School of Optometry and Vision Science, University of Auckland, New Zealand.
School of Pharmacy, University of Otago, New Zealand.
Neural Plast. 2019 Jun 9;2019:5857243. doi: 10.1155/2019/5857243. eCollection 2019.
Nonhuman animal models have demonstrated that selective serotonin reuptake inhibitors (SSRIs) can enhance plasticity within the mature visual cortex and enable recovery from amblyopia. The aim of this study was to test the hypothesis that the SSRI citalopram combined with part-time patching of the fellow fixing eye would improve amblyopic eye visual acuity in adult humans. Following a crossover, randomized, double-blind, placebo-controlled design, participants completed two 2-week blocks of fellow fixing eye patching. One block combined patching with citalopram (20 mg/day) and the other with a placebo tablet. The blocks were separated by a 2-week washout period. The primary outcome was change in amblyopic eye visual acuity. Secondary outcomes included stereoacuity and electrophysiological measures of retinal and cortical function. Seven participants were randomized, fewer than our prespecified sample size of 20. There were no statistically significant differences in amblyopic eye visual acuity change between the active (mean ± SD change = 0.08 ± 0.16 logMAR) and the placebo (mean change = -0.01 ± 0.03 logMAR) blocks. No treatment effects were observed for any secondary outcomes. However, 3 of 7 participants experienced a 0.1 logMAR or greater improvement in amblyopic eye visual acuity in the active but not the placebo blocks. These results from a small sample suggest that larger-scale trials of SSRI treatment for adult amblyopia may be warranted. Considerations for future trials include drug dose, treatment duration, and recruitment challenges. This study was preregistered as a clinical trial (ACTRN12611000669998).
非人类动物模型表明,选择性 5-羟色胺再摄取抑制剂(SSRIs)可以增强成熟视皮层的可塑性,并使弱视恢复。本研究旨在检验这样一个假设,即 SSRIs 西酞普兰与同眼部分时间遮盖相结合,是否能提高成人弱视眼的视力。采用交叉、随机、双盲、安慰剂对照设计,参与者完成了两个为期 2 周的同眼遮盖周期。一个周期结合了西酞普兰(20mg/天)和安慰剂片的遮盖,另一个周期则不进行遮盖。两个周期之间有 2 周的洗脱期。主要结果是弱视眼视力的变化。次要结果包括立体视锐度和视网膜及皮质功能的电生理测量。有 7 名参与者被随机分配到治疗组和安慰剂组,低于我们预先指定的 20 名参与者的样本量。在治疗组(弱视眼视力变化的平均±SD 变化=0.08±0.16logMAR)和安慰剂组(弱视眼视力变化的平均变化=-0.01±0.03logMAR)之间,弱视眼视力变化没有统计学上的显著差异。任何次要结果均未观察到治疗效果。然而,在治疗组的 7 名参与者中,有 3 名在治疗周期中弱视眼视力提高了 0.1 logMAR 或以上,而在安慰剂组中则没有。这项来自小样本的研究结果表明,对于成人弱视的 SSRI 治疗可能需要更大规模的试验。未来试验需要考虑药物剂量、治疗持续时间和招募挑战。本研究已预先注册为临床试验(ACTRN12611000669998)。