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Published Online First: 29 May 2008. doi:10.1136/bjo.2007.130013 British Journal of Ophthalmology 2008;92:896-900 Copyright © 2008 by the BMJ Publishing Group Ltd.
Open clinical study of eye-drops containing tetrapeptides derived from substance P and insulin-like growth factor-1 for treatment of persistent corneal epithelial defects associated with neurotrophic keratopathyN Yamada1, R Matsuda1, N Morishige1, R Yanai1, T-i Chikama2, T Nishida1, T Ishimitsu3, A Kamiya3
1 Department of Ophthalmology, Yamaguchi University Graduate School of Medicine, Ube City, Japan
Correspondence to: Background/aims: Loss of corneal sensation results in the development of persistent corneal epithelial defects. The combination of a substance P-derived peptide (FGLM-amide) and an insulin-like growth factor-1 (IGF-1)-derived peptide (SSSR) stimulates rabbit corneal epithelial migration in vitro and rabbit corneal epithelial wound closure in vivo. The clinical efficacy of eye-drops containing FGLM-amide and SSSR for the treatment of persistent corneal epithelial defects in individuals with neurotrophic keratopathy was examined in a prospective open study. Methods: Twenty-five consecutive patients (26 eyes) with persistent corneal epithelial defects associated with neurotrophic keratopathy were treated by administration of eye-drops containing FGLM-amide and SSSR. The course of epithelial healing was monitored by slit-lamp examination. Results: Epithelial defects resurfaced completely in 19 of the 26 eyes (73%) within 4 weeks after treatment initiation. Complete resurfacing of epithelial defects was apparent in 18 of 22 (82%) or in one of four (25%) eyes without or with limbal stem cell deficiency, respectively. No adverse effects of treatment were observed in any subject. Conclusion: Eye-drops containing FGLM-amide and SSSR induced the rapid resurfacing of persistent epithelial defects in stem cell-positive individuals with neurotrophic keratopathy.
Competing interests: None. Ethics approval: The open non-randomised clinical study was approved by the Institutional Review Board of Yamaguchi University Hospital. Patient consent: Written informed consent was obtained from all subjects.
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