Literature DB >> 15503241

Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease.

Keiko Yamazaki1, Masakazu Takazoe2, Torao Tanaka2, Toshiki Ichimori3, Susumu Saito4, Aritoshi Iida4, Yoshihiro Onouchi5, Akira Hata5, Yusuke Nakamura6.   

Abstract

Crohn disease (CD) is an inflammatory bowel disease characterized by chronic transmural, segmental, and typically granulomatous inflammation of the gut. Recently, two novel candidate gene loci associated with CD, SLC22A4 and SLC22A5 on chromosome 5 known as IBD5 and DLG5 on chromosome 10, were identified through association analysis of Caucasian CD patients. We validated these candidate genes in Japanese patients with CD and found a weak but possible association with both SLC22A4 (P=0.028) and DLG5 (P=0.023). However, the reported genetic variants that were indicated to be causative in the Caucasian population were completely absent in or were not associated with Japanese CD patients. These findings imply significant differences in genetic background with CD susceptibility among different ethnic groups and further indicate some difficulty of population-based studies.

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Year:  2004        PMID: 15503241     DOI: 10.1007/s10038-004-0204-x

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  30 in total

1.  Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease.

Authors:  K Kyo; T Muto; H Nagawa; G M Lathrop; Y Nakamura
Journal:  J Hum Genet       Date:  2001       Impact factor: 3.172

2.  A high-throughput SNP typing system for genome-wide association studies.

Authors:  Y Ohnishi; T Tanaka; K Ozaki; R Yamada; H Suzuki; Y Nakamura
Journal:  J Hum Genet       Date:  2001       Impact factor: 3.172

3.  Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism.

Authors:  Hisanori Haga; Ryo Yamada; Yozo Ohnishi; Yusuke Nakamura; Toshihiro Tanaka
Journal:  J Hum Genet       Date:  2002       Impact factor: 3.172

4.  Functional variants of OCTN cation transporter genes are associated with Crohn disease.

Authors:  Vanya D Peltekova; Richard F Wintle; Laurence A Rubin; Christopher I Amos; Qiqing Huang; Xiangjun Gu; Bill Newman; Mark Van Oene; David Cescon; Gordon Greenberg; Anne M Griffiths; Peter H St George-Hyslop; Katherine A Siminovitch
Journal:  Nat Genet       Date:  2004-04-11       Impact factor: 38.330

5.  Association of ulcerative colitis with rare VNTR alleles of the human intestinal mucin gene, MUC3.

Authors:  K Kyo; M Parkes; Y Takei; H Nishimori; P Vyas; J Satsangi; J Simmons; H Nagawa; S Baba; D Jewell; T Muto; G M Lathrop; Y Nakamura
Journal:  Hum Mol Genet       Date:  1999-02       Impact factor: 6.150

6.  Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.

Authors:  J D Rioux; M S Silverberg; M J Daly; A H Steinhart; R S McLeod; A M Griffiths; T Green; T S Brettin; V Stone; S B Bull; A Bitton; C N Williams; G R Greenberg; Z Cohen; E S Lander; T J Hudson; K A Siminovitch
Journal:  Am J Hum Genet       Date:  2000-04-21       Impact factor: 11.025

7.  HLA-linked susceptibility and resistance genes in Crohn's disease.

Authors:  A Nakajima; N Matsuhashi; T Kodama; Y Yazaki; M Takazoe; A Kimura
Journal:  Gastroenterology       Date:  1995-11       Impact factor: 22.682

8.  Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease.

Authors:  Keiko Yamazaki; Masakazu Takazoe; Torao Tanaka; Toshiki Kazumori; Yusuke Nakamura
Journal:  J Hum Genet       Date:  2002       Impact factor: 3.172

9.  Lack of common NOD2 variants in Japanese patients with Crohn's disease.

Authors:  Nagamu Inoue; Kazuo Tamura; Yoshitaka Kinouchi; Yoshihiro Fukuda; Seiichi Takahashi; Yasunori Ogura; Naohiro Inohara; Gabriel Núñez; Yusuke Kishi; Yuji Koike; Tooru Shimosegawa; Takashi Shimoyama; Toshifumi Hibi
Journal:  Gastroenterology       Date:  2002-07       Impact factor: 22.682

10.  Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations.

