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Sjögren Disease and the Corneal Surface
1Department of Ophthalmology (R.K., S.K.), The University of Osaka Graduate School of Medicine, Osaka, Japan; and Department of Innovative Visual Science (S.K.), The University of Osaka Graduate School of Medicine Graduate School of Medicine, Osaka, Japan.
Dry eye in Sjögren disease involves lacrimal gland dysfunction and corneal nerve abnormalities. Understanding these nerve issues can lead to personalized treatments for patients with Sjögren disease.
Area of Science:
- Ophthalmology
- Neuroscience
- Immunology
Background:
- Sjögren disease causes dry eye via lacrimal gland dysfunction, leading to reduced tear secretion and ocular surface damage.
- Corneal nerves are critical in Sjögren disease, with abnormalities influencing patient symptoms.
- Two distinct phenotypes exist: neurotrophic (reduced symptoms despite signs) and neuropathic (disproportionate symptoms).
Purpose of the Study:
- To explore the role of corneal nerve status in Sjögren disease.
- To differentiate between neurotrophic and neuropathic aspects of dry eye in Sjögren disease.
- To highlight the potential for personalized treatment based on corneal nerve evaluation.
Main Methods:
- Clinical assessment of ocular surface signs.
- Evaluation of corneal nerve structure and function.
- Symptom analysis including pain and sensitivity.
Main Results:
- Patients with Sjögren disease display varied corneal nerve abnormalities.
- Distinct symptom profiles correlate with specific nerve phenotypes (neurotrophic vs. neuropathic).
- Clinical signs may not always align with reported symptoms, particularly in the neurotrophic type.
Conclusions:
- Corneal nerve status is a key factor in the presentation of dry eye in Sjögren disease.
- Identifying neurotrophic and neuropathic phenotypes is crucial for understanding patient experience.
- Comprehensive assessment of corneal nerves can guide personalized therapeutic strategies for Sjögren disease patients.
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