Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population (original) (raw)
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- Published: 05 May 2005
Genes & Immunity volume 6, pages 459–461 (2005) Cite this article
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Abstract
Protein tyrosine phosphatase PTPN22 is involved in the negative regulation of T-cell responsiveness. Recently, the association of a coding variant of the PTPN22 gene-R620W(1858C>T) with a number of autoimmune diseases has been described. Therefore, we tested the association of PTPN22 1858*T allele in Dutch early onset type 1 diabetes (T1D) and rheumatoid arthritis (RA) patients, as well as celiac disease (CD) patients, for which no previous study of PTPN22 has been reported. The PTPN22 variant was strongly associated with T1D in cases vs controls (P=2 × 10−7, OR=2.3, 95% CI=1.7–3.1) as well as in a transmission disequilibrium test in nuclear trio's (P=9 × 10−9, OR=3.3, CI=2.1–5.0), RA (case/control: P=0.003, OR=1.8 CI =1.2–2.6), but not CD, in spite of a trend of increased homozygosity (P=0.05) and early age at onset (P=0.01). PTPN22 is not generally associated with T-cell mediated autoimmune diseases, although it might play a role in the CD patients with early clinical manifestation.
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References
- Raman K, Mohan C . Genetic underpinnings of autoimmunity—lessons from studies in arthritis, diabetes, lupus and multiple sclerosis. Curr Opin Immunol 2003; 15: 651–659.
Article CAS Google Scholar - Becker KG . Comparative genetics of type 1 diabetes and autoimmune disease: common loci, common pathways? Diabetes 1999; 48: 1353–1358.
Article CAS Google Scholar - Aune TM, Parker JS, Maas K, Liu Z, Olsen NJ, Moore JH . Co-localization of differentially expressed genes and shared susceptibility loci in human autoimmunity. Genet Epidemiol 2004; 27: 162–172.
Article Google Scholar - Bottini N, Musumeci L, Alonso A et al. A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes. Nat Genet 2004; 36: 337–338.
Article CAS Google Scholar - Smyth D, Cooper JD, Collins JE et al. Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus. Diabetes 2004; 53: 3020–3023.
Article CAS Google Scholar - Onengut-Gumuscu S, Ewens KG, Spielman RS, Concannon P . A functional polymorphism (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families. Genes Immun 2004; 5: 678–680.
Article CAS Google Scholar - Begovich AB, Carlton VE, Honigberg LA et al. A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am J Hum Genet 2004; 75: 330–337.
Article CAS Google Scholar - Kyogoku C, Langefeld CD, Ortmann WA et al. Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE. Am J Hum Genet 2004; 75: 504–507.
Article CAS Google Scholar - Velaga MR, Wilson V, Jennings CE et al. The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease. J Clin Endocrinol Metab 2004; 89: 5862–5865.
Article CAS Google Scholar - Hasegawa K, Martin F, Huang G, Tumas D, Diehl L, Chan AC . PEST domain-enriched tyrosine phosphatase (PEP) regulation of effector/memory T cells. Science 2004; 303: 685–689.
Article CAS Google Scholar - Siminovitch KA . PTPN22 and autoimmune disease. Nat Genet 2004; 36: 1248–1249.
Article CAS Google Scholar - Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition. Arch Dis Child 1990; 65: 909–911.
- Van Belzen MJ, Meijer JW, Sandkuijl LA et al. A major non-HLA locus in celiac disease maps to chromosome 19. Gastroenterology 2003; 125: 1032–1041.
Article CAS Google Scholar - Begovich AB, Caillier SJ, Alexander HC et al. The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis. Am J Hum Genet 2005; 76: 184–187.
Article CAS Google Scholar
Acknowledgements
We thank all patients and their families participating in the study. We thank physicians participating in the study—Chris Mulder, Roderick Houwen, Maria Luisa Mearin, Jan Bruining. We also thank Alienke Monsuur and Martine van Belzen for the samples collection and Jackie Senior for improving the manuscript. The study was supported by grants from the Dutch Diabetes Research Foundation (97.137), The Dutch Digestive Disease Foundation (WS 03-06), The Netherlands Organisation for Health Research and Development (ZonMW 912-02-028), The Juvenile Diabetes Research Foundation Internationdal (JDRF) (2001.10.004) and the Celiac Disease Consortium, an Innovative Cluster approved by the Netherlands Genomics Initiative and partially funded by the Dutch Government (BSIK03009).
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Authors and Affiliations
- Division of Biomedical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands
A Zhernakova, C Wijmenga & B P C Koeleman - Department of Immunohaematology and Blood Transfusion, Leiden University Medical Centre, Leiden, The Netherlands
P Eerligh, B O Roep & B P C Koeleman - Rheumatology Department, University Hospital St Radboud Nijmegen, The Netherlands
P Barrera
Authors
- A Zhernakova
- P Eerligh
- C Wijmenga
- P Barrera
- B O Roep
- B P C Koeleman
Corresponding author
Correspondence toB P C Koeleman.
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Zhernakova, A., Eerligh, P., Wijmenga, C. et al. Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population.Genes Immun 6, 459–461 (2005). https://doi.org/10.1038/sj.gene.6364220
- Received: 18 January 2005
- Revised: 09 March 2005
- Accepted: 09 March 2005
- Published: 05 May 2005
- Issue date: 01 September 2005
- DOI: https://doi.org/10.1038/sj.gene.6364220