Department of Ophthalmology, Boston Children's Hospital, Boston, MA, USA.
Department of Ophthalmology, Harvard Medical School, Boston, MA, USA.
Sci Rep. 2023 Jun 22;13(1):10161. doi: 10.1038/s41598-023-34891-5.
An elevated threshold for neuroplasticity limits visual gains with treatment of residual amblyopia in older children and adults. Acetylcholinesterase inhibitors (AChEI) can enable visual neuroplasticity and promote recovery from amblyopia in adult mice. Motivated by these promising findings, we sought to determine whether donepezil, a commercially available AChEI, can enable recovery in older children and adults with residual amblyopia. In this open-label pilot efficacy study, 16 participants (mean age 16 years; range 9-37 years) with residual anisometropic and/or strabismic amblyopia were treated with daily oral donepezil for 12 weeks. Donepezil dosage was started at 2.5 or 5.0 mg based on age and increased by 2.5 mg if the amblyopic eye visual acuity did not improve by 1 line from the visit 4 weeks prior for a maximum dosage of 7.5 or 10 mg. Participants < 18 years of age further patched the dominant eye. The primary outcome was visual acuity in the amblyopic eye at 22 weeks, 10 weeks after treatment was discontinued. Mean amblyopic eye visual acuity improved 1.2 lines (range 0.0-3.0), and 4/16 (25%) improved by ≥ 2 lines after 12 weeks of treatment. Gains were maintained 10 weeks after cessation of donepezil and were similar for children and adults. Adverse events were mild and self-limited. Residual amblyopia improves in older children and adults treated with donepezil, supporting the concept that the critical window of visual cortical plasticity can be pharmacologically manipulated to treat amblyopia. Placebo-controlled studies are needed.
神经可塑性的阈值升高限制了大龄儿童和成年人弱视治疗的视觉改善。乙酰胆碱酯酶抑制剂(AChEI)可增强视觉神经可塑性,促进成年小鼠弱视恢复。受这些有前景的发现的启发,我们试图确定是否可以使用一种商业上可获得的 AChEI 多奈哌齐(donepezil)来帮助大龄儿童和成人弱视患者恢复视力。在这项开放性、单臂、疗效研究中,招募了 16 名患有残余斜视性和/或屈光不正性弱视的参与者(平均年龄 16 岁;9-37 岁),每天接受口服多奈哌齐治疗 12 周。多奈哌齐剂量根据年龄从 2.5 或 5.0mg 开始,如果治疗 4 周后,弱视眼视力没有提高 1 行,则增加 2.5mg,最大剂量为 7.5 或 10mg。年龄小于 18 岁的患者还需要对优势眼进行遮盖。主要结局是治疗结束后 22 周时弱视眼的视力。治疗 12 周后,平均弱视眼视力提高了 1.2 行(0.0-3.0),16 名患者中有 4 名(25%)提高了≥2 行。停止使用多奈哌齐 10 周后,仍保持疗效,且儿童和成人的疗效相似。不良反应轻微且自行缓解。使用多奈哌齐治疗后,大龄儿童和成人的弱视得到改善,这支持了一个观点,即视觉皮质可塑性的关键窗口可以通过药物干预来治疗弱视。需要进行安慰剂对照研究。