Apolipoprotein E and obstructive sleep apnea: evaluating whether a candidate gene explains a linkage peak
✍ Scribed by Emma K. Larkin; Sanjay R. Patel; Susan Redline; Emmanuel Mignot; Robert C. Elston; Joachim Hallmayer
- Book ID
- 102222523
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 154 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0741-0395
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✦ Synopsis
Abstract
Evidence from both linkage analyses and association‐based analyses has implicated Apoliprotein E (ApoE) as a disease susceptibility locus for obstructive sleep apnea. To further assess the putative role of ApoE in sleep apnea, we performed genotyping, association, and linkage analyses in a cohort assembled to investigate the genetic epidemiology of sleep apnea. Among a subset of the Caucasian families, ten microsatellites, spanning 20 cM, were genotyped in a region near ApoE on chromosome 19 where previous suggestive linkage had been demonstrated using a 9.1‐cM genome‐wide scan. Haseman‐Elston regression analysis, conducted with these fine mapping markers (n=196 sibling pairs, 56 families), showed evidence for linkage to marker AFM210yg9 (p=0.00034), which was increased over that observed with the original scan. ApoE genotyping also was performed on a larger set of data (n=1,211 from 271 families, ages 3–85 years) from the cohort with available DNA. To determine whether the ApoE genotype explains the linkage peak, we included the ApoE genotype as a covariate in regression models. Inclusion of ApoE E2 allele as a covariate reduced the regression coefficient by 18%, suggesting that ApoE does not substantively explain the linkage signal. Finally, we repeated an association‐based analysis in the larger sample of 1,211 individuals, and observed a higher prevalence of sleep apnea among individuals with the ApoE E2 allele. Overall, the evidence suggests that there is a disease susceptibility locus for obstructive sleep apnea in the region of ApoE, but ApoE itself is unlikely to be the causative locus. Genet. Epidemiol. 2006. © 2005 Wiley‐Liss, Inc.