Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease

被引:93
作者
Ozen, S. [1 ]
Aktay, N. [1 ]
Lainka, E. [2 ]
Duzova, A. [1 ]
Bakkaloglu, A. [1 ]
Kallinich, T. [3 ]
机构
[1] Hacettepe Univ, Fac Med, Dept Paediat, TR-06100 Ankara, Turkey
[2] Univ Duisburg Essen, Ctr Pediat, Essen, Germany
[3] Charite Univ Med Berlin, Berlin, Germany
关键词
TURKISH POPULATION; RENAL AMYLOIDOSIS; FREQUENCY; MUTATION; SAA1;
D O I
10.1136/ard.2008.092031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Worldwide, familial Mediterranean fever (FMF) is the most common autoinflammatory disease. It has been suggested that environmental factors affect the phenotype as some patients do not develop the complication of secondary amyloidosis. Objective: To analyse whether disease severity in Turkish children with FMF, living in Turkey and Germany is different. Patients and methods: A total of 55 Turkish children living in Turkey were compared with 45 Turkish children born and raised in Germany. Mean age among the group from Turkey and Germany was 42.2 and 44.29 months, respectively. M694V was the leading mutation in both groups. The severity scores were compared with two scoring systems, modified according to published paediatric data for dosage. Results: There was no significant difference between the mean C-reactive protein and erythrocyte sedimentation rate levels of the two groups. According to the modified Sheba Center score, 78.2% of patients from the group living in Turkey had a severe course compared with 34.1% from the group living in Germany. The modified score of Pras et al also showed more severe disease in the patients from Turkey. The difference between the two groups for both scoring systems were significant (both p < 0.05). Conclusions: We believe the modified scores that we introduce can be widely used for children. Our results suggest that the environment affects the phenotype of a monogenic disease of the innate inflammatory pathway.
引用
收藏
页码:246 / 248
页数:3
相关论文
共 16 条
[1]   Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population [J].
Aksentijevich, I ;
Torosyan, Y ;
Samuels, J ;
Centola, M ;
Pras, E ;
Chae, JJ ;
Oddoux, C ;
Wood, G ;
Azzaro, MP ;
Palumbo, G ;
Giustolisi, R ;
Pras, M ;
Ostrer, H ;
Kastner, DL .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (04) :949-962
[2]  
Bakkaloglu A, 2004, J RHEUMATOL, V31, P1139
[3]   The contribution of genotypes at the MEFV and SAA1 loci to amyloidosis and disease severity in patients with familial Mediterranean fever [J].
Gershoni-Baruch, R ;
Brik, R ;
Zacks, N ;
Shinawi, M ;
Lidar, M ;
Livneh, A .
ARTHRITIS AND RHEUMATISM, 2003, 48 (04) :1149-1155
[4]   Cultural adaptation is associated with atopy and wheezing among children of Turkish origin living in Germany [J].
Grüber, C ;
Illi, S ;
Plieth, A ;
Sommerfeld, C ;
Wahn, U .
CLINICAL AND EXPERIMENTAL ALLERGY, 2002, 32 (04) :526-531
[5]   Colchicine use in children and adolescents with familial Mediterranean fever: Literature review and consensus statement [J].
Kallinich, Tilmann ;
Haffner, Dieter ;
Niehues, Tim ;
Huss, Kristina ;
Lainka, Elke ;
Neudorf, Ulrich ;
Schaefer, Christof ;
Stojanov, Silvia ;
Timmann, Christian ;
Keitzer, Rolf ;
Ozdogan, Huri ;
Ozen, Seza .
PEDIATRICS, 2007, 119 (02) :E474-E483
[6]   Diagnostic and treatment concerns in familial Mediterranean fever [J].
Livneh, A ;
Langevitz, P .
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2000, 14 (03) :477-498
[7]   Evaluation of disease severity in familial Mediterranean fever [J].
Mor, A ;
Shinar, Y ;
Zaks, N ;
Langevitz, P ;
Chetrit, A ;
Shtrasburg, S ;
Rabinovitz, E ;
Livneh, A .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2005, 35 (01) :57-64
[8]   Childhood vasculitides in Turkey: a nationwide survey [J].
Ozen, Seza ;
Bakkaloglu, Aysin ;
Dusunsel, Ruhan ;
Soylemezoglu, Oguz ;
Ozaltin, Fatih ;
Poyrazoglu, Hakan ;
Kasapcopur, Ozgur ;
Ozkaya, Ozan ;
Yalcinkaya, Fatos ;
Balat, Ayse ;
Kural, Nurdan ;
Donmez, Osman ;
Alpay, Harika ;
Anarat, Ali ;
Mir, Sevgi ;
Gur-Guven, Ayfer ;
Sonmez, Ferah ;
Gok, Faysal .
CLINICAL RHEUMATOLOGY, 2007, 26 (02) :196-200
[9]  
Ozen S, 2006, J RHEUMATOL, V33, P2498
[10]  
Pras E, 1998, AM J MED GENET, V75, P216, DOI 10.1002/(SICI)1096-8628(19980113)75:2<216::AID-AJMG20>3.0.CO