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Ex Vivo OCT-Based Multimodal Imaging of Human Donor Eyes for Research into Age-Related Macular Degeneration
Published on: May 26, 2023
Cardiovascular Disease and Age-Related Macular Degeneration
R Theodore Smith1, Philip J Rosenfeld2
1From the New York Eye and Ear Infirmary of Mount Sinai (R.T.S.), New York City, New York, USA.
Insights
Cardiovascular disease (CVD) and age-related macular degeneration (AMD) are linked, particularly high-risk CVDs impacting choroidal perfusion, which may drive subretinal drusenoid deposit (SDD) formation. Further research into these connections is crucial for patient care.
Area of Science:
- Ophthalmology
- Cardiology
- Genetics
Background:
- Cardiovascular disease (CVD) is a leading global cause of death.
- Age-related macular degeneration (AMD) is a primary cause of irreversible blindness in the elderly.
- Both CVD and AMD share risk factors like hypertension and smoking.
Purpose of the Study:
- To review and update the understanding of associations between CVD and AMD.
- To explore the specific links between subsets of CVD and AMD.
Main Methods:
- Evidence-based literature review.
- Analysis of authors' clinical experience.
- Synthesis of current research findings.
Main Results:
- A general association between CVD and AMD is not consistently demonstrated.
- Specific high-risk cardiovascular diseases (HRCVDs) are strongly associated with subretinal drusenoid deposits (SDDs), not soft drusen.
- Compromised choroidal perfusion due to HRCVDs is proposed as a mechanism for SDD formation, disrupting metabolic support to photoreceptors.
Conclusions:
- The link between SDDs and HRCVDs warrants further investigation, particularly in patients with AMD genetic risk alleles.
- Prospective studies are needed to identify clinical and genetic factors driving AMD progression.
- Disease models can guide referrals between ophthalmology and cardiology for comprehensive patient management.
Purpose:
To provide an update on the published associations between cardiovascular disease (CVD) and age-related macular degeneration (AMD).
Design:
Evidence-based perspective.
Methods:
Review of literature and experience of authors.
Results:
CVD is the leading cause of death worldwide, and AMD is the leading cause of irreversible blindness among the elderly. Both these conditions are associated with hypertension and smoking. Thus, it was expected that patients with CVD might be at higher risk for AMD, and AMD would be closely associated with CVD. However, such a general association has never been shown in dozens of studies. Instead, current evidence suggests that there are associations only between certain subsets of CVD and AMD. A strong association was shown to exist between specific high-risk cardiovascular diseases (HRCVDs) that confer compromised choroidal perfusion and the presence of subretinal drusenoid deposit (SDD), not ordinary soft drusen, which are considered the hallmark of intermediate AMD. We propose that this compromised choroidal perfusion is the underlying mechanism driving the formation of SDDs. We also propose, more generally, that the formation of SDDs result from the disruption of the normal metabolic support between the choriocapillaris and photoreceptors (PRs). We recommend that HRCVDs need to be studied in association with genetic risk-alleles to better understand the association between decreased choroidal perfusion and AMD progression.
Conclusion:
The strong association between SDDs to HRCVDs merits further investigation, especially in cardiovascular patients with SDDs carrying the high-risk alleles for AMD. Further prospective studies in both HRCVD and AMD patients are needed to elucidate the totality of clinical and genetic factors that drive AMD. These disease models can then be deployed to identify vasculopathic patients who need a retinal referral for AMD as well as AMD patients who need a cardiovascular workup to address undetected HRCVDs in patients with SDDs.
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