Literature DB >> 30973406

Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients With Fuchs Endothelial Corneal Dystrophy.

Naoki Okumura1, Ryousuke Hayashi1, Masakazu Nakano2, Kei Tashiro2, Kengo Yoshii3, Ross Aleff4, Malinda Butz5, Edward W Highsmith5, Eric D Wieben4, Michael P Fautsch6, Keith H Baratz6, Yuya Komori1, Emi Ueda1, Makiko Nakahara1, Julia Weller7, Theofilos Tourtas7, Ursula Schlötzer-Schrehardt7, Friedrich Kruse7, Noriko Koizumi1.   

Abstract

PURPOSE: To investigate single nucleotide polymorphisms (SNPs) and trinucleotide repeat (TNR) expansion in the transcription factor 4 (TCF4) gene in a large cohort of German patients with Fuchs endothelial corneal dystrophy (FECD).
METHODS: Genomic DNA was obtained from 398 patients with FECD and from 58 non-FECD controls. Thirty-seven previously reported SNPs were evaluated by genotyping. The 398 FECD samples were analyzed for TNR expansions by short tandem repeat assays and Southern blotting. The possible associations between the TNR length and clinical parameters (age, sex, visual acuity, and central corneal thickness) were analyzed in 132 patients.
RESULTS: The SNPs in COL8A2, TCF8, LOXHD1, and AGBL1 showed no heterogeneity in 36 cases, although SLCA411 showed 3 nonsense mutations. SNPs were detected for TCF4 (rs613872, rs2123392, rs17089887, rs1452787, and rs1348047), but only rs613872 showed a significant association with FECD (P = 9.93 × 10). Overall, 315/398 (79%) patients harbored TNR lengths >50, whereas no non-FECD controls harbored TNR lengths >50. The TCF4 SNP rs613872 genotype was TT: 39 (67%), TG: 18 (31%), and GG: 1 (2%) in non-FECD controls; TT: 39 (47%), TG: 38 (46%), and GG: 6 (7%) in FECD cases harboring TNR <50; and TT: 23 (8%), TG: 224 (79%), and GG: 38 (13%) in FECD cases harboring TNR >50 (P = 2.93 × 10). No significant association was detected between the TNR length and clinical parameters.
CONCLUSIONS: Our large German cohort demonstrated a significant association between the risk allele G in rs613872 and FECD, irrespective of TNR expansion, although this risk allele was more frequent in FECD cases with TNR expansion than without.

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Year:  2019        PMID: 30973406      PMCID: PMC6554040          DOI: 10.1097/ICO.0000000000001952

Source DB:  PubMed          Journal:  Cornea        ISSN: 0277-3740            Impact factor:   2.651


  31 in total

1.  Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13pTel-13q12.13.

Authors:  Olof H Sundin; Albert S Jun; Karl W Broman; Sammy H Liu; Siobhan E Sheehan; Elizabeth C L Vito; Walter J Stark; John D Gottsch
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-01       Impact factor: 4.799

2.  A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32.

Authors:  Olof H Sundin; Karl W Broman; Howard H Chang; Elizabeth C L Vito; Walter J Stark; John D Gottsch
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-09       Impact factor: 4.799

3.  Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.

Authors:  S Biswas; F L Munier; J Yardley; N Hart-Holden; R Perveen; P Cousin; J E Sutphin; B Noble; M Batterbury; C Kielty; A Hackett; R Bonshek; A Ridgway; D McLeod; V C Sheffield; E M Stone; D F Schorderet; G C Black
Journal:  Hum Mol Genet       Date:  2001-10-01       Impact factor: 6.150

4.  Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy.

