Literature DB >> 24917144

Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.

Yi-Ju Li1, Mollie A Minear2, Xuejun Qin2, Jacqueline Rimmler2, Michael A Hauser2, R Rand Allingham3, Robert P Igo4, Jonathan H Lass4, Sudha K Iyengar4, Gordon K Klintworth5, Natalie A Afshari6, Simon G Gregory2.   

Abstract

PURPOSE: We investigated whether mitochondrial DNA (mtDNA) variants affect the susceptibility of Fuchs endothelial corneal dystrophy (FECD).
METHODS: Ten mtDNA variants defining European haplogroups were genotyped in a discovery dataset consisting of 530 cases and 498 controls of European descent from the Duke FECD cohort. Association tests for mtDNA markers and haplogroups were performed using logistic regression models with adjustment of age and sex. Subset analyses included controlling for additional effects of either the TCF4 SNP rs613872 or cigarette smoking. Our replication dataset was derived from the genome-wide association study (GWAS) of the FECD Genetics Consortium, where genotypes for three of 10 mtDNA markers were available. Replication analyses were performed to compare non-Duke cases to all GWAS controls (GWAS1, N = 3200), and to non-Duke controls (GWAS2, N = 3043).
RESULTS: The variant A10398G was significantly associated with FECD (odds ratio [OR] = 0.72; 95% confidence interval [CI] = [0.53, 0.98]; P = 0.034), and remains significant after adjusting for smoking status (min P = 0.012). This variant was replicated in GWAS1 (P = 0.019) and GWAS2 (P = 0.036). Haplogroup I was significantly associated with FECD (OR = 0.46; 95% CI = [0.22, 0.97]; P = 0.041) and remains significant after adjusting for the effect of smoking (min P = 0.008) or rs613872 (P = 0.034).
CONCLUSIONS: The 10398G allele and Haplogroup I appear to confer significant protective effects for FECD. The effect of A10398G and Haplogroup I to FECD is likely independent of the known TCF4 variant. More data are needed to decipher the interaction between smoking and mtDNA haplogroups. Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.

Entities:  

Keywords:  TCF4; genetic association; mitochondrial haplogroup; oxidative stress; smoking

Mesh:

Substances:

Year:  2014        PMID: 24917144      PMCID: PMC4109404          DOI: 10.1167/iovs.13-13517

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  53 in total

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

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Journal:  Ocul Surf       Date:  2010-10       Impact factor: 5.033

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9.  Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy.

Authors:  Robert P Igo; Laura J Kopplin; Peronne Joseph; Barbara Truitt; Jeremy Fondran; David Bardenstein; Anthony J Aldave; Christopher R Croasdale; Marianne O Price; Miriam Rosenwasser; Jonathan H Lass; Sudha K Iyengar
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10.  Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.

Authors:  Mollie A Minear; Yi-Ju Li; Jacqueline Rimmler; Elmer Balajonda; Shera Watson; R Rand Allingham; Michael A Hauser; Gordon K Klintworth; Natalie A Afshari; Simon G Gregory
Journal:  Mol Vis       Date:  2013-12-12       Impact factor: 2.367

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Review 3.  Association of TCF4 polymorphisms and Fuchs' endothelial dystrophy: a meta-analysis.

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Review 5.  Update on the genetics of corneal endothelial dystrophies.

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Review 6.  Fuchs endothelial corneal dystrophy: The vicious cycle of Fuchs pathogenesis.

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