Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree

Genome Res. 1995 Sep;5(2):105-15. doi: 10.1101/gr.5.2.105.

Abstract

An X-chromosomal predisposing locus to manic-depressive illness has been suggested since 1969 on the basis of the cosegregation of this trait in some families with phenotypic markers, such as color blindness, the glucose-6-phosphate dehydrogenase deficiency, and the coagulation factor IX deficiency. However, the conclusive evidence and the exact location of the putative X-chromosomal locus have remained controversial. We report here a linkage between DNA markers near the coagulation factor IX gene and bipolar disorder in an extended pedigree rising from the genetically isolated population of Finland. A distinct chromosomal haplotype covering a 20-cM region on Xq24-q27.1 could be demonstrated to segregate with bipolar disorder. These findings should encourage research groups to study extended family materials with Xq24-q27.1 markers to finally resolve the question of the X-chromosomal linkage of bipolar disorder.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Bipolar Disorder / genetics*
  • Chromosome Mapping
  • DNA Primers
  • Female
  • Finland
  • Haplotypes
  • Humans
  • Hypoxanthine Phosphoribosyltransferase / genetics
  • Male
  • Molecular Sequence Data
  • Pedigree
  • X Chromosome*

Substances

  • DNA Primers
  • Hypoxanthine Phosphoribosyltransferase