Literature DB >> 18077767

Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association.

L L E Koskinen1, I R Korponay-Szabo, K Viiri, K Juuti-Uusitalo, K Kaukinen, K Lindfors, K Mustalahti, K Kurppa, R Adány, Z Pocsai, G Széles, E Einarsdottir, C Wijmenga, M Mäki, J Partanen, J Kere, P Saavalainen.   

Abstract

BACKGROUND: Coeliac disease is caused by dietary gluten, which triggers chronic inflammation of the small intestine in genetically predisposed individuals. In one quarter of the patients the disease manifests in the skin as dermatitis herpetiformis. Recently, a novel candidate gene, myosin IXB on chromosome 19p13, was shown to be associated with coeliac disease in the Dutch and Spanish populations. The same gene has previously been associated with inflammatory bowel disease, systemic lupus erythematosus and rheumatoid arthritis risk, making myosin IXB a potential shared risk factor in these inflammatory disorders.
METHODS: In this study, previously reported myosin IXB variants were tested for genetic linkage and association with coeliac disease in 495 Hungarian and Finnish families and in an additional 270 patients and controls. RESULTS AND
CONCLUSION: The results show significant linkage (logarithm of odds (LOD) 3.76, p = 0.00002) to 19p13 which supports the presence of a genuine risk factor for coeliac disease in this locus. Myosin IXB variants were not associated with coeliac disease in this study; however, weak evidence of association with dermatitis herpetiformis was found. The association could not explain the strong linkage seen in both phenotypes, indicating that the role of other neighbouring genes in the region cannot be excluded. Therefore, more detailed genetic and functional studies are required to characterise the role of the myosin IXB gene in both coeliac disease and dermatitis herpetiformis.

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Year:  2007        PMID: 18077767     DOI: 10.1136/jmg.2007.053991

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  6 in total

Review 1.  The myosin superfamily at a glance.

Authors:  M Amanda Hartman; James A Spudich
Journal:  J Cell Sci       Date:  2012-04-01       Impact factor: 5.285

2.  Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations.

Authors:  Elisabet Einarsdottir; Marianna R Bevova; Alexandra Zhernakova; Alienke Monsuur; Lotta L E Koskinen; Ruben van't Slot; Chris Mulder; M Luisa Mearin; Ilma R Korponay-Szabo; Katri Kaukinen; Kalle Kurppa; Juha Kere; Markku Mäki; Cisca Wijmenga; Päivi Saavalainen
Journal:  Eur J Hum Genet       Date:  2011-02-16       Impact factor: 4.246

3.  Cost-effective HLA typing with tagging SNPs predicts celiac disease risk haplotypes in the Finnish, Hungarian, and Italian populations.

Authors:  Lotta Koskinen; Jihane Romanos; Katri Kaukinen; Kirsi Mustalahti; Ilma Korponay-Szabo; Donatella Barisani; Maria Teresa Bardella; Fabiana Ziberna; Serena Vatta; György Széles; Zsuzsa Pocsai; Kati Karell; Katri Haimila; Róza Adány; Tarcisio Not; Alessandro Ventura; Markku Mäki; Jukka Partanen; Cisca Wijmenga; Päivi Saavalainen
Journal:  Immunogenetics       Date:  2009-03-03       Impact factor: 2.846

Review 4.  Dermatitis herpetiformis: from the genetics to the development of skin lesions.

Authors:  Diletta Bonciani; Alice Verdelli; Veronica Bonciolini; Antonietta D'Errico; Emiliano Antiga; Paolo Fabbri; Marzia Caproni
Journal:  Clin Dev Immunol       Date:  2012-06-07

5.  Effects of In Vivo Gluten Challenge on PBMC Gene Expression Profiles in Diet Treated Celiac Disease.

Authors:  Dawit A Yohannes; Andrea de Kauwe; Katri Kaukinen; Kalle Kurppa; Markku Mäki; Robert P Anderson; Sten Linnarsson; Dario Greco; Päivi Saavalainen
Journal:  Front Immunol       Date:  2020-12-11       Impact factor: 7.561

6.  IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease.

Authors:  Elisabet Einarsdottir; Lotta L E Koskinen; Emma Dukes; Kati Kainu; Sari Suomela; Maarit Lappalainen; Fabiana Ziberna; Ilma R Korponay-Szabo; Kalle Kurppa; Katri Kaukinen; Róza Adány; Zsuzsa Pocsai; György Széles; Martti Färkkilä; Ulla Turunen; Leena Halme; Paulina Paavola-Sakki; Tarcisio Not; Serena Vatta; Alessandro Ventura; Robert Löfberg; Leif Torkvist; Francesca Bresso; Jonas Halfvarson; Markku Mäki; Kimmo Kontula; Ulpu Saarialho-Kere; Juha Kere; Mauro D'Amato; Päivi Saavalainen
Journal:  BMC Med Genet       Date:  2009-01-28       Impact factor: 2.103

  6 in total

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