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Gene–environment interactions in Leber hereditary optic neuropathy

Leber hereditary optic neuropathy (LHON) is a genetic disorder primarily due to mutations of mitochondrial DNA (mtDNA). Environmental factors are thought to precipitate the visual failure and explain the marked incomplete penetrance of LHON, but previous small studies have failed to confirm this to...

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Autores principales: Kirkman, Matthew Anthony, Yu-Wai-Man, Patrick, Korsten, Alex, Leonhardt, Miriam, Dimitriadis, Konstantin, De Coo, Ireneaus F., Klopstock, Thomas, Chinnery, Patrick Francis
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732267/
https://www.ncbi.nlm.nih.gov/pubmed/19525327
http://dx.doi.org/10.1093/brain/awp158
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author Kirkman, Matthew Anthony
Yu-Wai-Man, Patrick
Korsten, Alex
Leonhardt, Miriam
Dimitriadis, Konstantin
De Coo, Ireneaus F.
Klopstock, Thomas
Chinnery, Patrick Francis
author_facet Kirkman, Matthew Anthony
Yu-Wai-Man, Patrick
Korsten, Alex
Leonhardt, Miriam
Dimitriadis, Konstantin
De Coo, Ireneaus F.
Klopstock, Thomas
Chinnery, Patrick Francis
author_sort Kirkman, Matthew Anthony
collection PubMed
description Leber hereditary optic neuropathy (LHON) is a genetic disorder primarily due to mutations of mitochondrial DNA (mtDNA). Environmental factors are thought to precipitate the visual failure and explain the marked incomplete penetrance of LHON, but previous small studies have failed to confirm this to be the case. LHON has no treatment, so identifying environmental triggers is the key to disease prevention, whilst potentially revealing new mechanisms amenable to therapeutic manipulation. To address this issue, we conducted a large, multicentre epidemiological study of 196 affected and 206 unaffected carriers from 125 LHON pedigrees known to harbour one of the three primary pathogenic mtDNA mutations: m.3460G>A, m.11778G>A and m.14484T>C. A comprehensive history of exposure to smoking, alcohol and other putative environmental insults was collected using a structured questionnaire. We identified a strong and consistent association between visual loss and smoking, independent of gender and alcohol intake, leading to a clinical penetrance of 93% in men who smoked. There was a trend towards increased visual failure with alcohol, but only with a heavy intake. Based on these findings, asymptomatic carriers of a LHON mtDNA mutation should be strongly advised not to smoke and to moderate their alcohol intake.
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spelling pubmed-27322672009-08-27 Gene–environment interactions in Leber hereditary optic neuropathy Kirkman, Matthew Anthony Yu-Wai-Man, Patrick Korsten, Alex Leonhardt, Miriam Dimitriadis, Konstantin De Coo, Ireneaus F. Klopstock, Thomas Chinnery, Patrick Francis Brain Original Articles Leber hereditary optic neuropathy (LHON) is a genetic disorder primarily due to mutations of mitochondrial DNA (mtDNA). Environmental factors are thought to precipitate the visual failure and explain the marked incomplete penetrance of LHON, but previous small studies have failed to confirm this to be the case. LHON has no treatment, so identifying environmental triggers is the key to disease prevention, whilst potentially revealing new mechanisms amenable to therapeutic manipulation. To address this issue, we conducted a large, multicentre epidemiological study of 196 affected and 206 unaffected carriers from 125 LHON pedigrees known to harbour one of the three primary pathogenic mtDNA mutations: m.3460G>A, m.11778G>A and m.14484T>C. A comprehensive history of exposure to smoking, alcohol and other putative environmental insults was collected using a structured questionnaire. We identified a strong and consistent association between visual loss and smoking, independent of gender and alcohol intake, leading to a clinical penetrance of 93% in men who smoked. There was a trend towards increased visual failure with alcohol, but only with a heavy intake. Based on these findings, asymptomatic carriers of a LHON mtDNA mutation should be strongly advised not to smoke and to moderate their alcohol intake. Oxford University Press 2009-09 2009-06-12 /pmc/articles/PMC2732267/ /pubmed/19525327 http://dx.doi.org/10.1093/brain/awp158 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Kirkman, Matthew Anthony
Yu-Wai-Man, Patrick
Korsten, Alex
Leonhardt, Miriam
Dimitriadis, Konstantin
De Coo, Ireneaus F.
Klopstock, Thomas
Chinnery, Patrick Francis
Gene–environment interactions in Leber hereditary optic neuropathy
title Gene–environment interactions in Leber hereditary optic neuropathy
title_full Gene–environment interactions in Leber hereditary optic neuropathy
title_fullStr Gene–environment interactions in Leber hereditary optic neuropathy
title_full_unstemmed Gene–environment interactions in Leber hereditary optic neuropathy
title_short Gene–environment interactions in Leber hereditary optic neuropathy
title_sort gene–environment interactions in leber hereditary optic neuropathy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732267/
https://www.ncbi.nlm.nih.gov/pubmed/19525327
http://dx.doi.org/10.1093/brain/awp158
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