Genome-wide scan of additional Jewish families confirms linkage of a myopia susceptibility locus to chromosome 22q12

Mol Vis. 2006 Dec 4:12:1499-505.

Abstract

Purpose: A genome-wide scan was previously reported for myopia in Ashkenazi Jews. In order to confirm the previous linkage peaks, a collection of DNA samples from 19 new Ashkenazi Jewish families were tested for linkage in a genome wide scan.

Methods: Families were ascertained from an Orthodox Ashkenazi Jewish community through mailings. Myopia was defined as equal to or greater than -1 diopter in both meridians in both eyes. The genome wide scan used markers from a modified Cooperative Human Linkage Center version 9 (402 markers). Parametric two-point linkage was calculated with FASTLINK while multipoint linkage was calculated with GENEHUNTER.

Results: The results for the 19 families demonstrated several regions of suggestive linkage on chromosomes 7, 1, 17, and 22. A combined analysis of the 19 families and 44 previously reported families demonstrated an increase in the LOD score to 4.73 for the chromosome 22 locus.

Conclusions: Multiple chromosomal regions have exhibited some evidence of linkage to a myopia susceptibility gene in this Ashkenazi Jewish population. The strongest evidence of linkage to such a susceptibility gene in these data is on chromosome 22.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 1
  • Chromosomes, Human, Pair 17
  • Chromosomes, Human, Pair 22*
  • Chromosomes, Human, Pair 7
  • Female
  • Genetic Linkage*
  • Genetic Predisposition to Disease*
  • Genome, Human*
  • Humans
  • Jews / genetics*
  • Lod Score
  • Male
  • Middle Aged
  • Myopia / genetics*