J Korean Ophthalmol Soc.  2015 May;56(5):680-686. 10.3341/jkos.2015.56.5.680.

Corneal Microstructural Changes in Non-Sjogren Dry Eye Using Confocal Microscopy: Clinical Correlation

Affiliations
  • 1Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea. shadik@yuhs.ac
  • 2Institute of Corneal Dystrophy Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.

Abstract

PURPOSE
To investigate the relationship between changes of corneal epithelium and subbasal nerves in non-Sjogren dry eye using in vivo confocal microscope (IVCM) and self-reported clinical symptoms.
METHODS
The present study included 40 patients with dry eye and 18 healthy control subjects. The dry eye group underwent an evaluation of dry eye symptoms using visual analogue scale (VAS) score and was subdivided into 2 groups; score 0-5 as the low VAS score (LVS) group and score 6 - 10 as the high VAS score (HVS) group. The tear film break-up time, fluorescein staining, Schirmer test and microstructural imaging of epithelium, and subbasal nerve at cornea center with IVCM were performed on both eyes of each patient. Twenty-three normal eyes and 54 eyes of dry eye patients were included in the study. Cell densities and morphological characteristics were analyzed using ImageJ and NeuronJ softwares.
RESULTS
Both LVS and HVS groups had decreased cell density of superficial, intermediate, and basal epithelium (p < 0.001). Intermediate epithelial cells were more decreased in the dry eye group with more severe symptoms (p < 0.0001). Subbasal nerve density (p < 0.005) was more decreased and nerve beadings, tortuosity, and reflectivity increased in the HVS group than both LVS and control groups (p < 0.05).
CONCLUSIONS
The alterations of corneal cellular level in dry eye patients visualized using IVCM are correlated with pathology and clinical symptoms and may be useful objective criteria in diagnosis and monitoring treatment efficacy.

Keyword

Confocal microscopy; Dry eye; In vivo confocal microscopy (IVCM); Non-Sjogren dry eye

MeSH Terms

Cell Count
Cornea
Diagnosis
Epithelial Cells
Epithelium
Epithelium, Corneal
Fluorescein
Humans
Microscopy, Confocal*
Pathology
Tears
Treatment Outcome
Fluorescein

Figure

  • Figure 1. In vivo confocal images of cornea. Superficial epithelium. Compared with (A), (B), and (C) had more decreased cell density. (A) Showing regularly arranged cells with dark nuclei. (B) and (C) showing squamous metaplasia, hyperreflectivity as compared to control. Intermediate epithelium. Compared with (D) and (E), (F) had more decreased cell density. Basal epithelium. Compared with (G), (H) and (I) had more decreased cell density. Bar, 100 μ m. LVS = low visual analogue scale score; HVS = high visual analogue scale score.

  • Figure 2. In vivo confocal images of cornea. Subbasal nerve. Compared with (A) and (B), (C) had more decreased subbasal nerve density and had more increased subbasal nerve beadings, tortuosity, and reflectivity. Bar, 100 μ m. LVS = low visual analogue scale score; HVS = high visual analogue scale score.


