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Evaluation of the effect of unilateral late blindness on the retina, optic nerve and choroid parameters in the sighted eye

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Abstract

Background

To investigate whether unilateral late blindness alters the peripapillary retinal nerve fiber layer (RNFL), ganglion cell complex (GCC), central macular thickness (CMT) and choroidal thickness (CT).

Methods

The 17 healthy eyes of 17 monocular patients with late blindness due to isolated eye trauma in one eye and the 19 eyes of 19 healthy individuals were evaluated in this retrospective study. Patients with at least 10 years of monocular blindness, a refractive error between + 1.5 and -1.5 D in the sighted eye, a best-corrected visual acuity of at least 20/20 and an axial length (AL) < 25 mm were included in the study. Following ophthalmologic examination, the RNFL, GCC, CMT and CT values were measured with spectral domain optic tomography (SD-OCT). Those with ocular, systemic or neurological disease that could influence the measured parameters were excluded from the study.

Results

A total of 17 (14 males, 3 females) monocular patients [mean age 41.00 ± 11.95 (24–64)] and 19 (16 males, 3 females) healthy individuals [mean age 39.79 ± 6.74 (30–56)], similar in age and gender (p = 0.949 and p = 0.881), were included in the study. The mean duration of being monocular was 22.76 ± 11.76 (10–49) years. No difference was present between the RNFL, GCC, CMT and CT measurements of the monocular patients and the healthy individuals (p = 0.692, p = 0.294, p = 0.113, p = 0.623, respectively). No significant correlation was found between the duration of monocularity and the retinal and optic nerve parameters.

Conclusion

The results of our study indicate no difference in the optic nerve, retina and choroid OCT findings in the sighted eyes of subjects with long-term monocular blindness compared to subjects with bilateral normal eyes. Although functional and volumetric neuroimaging studies suggest the possibility of compensation in these patients, our findings indicate that this is not at the ocular level.

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References

  1. (2014) WHO data Visual impairment and blindness Fact Sheet N°282". Archived from the original on 12 May 2015. Retrieved 23 May 2015.

  2. Maberley DA, Hollands H, Chuo J et al (2006) The prevalence of low vision and blindness in Canada. Eye 20(3):341–346

    Article  CAS  Google Scholar 

  3. Vos T, Allen C, Arora M, Barber RM, Bhutta ZA, Brown A (2016) Global, regional and national incidence, prevalence and years lived with disability for 310 diseases and injuries, 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet 388(10053):1545–1602

    Article  Google Scholar 

  4. Bourne RRA, Flaxman SR, Braithwaite T et al (2017) Magnitude, temporal trends and projections of the global prevalence of blindness and distance and near vision impairment: a systematic review and meta-analysis. Lancet Glob Health 5(9):e888–e897

    Article  Google Scholar 

  5. Baarah BT, Shatnawi RA, Khatatbeh AE (2018) Causes of Permanent Severe Visual Impairment and Blindness among Jordanian Population. Middle East Afr J Ophthalmol 25(1):25–29

    Article  Google Scholar 

  6. Thapa R, Bajimaya S, Paudyal G, Khanal S, Tan S, Thapa SS, van Rens GHMB (2018) Prevalence and causes of low vision and blindness in an elderly population in Nepal: the Bhaktapur retina study. BMC Ophthalmol 18(1):42

    Article  Google Scholar 

  7. Buch H, Vinding T, La Cour M, Nielsen NV (2001) The prevalence and causes of bilateral and unilateral blindness in an elderly urban Danish population. The Copenhagen City Eye Study. Acta Ophthalmol Scand 79(5):441–449

  8. Foreman J, Xie J, Keel S, Ang GS, Lee PY, Bourne R, Crowston JG, Taylor HR, Dirani M (2018) Prevalence and causes of unilateral vision impairment and unilateral blindness in Australia the National Eye Health Survey. JAMA Ophthalmol 136(3):240–248

    Article  Google Scholar 

  9. Steeves JKE, González EG, Steinbach MJ (2008) Vision with one eye: a review of visual function following unilateral enucleation. Spat Vis 21(6):509–529

    Article  Google Scholar 

  10. Prins D, Jansonius NM, Cornelissen FW (2017) Loss of binocular vision in monocularly blind patients causes selective degeneration of the superior lateral occipital cortices. Invest Ophthalmol Vis Sci 58(2):1304–1313

    Article  Google Scholar 

  11. Li Q, Huang X, Ye L, Wei R, Zhang Y, Zhong YL, Jiang N, Shao Y (2016) Altered spontaneous brain activity pattern in patients with late monocular blindness in middle-age using amplitude of low-frequency fluctuation: a resting-state functional MRI study. Clin Interv Aging 11:1773–1780

