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脆性X综合征的靶向治疗

Targeted Treatments for Fragile X Syndrome.

作者信息

Johnson Devon, Clark Courtney, Hagerman Randi

机构信息

MIND Institute, University of California Davis Health, Sacramento, CA, USA.

Department of Pediatrics, University of California Davis Health, Sacramento, CA, USA.

出版信息

Adv Neurobiol. 2023;30:225-253. doi: 10.1007/978-3-031-21054-9_10.

Abstract

The histories of targeted treatment trials in fragile X syndrome (FXS) are reviewed in animal studies and human trials. Advances in understanding the neurobiology of FXS have identified a number of pathways that are dysregulated in the absence of FMRP and are therefore pathways that can be targeted with new medication. The utilization of quantitative outcome measures to assess efficacy in multiple studies has improved the quality of more recent trials. Current treatment trials including the use of cannabidiol (CBD) topically and metformin orally have positive preliminary data, and both of these medications are available clinically. The use of the phosphodiesterase inhibitor (PDE4D), BPN1440, which raised the level of cAMP that is low in FXS has very promising results for improving cognition in adult males who underwent a controlled trial. There are many more targeted treatments that will undergo trials in FXS, so the future looks bright for new treatments.

摘要

本文回顾了脆性X综合征(FXS)靶向治疗试验在动物研究和人体试验中的历史。对FXS神经生物学理解的进展已经确定了一些在缺乏FMRP的情况下失调的通路,因此这些通路可以成为新药的靶向目标。在多项研究中使用定量结果指标来评估疗效提高了近期试验的质量。目前的治疗试验,包括局部使用大麻二酚(CBD)和口服二甲双胍,都有积极的初步数据,并且这两种药物都已在临床上可用。磷酸二酯酶抑制剂(PDE4D)BPN1440可提高FXS中较低的cAMP水平,在一项针对成年男性的对照试验中,该药物在改善认知方面取得了非常有前景的结果。还有更多的靶向治疗将在FXS中进行试验,因此新治疗方法的前景一片光明。

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