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Retinitis pigmentosa-associated anterior subcapsular cataract: morphological features and visual performance

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Abstract

Purpose

To investigate the morphological features and surgical outcomes of retinitis pigmentosa (RP)-associated anterior subcapsular cataract (ASC).

Methods

Consecutive RP-associated ASC cases were reviewed, and one hundred patients (171 eyes) were included. Anterior segment photographed images by slit-lamp microscope were reviewed. Best-corrected visual acuity (BCVA) was recorded. The cases were classified according to preoperative best BCVA, the area (central, midperipheral and peripheral) and the density (Grade 1, vacuolar/bubble-like; Grade 2, plaque-like/translucent; and Grade 3, fibrotic/opaque) of ASC; subgroup analysis of surgical outcomes was then performed.

Results

The mean age was 52.1 ± 13.7 years, and the 41–50-year group had the best BCVA. 13.5% of eyes had BCVA better than 20/63, 30.4% were between 20/400 and 20/63, and 56.1% were worse than 20/400. The percentage of ASCs in the central, midperipheral and peripheral areas was 55.0%, 37.4% and 7.6%, respectively. Postoperative BCVA was improved in the central and midperipheral groups (P < 0.001) but was not in the peripheral group (P = 0.07). The percentage of ASCs in density of Grade 1, 2 and 3 was 11.1%, 38.6% and 50.3%, respectively. Grade 2 and 3 achieved improved postoperative BCVA (P < 0.001), but Grade 1 did not (P = 0.693).

Conclusions

Mostly, ASC is located at the center of the pupillary area and affected the residual vision of RP patients. The patients benefited from cataract removal except for those with ASC extended to peripheral area. Surgery was also recommended for RP with ASC developed to be plaque-like and even fibrotic.

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Data availability

The data used to support the findings of this study are available from the corresponding author upon request.

References

  1. Hartong DT, Berson EL, Dryja TP (2006) Retinitis pigmentosa. Lancet 368:1795–1809. https://doi.org/10.1016/S0140-6736(06)69740-7

    Article  CAS  PubMed  Google Scholar 

  2. Ferrari S, Di Iorio E, Barbaro V, Ponzin D, Sorrentino FS, Parmeggiani F (2011) Retinitis pigmentosa: genes and disease mechanisms. Curr Genomics 12:238–249. https://doi.org/10.2174/138920211795860107

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Kim YJ, Joe SG, Lee DH, Lee JY, Kim JG, Yoon YH (2013) Correlations between spectral-domain OCT measurements and visual acuity in cystoid macular edema associated with retinitis pigmentosa. Invest Ophth Vis Sci 54:1303–1309. https://doi.org/10.1167/iovs.12-10149

    Article  Google Scholar 

  4. Sato H, Wada Y, Abe T, Kawamura M, Wakusawa R, Tamai M (2002) Retinitis pigmentosa associated with ectopia lentis. Arch Ophthalmol 120:852–854

    PubMed  Google Scholar 

  5. Triolo G, Pierro L, Parodi MB et al (2013) Spectral domain optical coherence tomography findings in patients with retinitis pigmentosa. Ophthalmic Res 50:160–164. https://doi.org/10.1159/000351681

    Article  PubMed  Google Scholar 

  6. Testa F, Rossi S, Colucci R et al (2014) Macular abnormalities in Italian patients with retinitis pigmentosa. Br J Ophthalmol 98:946–950. https://doi.org/10.1136/bjophthalmol-2013-304082

    Article  PubMed  Google Scholar 

  7. Jackson H, Garway-Heath D, Rosen P, Bird AC, Tuft SJ (2001) Outcome of cataract surgery in patients with retinitis pigmentosa. Br J Ophthalmol 85:936–938. https://doi.org/10.1136/bjo.85.8.936

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Dikopf MS, Chow CC, Mieler WF, Tu EY (2013) Cataract extraction outcomes and the prevalence of zonular insufficiency in retinitis pigmentosa. Am J Ophthalmol 156(82–88):e82. https://doi.org/10.1016/j.ajo.2013.02.002

    Article  Google Scholar 

  9. Yoshida N, Ikeda Y, Murakami Y et al (2015) Factors affecting visual acuity after cataract surgery in patients with retinitis pigmentosa. Ophthalmology 122:903–908. https://doi.org/10.1016/j.ophtha.2014.12.003

