Choroideremia: The Endpoint Endgame

被引:12
作者
Elsayed, Maram E. A. Abdalla [1 ,2 ]
Taylor, Laura J. [1 ,2 ]
Josan, Amandeep S. [1 ,2 ]
Fischer, M. Dominik [1 ,2 ]
MacLaren, Robert E. [1 ,2 ]
机构
[1] Oxford Univ Hosp Natl Hlth Serv Fdn Trust, Oxford Eye Hosp, Oxford OX3 9DU, England
[2] Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England
关键词
choroideremia; CHM gene; REP1; AAV; nonsense suppression therapy; antisense oligonucleotides; gene therapy; clinical trials; endpoints; outcome measures; QUALITY-OF-LIFE; RETINAL GENE-THERAPY; OPTICAL COHERENCE TOMOGRAPHY; TERM NATURAL-HISTORY; VISUAL-FIELD LOSS; OUTER RETINA; DELIVERY; VISION; AUTOFLUORESCENCE; METAANALYSIS;
D O I
10.3390/ijms241814354
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Choroideremia is an X-linked retinal degeneration resulting from the progressive, centripetal loss of photoreceptors and choriocapillaris, secondary to the degeneration of the retinal pigment epithelium. Affected individuals present in late childhood or early teenage years with nyctalopia and progressive peripheral visual loss. Typically, by the fourth decade, the macula and fovea also degenerate, resulting in advanced sight loss. Currently, there are no approved treatments for this condition. Gene therapy offers the most promising therapeutic modality for halting or regressing functional loss. The aims of the current review are to highlight the lessons learnt from clinical trials in choroideremia, review endpoints, and propose a future strategy for clinical trials.
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页数:18
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