evidence that environmental factors (EFs) and genetic factors, including MEFV mutations (such as M694V, E148Q) and background modifier genes (MGs), affect the clinical manifestations of FMF, the relative contribution of each remains unknown. Methods: To investigate the relative contribution of environmental and genetic factors to the phenotype of FMF, we compared the intra-pair clinical concordance of 10 mono and 7 dizygotic twins with FMF. The part played by EFs was determined by the phenotypic discordance of the monozygous twins, and the MGs effect was determined by deducing the environmental effect, computed for MZ twins, from the phenotypic discordance of the dizygous twins. Results: The mean +/- SD of intra-pair concordance was higher in the MZ than in DZ twin group (88.1 +/- 13.2 vs. 70.7 +/- 14.1 respectively, P value<0.05). Based on the concordance in clinical manifestations in MZ and DZ twins, the environmental effect on the phenotype of FMF is estimated as 11.9% +/- 6.6% and the MGs effect as 17.4% +/- 15.5% in average. Conclusions: In FMF the phenotype is affected by MEFV mutations. MGs and EFs in an estimated ratio of about 6:1.5:1 respectively. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:260 / 263
页数:4
相关论文
共 37 条
[1]  
Akar N, 2006, J NEPHROL, V19, P318
[2]   The relations between attacks and menstrual periods and pregnancies of familial Mediterranean fever patients [J].
Akar, S ;
Soyturk, M ;
Onen, F ;
Tunca, M .
RHEUMATOLOGY INTERNATIONAL, 2006, 26 (07) :676-679
[3]   A severe autosomal-dominant periodic inflammatory disorder with renal AA amyloidosis and colchicine resistance associated to the MEFV H478Y variant in a Spanish kindred:: An unusual familial Mediterranean fever phenotype or another MEFV-associated periodic inflammatory disorder? [J].
Aldea, A ;
Campistol, JM ;
Arostegui, JI ;
Rius, J ;
Maso, M ;
Vives, J ;
Yagüe, J .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 124A (01) :67-73
[4]  
Bakkaloglu A, 2004, J RHEUMATOL, V31, P1139
[5]   Vasculitis in siblings with familial Mediterranean fever: a report of three cases and review of the literature [J].
Balbir-Gurman, Alexandra ;
Nahir, Abraham Menahem ;
Braun-Moscovici, Yolanda .
CLINICAL RHEUMATOLOGY, 2007, 26 (07) :1183-1185
[6]   Chronic inflammation in FmF: markers, risk factors, outcomes and therapy [J].
Ben-Zvi, Ilan ;
Livneh, Avi .
NATURE REVIEWS RHEUMATOLOGY, 2011, 7 (02) :105-112
[7]   The genetic basis of autosomal dominant familial Mediterranean fever [J].
Booth, DR ;
Gillmore, JD ;
Lachmann, HJ ;
Booth, SE ;
Bybee, A ;
Soytürk, M ;
Akar, S ;
Pepys, MB ;
Tunca, M ;
Hawkins, PN .
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2000, 93 (04) :217-221
[8]   Familial Mediterranean Fever With a Single MEFV Mutation Where Is the Second Hit? [J].
Booty, Matthew G. ;
Chae, Jae Jin ;
Masters, Seth L. ;
Remmers, Elaine F. ;
Barham, Beverly ;
Le, Julie M. ;
Barron, Karyl S. ;
Holland, Steve M. ;
Kastner, Daniel L. ;
Aksentijevich, Ivona .
ARTHRITIS AND RHEUMATISM, 2009, 60 (06) :1851-1861
[9]   Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever [J].
Cazeneuve, C ;
Ajrapetyan, H ;
Papin, S ;
Roudot-Thoraval, F ;
Geneviève, D ;
Mndjoyan, E ;
Papazian, M ;
Sarkisian, A ;
Babloyan, A ;
Boissier, B ;
Duquesnoy, P ;
Kouyoumdjian, JC ;
Girodon-Boulandet, E ;
Grateau, G ;
Sarkisian, T ;
Amselem, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (05) :1136-1143
[10]   Gain-of-Function Pyrin Mutations Induce NLRP3 Protein-Independent Interleukin-1β Activation and Severe Autoinflammation in Mice [J].
Chae, Jae Jin ;
Cho, Young-Hun ;
Lee, Geun-Shik ;
Cheng, Jun ;
Liu, P. Paul ;
Feigenbaum, Lionel ;
Katz, Stephen I. ;
Kastner, Daniel L. .
IMMUNITY, 2011, 34 (05) :755-768