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Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy

. 2023 Sep ; 101 (6) : 679-686. [epub] 20230307

Language English Country England, Great Britain Media print-electronic

Document type Journal Article

Grant support
GACR 20-19278S Czech Republic Cooperation Program - Medical Diagnostics and Basic Medical Sciences
SVV 2016/260148 Czech Republic Cooperation Program - Medical Diagnostics and Basic Medical Sciences
MR/X006271/1 Medical Research Council - United Kingdom
MR/S031820/1 UKRI Future Leader Fellowship
UNCE/MED/007 Czech Republic Cooperation Program - Medical Diagnostics and Basic Medical Sciences

PURPOSE: To characterise the phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy (KC + FECD). METHODS: We recruited 20 patients with concurrent KC + FECD for a retrospective observational case series from the United Kingdom and the Czech Republic. We compared eight parameters of corneal shape (Pentacam, Oculus) with two groups of age-matched controls who had either isolated keratoconus (KC) or isolated FECD. We genotyped probands for an intronic triplet TCF4 repeat expansion (CTG18.1) and the ZEB1 variant c.1920G >T p.(Gln640His). RESULTS: The median age at diagnosis of patients with KC + FECD was 54 (interquartile range 46 to 66) years, with no evidence of KC progression (median follow-up 84 months, range 12 to 120 months). The mean (standard deviation (SD)) of the minimum corneal thickness, 493 (62.7) μm, was greater than eyes with KC, 458 (51.1) μm, but less than eyes with FECD, 590 (55.6) μm. Seven other parameters of corneal shape were more like KC than FECD. Seven (35%) probands with KC + FECD had a TCF4 repeat expansion of ≥50 compared to five controls with isolated FECD. The average of the largest TCF4 expansion in cases with KC + FECD (46 repeats, SD 36 repeats) was similar to the age-matched controls with isolated FECD (36 repeats, SD 28 repeats; p = 0.299). No patient with KC + FECD harboured the ZEB1 variant. CONCLUSIONS: The KC + FECD phenotype is consistent with KC but with superimposed stromal swelling from endothelial disease. The proportion of cases with a TCF4 expansion is similar in concurrent KC + FECD and age-matched controls with isolated FECD.

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Afshari, N.A., Igo, R.P., Jr., Morris, N.J., Stambolian, D., Sharma, S., Pulagam, V.L. et al. (2017) Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nature Communications, 8, 14898.

Alnawaiseh, M., Rosentreter, A., Eter, N. & Zumhagen, L. (2016) Changes in corneal refractive power for patients with Fuchs endothelial dystrophy after DMEK. Cornea, 35, 1073-1077.

Arnalich-Montiel, F., Mingo-Botín, D. & Diaz-Montealegre, A. (2019) Keratometric, Pachymetric, and surface elevation characterization of corneas with Fuchs endothelial corneal dystrophy treated with DMEK. Cornea, 38, 535-541.

Chan, E., Chong, E.W., Lingham, G., Stevenson, L.J., Sanfilippo, P.G., Hewitt, A.W. et al. (2021) Prevalence of keratoconus based on Scheimpflug imaging: the Raine study. Ophthalmology, 128, 515-521.

Davidson, A.E., Hayes, S., Hardcastle, A.J. & Tuft, S.J. (2014) The pathogenesis of keratoconus. Eye, 28, 189-195.

Evans, C.J., Liskova, P., Dudakova, L., Hrabcikova, P., Horinek, A., Jirsova, K. et al. (2015) Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3. Annals of Human Genetics, 79, 1-9.

Fautsch, M.P., Wieben, E.D., Baratz, K.H., Bhattacharyya, N., Sadan, A.N., Hafford-Tear, N.J. et al. (2020) TCF4-mediated Fuchs endothelial corneal dystrophy: insights into a common trinucleotide repeat-associated disease. Progress in Retinal and Eye Research, 81, 100883.

Godefrooij, D.A., Gans, R., Imhof, S.M. & Wisse, R.P.L. (2016) Nationwide reduction in the number of corneal transplantations for keratoconus following the implementation of cross-linking. Acta Ophthalmologica, 94, 675-678.

Goebels, S., Eppig, T., Seitz, B., Szentmàry, N., Cayless, A. & Langenbucher, A. (2018) Endothelial alterations in 712 keratoconus patients. Acta Ophthalmologica, 96, e134-e139.