Authors:  S Amer Riazuddin; Eranga N Vithana; Li-Fong Seet; Yangjian Liu; Amr Al-Saif; Li Wei Koh; Yee Meng Heng; Tin Aung; Danielle N Meadows; Allen O Eghrari; John D Gottsch; Nicholas Katsanis
Journal:  Hum Mutat       Date:  2010-10-14       Impact factor: 4.878

5.  E2-2 protein and Fuchs's corneal dystrophy.

Authors:  Keith H Baratz; Nirubol Tosakulwong; Euijung Ryu; William L Brown; Kari Branham; Wei Chen; Khoa D Tran; Katharina E Schmid-Kubista; John R Heckenlively; Anand Swaroop; Goncalo Abecasis; Kent R Bailey; Albert O Edwards
Journal:  N Engl J Med       Date:  2010-08-25       Impact factor: 91.245

6.  Linkage of a mild late-onset phenotype of Fuchs corneal dystrophy to a novel locus at 5q33.1-q35.2.

Authors:  S Amer Riazuddin; Allen O Eghrari; Amr Al-Saif; Lisa Davey; Danielle N Meadows; Nicholas Katsanis; John D Gottsch
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-07-15       Impact factor: 4.799

7.  SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

Authors:  Eranga N Vithana; Patricio E Morgan; Vedam Ramprasad; Donald T H Tan; Victor H K Yong; Divya Venkataraman; Anandalakshmi Venkatraman; Gary H F Yam; Soumittra Nagasamy; Ricky W K Law; Rama Rajagopal; Chi P Pang; Govindsamy Kumaramanickevel; Joseph R Casey; Tin Aung
Journal:  Hum Mol Genet       Date:  2007-11-16       Impact factor: 6.150

8.  Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy.

Authors:  Jodhbir S Mehta; Eranga N Vithana; Donald T H Tan; Victor H K Yong; Gary H F Yam; Ricky W K Law; Wesley G W Chong; Calvin P Pang; Tin Aung
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-01       Impact factor: 4.799

9.  Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.

Authors:  S Amer Riazuddin; Norann A Zaghloul; Amr Al-Saif; Lisa Davey; Bill H Diplas; Danielle N Meadows; Allen O Eghrari; Mollie A Minear; Yi-Ju Li; Gordon K Klintworth; Natalie Afshari; Simon G Gregory; John D Gottsch; Nicholas Katsanis
Journal:  Am J Hum Genet       Date:  2009-12-31       Impact factor: 11.025

10.  Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.

Authors:  Yi-Ju Li; Mollie A Minear; Jacqueline Rimmler; Bei Zhao; Elmer Balajonda; Michael A Hauser; R Rand Allingham; Allen O Eghrari; S Amer Riazuddin; Nicholas Katsanis; John D Gottsch; Simon G Gregory; Gordon K Klintworth; Natalie A Afshari
Journal:  PLoS One       Date:  2011-04-20       Impact factor: 3.240

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  4 in total

1.  A 20-year bibliometric analysis of Fuchs endothelial corneal dystrophy: from 2001 to 2020.

Authors:  Feng Lin; Luoli Zhang; Yimin Wang; Dan Fu; Yuliang Wang; Xingtao Zhou
Journal:  BMC Ophthalmol       Date:  2022-06-08       Impact factor: 2.086

Review 2.  Fuchs endothelial corneal dystrophy: The vicious cycle of Fuchs pathogenesis.

Authors:  Stephan Ong Tone; Viridiana Kocaba; Myriam Böhm; Adam Wylegala; Tomas L White; Ula V Jurkunas
Journal:  Prog Retin Eye Res       Date:  2020-05-08       Impact factor: 21.198

Review 3.  TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease.

Authors:  Michael P Fautsch; Eric D Wieben; Keith H Baratz; Nihar Bhattacharyya; Amanda N Sadan; Nathaniel J Hafford-Tear; Stephen J Tuft; Alice E Davidson
Journal:  Prog Retin Eye Res       Date:  2020-07-28       Impact factor: 21.198

Review 4.  Genetic mutations and molecular mechanisms of Fuchs endothelial corneal dystrophy.

Authors:  Xuerui Liu; Tao Zheng; Chuchu Zhao; Yi Zhang; Hanruo Liu; Liyuan Wang; Ping Liu
Journal:  Eye Vis (Lond)       Date:  2021-06-15
  4 in total

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