Authors:  J Hampe; A Cuthbert; P J Croucher; M M Mirza; S Mascheretti; S Fisher; H Frenzel; K King; A Hasselmeyer; A J MacPherson; S Bridger; S van Deventer; A Forbes; S Nikolaus; J E Lennard-Jones; U R Foelsch; M Krawczak; C Lewis; S Schreiber; C G Mathew
Journal:  Lancet       Date:  2001-06-16       Impact factor: 79.321

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  32 in total

1.  Contribution of the IBD5 locus to inflammatory bowel disease: a meta-analysis.

Authors:  Jian Wang; Xi Wang; Hong Yang; Dong Wu; Li Wang; Jiaming Qian
Journal:  Hum Genet       Date:  2011-01-30       Impact factor: 4.132

2.  Ethnic differences in allele frequency of autoimmune-disease-associated SNPs.

Authors:  Mikako Mori; Ryo Yamada; Kyoko Kobayashi; Reimi Kawaida; Kazuhiko Yamamoto
Journal:  J Hum Genet       Date:  2005-05-10       Impact factor: 3.172

3.  Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population.

Authors:  Alexandra V Pearce; Sheila A Fisher; Natalie J Prescott; Clive M Onnie; Reenal Pattni; Peter Green; Alastair Forbes; John Mansfield; Jeremy Sanderson; Stefan Schreiber; Cathryn M Lewis; Christopher G Mathew
Journal:  Int J Colorectal Dis       Date:  2006-05-31       Impact factor: 2.571

Review 4.  Genetics of inflammatory bowel disease: current status and future directions.

Authors:  Thomas D Walters; Mark S Silverberg
Journal:  Can J Gastroenterol       Date:  2006-10       Impact factor: 3.522

5.  Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease.

Authors:  Maria Gazouli; Gerassimos Mantzaris; Athanassios J Archimandritis; George Nasioulas; Nicholas P Anagnou
Journal:  World J Gastroenterol       Date:  2005-12-21       Impact factor: 5.742

Review 6.  Genetic factors associated with the development of inflammatory bowel disease.

Authors:  Jesus-K Yamamoto-Furusho
Journal:  World J Gastroenterol       Date:  2007-11-14       Impact factor: 5.742

7.  Spontaneous development of intestinal and colonic atrophy and inflammation in the carnitine-deficient jvs (OCTN2(-/-)) mice.

Authors:  Prem S Shekhawat; Sonne R Srinivas; Dietrich Matern; Michael J Bennett; Richard Boriack; Varghese George; Hongyan Xu; Puttur D Prasad; Penny Roon; Vadivel Ganapathy
Journal:  Mol Genet Metab       Date:  2007-09-19       Impact factor: 4.797

8.  Contribution of genetics to a new vision in the understanding of inflammatory bowel disease.

Authors:  A S Peña
Journal:  World J Gastroenterol       Date:  2006-08-14       Impact factor: 5.742

9.  Association between OCTN1/2 gene polymorphisms (1672C-T, 207G-C) and susceptibility of Crohn's disease: a meta-analysis.

Authors:  Chao Xuan; Bei-Bei Zhang; Tao Yang; Kai-Feng Deng; Ming Li; Rui-Juan Tian
Journal:  Int J Colorectal Dis       Date:  2011-06-25       Impact factor: 2.571

Review 10.  OCTNs: will the real IBD5 gene please stand up?

Authors:  Mark-S Silverberg
Journal:  World J Gastroenterol       Date:  2006-06-21       Impact factor: 5.742

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