TNF promoter polymorphisms and modulation of growth retardation and disease severity in pediatric Crohn's disease

被引:41
作者
Levine, A
Shamir, R
Wine, E
Weiss, B
Karban, A
Shaoul, RR
Reif, SS
Yakir, B
Friedlander, M
Kaniel, Y
Leshinsky-Silver, E
机构
[1] E Wolfson Med Ctr, Pediat Gastroenterol Serv, Pediat Gastroenterol & Nutr Unit, IL-58100 Holon, Israel
[2] Meyer Childrens Hosp, Pediat Gastroenterol Unit, Haifa, Israel
[3] Meyer Childrens Hosp, Nutr Unit, Haifa, Israel
[4] Tel Hashomer Med Ctr, Tel Aviv, Israel
[5] Rambam Med Ctr, Div Gastroenterol, Haifa, Israel
[6] Bnei Zion Med Ctr, Haifa, Israel
[7] Tel Aviv Med Ctr & Sch Med, Dana Childrens Hosp, IL-64239 Tel Aviv, Israel
[8] Hebrew Univ Jerusalem, Dept Stat, IL-91905 Jerusalem, Israel
[9] Daniel Biotech Weizman, Rehovot, Israel
[10] E Wolfson Med Ctr, Genet Mol Lab, Holon, Israel
[11] Tel Aviv Univ, Sackler Sch Med, IL-69978 Tel Aviv, Israel
关键词
D O I
10.1111/j.1572-0241.2005.41737.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Delayed growth is common in pediatric Crohn's disease (CD). Multiple factors have been shown to affect growth in this situation, the most prominent being the presence and severity of inflammation and inadequate nutritional intake. Inflammation, anorexia, and weight loss are all manifestations of circulating TNF-alpha, which is elevated in CD. The ability to secrete TNF-alpha may be affected by polymorphisms in the TNF-alpha promoter. The aim of our study was to determine whether growth retardation and disease severity in pediatric onset CD are affected by TNF promoter genotype. METHODS: Genotyping for TNF-alpha and NOD2/CARD15 single nucleotide polymorphisms was performed in 87 patients with detailed growth records. Parameters including disease location and disease severity were recorded, and the effect of these polymorphisms on Z-scores for height and weight at disease onset and during follow-up were analyzed. RESULTS: Lower age of onset was linked to more height retardation, while the presence of colonic disease and the absence of ileal disease were more likely to predict the absence of growth retardation. The presence of two polymorphisms thought to decrease circulating TNF-alpha was associated with higher mean Z-scores for height and a trend toward less growth retardation. Two other polymorphisms were modestly associated with disease severity. CONCLUSION: Polymorphisms in the TNF-alpha promoter may independently modulate growth and disease severity in pediatric onset CD. The effect of these polymorphisms does not appear to be mediated via weight loss, and is relatively modest.
引用
收藏
页码:1598 / 1604
页数:7
相关论文
共 48 条
[41]   THE MOUSE-HUMAN CHIMERIC MONOCLONAL-ANTIBODY CA2 NEUTRALIZES TNF IN-VITRO AND PROTECTS TRANSGENIC MICE FROM CACHEXIA AND TNF LETHALITY IN-VIVO [J].
SIEGEL, SA ;
SHEALY, DJ ;
NAKADA, MT ;
LE, JM ;
WOLFE, DS ;
PROBERT, L ;
KOLLIAS, G ;
GHRAYEB, J ;
VILCEK, J ;
DADDONA, PE .
CYTOKINE, 1995, 7 (01) :15-25
[42]   A common functional polymorphism (C -> A substitution at position-863) in the promoter region of the tumour necrosis factor-alpha (TNF-alpha) gene associated with reduced circulating levels of TNF-alpha [J].
Skoog, T ;
van't Hooft, FM ;
Kallin, B ;
Jovinge, S ;
Boquist, S ;
Nilsson, J ;
Eriksson, P ;
Hamsten, A .
HUMAN MOLECULAR GENETICS, 1999, 8 (08) :1443-1449
[43]  
STALLMACH A, 2003, INT J COLORECTAL DIS, V19, P308
[44]   NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease [J].
Tomer, G ;
Ceballos, C ;
Concepcion, E ;
Benkov, KJ .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2003, 98 (11) :2479-2484
[45]   Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF-κB transcription factors [J].
van Heel, DA ;
Udalova, IA ;
De Silva, AP ;
McGovern, DP ;
Kinouchi, Y ;
Hull, J ;
Lench, NJ ;
Cardon, LR ;
Carey, AH ;
Jewell, DP ;
Kwiatkowski, D .
HUMAN MOLECULAR GENETICS, 2002, 11 (11) :1281-1289
[46]   Relationship between the tumor necrosis factor alpha polymorphism and the serum C-reactive protein levels in inflammatory bowel disease [J].
Vatay, A ;
Bene, L ;
Kovács, A ;
Prohászka, Z ;
Szalai, C ;
Romics, L ;
Fekete, B ;
Karádi, I ;
Füst, G .
IMMUNOGENETICS, 2003, 55 (04) :247-252
[47]   Tumour necrosis factor 5′ promoter single nucleotide polymorphisms influence susceptibility to rheumatoid arthritis (RA) in immunogenetically defined multiplex RA families [J].
Waldron-Lynch, F ;
Adams, C ;
Amos, C ;
Zhu, DK ;
McDermott, MF ;
Shanahan, F ;
Molloy, MG ;
O'Gara, F .
GENES AND IMMUNITY, 2001, 2 (02) :82-87
[48]   Pediatric Crohn's disease and growth retardation: The role of genotype, phenotype, and disease severity [J].
Wine, E ;
Reif, SS ;
Leshinsky-Silver, E ;
Weiss, B ;
Shaoul, RR ;
Shamir, R ;
Wasserman, D ;
Lerner, A ;
Boaz, M ;
Levine, A .
PEDIATRICS, 2004, 114 (05) :1281-1286