Jackson Gregory R, Clark Mark E, Scott Ingrid U, Walter Laura E, Quillen David A, Brigell Mitchell G
*PhD †BS ‡MD, MPH §COA ∥MD Penn State Hershey Eye Center, Penn State College of Medicine, Hershey, Pennsylvania (GRJ, IUS, LEW, DAQ); Department of Ophthalmology, University of Alabama at Birmingham, Birmingham, Alabama (MEC); and Translational Medicine, Novartis Institute for BioMedical Research, Cambridge, Massachusetts (MGB).
Optom Vis Sci. 2014 Aug;91(8):925-31. doi: 10.1097/OPX.0000000000000247.
A sensitive endpoint is required for clinical trials evaluating preventative therapies for early age-related macular degeneration (AMD). Dark adaptation (DA) is a sensitive marker of AMD and has been proposed as a potential endpoint. This study evaluated whether significant changes in DA speed could be detected in participants with early to intermediate AMD at 12 months following baseline DA measurement.
Dark adaptation, visual acuity (VA), and fundus photography were obtained at baseline and at 6 and 12 months in 26 subjects with AMD and in 6 subjects with normal retinal health. Disease severity was assessed by the Nine-Step Age-Related Eye Disease Study AMD severity scale.
At 12 months, significant progression of DA impairment occurred in 5 of 26 (19%) participants with AMD. None of the participants with AMD exhibited a significant worsening of fundus grade or decrease of acuity related to disease progression. The normal group exhibited stable DA and VA during the observation period.
Significant worsening of DA was observed in 19% of subjects with AMD in 12 months of observation, despite stable VA and fundus appearance. This study suggests that DA may be a suitable functional endpoint for early clinical studies evaluating novel treatments for early to intermediate AMD.
在评估早期年龄相关性黄斑变性(AMD)预防疗法的临床试验中,需要一个敏感的终点指标。暗适应(DA)是AMD的一个敏感标志物,并已被提议作为一个潜在的终点指标。本研究评估了在基线DA测量后12个月,早期至中期AMD参与者的DA速度是否能检测到显著变化。
对26名AMD患者和6名视网膜健康正常的受试者在基线、6个月和12个月时进行暗适应、视力(VA)和眼底照相检查。通过九步年龄相关性眼病研究AMD严重程度量表评估疾病严重程度。
12个月时,26名(19%)AMD参与者中有5人出现了DA损伤的显著进展。没有AMD参与者表现出与疾病进展相关的眼底分级显著恶化或视力下降。正常组在观察期内DA和VA保持稳定。
在12个月的观察期内,19%的AMD受试者出现了DA的显著恶化,尽管VA和眼底外观保持稳定。本研究表明,DA可能是评估早期至中期AMD新疗法的早期临床研究的一个合适的功能终点指标。