You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 125 No. 1, January 2007 TABLE OF CONTENTS
  Archives
  •  Online Features
  Ophthalmic Molecular Genetics
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on Web of Science (14)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Topic Collections
 •Optics/ Refraction
 •Articles for Residents
 •Genetics
 •Genetic Disorders
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Confirmation of Linkage to Ocular Refraction on Chromosome 22q and Identification of a Novel Linkage Region on 1q

Alison P. Klein, PhD, MHS; Priya Duggal, PhD, MPH; Kristine E. Lee, MS; Ronald Klein, MD, MPH; Joan E. Bailey-Wilson, PhD; Barbara E. K. Klein, MD, MPH

Arch Ophthalmol. 2007;125(1):80-85.

Objective  To localize genes influencing ocular refraction in subjects in the Beaver Dam Eye Study. Previous studies establish that myopia clusters within families and linkage to myopia has been demonstrated on 2q, 4q, 12q, 17q, 18q, 22q, and Xq. Few studies have examined genetic effects across the entire range of refraction, though linkages to 1p, 3q, 4q, 8p, and 11p have been reported, and our previous analysis of the Beaver Dam Eye Study demonstrated substantial heritability for refraction (68%).

Methods  We conducted nonparametric sibling-pair and genome-wide linkage analyses on spherical equivalent adjusting for age, education, and nuclear sclerosis, in 834 sibling pairs in 486 extended pedigrees.

Results  We identified a novel region of suggestive linkage on 1q (multipoint, P<.00019) and replicated the 22q region (multipoint, P = .0033) previously linked to myopia. Additionally, there was some evidence of linkage to 7p (multipoint, P = .0023).

Conclusion  Refraction is a complex trait influenced by both genes and environment. Our work confirms a previously reported linkage region on 22q and identifies 2 novel regions of linkage on 1q and 7p.

Clinical Relevance  Further, genetic research is needed to finemap this trait to identify the causative gene. Modifying the actions of such a gene might lead to a reduction in the risk of refractive error.


Author Affiliations: Departments of Oncology and Pathology, Johns Hopkins School of Medicine, and Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health (Dr A. P. Klein), and Statistical Genetics Section, National Institutes of Health, National Human Genome Research Institute, Inherited Disease Research Branch, Baltimore, Md (Drs Duggal and Bailey-Wilson); and Department of Ophthalmology and Visual Sciences, University of Wisconsin Medical School, Madison (Ms Lee and Drs R. Klein and B. E. K. Klein).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

An International Collaborative Family-Based Whole-Genome Linkage Scan for High-Grade Myopia
Li et al.
IOVS 2009;50:3116-3127.
ABSTRACT | FULL TEXT  

Genomewide Linkage Scans for Ocular Refraction and Meta-analysis of Four Populations in the Myopia Family Study
Wojciechowski et al.
IOVS 2009;50:2024-2032.
ABSTRACT | FULL TEXT  

Heritability Analysis of Spherical Equivalent, Axial Length, Corneal Curvature, and Anterior Chamber Depth in the Beaver Dam Eye Study
Klein et al.
Arch Ophthalmol 2009;127:649-655.
ABSTRACT | FULL TEXT  

Assessment of TGIF as a Candidate Gene for Myopia
Pertile et al.
IOVS 2008;49:49-54.
ABSTRACT | FULL TEXT  

Genetic Mapping of Myopia Susceptibility Loci
Schache et al.
IOVS 2007;48:4924-4929.
ABSTRACT | FULL TEXT  

Linkage Replication of the MYP12 Locus in Common Myopia
Chen et al.
IOVS 2007;48:4433-4439.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2007 American Medical Association. All Rights Reserved.