No association of polymorphisms in human endogenous retrovirus K18 and CD48 with schizophrenia

Research output: Contribution to journalJournal articleResearchpeer-review

  • Mette Nyegaard
  • Ditte Demontis
  • Britta Boserup Thestrup
  • Anne Hedemand
  • Karina Meden Sørensen
  • Thomas Hansen
  • Werge, Thomas
  • David Michael Hougaard
  • Robert H Yolken
  • Preben Bo Mortensen
  • Ole Mors
  • Anders Børglum
The human endogenous retrovirus HERV-K18 is located within intron 1 of CD48 on chromosome 1q and is still active in the human genome. Genetic variation in HERV-K18 single-nucleotide polymorphisms (SNPs) has previously been associated with an increased risk of schizophrenia (SZ) and with type 2 diabetes (T2D) among individuals with SZ. Here, we present a replication study of association of two SNPs in HERV-K18 and 19 tagSNPs in CD48 with (a) SZ and (b) T2D in patients with SZ in two Danish samples (total number of cases=750 and controls=1214). No association was found with SZ or with T2D among individuals with SZ for any of the investigated SNPs. However, one HERV-K18 SNP showed a tendency toward an association with T2D in younger SZ patients, in agreement with previous findings, but due to a very low sample size, this result needs to be further investigated.
Original languageEnglish
JournalPsychiatric Genetics
Volume22
Issue number3
Pages (from-to)146-8
Number of pages3
ISSN0955-8829
DOIs
Publication statusPublished - Jun 2012

ID: 48611319