Reference

References

1. Uchino M, Schaumberg DA, Dogru M, et al. Prevalence of dry eye disease among Japanese visual display terminal users. Ophthalmology. 2008; 115:1982–8.
Article
2. Guo B, Lu P, Chen X, et al. Prevalence of dry eye disease in Mongolians at high altitude in China: the Henan eye study. Ophthalmic Epidemiol. 2010; 17:234–41.
Article
3. Kim WJ, Kim HS, Kim MS. Current trends in the recognition and treatment of dry eye: a survey of ophthalmologists. J Korean Ophthalmol Soc. 2007; 48:1614–22.
Article
4. Schiffman RM, Walt JG, Jacobsen G, et al. Utility assessment among patients with dry eye disease. Ophthalmology. 2003; 110:1412–9.
Article
5. Buchholz P, Steeds CS, Stern LS, et al. Utility assessment to measure the impact of dry eye disease. Ocul Surf. 2006; 4:155–61.
Article
6. Yamada M, Mizuno Y, Shigeyasu C. Impact of dry eye on work productivity. Clinicoecon Outcomes Res. 2012; 4:307–12.
Article
7. Uchino M, Uchino Y, Dogru M, et al. Dry eye disease and work productivity loss in visual display users: the Osaka study. Am J Ophthalmol. 2014; 157:294–300.
Article
8. Cho BJ, Lee JH, Shim OJ. The relation between clinical manifes-tations of dry eye patients and their BUTs. J Korean Ophthalmol Soc. 1992; 33:297–302.
9. Zhang X, Chen Q, Chen W, et al. Tear dynamics and corneal confocal microscopy of subjects with mild self-reported office dry eye. Ophthalmology. 2011; 118:902–7.
Article
10. Cavanagh HD, Jester JV, Essepian J, et al. Confocal microscopy of the living eye. CLAO J. 1990; 16:65–73.
11. Alhatem A, Cavalcanti B, Hamrah P. In vivo confocal microscopy in dry eye disease and related conditions. Semin Ophthalmol. 2012; 27:138–48.
12. Qazi Y, Aggarwal S, Hamrah P. Image-guided evaluation and monitoring of treatment response in patients with dry eye disease. Graefes Arch Clin Exp Ophthalmol. 2014; 252:857–72.
Article
13. Benítez del Castillo JM, Wasfy MA, Fernandez C, Garcia-Sanchez J. An in vivo confocal masked study on corneal epithelium and subbasal nerves in patients with dry eye. Invest Ophthalmol Vis Sci. 2004; 45:3030–5.
14. Tuominen IS, Konttinen YT, Vesaluoma MH, et al. Corneal in-nervation and morphology in primary Sjögren's syndrome. Invest Ophthalmol Vis Sci. 2003; 44:2545–9.
15. Zhang M, Chen J, Luo L, et al. Altered corneal nerves in aqueous tear deficiency viewed by in vivo confocal microscopy. Cornea. 2005; 24:818–24.
Article
16. Villani E, Galimberti D, Viola F, et al. The cornea in Sjogren's syndrome: an in vivo confocal study. Invest Ophthalmol Vis Sci. 2007; 48:2017–22.
Article
17. Labbé A, Alalwani H, Van Went C, et al. The relationship between subbasal nerve morphology and corneal sensation in ocular surface disease. Invest Ophthalmol Vis Sci. 2012; 53:4926–31.
Article
18. Vitali C, Bombardieri S, Jonsson R, et al. Classification criteria for Sjögren's syndrome: a revised version of the European criteria pro-posed by the American-European Consensus Group. Ann Rheum Dis. 2002; 61:554–8.
19. Oliveira-Soto L, Efron N. Morphology of corneal nerves using confocal microscopy. Cornea. 2001; 20:374–84.
Article
20. Wang J, Palakuru JR, Aquavella JV. Correlations among upper and lower tear menisci, noninvasive tear break-up time, and the Schirmer test. Am J Ophthalmol. 2008; 145:795–800.
Article
21. Hoşal BM, Ornek N, Zilelioğlu G, Elhan AH. Morphology of corneal nerves and corneal sensation in dry eye: a preliminary study. Eye (Lond). 2005; 19:1276–9.
Article
22. Shim J, Park C, Lee HS, et al. Change in prostaglandin expression levels and synthesizing activities in dry eye disease. Ophthalmology. 2012; 119:2211–9.
Article
23. Parra A, Madrid R, Echevarria D, et al. Ocular surface wetness is regulated by TRPM8-dependent cold thermoreceptors of the cornea. Nat Med. 2010; 16:1396–9.
Article
24. Labbé A, Liang Q, Wang Z, et al. Corneal nerve structure and function in patients with non-sjogren dry eye: clinical correlations. Invest Ophthalmol Vis Sci. 2013; 54:5144–50.
25. Erdélyi B, Kraak R, Zhivov A, et al. In vivo confocal laser scanning microscopy of the cornea in dry eye. Graefes Arch Clin Exp Ophthalmol. 2007; 245:39–44.
Article
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