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Association between Age-Related Macular Degeneration and Mortality in a High Cardiovascular Risk Cohort: A
Richard Kha1, George Burlutsky1, Aravinda Thiagalingam2
1Centre for Vision Research, Westmead Institute for Medical Research, Westmead, New South Wales, Australia.
Insights
Age-related macular degeneration (AMD) independently predicts higher all-cause mortality in individuals at high risk for cardiovascular disease (CVD). Early AMD also increases the risk of CVD mortality, suggesting shared underlying pathways.
Area of Science:
- Ophthalmology
- Cardiology
- Public Health
Background:
- Age-related macular degeneration (AMD) is a leading cause of vision loss.
- Cardiovascular disease (CVD) remains a major global health concern.
- The potential link between AMD and CVD mortality risk is not fully understood.
Purpose of the Study:
- To determine if AMD predicts all-cause and CVD mortality in a high-risk cohort.
- To investigate the association between different stages of AMD and mortality outcomes.
Main Methods:
- Prospective cohort study of 1545 adults evaluated for acute coronary syndrome.
- AMD assessed from fundus photographs; coronary artery disease severity graded by Gensini score.
- Mortality data collected over 9 years via linkage with the Australian National Death Index; Cox regression used.
Main Results:
- Any AMD (6.9%) was present in 107 participants; 15.1% died over 9 years, with 11.3% from CVD.
- After adjusting for confounders, any AMD, early AMD, and late AMD predicted increased all-cause mortality.
- Any AMD and early AMD were associated with increased CVD mortality; late AMD was not.
Conclusions:
- AMD at any stage independently predicts higher all-cause mortality in high-CVD-risk individuals.
- Early AMD is also linked to increased CVD mortality, suggesting shared pathophysiological mechanisms.
- Further research is needed to elucidate the shared pathways between AMD and CVD.
Objective:
To investigate whether age-related macular degeneration (AMD) predicts the risk of all-cause and cardiovascular disease (CVD) mortality in a high CVD risk cohort.
Design:
Prospective cohort study.
Participants:
A total of 1545 adult participants who presented to a tertiary Australian hospital for evaluation of acute coronary syndrome were included in this study.
Methods:
Participants were evaluated for acute coronary syndrome using coronary angiography. Participants were concurrently examined for AMD from mydriatic fundus photographs, which were graded using the Wisconsin grading system into categories of any AMD, early AMD, and late AMD. Coronary artery disease was graded from coronary angiograms using the Gensini score. Mortality data were obtained 9 years after baseline examination through data linkage with the Australian National Death Index. Hazard ratios (HRs) were obtained using Cox regression analysis.
Main Outcome Measures:
All-cause and CVD mortality data were obtained through data linkage with the Australian National Death Index. Death rates through June 2018 were compared by demographics and potential confounders.
Results:
Any AMD was identified in 107 (6.9%) participants, including those with early (n = 86) and late AMD (n = 21). Over 9 years of follow-up, 234 (15.1%) participants had died, including 174 (11.3%) participants from fatal CVD events. After controlling for age, sex, body mass index, total cholesterol, smoking status, history of diabetes, hypertension, myocardial infarction, stroke, and macrovascular coronary artery disease severity using the Gensini score, there was an increased rate of all-cause mortality for those with any AMD (HR, 2.37; 95% confidence interval [CI], 1.54-3.64), early AMD (HR, 2.42; 95% CI, 1.48-3.94), and late AMD (HR, 2.25; 95% CI, 1.08-4.71). Any AMD (HR, 2.62; 95% CI, 1.61-4.26) and early AMD (HR, 2.61; 95% CI, 1.50-4.64) were also associated with a greater likelihood of CVD mortality. Late AMD was not associated with CVD mortality.
Conclusions:
In individuals with high CVD risk, the presence of AMD at any stage independently predicted increased all-cause mortality. Meanwhile, any AMD and early AMD increased the risk of CVD mortality. Although mechanisms are unclear, this potentially reflects shared pathways between AMD and CVD.
Financial Disclosure(S):
The authors have no proprietary or commercial interest in any materials discussed in this article.
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