Gomes, J.A.P., Tan, D., Rapuano, C.J., Belin, M.W., Ambrósio, R., Jr., Guell, J.L. et al. (2015) Global consensus on keratoconus and ectatic diseases. Cornea, 34, 359-369.

Gordon, M.O., Steger-May, K., Szczotka-Flynn, L., Riley, C., Joslin, C.E., Weissman, B.A. et al. (2006) Baseline factors predictive of incident penetrating keratoplasty in keratoconus. American Journal of Ophthalmology, 142, 923-930.

Gupta, R., Kinderyte, R., Jacobs, D.S. & Jurkunas, U.V. (2017) Elimination of anterior corneal steepening with Descemet membrane endothelial Keratoplasty in a patient with Fuchs dystrophy and Keratoconus: implications for IOL calculation. Cornea, 36, 1260-1262.

Gurnani, B., Kaur, K. & Tripathy, K. (2021) Is there a genetic link between Keratoconus and Fuch's endothelial corneal dystrophy? Medical Hypotheses, 157, 110699.

Ham, L., Dapena, I., Moutsouris, K., Balachandran, C., Frank, L.E., van Dijk, K. et al. (2011) Refractive change and stability after Descemet membrane endothelial keratoplasty. Effect of corneal dehydration-induced hyperopic shift on intraocular lens power calculation. Journal of Cataract and Refractive Surgery, 37, 1455-1464.

Hardcastle, A.J., Liskova, P., Bykhovskaya, Y., McComish, B.J., Davidson, A.E., Inglehearn, C.F. et al. (2021) A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. Communications Biology, 4, 266.

Hashemi, H., Beiranvand, A., Yekta, A., Maleki, A., Yazdani, N. & Khabazkhoob, M. (2016) Pentacam top indices for diagnosing subclinical and definite keratoconus. Journal of Current Ophthalmology, 28, 21-26.

Herber, R., Pillunat, L.E. & Raiskup, F. (2021) Development of a classification system based on corneal biomechanical properties using artificial intelligence predicting keratoconus severity. Eye and Vision, 8, 21.

Jurkunas, U. & Azar, D.T. (2006) Potential complications of ocular surgery in patients with coexistent keratoconus and Fuchs' endothelial dystrophy. Ophthalmology, 113, 2187-2197.

Kennedy, R.H., Bourne, W.M. & Dyer, J.A. (1986) A 48-year clinical and epidemiologic study of keratoconus. American Journal of Ophthalmology, 101, 267-273.

Krachmer, J.H., Purcell, J.J., Jr., Young, C.W. & Bucher, K.D. (1978) Corneal endothelial dystrophy. A study of 64 families. Archives of Ophthalmology, 96, 2036-2039.

Laing, R.A., Leibowitz, H.M., Oak, S.S., Chang, R., Berrospi, A.R. & Theodore, J. (1981) Endothelial mosaic in Fuchs' dystrophy. A qualitative evaluation with the specular microscope. Archives of Ophthalmology, 99, 80-83.

Lechner, J., Dash, D.P., Muszynska, D., Hosseini, M., Segev, F., George, S. et al. (2013) Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation. Investigative Ophthalmology and Visual Science, 54, 3215-3223.

Lee, W.B., Jacobs, D.S., Musch, D.C., Kaufman, S.C., Reinhart, W.J. & Shtein, R.M. (2009) Descemet's stripping endothelial keratoplasty: safety and outcomes: a report by the American Academy of ophthalmology. Ophthalmology, 116, 1818-1830.

Liu, H., Chen, Y., Wang, P., Li, B., Wang, W., Su, Y. et al. (2015) Efficacy and safety of deep anterior lamellar keratoplasty vs. penetrating keratoplasty for keratoconus: a meta-analysis. PLoS One, 10, e0113332.

Mazzotta, C., Traversi, C., Raiskup, F., Rizzo, C.L. & Renieri, A. (2014) First identification of a triple corneal dystrophy association: keratoconus, epithelial basement membrane corneal dystrophy and fuchs' endothelial corneal dystrophy. Case Reports in Ophthalmology, 5, 281-288.

Mootha, V.V., Gong, X., Ku, H.-C. & Xing, C. (2014) Association and familial segregation of CTG18.1 trinucleotide repeat expansion of TCF4 gene in Fuchs' endothelial corneal dystrophy. Investigative Ophthalmology and Visual Science, 55, 33-42.

