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Research
grants Blue Mountains Eye Study
The Blue Mountains Eye Study (BMES) was the first large population-based assessment of visual impairment and common eye diseases of a representative older Australian community sample. The project was conducted in an area that included Katoomba, Leura, Medlow Bath (postcode 2780) and Wentworth Falls (postcode 2782). This area was chosen as its demography is similar to the overall Australian population of this age. The Population In late 1992 the target population was identified by a door-to-door census of all dwellings in the two postcode areas. 3,654 residents aged 49-97 were examined during the period 1992-1994 (an overall response of 82.4% of non-institutionalised residents - BMES-1) During 1997-1999, all surviving participants were invited to attend a 5-year follow up examination, for which 2,334 persons returned (75% of survivors - BMES-2). A second census of the same postcode areas was conducted in 1999, identifying a further 1,510 residents now eligible to participte of which 1,206 were examined as part of an extension study during 1999-2000 (BMES-E). In 2002, participants were invited to return for 10-year follow-up exams, and during 2002-2004 1952 original participants were re-examined (BMES-3) Commencing in 2007, all participants are again being asked to return for 15-year follow-up exams (BMES-4).
At each examination, a detailed assessment of eye disease and other general health measures was conducted. Participants were also asked to attend fasting blood tests after each examination and complete a detailed questionnaire about the types of food they consumed. At the 5 and 10 year exams, a test of memory and cognition (Mini Mental State Examination), questions about quality of life (Short Form 36) and visual functioning were also conducted. Eye conditions were assessed at each examination by taking a series of photographs of the eye. Photographs of the retina (the back of the eye) were used to assess the presence of diseases like macular degeneration or diabetic eye damage. Stereo photographs of the optic nerve (which enters at the back of the optic disc) were taken to assess changes that, together with an automated test of the field of vision, indicate the presence of glaucoma. Two types of photographs were taken of the lens inside the eye to grade the presence of the different types of cataract. All of these photographs are graded using standard protocols (developed for the Beaver Dam Eye Study in Wisconsin, USA). Participants at 5 and 10 years were also asked to attend a detailed hearing assessment (BMHS). The hearing tests were conducted in sound booths by audiologists.
Visual impairment Both impaired vision and reduced visual field were found to double the risk of falls. For those aged 75 or older, moderate visual impairment was associated with a nine-fold increase in risk of hip fracture during the subsequent two years. People with any visual impairment were three times as likely to use community support services, including 'meals-on-wheels', home care or home nursing care, and were six times as likely to state that they felt unable to go out alone. They were also more likely to rank their general health as poorer. Self-reported car accidents as driver were also twice as high among those with visual impairment compared to those without. After taking into account a range of factors predicting placement, older people with visual impairment were significantly more likely to be admitted permanently to a nursing home. We previously found a high rate of visual impairment and a ten-fold higher rate of blindness among nursing home residents in this region than in the community. After adjusting for age and all of the factors found associated with mortality, those who were visually impaired had an 80% higher risk of dying than people with good vision. The mechanism of this impact is not known but it could act via depression. Cataract Age-related maculopathy
(macular degeneration) Other than age, several groups of factors appear to either increase or decrease the risk of age-related maculopathy, including smoking, vascular, familial, racial or ethnic, nutritional, hormonal, ocular or sunlight-related factors. The BMES confirmed the highest risk of late-stage macular degeneration among current smokers, who had a four-fold increased risk compared with past or non-smokers, including a smoking exposure gradient. Using population attributable risk calculations, we estimated that smoking may thus substantially contribute to around 20% of blindness in Australians aged over 50. This finding has been confirmed internationally, with the smoking relationship strongly confirmed in the pooled three-continent data. Our 5-year incidence data demonstrated associations between current smoking at baseline and new late lesions. Importantly, we also showed that smokers developed late-stage macular degeneration an average 10 years before nonsmokers. We plan to pool age-related maculopathy incidence data from the Beaver Dam and Rotterdam studies to improve study power. Interestingly, we found no micronutrient associations with age-related maculopathy, but we did observe a significant protective association from higher fish consumption and an increased risk associated with higher consumption of dietary fat. Glaucoma Diabetic and other vascular
retinopathy Diabetic eye damage (retinopathy) was present in one third of those with diabetes, including 16% of those with previously undiagnosed diabetes. The presence of diabetic retinopathy was related to higher levels of blood glucose in this population. People with diabetes had significantly worse vision that those without this condition. The cumulative 5-year incidence of diabetic retinopathy was 22.2%. Progression of retinopathy by one step on the standard scale was found in one in four of those with retinopathy at baseline. Isolated retinopathy lesions (microaneurysms, haemorrhages) were also found in 9.8% of subjects without a history or blood test findings suggesting diabetes. This rate was higher than in some earlier studies. The finding of retinopathy was strongly related to hypertension in a dose-dependent manner, as well as to other vascular risk factors. A number of other retinal vascular signs (focal narrowing and an opaque appearance of the small retinal arterioles, nipping of the retinal veins and signs of small cholesterol crystals in the lumen of branch retinal arterioles were identified. All of these signs were shown to predict stroke or cerebrovascular death during the 5-year follow-up, independently of age and sex, as well as measures of hypertension and smoking. Hearing Loss
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