TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy
Purpose: Fuchs' endothelial corneal dystrophy (FECD) has been considered a genetically heterogeneous disease but is increasingly associated with the transcription factor 4 (TCF4) gene. This study investigates the prevalence of the cytosine-thymine-guanine (CTG)n repeat expansion in TCF4 among F...
Published in: | Acta Ophthalmologica |
---|---|
Main Authors: | , , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Umeå universitet, Oftalmiatrik
2022
|
Subjects: | |
Online Access: | http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-187710 https://doi.org/10.1111/aos.15032 |
_version_ | 1821663416924766208 |
---|---|
author | Viberg, Andreas Westin, Ida Maria Golovleva, Irina Byström, Berit |
author_facet | Viberg, Andreas Westin, Ida Maria Golovleva, Irina Byström, Berit |
author_sort | Viberg, Andreas |
collection | Umeå University: Publications (DiVA) |
container_title | Acta Ophthalmologica |
description | Purpose: Fuchs' endothelial corneal dystrophy (FECD) has been considered a genetically heterogeneous disease but is increasingly associated with the transcription factor 4 (TCF4) gene. This study investigates the prevalence of the cytosine-thymine-guanine (CTG)n repeat expansion in TCF4 among FECD patients in northern Sweden coupled to the phenotype. Methods: Blood samples were collected from 85 FECD cases at different stages. Short tandem repeat PCR and triplet repeat-primed PCR were applied in order to determine TCF4 (CTG)n genotype. Results: A (CTG)n repeat expansion (n > 50) in TCF4 was identified in 76 of 85 FECD cases (89.4%) and in four of 102 controls (3.9%). The median (CTG)n repeat length was 81 (IQR 39.3) in mild FECD and 87 (IQR 13.0) in severe FECD (p = 0.01). A higher number of (CTG)n repeats in an expanded TCF4 allele increased the probability of severe FECD. Other ocular surgery was overrepresented in FECD cases without a (CTG)n repeat expansion (44.4%, n = 4) compared with 3.9% (n = 3) in FECD cases with an (CTG)n repeat expansion (p < 0.001). Conclusion: In northern Sweden, the FECD phenotype is associated with (CTG)n expansion in the TCF4 gene, with nearly 90% of patients being hetero- or homozygous for (CTG)n expansion over 50 repeats. Furthermore, the severity of FECD was associated with the repeat length in the TCF4 gene. Ocular surgery might act as an environmental factor explaining the clinical disease in FECD without a repeat expansion in TCF4. Previously included in thesis in manuscript form. |
format | Article in Journal/Newspaper |
genre | Northern Sweden |
genre_facet | Northern Sweden |
geographic | Fuchs |
geographic_facet | Fuchs |
id | ftumeauniv:oai:DiVA.org:umu-187710 |
institution | Open Polar |
language | English |
long_lat | ENVELOPE(-68.666,-68.666,-67.233,-67.233) |
op_collection_id | ftumeauniv |
op_doi | https://doi.org/10.1111/aos.15032 |
op_relation | Acta Ophthalmologica, 1755-375X, 2022, 100:5, s. 541-548 orcid:0000-0002-1292-1945 orcid:0000-0001-8741-0616 orcid:0000-0002-7965-8889 http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-187710 urn:isbn:978-91-7855-588-8 urn:isbn:978-91-7855-589-5 doi:10.1111/aos.15032 PMID 34644448 ISI:000706786900001 Scopus 2-s2.0-85116925455 |
op_rights | info:eu-repo/semantics/openAccess |
publishDate | 2022 |
publisher | Umeå universitet, Oftalmiatrik |
record_format | openpolar |
spelling | ftumeauniv:oai:DiVA.org:umu-187710 2025-01-16T23:55:09+00:00 TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy Viberg, Andreas Westin, Ida Maria Golovleva, Irina Byström, Berit 2022 application/pdf http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-187710 https://doi.org/10.1111/aos.15032 eng eng UmeÃ¥ universitet, Oftalmiatrik UmeÃ¥ universitet, Medicinsk och klinisk genetik Acta Ophthalmologica, 1755-375X, 2022, 100:5, s. 541-548 orcid:0000-0002-1292-1945 orcid:0000-0001-8741-0616 orcid:0000-0002-7965-8889 http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-187710 urn:isbn:978-91-7855-588-8 urn:isbn:978-91-7855-589-5 doi:10.1111/aos.15032 PMID 34644448 ISI:000706786900001 Scopus 2-s2.0-85116925455 info:eu-repo/semantics/openAccess cornea Fuchs’ endothelial corneal dystrophy genetic aetiology TCF4 trinucleotide repeat disorders Ophthalmology Oftalmologi Article in journal info:eu-repo/semantics/article text 2022 ftumeauniv https://doi.org/10.1111/aos.15032 2024-08-13T23:39:05Z Purpose: Fuchs' endothelial corneal dystrophy (FECD) has been considered a genetically heterogeneous disease but is increasingly associated with the transcription factor 4 (TCF4) gene. This study investigates the prevalence of the cytosine-thymine-guanine (CTG)n repeat expansion in TCF4 among FECD patients in northern Sweden coupled to the phenotype. Methods: Blood samples were collected from 85 FECD cases at different stages. Short tandem repeat PCR and triplet repeat-primed PCR were applied in order to determine TCF4 (CTG)n genotype. Results: A (CTG)n repeat expansion (n > 50) in TCF4 was identified in 76 of 85 FECD cases (89.4%) and in four of 102 controls (3.9%). The median (CTG)n repeat length was 81 (IQR 39.3) in mild FECD and 87 (IQR 13.0) in severe FECD (p = 0.01). A higher number of (CTG)n repeats in an expanded TCF4 allele increased the probability of severe FECD. Other ocular surgery was overrepresented in FECD cases without a (CTG)n repeat expansion (44.4%, n = 4) compared with 3.9% (n = 3) in FECD cases with an (CTG)n repeat expansion (p < 0.001). Conclusion: In northern Sweden, the FECD phenotype is associated with (CTG)n expansion in the TCF4 gene, with nearly 90% of patients being hetero- or homozygous for (CTG)n expansion over 50 repeats. Furthermore, the severity of FECD was associated with the repeat length in the TCF4 gene. Ocular surgery might act as an environmental factor explaining the clinical disease in FECD without a repeat expansion in TCF4. Previously included in thesis in manuscript form. Article in Journal/Newspaper Northern Sweden Umeå University: Publications (DiVA) Fuchs ENVELOPE(-68.666,-68.666,-67.233,-67.233) Acta Ophthalmologica |
spellingShingle | cornea Fuchs’ endothelial corneal dystrophy genetic aetiology TCF4 trinucleotide repeat disorders Ophthalmology Oftalmologi Viberg, Andreas Westin, Ida Maria Golovleva, Irina Byström, Berit TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy |
title | TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy |
title_full | TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy |
title_fullStr | TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy |
title_full_unstemmed | TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy |
title_short | TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs’ endothelial corneal dystrophy |
title_sort | tcf4 trinucleotide repeat expansion in swedish cases with fuchs’ endothelial corneal dystrophy |
topic | cornea Fuchs’ endothelial corneal dystrophy genetic aetiology TCF4 trinucleotide repeat disorders Ophthalmology Oftalmologi |
topic_facet | cornea Fuchs’ endothelial corneal dystrophy genetic aetiology TCF4 trinucleotide repeat disorders Ophthalmology Oftalmologi |
url | http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-187710 https://doi.org/10.1111/aos.15032 |