Literature DB >> 19623168

Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children.

Devendra K Amre1, David R Mack, Kenneth Morgan, Mary Fujiwara, David Israel, Colette Deslandres, Ernest G Seidman, Phlippe Lambrette, Irina Costea, Alfreda Krupoves, Houda Fegury, Jinsong Dong, Guy Grimard, Emile Levy.   

Abstract

OBJECTIVES: A recent pediatric-focused genome-wide association study has reported novel associations of the 20q13 and 21q22 loci with inflammatory bowel disease (IBD). We aimed to investigate these associations with Crohn's disease (CD) in Canadian children.
METHODS: A combined case-control and case-parent design was implemented at three pediatric gastroenterology clinics in Canada. Children less than 20 years of age with a confirmed diagnosis of CD were recruited along with controls. For a subset of the patients, biological parents were also recruited. Three single-nucleotide polymorphisms (SNPs) at the 20q13 locus and 1 SNP at the 21q22 locus were genotyped. Associations between individual SNPs and haplotypes were examined.
RESULTS: A total of 410 cases, 415 controls, and 302 parents were studied. The mean (+/-s.d.) age for the cases was 12.3 (+/-3.2) years. Most cases were men (56.1%) who had ileocolonic disease (L3+/-L4, 52.2%) and inflammatory behavior (B1+/-B4, 87.0%) at diagnosis. Single SNP analysis showed that all 3 SNPs at the 20q13 locus were significantly associated with CD (rs2297441, P=2.24x10(-4); rs2315008, P=4.77x10(-4); rs4809330, P=6.08x10(-3)). Haplotype analysis suggested that the association signal at 20q13 resided on a common haplotype comprising the minor allele of rs2297441 (P=2.8x10(-5)). SNP rs2836878 at the 21q22 locus showed a trend for association with CD that was statistically not significant (P=0.06).
CONCLUSIONS: Our results support an association between the 20q13 locus and CD in Canadian children. Positional cloning studies are required to further dissect the potential causative genes in the region.

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Year:  2009        PMID: 19623168     DOI: 10.1038/ajg.2009.430

Source DB:  PubMed          Journal:  Am J Gastroenterol        ISSN: 0002-9270            Impact factor:   10.864


  17 in total

1.  Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children.

Authors:  Devendra K Amre; David R Mack; Kenneth Morgan; David Israel; Colette Deslandres; Ernest G Seidman; Phlippe Lambrette; Irina Costea; Alfreda Krupoves; Houda Fegury; Jinsong Dong; Zia Xhu; Guy Grimard; Emile Levy
Journal:  Hum Genet       Date:  2010-05-16       Impact factor: 4.132

Review 2.  Early-Onset Inflammatory Bowel Disease.

Authors:  Judith R Kelsen; Pierre Russo; Kathleen E Sullivan
Journal:  Immunol Allergy Clin North Am       Date:  2019-02       Impact factor: 3.479

Review 3.  Role of genetics in the diagnosis and prognosis of Crohn's disease.

Authors:  Epameinondas V Tsianos; Konstantinos H Katsanos; Vasileios E Tsianos
Journal:  World J Gastroenterol       Date:  2011-12-28       Impact factor: 5.742

4.  Inflammatory bowel disease in pediatric and adolescent patients: a biomolecular and histopathological review.

Authors:  Luciana Rigoli; Rosario Alberto Caruso
Journal:  World J Gastroenterol       Date:  2014-08-14       Impact factor: 5.742

Review 5.  Role of genetics in the diagnosis and prognosis of Crohn's disease.

Authors:  Epameinondas V Tsianos; Konstantinos H Katsanos; Vasileios E Tsianos
Journal:  World J Gastroenterol       Date:  2012-01-14       Impact factor: 5.742

6.  Interaction of Crohn's disease susceptibility genes in an Australian paediatric cohort.

Authors:  Josef Wagner; Winnie H Sim; Justine A Ellis; Eng K Ong; Anthony G Catto-Smith; Donald J S Cameron; Ruth F Bishop; Carl D Kirkwood
Journal:  PLoS One       Date:  2010-11-08       Impact factor: 3.240

7.  Genome-wide association studies--a summary for the clinical gastroenterologist.

Authors:  Espen Melum; Andre Franke; Tom H Karlsen
Journal:  World J Gastroenterol       Date:  2009-11-21       Impact factor: 5.742

8.  Genes involved in the metabolism of poly-unsaturated fatty-acids (PUFA) and risk for Crohn's disease in children & young adults.

Authors:  Irina Costea; David R Mack; David Israel; Kenneth Morgan; Alfreda Krupoves; Ernest Seidman; Colette Deslandres; Philippe Lambrette; Guy Grimard; Emile Levy; Devendra K Amre
Journal:  PLoS One       Date:  2010-12-20       Impact factor: 3.240

9.  Investigation of multiple susceptibility loci for inflammatory bowel disease in an Italian cohort of patients.

Authors:  Anna Latiano; Orazio Palmieri; Tiziana Latiano; Giuseppe Corritore; Fabrizio Bossa; Giuseppina Martino; Giuseppe Biscaglia; Daniela Scimeca; Maria Rosa Valvano; Maria Pastore; Antonio Marseglia; Renata D'Incà; Angelo Andriulli; Vito Annese
Journal:  PLoS One       Date:  2011-07-27       Impact factor: 3.240

10.  A non-synonymous coding variant (L616F) in the TLR5 gene is potentially associated with Crohn's disease and influences responses to bacterial flagellin.

Authors:  Jared Sheridan; David R Mack; Devendra K Amre; David M Israel; Artem Cherkasov; Huifang Li; Guy Grimard; Theodore S Steiner
Journal:  PLoS One       Date:  2013-04-11       Impact factor: 3.240

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