Neither an intronic CA repeat within the CD48 gene nor the HERV-K18 polymorphisms are associated with type 1 diabetes.

E Ramos-Lopez, S Ghebru, Jan Van Autreve, Folefac Aminkeng, J. Herwig, E. Seifried, C. Seidl, Bart Van Der Auwera, Klaus Badenhoop

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)

Abstract

Type 1 diabetes is an autoimmune heterogeneous disease that is determined by environmental and genetic factors. A possible retroviral etiology has been inferred from the observation that human endogenous retrovirus (HERV)-K18 encoding a superantigen (SAg) has a polymorphism associated with this disease. Type 1 diabetes families from Germany and Belgium were genotyped for the novel HERV-8914 (303 families) and for the known HERV-8594 (284 families) polymorphisms within the SAg-coding region on the HERV-K18. Case-control analysis was performed for the HERV-8914 polymorphism (506 patients) and for the HERV-8594 polymorphism (370 patients) and compared with 350 German controls. Haplotypes were constructed. Additionally, a microsatellite within the CD48 gene was analyzed in German type 1 diabetes families (n=125) as well as in patients (n=375) and in healthy controls (n=350). No association was found for HERV-K18 polymorphisms or the CA repeat within the CD48 gene with type 1 diabetes mellitus either in families or by comparing patients and controls. In conclusion, we cannot confirm a role of HERV-K18 polymorphisms -HERV-8914 and HERV-8594- or of the CD48 CA repeat for type 1 diabetes susceptibility.
Original languageEnglish
Pages (from-to)147-152
Number of pages6
JournalTissue Antigens
Volume2
Issue number68
Publication statusPublished - 19 Aug 2006

Keywords

  • CD48
  • HERV-K18
  • type 1 diabetes

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