Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.humimm.2006.02.032
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dc.titleMICA is associated with type 1 diabetes in the Belgian population, independent of HLA-DQ
dc.contributor.authorVan Autreve, Jan E
dc.contributor.authorKoeleman, Bobby PC
dc.contributor.authorQuartier, Erik
dc.contributor.authorAminkeng, Folefac
dc.contributor.authorWeets, Ilse
dc.contributor.authorGorus, Frans K
dc.contributor.authorVan der Auwera, Bart JR
dc.date.accessioned2022-12-05T04:22:22Z
dc.date.available2022-12-05T04:22:22Z
dc.date.issued2006-01-01
dc.identifier.citationVan Autreve, Jan E, Koeleman, Bobby PC, Quartier, Erik, Aminkeng, Folefac, Weets, Ilse, Gorus, Frans K, Van der Auwera, Bart JR (2006-01-01). MICA is associated with type 1 diabetes in the Belgian population, independent of HLA-DQ. HUMAN IMMUNOLOGY 67 (1-2) : 94-101. ScholarBank@NUS Repository. https://doi.org/10.1016/j.humimm.2006.02.032
dc.identifier.issn0198-8859
dc.identifier.issn1879-1166
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/235318
dc.description.abstractTo ascertain association of MICA with type 1 diabetes (T1D) in the Belgian population, well-characterized antibody-positive patients were analyzed for MICA transmembrane gene polymorphism in both an association study and a nuclear family study. The frequency of MICA5 was significantly increased in the T1D patient group (18%) compared with the control population (12%, OR = 1.6, pc < 10-3), whereas MICA9 was decreased (11% versus 16%, OR = 0.7, pc < 0.01). A p value <10-3 for the association of MICA conditional on HLA class II and p = 0.01 for the conditional extended transmission disequilibrium test were obtained, indicating that MICA is associated with type 1 diabetes, independent of HLA-DQ. Analysis of estimated extended HLA-DQ-MICA haplotypes revealed individual effects of MICA alleles. The most significant effect was seen for MICA5 on the HLA-DQA1*03-DQB1*0302-MICA haplotype (OR = 2.5, p < 10-3). A significant protective effect was seen for the combination of DQA1*01-DQB1*0602/3 and MICA5.1 (OR = 0.3, p < 10-3). However, patients stratified according to the presence or absence of the different MICA alleles did not differ in terms of age at onset, sex, or other diabetes-related clinical and epidemiological data. In conclusion, MICA is associated with type 1 diabetes in the Belgian population and the observed association does not result from the HLA-DQ associated risk. © 2006 American Society for Histocompatibility and Immunogenetics.
dc.language.isoen
dc.publisherELSEVIER SCIENCE INC
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectImmunology
dc.subjectMICA
dc.subjectHLA
dc.subjectrisk
dc.subjecttype 1 diabetes
dc.subjectCHAIN-RELATED GENE
dc.subjectMAJOR HISTOCOMPATIBILITY COMPLEX
dc.subjectBODY-MASS INDEX
dc.subjectCLASS-I REGION
dc.subjectTRANSMEMBRANE REGION
dc.subjectLINKAGE DISEQUILIBRIUM
dc.subjectNUCLEOTIDE-SEQUENCE
dc.subjectMELLITUS
dc.subjectPOLYMORPHISM
dc.subjectDISEASE
dc.typeArticle
dc.date.updated2022-11-30T19:56:35Z
dc.contributor.departmentMEDICINE
dc.description.doi10.1016/j.humimm.2006.02.032
dc.description.sourcetitleHUMAN IMMUNOLOGY
dc.description.volume67
dc.description.issue1-2
dc.description.page94-101
dc.published.statePublished
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