    Article  PubMed  Google Scholar 

  10. Pruett RC (1983) Retinitis pigmentosa: clinical observations and correlations. Trans Am Ophthalmol Soc 81:693–735

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Vasavada AR, Mamidipudi PR, Sharma PS (2004) Morphology of and visual performance with posterior subcapsular cataract. J Cataract Refract Surg 30:2097–2104. https://doi.org/10.1016/j.jcrs.2004.02.076

    Article  PubMed  Google Scholar 

  12. Fishman GA, Anderson RJ, Lourenco P (1985) Prevalence of posterior subcapsular lens opacities in patients with retinitis pigmentosa. Br J Ophthalmol 69:263–266. https://doi.org/10.1136/bjo.69.4.263

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Dilley KJ, Bron AJ, Habgood JO (1976) Anterior polar and posterior subcapsular cataract in a patient with retinitis pigmentosa: a light-microscopic and ultrastructural study. Exp Eye Res 22:155–167. https://doi.org/10.1016/0014-4835(76)90042-7

    Article  CAS  PubMed  Google Scholar 

  14. Eshaghian J, Rafferty NS, Goossens W (1980) Ultrastructure of human cataract in retinitis pigmentosa. Arch Ophthalmol 98:2227–2230. https://doi.org/10.1001/archopht.1980.01020041079018

    Article  CAS  PubMed  Google Scholar 

  15. Wang Y, Guo L, Cai SP et al (2012) Exome sequencing identifies compound heterozygous mutations in CYP4V2 in a pedigree with retinitis pigmentosa. PLoS ONE 7:e33673. https://doi.org/10.1371/journal.pone.0033673

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Andjelic S, Draslar K, Hvala A, Hawlina M (2017) Anterior lens epithelium in cataract patients with retinitis pigmentosa - scanning and transmission electron microscopy study. Acta Ophthalmol 95:e212–e220. https://doi.org/10.1111/aos.13250

    Article  PubMed  Google Scholar 

  17. He Y, Zhang Y, Su G (2015) Recent advances in treatment of retinitis pigmentosa. Curr Stem Cell Res Ther 10:258–265. https://doi.org/10.2174/1574888x09666141027103552

    Article  CAS  PubMed  Google Scholar 

  18. Hamel C (2006) Retinitis pigmentosa. Orphanet J Rare Dis 1:40. https://doi.org/10.1186/1750-1172-1-40

    Article  PubMed  PubMed Central  Google Scholar 

  19. Hayashi K, Hayashi H, Matsuo K, Nakao F, Hayashi F (1998) Anterior capsule contraction and intraocular lens dislocation after implant surgery in eyes with retinitis pigmentosa. Ophthalmology 105:1239–1243. https://doi.org/10.1016/S0161-6420(98)97028-2

    Article  CAS  PubMed  Google Scholar 

  20. Srinivasan Y, Lovicu FJ, Overbeek PA (1998) Lens-specific expression of transforming growth factor beta1 in transgenic mice causes anterior subcapsular cataracts. J Clin Invest 101:625–634. https://doi.org/10.1172/JCI1360

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Lovicu FJ, Schulz MW, Hales AM et al (2002) TGFbeta induces morphological and molecular changes similar to human anterior subcapsular cataract. Br J Ophthalmol 86:220–226. https://doi.org/10.1136/bjo.86.2.220

    Article  PubMed  PubMed Central  Google Scholar 

  22. Xiao W, Chen X, Li W et al (2015) Quantitative analysis of injury-induced anterior subcapsular cataract in the mouse: a model of lens epithelial cells proliferation and epithelial-mesenchymal transition. Sci Rep 5:8362. https://doi.org/10.1038/srep08362

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Eldred JA, Dawes LJ, Wormstone IM (2011) The lens as a model for fibrotic disease. Philos T R Soc B 366:1301–1319. https://doi.org/10.1098/rstb.2010.0341

    Article  CAS  Google Scholar 

  24. Stunf S, Hvala A, Valentincic NV, Kraut A, Hawlina M (2012) Ultrastructure of the anterior lens capsule and epithelium in cataracts associated with uveitis. Ophthalmic Res 48:12–21. https://doi.org/10.1159/000333219

