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State‐of‐the‐art therapy for Down syndrome

医学 疾病 重症监护医学 临床试验 心理干预 人口 认知 精神科 病理 环境卫生
作者
Nicola Lorenzón,Juanluis Musoles‐Lleó,Federica Turrisi,Maria Gomis‐González,Rafael de la Torre,Mara Dierssen
出处
期刊:Developmental Medicine & Child Neurology [Wiley]
卷期号:65 (7): 870-884 被引量:17
标识
DOI:10.1111/dmcn.15517
摘要

Abstract In the last decade, an important effort was made in the field of Down syndrome to find new interventions that improve cognition. These therapies have added to the traditional symptomatic treatments and to the drugs for treating Alzheimer disease in the general population repurposed for Down syndrome. Defining next‐generation therapeutics will involve biomarker‐based therapeutic decision‐making, and preventive and multimodal interventions. However, translation of specific findings into effective therapeutic strategies has been disappointingly slow and has failed in many cases at the clinical level, leading to reduced credibility of mouse studies. This is aggravated by a tendency to favour large‐magnitude effects and highly significant findings, leading to high expectations but also to a biased view of the complex pathophysiology of Down syndrome. Here, we review some of the most recent and promising strategies for ameliorating the cognitive state of individuals with Down syndrome. We studied the landscape of preclinical and clinical studies and conducted a thorough literature search on PubMed and ClinicalTrials.gov for articles published between June 2012 and August 2022 on therapies for ameliorating cognitive function in individuals with Down syndrome. We critically assess current therapeutic approaches, why therapies fail in clinical trials in Down syndrome, and what could be the path forward. We discuss some intrinsic difficulties for translational research, and the need for a framework that improves the detection of drug efficacy to avoid discarding compounds too early from the companies’ pipelines.

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