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Cracking the Code: Which Ocular Symptoms Predict Dry Eye Signs? Insights From a Large International Sicca Registry
Pragnya R Donthineni1,2, Chloe Shields1,3,4, Rohit Muralidhar5
1Bascom Palmer Eye Institute, University of Miami, Miami, Florida.
Artificial tear use and blurred vision predict dry eye disease (DED) signs better than pain. Identifying symptom clusters in DED patients is crucial for targeted therapies.
Area of Science:
- Ophthalmology
- Dry Eye Disease Research
- Clinical Diagnostics
Background:
- Dry eye disease (DED) is a multifactorial condition affecting the ocular surface.
- Identifying reliable predictors of DED signs is essential for accurate diagnosis and management.
- The Sjögrens International Collaborative Clinical Alliance (SICCA) cohort provides a valuable dataset for DED research.
Purpose of the Study:
- To identify symptom-based predictors of objective dry eye disease (DED) signs within the SICCA cohort.
- To explore the relationship between ocular symptoms, artificial tear use, and DED diagnostic signs.
- To investigate symptom clusters and their association with disease characteristics.
Main Methods:
- Retrospective analysis of 16 ocular symptoms and artificial tear (AT) use.
- Logistic regression models were employed for univariable and multivariable analyses.
- Hierarchical cluster analysis was used to identify distinct symptom-based groups.
Main Results:
- Artificial tear use, eye redness, and blurred vision were positively associated with abnormal ocular surface staining (OSS).
- Dry eye sensation, AT use, and blurred vision correlated with abnormal Schirmer test (ST) results.
- Cluster analysis identified three groups with varying symptom burdens, with a mild-moderate cluster showing more abnormal ocular signs and positive serologies.
Conclusions:
- Artificial tear use and blurred vision are stronger indicators of ocular surface and tear film abnormalities than pain.
- Symptom-based clustering reveals heterogeneity in sicca presentations, potentially linked to neurotrophic/neuropathic mechanisms.
- These findings underscore the need for phenotype-based targeted therapies for DED.
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