Geneenvironment interactions in Leber hereditary optic neuropathy

被引:255
作者
Kirkman, Matthew Anthony [1 ]
Yu-Wai-Man, Patrick [1 ,2 ]
Korsten, Alex [3 ]
Leonhardt, Miriam [4 ]
Dimitriadis, Konstantin [4 ]
De Coo, Ireneaus F. [3 ]
Klopstock, Thomas [4 ]
Chinnery, Patrick Francis [1 ]
机构
[1] Newcastle Univ, Sch Med, Mitochondrial Res Grp, Inst Ageing & Hlth, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Royal Victoria Infirm, Dept Ophthalmol, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[3] Univ Med Ctr Rotterdam, Erasmus Med Ctr, Dept Child Neurol, Rotterdam, Netherlands
[4] Univ Munich, Friedrich Baur Inst, Dept Neurol, Munich, Germany
基金
英国惠康基金;
关键词
Leber hereditary optic neuropathy; mitochondrial DNA; alcohol; tobacco; epigenetics; MITOCHONDRIAL-DNA MUTATIONS; CLINICAL EXPRESSION; IDENTICAL-TWINS; DISCORDANT; PEDIGREES; EXPOSURE; SMOKING; DISEASE; TOBACCO; LOCUS;
D O I
10.1093/brain/awp158
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.3460GA, m.11778GA and m.14484TC. 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.
引用
收藏
页码:2317 / 2326
页数:10
相关论文
共 39 条
[1]   De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy [J].
Biousse, V ;
Brown, MD ;
Newman, NJ ;
Allen, JC ;
Rosenfeld, J ;
Meola, G ;
Wallace, DC .
NEUROLOGY, 1997, 49 (04) :1136-1138
[2]  
Bland M., 1995, INTRO MED STAT, V2nd
[3]  
BROWN MD, 1994, CLIN NEUROSCI, V2, P138
[4]   Grand rounds:: Could occupational exposure to n-hexane and other solvents precipitate visual failure in Leber hereditary optic neuropathy? [J].
Carelli, Valerio ;
Franceschini, Flavia ;
Venturi, Silvia ;
Barboni, Piero ;
Savini, Giacomo ;
Barbieri, Giuseppe ;
Pirro, Ettore ;
La Morgia, Chiara ;
Valentino, Maria L. ;
Zanardi, Francesca ;
Violante, Francesco S. ;
Mattioli, Stefano .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2007, 115 (01) :113-115
[5]   A case-control study of Leber's hereditary optic neuropathy [J].
Chalmers, RM ;
Harding, AE .
BRAIN, 1996, 119 :1481-1486
[6]   LEBERS HEREDITARY OPTIC NEUROPATHY MASQUERADING AS TOBACCO-ALCOHOL AMBLYOPIA [J].
CULLOM, ME ;
HEHER, KL ;
MILLER, NR ;
SAVINO, PJ ;
JOHNS, DR .
ARCHIVES OF OPHTHALMOLOGY, 1993, 111 (11) :1482-1485
[7]  
DUBOIS LG, 1992, J CLIN NEURO-OPHTHAL, V12, P15
[8]   Pathogenic mitochondrial DNA mutations are common in the general population [J].
Elliott, Hannah R. ;
Samuels, David C. ;
Eden, James A. ;
Relton, Caroline L. ;
Chinnery, Patrick F. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 83 (02) :254-260
[9]  
GOLNIK KC, 1994, J NEURO-OPHTHALMOL, V14, P163
[10]  
Gvozdjak J, 1987, Czech Med, V10, P47