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Association between cognitive function and large optic nerve cupping, accounting for cup-disc-ratio genetic risk
Sasha Kravets1,2, Rawan Allozi Rupnow1,2, Abhishek Sethi1,3
1Department of Ophthalmology and Visual Sciences, Illinois Eye and Ear Infirmary, University of Illinois at Chicago, Chicago, Illinois, United States of America.
Plos One
|October 31, 2022
Summary
Large cup-to-disc ratio (CDR) is linked to lower cognitive function in women, regardless of genetic risk score. This finding highlights CDR as a potential indicator for cognitive health assessments.
Area of Science:
- Ophthalmology
- Neuroscience
- Genetics
Background:
- Large cup-to-disc ratio (CDR) is a risk factor for glaucoma.
- Cognitive function can be influenced by various physiological factors.
- Genetic predisposition may play a role in ocular and cognitive health.
Purpose of the Study:
- To determine if a cup-to-disc ratio (CDR) genetic risk score (GRS) modifies the association between large CDR and cognitive function in women.
- To explore the relationship between CDR GRS, CDR status, and cognitive performance.
Main Methods:
- Retrospective analysis of data from the Women's Health Initiative.
- Exclusion of participants with glaucoma or ocular hypertension.
- Calculation of CDR GRS using 13 single nucleotide polymorphisms (SNPs).
- Assessment of cognitive function using the Modified Mini-Mental State Examination (3MSE).
- Logistic and linear regression analyses to evaluate associations between GRS, CDR, and 3MSE scores.
Main Results:
- A significant association was found between CDR GRS and large CDR (p=0.011).
- Women with large CDR had significantly lower 3MSE scores (mean difference of 0.84, p=0.007), even after accounting for GRS.
- The mean GRS was higher in women with large CDR compared to those without (p=0.004).
Conclusions:
- Large CDR is independently associated with lower cognitive function in women.
- The CDR GRS did not modify the negative association between large CDR and cognitive function.
- Findings suggest that large CDR is a significant indicator of reduced cognitive function, irrespective of genetic risk.
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