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Association of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population.

TitleAssociation of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population.
Publication TypeJournal Article
Year of Publication2010
AuthorsWirtz, M. K., Samples J. R., Toumanidou V., Charlesworth J., Mikropoulos D. G., Kaltsos K., Economou A., Dimopoulos A., Georgiadou I. N., Moumtzis G., Papanastasiou A., Kramer P. L., Dyer T., Blangero J., & Konstas A. G. P.
JournalInvest Ophthalmol Vis Sci
Volume51
Issue6
Pagination3055-60
Date Published2010 Jun
ISSN1552-5783
KeywordsAdolescent, Adult, Aged, Aged, 80 and over, Child, Cytoskeletal Proteins, European Continental Ancestry Group, Exons, Eye Proteins, Female, Genotype, Glaucoma, Open-Angle, Glycoproteins, Greece, Humans, Incidence, Intraocular Pressure, Male, Middle Aged, Pedigree, Phenotype, Point Mutation, Risk Factors, Rural Population
Abstract

PURPOSE: To characterize the MYOC genotype correlation with phenotypes in an isolated Greek population with a high incidence of glaucoma.METHODS: Five hundred thirty-one villagers were enrolled in the study. Participants underwent a comprehensive ophthalmic examination. All three exons of myocilin were bidirectionally sequenced. Power calculations and measured genotype analysis was conducted using the genetic variance analysis program, SOLAR version 4.2, to account for the relatedness between individuals.RESULTS: The participants, 376 of whom were linked in a single 11-generation pedigree, ranged in age from 10 to 95 years with a mean age of 49. Sixty-five individuals had POAG, and 27 of those carried the Thr377Met MYOC mutation. Both peak intraocular pressure and vertical cup-to dis- ratio were significantly associated with the MYOC Thr377Met variant (P = 9 x 10(-14) and P = 9 x 10(-8), respectively), whereas central corneal thickness showed no significant association (P < 0.7).CONCLUSIONS: This village had a high frequency of glaucoma, with 12% of the participants aged 10 to 95 years having the disease. In this cohort, the Thr377Met MYOC mutation was significantly associated with both high intraocular pressures and high vertical cup-to-disc ratios. No association was found with central corneal thickness.

DOI10.1167/iovs.09-4652
Alternate JournalInvest. Ophthalmol. Vis. Sci.
PubMed ID20107173
PubMed Central IDPMC2891465
Grant List5P30EY010572 / EY / NEI NIH HHS / United States
5R01EY010555 / EY / NEI NIH HHS / United States
5R01EY011650 / EY / NEI NIH HHS / United States
5R37MH059490 / MH / NIMH NIH HHS / United States

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