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Ocular surface changes in type II diabetic patients with proliferative diabetic retinopathy
Authors:Yan Gao  Yan Zhang  Yu-Sha Ru  Xiao-Wu Wang  Ji-Zhong Yang  Chun-Hui Li  Hong-Xing Wang  Xiao-Rong Li  Bing Li
Affiliation:Shanxi Eye Hospital, Taiyuan 030002, Shanxi Province, China;College of Optometry and Ophthalmology, Tianjin Medical University, Tianjin Medical University Eye Institute, Tianjin Medical University Eye Hospital, Tianjin 300384, China;College of Optometry and Ophthalmology, Tianjin Medical University, Tianjin Medical University Eye Institute, Tianjin Medical University Eye Hospital, Tianjin 300384, China;Shanxi Eye Hospital, Taiyuan 030002, Shanxi Province, China;Shanxi Eye Hospital, Taiyuan 030002, Shanxi Province, China;Department of Ophthalmology, Shanxi Medical University First Hospital, Taiyuan 030001, Shanxi Province, China;Department of Ophthalmology, Beijing Chuiyangliu Hospital Affiliated to Tsinghua University, Beijing 100022, China;College of Optometry and Ophthalmology, Tianjin Medical University, Tianjin Medical University Eye Institute, Tianjin Medical University Eye Hospital, Tianjin 300384, China;Shanxi Eye Hospital, Taiyuan 030002, Shanxi Province, China
Abstract:
AIM: To detect and analyze the changes on ocular surface and tear function in type II diabetic patients with proliferative diabetic retinopathy (PDR), an advanced stage of diabetic retinopathy (DR), using conventional ophthalmic tests and the high-resolution laser scanning confocal microscopy. METHODS: Fifty-eight patients with type II diabetes were selected. Based on the diagnostic criteria and stage classification of DR, the patients were divided into the non-DR (NDR) group and the PDR group. Thirty-six patients with cataract but no other ocular and systemic disease were included as non-diabetic controls. All the patients were subjected to the conventional clinical tests of corneal sensitivity, Schirmer I Test, and corneal fluorescein staining. The non-invasive tear film break-up time (NIBUT) and tear interferometry were conducted by a Tearscope Plus. The morphology of corneal epithelia and nerve fibers was examined using the high-resolution confocal microscopy. RESULTS: The NDR group exhibited significantly declined corneal sensitivity and Schirmer I test value, as compared to the non-diabetic controls (P< 0.001). The PDR group showed significantly reduced corneal sensitivity, Schirmer I test value, and NIBUT in comparison to the non-diabetic controls (P < 0.001). Corneal fluorescein staining revealed the progressively injured corneal epithelia in the PDR patients. Moreover, significant decrease in the corneal epithelial density and morphological abnormalities in the corneal epithelia and nerve fibers were also observed in the PDR patients. CONCLUSION: Ocular surface changes, including blunted corneal sensitivity, reduced tear secretion, tear film dysfunction, progressive loss of corneal epithelia and degeneration of nerve fibers, are common in type II diabetic patients, particularly in the diabetic patients with PDR. The corneal sensitivity, fluorescein staining scores, and the density of corneal epithelial cells and nerve fibers in the diabetic patients correlate with the duration of diabetes. Therefore, ocular surface of the patients with PDR should be examined regularly by conventional approaches and confocal microscopy to facilitate early diagnosis and treatment of keratopathy.
Keywords:type II diabetes   proliferative diabetic retinopathy   ocular surface   corneal sensitivity   confocal microscopy   tear film break-up time
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