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World J Gastroenterol. Sep 14, 2006; 12(34): 5550-5553
Published online Sep 14, 2006. doi: 10.3748/wjg.v12.i34.5550
Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn’s disease
Judit Bene, Lili Magyari, Gábor Talián, Katalin Komlósi, Beáta Gasztonyi, Beáta Tari, Ágnes Várkonyi, Gyula Mózsik, Béla Melegh
Judit Bene, MTA PTE Clinical Genetics Research Group of Hungarian Academy of Sciences at the University of Pécs, Pécs, Hungary
Judit Bene, Lili Magyari, Gábor Talián, Katalin Komlósi, Béla Melegh, Department of Medical Genetics and Child Development, University of Pécs, Pécs, Hungary
Beáta Tari, Ágnes Várkonyi, Department of Pediatrics and Child Health Center, University of Szeged, Szeged, Hungary
Beáta Gasztonyi, Gyula Mózsik, 1st Department of Medicine, School of Medicine, University of Pécs, Pécs, Hungary
Supported by the grant of Hungarian Science Foundation No. OTKA T 49589
Correspondence to: Dr. Béla Melegh, Professor of Medical Genetics and Pediatrics, Department of Medical Genetics and Child Development, University of Pécs, H-7624 Pécs, Szigeti 12, Hungary. bela.melegh@aok.pte.hu
Telephone: +36-72-536427 Fax: +36-72-536427
Received: June 13, 2006
Revised: June 28, 2006
Accepted: July 7, 2006
Published online: September 14, 2006
Abstract

AIM: To investigate the frequency of the common NOD2/CARD15 susceptibility variants and two functional polymorphisms of OCTN cation transporter genes in Hungarian pediatric patients with Crohn’s disease (CD).

METHODS: A cohort of 19 unrelated pediatric and 55 unrelated adult patients with Crohn’s disease and 49 healthy controls were studied. Genotyping of the three common CD-associated CARD15 variants (Arg702Trp, Gly908Arg and 1007finsC changes) with the SLC22A4 1672C→T, and SLC22A5 -207G→C mutations was performed by direct sequencing of the specific regions of these genes.

RESULTS: At least one CARD15 mutation was present in 52.6% of the children and in 34.5% of the adults compared to 14.3% in controls. Surprisingly, strongly different mutation profile was detected in the pediatric versus adult patients. While the G908R and 1007finsC variants were 18.4% and 21.1% in the pediatric group, they were 1.82% and 11.8% in the adults, and were 1.02% and 3.06% in the controls, respectively. The R702W allele was increased approximately two-fold in the adult subjects, while in the pediatric group it was only approximately 64% of the controls (9.09% in the adults, 2.63% in pediatric patients, and 4.08% in the controls). No accumulation of the OCTN variants was observed in any patient group versus the controls.

CONCLUSION: The frequency of the NOD2/CARD15 susceptibility variants in the Hungarian pediatric CD population is high and the profile differs from the adult CD patients, whereas the results for SLC22A4 and SLC22A5 mutation screening do not confirm the assumption that the carriage of these genotypes means an obligatory susceptibility to CD.

Keywords: OCTN1; OCTN2; NOD2/CARD15; Crohn’s disease