    Article  PubMed  Google Scholar 

  25. Sasaki K, Kojima M, Nakaizumi H, Kitagawa K, Yamada Y, Ishizaki H (1998) Early lens changes seen in patients with atopic dermatitis applying image analysis processing of scheimpflug and specular microscopic images. Ophthalmologica 212:88–94. https://doi.org/10.1159/000027285

    Article  CAS  PubMed  Google Scholar 

  26. Marcantonio JM, Syam PP, Liu CS, Duncan G (2003) Epithelial transdifferentiation and cataract in the human lens. Exp Eye Res 77:339–346. https://doi.org/10.1016/s0014-4835(03)00125-8

    Article  CAS  PubMed  Google Scholar 

  27. Yamazaki K, Yoneyama J, Hayashi T, Kimoto R, Shibata Y, Mimura T (2021) Efficacy of femtosecond laser-assisted cataract surgery for cataracts due to atopic dermatitis. Case Rep Ophthalmol 12:41–47. https://doi.org/10.1159/000510346

    Article  PubMed  PubMed Central  Google Scholar 

  28. Yoshida N, Ikeda Y, Notomi S et al (2013) Laboratory evidence of sustained chronic inflammatory reaction in retinitis pigmentosa. Ophthalmology 120:e5-12. https://doi.org/10.1016/j.ophtha.2012.07.008

    Article  PubMed  Google Scholar 

  29. Salom D, Diaz-Llopis M, Garcia-Delpech S, Udaondo P, Sancho-Tello M, Romero FJ (2008) Aqueous humor levels of vascular endothelial growth factor in retinitis pigmentosa. Invest Ophthalmol Vis Sci 49:3499–3502. https://doi.org/10.1167/iovs.07-1168

    Article  PubMed  Google Scholar 

  30. Ten Berge JC, Fazil Z, van den Born I et al (2019) Intraocular cytokine profile and autoimmune reactions in retinitis pigmentosa, age-related macular degeneration, glaucoma and cataract. Acta Ophthalmol 97:185–192. https://doi.org/10.1111/aos.13899

    Article  CAS  PubMed  Google Scholar 

  31. Lu B, Yin HF, Tang QM et al (2020) Multiple cytokine analyses of aqueous humor from the patients with retinitis pigmentosa. Cytokine. https://doi.org/10.1016/j.cyto.2019.154943

    Article  PubMed  Google Scholar 

  32. Salom D, Diaz-Llopis M, Quijada A et al (2010) Aqueous humor levels of hepatocyte growth factor in retinitis pigmentosa. Invest Ophthalmol Vis Sci 51:3157–3161. https://doi.org/10.1167/iovs.09-4390

    Article  PubMed  Google Scholar 

  33. Zigler JS Jr, Hess HH (1985) Cataracts in the royal college of surgeons rat: evidence for initiation by lipid peroxidation products. Exp Eye Res 41:67–76. https://doi.org/10.1016/0014-4835(85)90095-8

    Article  CAS  PubMed  Google Scholar 

  34. Dovrat A, Ding LL, Horwitz J (1993) Enzyme activities and crystallin profiles of clear and cataractous lenses of the RCS rat. Exp Eye Res 57:217–224. https://doi.org/10.1006/exer.1993.1117

    Article  CAS  PubMed  Google Scholar 

  35. Merin S, Auerbach E (1976) Retinitis pigmentosa. Surv Ophthalmol 20:303–346. https://doi.org/10.1016/s0039-6257(96)90001-6

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This study was financially supported by the grant from the National Key Research and Development Program of China (No. 2017YFC1104603) and the National Natural Science Foundation of China (No. 81470615)

Funding

This study was financially supported by the grant from the National Key Research and Development Program of China (No. 2017YFC1104603) and the National Natural Science Foundation of China (No. 81470615).

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Contributions

All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by Min Hou and Xuan Bao. The first draft of the manuscript was written by Min Hou and all authors commented on the previous versions of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Mingxing Wu.

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The authors declare that they have no conflict of interest.

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The participants have consented to the submission of case report to the journal.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. This retrospective study was approved by the Institutional Review Board of Zhongshan Ophthalmic Center, Sun Yat-sen University (No.2016MEKY047).

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Hou, M., Bao, X., Liu, L. et al. Retinitis pigmentosa-associated anterior subcapsular cataract: morphological features and visual performance. Int Ophthalmol 41, 3631–3639 (2021). https://doi.org/10.1007/s10792-021-01935-6

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