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Accuracy and implications of a reported family history of glaucoma - Experience from the glaucoma inheritance study in Tasmania

Citation

McNaught, A and Allen, J and Healey, D and McCartney, P and Coote, M and Wong, T and Craig, JE and Green, C and Rait, J and Mackey, DA, Accuracy and implications of a reported family history of glaucoma - Experience from the glaucoma inheritance study in Tasmania, Archives of Ophthalmology, 118, (7) pp. 900-904. ISSN 0003-9950 (2000) [Refereed Article]

Abstract

Objectives: To ascertain the prevalence of previously undiagnosed primary open-angle glaucoma (POAG) within 5 large POAG pedigrees and to evaluate the reliability of a reported family history of glaucoma within these pedigrees. Methods: The Glaucoma Inheritance Study in Tasmania (GIST) identified several large adult POAG pedigrees. Intraocular pressure (IOP), optic disc stereophotography, and automated perimetry were performed on all adult pedigree members. Participants were classified as normal (IOP <22 mm Hg and normal optic disc and field); glaucoma suspect (normal field, but an IOP ≥22 mm Hg and/or suspicious optic disc); or POAG (field defect and glaucomatous optic disc). Some individuals with POAG had been previously diagnosed by their local ophthalmologist; others were diagnosed as a result of the GIST project. Family members with a prior diagnosis of POAG were asked to report if they were aware of any relatives with POAG. This reported family history was then directly compared with the actual pedigree (before the diagnosis of new cases) to calculate agreement. Main Outcome Measure: The rate of glaucoma in pedigrees and percentage of previously diagnosed glaucoma cases who were aware of the positive family history of POAG. Results: Four hundred forty-two subjects (mean age, 54 years [range, 13-97 years]) from 5 pedigrees were examined: 316 subjects (71%) were normal, 47 (11%) were previously diagnosed with POAG, and 8 (2%) were previously diagnosed glaucoma suspects; 30 cases (7%) of POAG and 41 suspects (9%) were newly diagnosed as a direct result of the GIST examination. Of the 47 previously diagnosed POAG cases, 41 were questioned about their prior knowledge of any family history and 11 (27%) were unaware of their family history of POAG. Conclusions: Examination of all adult subjects from POAG families yields new cases. Even in large POAG pedigrees, 27% of previously diagnosed POAG patients were unaware of their positive family history. These findings suggest that a higher percentage of adult POAG may be inherited than hitherto reported.

Item Details

Item Type:Refereed Article
Research Division:Medical and Health Sciences
Research Group:Public Health and Health Services
Research Field:Epidemiology
Objective Division:Health
Objective Group:Clinical Health (Organs, Diseases and Abnormal Conditions)
Objective Field:Hearing, Vision, Speech and Their Disorders
Author:Wong, T (Ms Wong)
Author:Craig, JE (Mr Jamie Craig)
Author:Mackey, DA (Professor David Mackey)
ID Code:18833
Year Published:2000
Web of Science® Times Cited:51
Deposited By:Menzies Centre
Deposited On:2000-08-01
Last Modified:2011-09-21
Downloads:0

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