4.5 Article

The influence of overnight orthokeratology on ocular surface and dry eyerelated cytokines IL-17A, IL-6, and PGE2 in children

期刊

CONTACT LENS & ANTERIOR EYE
卷 44, 期 1, 页码 81-88

出版社

ELSEVIER
DOI: 10.1016/j.clae.2020.04.001

关键词

Overnight orthokeratology; Ocular surface; Meibomian glands; Dry eye-related cytokines

资金

  1. Natural Science Foundation of Zhejiang Province of China [LY20H120009]
  2. Science and Technology Planning Project of Zhejiang Province of China [2018ZH018]

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The study found that wearing orthokeratology lenses may increase ocular surface disease index and damage to the meibomian glands, with significant differences in noninvasive tear breakup time and corneal fluorescein staining compared to the control group.
Objective: To investigate the effect of overnight orthokeratology (OOK) on the ocular surface and dry eye-related cytokines in children. Methods: A non-randomized, prospective pilot study was conducted including sixty myopes treated with OOK and sixty age-matched spectacle wearing participants. The following tests were performed before and after 1, 3, 6 and 12 months: ocular surface disease index (OSDI), noninvasive tear breakup time (NITBUT), tear meniscus height (TMH), corneal fluorescein staining (CFS), meiboscore using noncontact meibography. Then the concentrations of interleukin-17A (IL-17A), interleukin-6 (IL-6), and prostaglandin E2 (PGE2) in tear samples were detected with a multiplex immunobead assay at different time points. Results: All parameters had no statistical differences between the two groups prior to treatment. No adverse events were observed except trace to moderate corneal staining and allergic conjunctivitis in the treatment group. NITBUT significantly decreased after 6 and 12 months OOK wearing (P = 0.003 and P = 0.001, respectively). After wearing OOK there was a significant increase in CFS at each follow-up time point compared with baseline (P = 0.023, P = 0.016, P = 0.001, and P < 0.001at 1, 3, 6, and 12 months, respectively). The upper meiboscore and the total meiboscore increased gradually and peaked at 12 months of OOK (both P < 0.001). The concentration of the three cytokines in the treatment group significantly increased after OOK wearing. These increases occurred at different time points: IL-17A increased significantly 3 months after 00K, IL-6 at 6 months, and PGE2 at 12 months (all P < 0.001). However, there were no significant changes in the above parameters in the control group. There were no significant differences in the OSDI or TMH at any followup time point compared to baseline in both groups (both P > 0.05). Conclusions: Short-term OOK may reduce the stability of the tear film and increase damage to the corneal epithelium. Long-term OOK could induce ocular inflammation through the disruption of meibomian glands.

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