Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene

被引:106
作者
Aung, T
Rezaie, T
Okada, K
Viswanathan, AC
Child, AH
Brice, G
Bhattacharya, SS
Lehmann, OJ
Sarfarazi, M
Hitchings, RA
机构
[1] Singapore Natl Eye Ctr, Glaucoma Serv, Singapore 168751, Singapore
[2] Moorfields Eye Hosp, London, England
[3] UCL, Inst Ophthalmol, London, England
[4] Univ Connecticut, Ctr Hlth, Farmington, CT USA
[5] Hiroshima Univ, Fac Med, Hiroshima, Japan
[6] Univ London St Georges Hosp, Sch Med, London SW17 0RE, England
[7] Univ Alberta, Edmonton, AB, Canada
关键词
D O I
10.1167/iovs.04-1133
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. To investigate the clinical features of subjects with glaucoma with the E50K mutation in the optineurin (OPTN) gene and to compare the onset, severity, and clinical course of these patients with a control group of subjects with glaucoma without this mutation. METHODS. The phenotype of well-characterized subjects from Moorfields Eye Hospital, London, who had been identified as carrying the OPTN E50K mutation was examined. A wide range of structural, psychophysical, and demographic factors were then compared with those in a control group of subjects with glaucoma without this mutation. RESULTS. Eleven subjects with glaucoma with the E50K mutation ( nine in two families and two sporadic cases) were studied. All 11 subjects had normal tension glaucoma (NTG), with presenting and highest IOP of 15.3 +/- 3.0 and 16.5 +/- 2.5 mm Hg ( +/- SD) on diurnal testing. Compared with 87 NTG control subjects who did not have this mutation, subjects with E50K presented at a younger age ( 40.8 +/- 15 years, P = 0.0001) and had more advanced optic disc cupping ( mean cup-disc ratio +/- SD 0.86 +/- 0.1, P = 0.001) and smaller neuroretinal rim area ( +/- SD; 0.5 +/- 0.28 mm(2), P = 0.001) at diagnosis. The rate of filtration surgery performed for progressive visual field loss in those with and without the E50K mutation was 72.7% and 25.3%, respectively ( P = 0.003), and all subjects with E50K were found to have progressing visual fields. In addition, seven E50K mutation-carrying individuals in two families ( age range, 23 - 58 years) presented with normal optic discs and visual fields and, as yet, no signs of glaucoma. CONCLUSIONS. In this study, subjects with glaucoma who had the OPTN E50K mutation were found to have NTG that appeared to be more severe than that in a control group of subjects with NTG without this mutation. The findings emphasize the importance of early detection and treatment of glaucoma in such individuals, to minimize visual loss.
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页码:2816 / 2822
页数:7
相关论文
共 43 条
[1]  
Allingham RR, 1998, INVEST OPHTH VIS SCI, V39, P2288
[2]  
Alward WL, 1998, AM J OPHTHALMOL, V126, P498
[3]   Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLCIA) [J].
Alward, WLM ;
Fingert, JH ;
Coote, MA ;
Johnson, AT ;
Lerner, SF ;
Junqua, D ;
Durcan, FJ ;
McCartney, PJ ;
Mackey, DA ;
Sheffield, VC ;
Stone, EM .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (15) :1022-1027
[4]  
Alward WLM, 2002, ARCH OPHTHALMOL-CHIC, V120, P1189
[6]  
Angius A, 2000, ARCH OPHTHALMOL-CHIC, V118, P674
[7]   Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing [J].
Aung, T ;
Ebenezer, ND ;
Brice, G ;
Child, AH ;
Prescott, Q ;
Lehmann, OJ ;
Hitchings, RA ;
Bhattacharya, SS .
JOURNAL OF MEDICAL GENETICS, 2003, 40 (08) :e101
[8]   Effect of surgery on visual field progression in normal-tension glaucoma [J].
Bhandari, A ;
Crabb, DP ;
Poinoosawmy, D ;
Fitzke, FW ;
Hitchings, RA ;
Noureddin, BN .
OPHTHALMOLOGY, 1997, 104 (07) :1131-1137
[9]   Prevalence of glaucoma and intraocular pressure distribution in a defined population -: The Egna-Neumarkt study [J].
Bonomi, L ;
Marchini, G ;
Marraffa, M ;
Bernardi, P ;
De Franco, I ;
Perfetti, S ;
Varotto, A ;
Tenna, V .
OPHTHALMOLOGY, 1998, 105 (02) :209-215
[10]  
Copt RP, 1999, ARCH OPHTHALMOL-CHIC, V117, P14