Heritable features of the optic disc: A novel twin method for determining genetic significance

被引:20
作者
Hewitt, Alex W.
Poulsen, Johan P.
Alward, Wallace L. M.
Bennett, Sonya L.
Budde, Wido M.
Cooper, Richard L.
Craig, Jamie E.
Fingert, John H.
Foster, Paul J.
Garway-Heath, David E.
Green, Catherine M.
Hammond, Christopher J.
Hayreh, Sohan S.
Jonas, Jost B.
Kaufman, Paul L.
Miller, Neil R.
Morgan, William H.
Newman, Nancy J.
Quigley, Harry A.
Samples, John R.
Spaeth, George L.
Pesudovs, Konrad
Mackey, David A.
机构
[1] Flinders Univ S Australia, NHMRC, Ctr Clin Eye Res, Dept Ophthalmol,Med Ctr, Adelaide, SA 5001, Australia
[2] Univ Melbourne, Ctr Res Australia, Royal Victorian Eye & Ear Hosp, Melbourne, Vic, Australia
[3] Univ Iowa, Dept Ophthalmol, Iowa City, IA 52242 USA
[4] Moorfields Eye Hosp, Glaucoma Res Unit, London, England
[5] Univ Heidelberg, Dept Ophthalmol, Fac Clin Med, D-6800 Mannheim, Germany
[6] Tasmanian Eye Clin, Launceston, Tas, Australia
[7] Royal Victorian Eye & Ear Hosp, Glaucoma Res Unit, Melbourne, Vic 3002, Australia
[8] St Thomas Hosp, Twin Res & Genet Epidemiol Unit, London, England
[9] Univ Wisconsin, Dept Ophthalmol & Visual Sci, Sch Med & Publ Hlth, Ctr Clin Sci, Madison, WI USA
[10] Johns Hopkins Med Inst, Dept Ophthalmol, Baltimore, MD 21205 USA
[11] Univ Western Australia, Lions Eye Inst, Nedlands, WA 6009, Australia
[12] Emory Univ, Sch Med, Dept Ophthalmol, Ctr Eye, Atlanta, GA 30322 USA
[13] Casey Eye Inst, Portland, OR USA
[14] Wills Eye Hosp & Res Inst, William & Anna Goldberg Glaucoma Serv & Res Labs, Jefferson Med Coll, Philadelphia, PA USA
[15] Univ Tasmania, Dept Ophthalmol, Royal Hobart Hosp, Hobart, Tas, Australia
关键词
OPEN-ANGLE GLAUCOMA; NERVE-FIBER LAYER; BEAVER DAM EYE; MONOZYGOTIC TWINS; PHYSIOLOGIC CUP; HEAD; HEREDITARY; IDENTIFICATION; NEUROPATHY; MUTATIONS;
D O I
10.1167/iovs.06-1470
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. Numerous genetic diseases and environmental stimuli affect optic nerve morphology. The purpose of this study was to identify the principal heritable components of visible optic nerve head structures in a population-based sample of twins. METHODS. Fifteen optic nerve specialists viewed stereoscopic optic nerve head photographs (Stereo Viewer-II; Pentax Corp., Tokyo, Japan) from 50 randomly selected monozygotic or dizygotic twin pairs. Before viewing, each expert was questioned about which optic nerve head traits they believed were inherited. After viewing a standardized reaching set, the experts indicated which twin pairs they thought were monozygotic. Participants were then questioned about how their decisions were reached. A rank-ordered Rasch analysis was used to determine the relative weighting and value applied to specific optic nerve head traits. RESULTS. The proportion of twin pairs for which zygosity was correctly identified ranged from 74% to 90% (median, 82%) across the panel. Experts who correctly identified the zygosity in more than 85% of cases placed most weighting on shape and size of the optic disc and cup, whereas experts with the lowest scores placed greater weighting on the optic nerve head vasculature in reaching their decisions. CONCLUSIONS. In determining the genetic components of the optic nerve head, the results of this study suggest that the shape and size of the optic disc and cup are more heritable and should receive a greater priority for quantification than should vascular features.
引用
收藏
页码:2469 / 2475
页数:7
相关论文
共 36 条
[1]  
AIRAKSINEN PJ, 1984, AM J OPHTHALMOL, V98, P566, DOI 10.1016/0002-9394(84)90242-3
[2]   OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 [J].
Alexander, C ;
Votruba, M ;
Pesch, UEA ;
Thiselton, DL ;
Mayer, S ;
Moore, A ;
Rodriguez, M ;
Kellner, U ;
Leo-Kottler, B ;
Auburger, G ;
Bhattacharya, SS ;
Wissinger, B .
NATURE GENETICS, 2000, 26 (02) :211-215
[3]  
ARMALY MF, 1967, ARCH OPHTHALMOL-CHIC, V78, P5
[4]  
BENGTSSON B, 1980, ACTA OPHTHALMOL, V58, P733
[5]   Determinants and heritability of intraocular pressure and cup-to-disc ratio in a defined older population [J].
Chang, TC ;
Congdon, NG ;
Wojciechowski, R ;
Muñoz, B ;
Gilbert, D ;
Chen, P ;
Friedman, DS ;
West, SK .
OPHTHALMOLOGY, 2005, 112 (07) :1186-1191
[6]   Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy [J].
Delettre, C ;
Lenaers, G ;
Griffoin, JM ;
Gigarel, N ;
Lorenzo, C ;
Belenguer, P ;
Pelloquin, L ;
Grosgeorge, J ;
Turc-Carel, C ;
Perret, E ;
Astarie-Dequeker, C ;
Lasquellec, L ;
Arnaud, B ;
Ducommun, B ;
Kaplan, J ;
Hamel, CP .
NATURE GENETICS, 2000, 26 (02) :207-210
[7]   A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation [J].
Duffy, David L. ;
Montgomery, Grant W. ;
Chen, Wei ;
Zhao, Zhen Zhen ;
Le, Lien ;
James, Michael R. ;
Hayward, Nicholas K. ;
Martin, Nicholas G. ;
Sturm, Richard A. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 80 (02) :241-252
[8]  
FitzGibbon T, 1996, J COMP NEUROL, V375, P238
[9]   Evaluation of heredity as a determinant of retinal nerve fiber layer thickness as measured by optical coherence tomography [J].
Hougaard, JL ;
Kessel, L ;
Sander, B ;
Kyvik, KO ;
Sorensen, TIA ;
Larsen, M .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (07) :3011-3016
[10]  
Huntzinger R S, 1978, Prog Clin Biol Res, V24 Pt C, P241