Neurosciences Research Programme, IMIM-Hospital del Mar Research Institute and CIBEROBN, Barcelona, Spain.
Prog Brain Res. 2012;197:1-14. doi: 10.1016/B978-0-444-54299-1.00001-7.
Clinical trials with drugs aimed at treatment of Alzheimer disease to decelerate cognitive decline and translated mimetically to demented and young nondemented Down syndrome patients have been unable to demonstrate improvements in cognitive performance and functioning. Unfortunately, results from clinical trials do not support the use of NMDA antagonists like memantine and we should await at the development of safer GABA(A) antagonists to conclude about the efficacy of approaching Down syndrome therapeutics by modulating neurotransmission systems altered in this pathology. The use of folinic acid or antioxidants in DS patients is not supported by scientific evidence and do not provide improvement in cognitive performance to patients. Alternatively to the modulation of neurotransmission systems, future therapeutic approaches should focus at normalizing the expression levels or function of candidate molecules. Epigallocatechin gallate, a green tea polyphenol, that modulates DYRK1A functioning has already shown preliminarily that this approach may prove useful in therapeutics.
针对阿尔茨海默病的药物的临床试验旨在减缓认知能力下降,并将其转化为痴呆和年轻非痴呆唐氏综合征患者的模型,但未能证明认知表现和功能的改善。不幸的是,临床试验的结果并不支持使用 NMDA 拮抗剂,如美金刚,我们应该等待更安全的 GABA(A)拮抗剂的发展,以确定通过调节改变这种病理的神经传递系统来治疗唐氏综合征的疗效。叶酸或抗氧化剂在 DS 患者中的使用没有科学证据支持,也不能改善患者的认知表现。作为神经传递系统调节的替代方法,未来的治疗方法应侧重于使候选分子的表达水平或功能正常化。表没食子儿茶素没食子酸酯(EGCG),一种绿茶多酚,可调节 DYRK1A 的功能,已经初步表明这种方法可能对治疗有用。