| Autor: |
Bennett, Sonya L., Hewitt, Alex W., Poulsen, Johan L., Kearns, Lisa S., Morgan, James E., Craig, Jamie E., Mackey, David A. |
| Zdroj: |
Archives of Ophthalmology; Jan2007, Vol. 125 Issue 1, p112-116, 5p |
| Abstrakt: |
Objective: To investigate whether structural differences of the optic nerve head are evident in young people who do not have manifest glaucoma but are known to carry myocilin mutations. Methods: A case-control design was adopted. Subjects from Australian pedigrees known to have either the Gln368STOP myocilin mutation (cutoff age, < 40 years) or the Thr377Met myocilin mutation (cutoff age, <30 years) were examined for signs of glaucoma. Stereoscopic disc photographs were digitalized. Analysis of the optic disc area, optic cup area, and neuroretinal rim area was performed using digital stereoscopy with a Z-screen. Mutation analysis was conducted using direct sequencing. The t test, corrected for multiple comparison testing, was used in analysis. Results: A total of 29 myocilin mutation-carrying (case) and 33 mutation-free (control) individuals were reviewed. The mean±SD ages were 19.9±9.0 and 22.1 ±9.5 years in the mutation and mutation-free groups, respectively (P = .35). There was no significant difference in intraocular pressure between mutation carriers and noncarriers (P = .44). There were no statistically significant differences in the mean disc, neuroretinal rim, and cup areas between the groups. The mean± SD neuroretinal rim area was 1.24±0.24 mm² in the noncarrier group and 1.25 ±0.23 mm² in the mutation group (P=.46). No notch, nerve fiber layer defect, or neuroretinal rim hemorrhage was noted in any eye examined. Conclusions: Although confounded by penetrance and expressivity, no quantified structural difference in the optic nerve head was observed in individuals who had a myocilin mutation prior to the diagnosis of glaucoma. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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