Moshirfar, M., Liu, H.Y., Vaidyanathan, U., Somani, A.N., Hopping, G.C., Barnes, J.R. et al. (2019) Diagnosis and Management of Pseudoguttata: a literature review. Medical Hypothesis, Discovery and Innovation in Ophthalmology, 8, 156-162.

Mylona, I., Tsinopoulos, I. & Ziakas, N. (2020) Comorbidity of Keratoconus and Fuchs' corneal endothelial dystrophy: a review of the literature. Ophthalmic Research, 63, 369-374.

Nakashima, Y., Yoshitomi, F. & Oshika, T. (2007) Clinical evaluation of cornea pseudoguttata. The British Journal of Ophthalmology, 91, 22-25.

Pearson, A.R., Soneji, B., Sarvananthan, N. & Sandford-Smith, J.H. (2000) Does ethnic origin influence the incidence or severity of keratoconus? Eye, 14(Pt 4), 625-628.

Rabinowitz, Y.S., Galvis, V., Tello, A., Rueda, D. & García, J.D. (2021) Genetics vs chronic corneal mechanical trauma in the etiology of keratoconus. Experimental Eye Research, 202, 108328.

Ramos, I.C., Valbon, B.F., Pimentel, L.N. & Caldas, D.L. (2012) Keratoconus associated with corneal Guttata. International Journal of Keratoconus and Ectatic Corneal Diseases., 1, 173-178.

Repp, D.J., Hodge, D.O., Baratz, K.H., McLaren, J.W. & Patel, S.V. (2013) Fuchs' endothelial corneal dystrophy: subjective grading versus objective grading based on the central-to-peripheral thickness ratio. Ophthalmology, 120, 687-694.

Sandvik, G.F., Thorsrud, A., Råen, M., Østern, A.E., Saethre, M. & Drolsum, L. (2015) Does corneal collagen cross-linking reduce the need for Keratoplasties in patients with Keratoconus? Cornea, 34, 991-995.

Seitzman, G.D., Gottsch, J.D. & Stark, W.J. (2005) Cataract surgery in patients with Fuchs' corneal dystrophy: expanding recommendations for cataract surgery without simultaneous keratoplasty. Ophthalmology, 112, 441-446.

Song, M., Fang, Q.Y., Seth, I., Baird, P.N., Daniell, M.D. & Sahebjada, S. (2022) Non-genetic risk factors for keratoconus. Clinical and Experimental Optometry, 1-11. Available from: https://doi.org/10.1080/08164622.2022.2062222

Tur, V.M., MacGregor, C., Jayaswal, R., O'Brart, D. & Maycock, N. (2017) A review of keratoconus: diagnosis, pathophysiology, and genetics. Survey of Ophthalmology, 62, 770-783.

Vira, S., Abugo, U., Shih, C.Y., Udell, I.J., Sperling, B., Hannush, S.B. et al. (2014) Descemet stripping endothelial keratoplasty for the treatment of combined fuchs corneal endothelial dystrophy and keratoconus. Cornea, 33, 1-5.

Waring, G.O., 3rd, Bourne, W.M., Edelhauser, H.F. & Kenyon, K.R. (1982) The corneal endothelium. Normal and pathologic structure and function. Ophthalmology, 89, 531-590.

Watson, M.P., Anand, S., Bhogal, M., Gore, D., Moriyama, A., Pullum, K. et al. (2014) Cataract surgery outcome in eyes with keratoconus. The British Journal of Ophthalmology, 98, 361-364.

Zarouchlioti, C., Sanchez-Pintado, B., Hafford Tear, N.J., Klein, P., Liskova, P., Dulla, K. et al. (2018) Antisense therapy for a common corneal dystrophy ameliorates TCF4 repeat expansion-mediated toxicity. American Journal of Human Genetics, 102, 528-539.

Zoega, G.M., Arnarsson, A., Sasaki, H., Söderberg, P.G. & Jonasson, F. (2013) The 7-year cumulative incidence of cornea guttata and morphological changes in the corneal endothelium in the Reykjavik eye study. Acta Ophthalmologica, 91, 212-218.

Zoega, G.M., Fujisawa, A., Sasaki, H., Kubota, A., Sasaki, K., Kitagawa, K. et al. (2006) Prevalence and risk factors for cornea guttata in the Reykjavik eye study. Ophthalmology, 113, 565-569.

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