Cosman Kelly M, Boyle Lisa L, Porsteinsson Anton P
University of Rochester School of Medicine, Alzheimer's Disease Care Research and Education Program (AD-CARE), Monroe Community Hospital, 435 East Henrietta Road, Rochester, NY 14620, USA.
Expert Opin Pharmacother. 2007 Feb;8(2):203-14. doi: 10.1517/14656566.8.2.203.
Memantine is the first and only medication that has been approved by European, US and Canadian regulatory agencies for the treatment of moderate-to-severe Alzheimer's disease (AD). It is an NMDA receptor antagonist that works to prevent excitotoxicity and cell death, which are mediated by the excessive influx of calcium during a sustained release of glutamate. Preclinical studies of memantine reveal that it has the potential to improve memory and learning processes after impairment has occurred, as well as to prevent further neuronal damage. Although memantine has been considered for the treatment of earlier AD, it has not yet been approved for this. Randomized controlled trials of memantine in the treatment of mild-to-moderate AD have demonstrated small treatment effects in measures of cognition, global assessment and behavior favoring the use of memantine. However, the differences between treatment groups were not consistently significant. Two ongoing long-term trials are further investigating the efficacy of memantine in the treatment of mild-to-moderate AD.
美金刚是首个且唯一已获欧洲、美国和加拿大监管机构批准用于治疗中重度阿尔茨海默病(AD)的药物。它是一种N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,作用是预防由谷氨酸持续释放期间钙的过度内流介导的兴奋性毒性和细胞死亡。美金刚的临床前研究表明,它有可能在损伤发生后改善记忆和学习过程,并防止进一步的神经元损伤。尽管美金刚已被考虑用于早期AD的治疗,但尚未获此批准。美金刚治疗轻至中度AD的随机对照试验已证明,在认知、整体评估和行为测量方面有小的治疗效果,支持使用美金刚。然而,治疗组之间的差异并非始终显著。两项正在进行的长期试验正在进一步研究美金刚治疗轻至中度AD的疗效。