    Article  Google Scholar 

  12. Huang X, Ye CL, Zhong YL, Ye L, Yang QC, Li HJ, Jiang N, Peng DC, Shao Y (2017) Altered regional homogeneity in patients with late monocular blindness: a resting-state functional MRI study. NeuroReport 28(16):1085–1091

    Article  Google Scholar 

  13. Chiquita S, Neves ACR, Baptista FI, Carecho R, Moreira PI, Castelo-Branco M, Ambrósio AF (2019) The retina as a window or mirror of the brain changes detected in Alzheimer’s Disease: Critical aspects to unravel. Mol Neurobiol 56(8):5416–5435

    Article  CAS  Google Scholar 

  14. Oktem EO, Derle E, Kibaroglu S, Oktem C, Akkoyun I, Can U (2015) The relationship between the degree of cognitive impairment and retinal nerve fiber layer thickness. Neurol Sci 36(7):1141–1146

    Article  Google Scholar 

  15. di Staso F, Cıancaglını M, Abdolrahımzadeh S, D’apolıto F, Scuderı G, (2019) Optical coherence tomography of choroid in common neurological diseases. Vivo 33(5):1403–1409

    Article  Google Scholar 

  16. Oktem C, Oktem EO, Kurt A, Kilic R (2019) Does choroidal thickness change in Parkinson's disease? Cesk Slov Neurol N 82 /115(6):677–681

  17. Bayhan HA, Aslan Bayhan S, Celikbilek A, Tanık N, Gürdal C (2015) Evaluation of the chorioretinal thickness changes in Alzheimer’s disease using spectral-domain optical coherence tomography. Clin Exp Ophthalmol 43(2):145–151

    Article  Google Scholar 

  18. Choi SE, Yoo S, You D, Jeong IG, Song C, Hong B, Hong JH, Ahn H, Kim CS (2017) Adaptive functional change of the contralateral kidney after partial nephrectomy. Am J Physiol Renal Physiol 313(2):192–198

    Article  Google Scholar 

  19. Funahashi Y, Hattori R, Yamamoto T, Kamihira O, Sassa N, Gotoh M (2011) Relationship between renal parenchymal volume and single kidney glomerular filtration rate before and after unilateral nephrectomy. Urology 77(6):1404–1408

    Article  Google Scholar 

  20. Ashmead DH, Wall RS, Ebinger KA, Eaton SB, Snook-Hill MM, Yang X (1998) Spatial hearing in children with visual disabilities. Perception 27(1):105–122

    Article  CAS  Google Scholar 

  21. Collignon O, Lassonde M, Lepore F, Bastien D, Veraart C (2007) Functional cerebral reorganization for auditory spatial processing and auditory substitution of vision in early blind subjects. Cereb Cortex 17(2):457–465

    Article  Google Scholar 

  22. Karmarkar UR, Dan Y (2006) Experience-dependent plasticity in adult visual cortex. Neuron 52(4):577–585

    Article  CAS  Google Scholar 

  23. Kiorpes L, Movshon JA (2004) Development of sensitivity to visual motion in macaque monkeys. Vis Neurosci 21(6):851–859

    Article  Google Scholar 

  24. Fox K, Wong RO (2005) A comparison of experience-dependent plasticity in the visual and somatosensory systems. Neuron 48(3):465–477

    Article  CAS  Google Scholar 

  25. Guillery RW (1989) ‘‘Competition in the development of the visual pathways,’’ In: The Making of the Nervous System, eds J. G. Parnavelas, C. D. Stern and R. V. Stirling (Oxford: Oxford University Press), 319–339

  26. Stilla R, Hanna R, Mariola E, Deshpande G, Hu X, Sathian K (2008) Neural processing underlying tactile microspatial discrimination in the blind: a functional magnetic resonance imaging study. J Vis 8(10):13.1–19

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Authors

Contributions

All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by [Caglar Oktem] and [Fatih Aslan]. The first draft of the manuscript was written by [Caglar Oktem and Ece Ozdemir Oktem] and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

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Correspondence to Caglar Oktem.

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Ethical approval

The study procedures were carried out in accordance with the Helsinki Declaration. The study protocol was approved by the Alanya Alaaddin Keykubat University Clinical Research Ethics Committee (No. 22–30 dated 2020/8).

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Oktem, C., Aslan, F. & Oktem, E.O. Evaluation of the effect of unilateral late blindness on the retina, optic nerve and choroid parameters in the sighted eye. Int Ophthalmol 41, 4083–4089 (2021). https://doi.org/10.1007/s10792-021-01981-0

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  • DOI: https://doi.org/10.1007/s10792-021-01981-0

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