Advances in clinical endpoints for neurocognitive rehabilitation in down syndrome

Jamie Edgin, Goffredina Spanō, Lynn Nadel

Research output: Chapter in Book/Report/Conference proceedingChapter

2 Scopus citations


Considerable progress in our understanding of the cognitive profile of Down syndrome (DS) has occurred in the last decade. Complementing this progress has been a series of landmark studies highlighting promise for pharmacological intervention for cognitive deficits in this population (Fernandez et al., 2007; Salehi et al., 2009). Movement forward has also been demonstrated by the development of behavioral cognitive interventions targeting specific aspects of the cognitive profile (e.g. Fidler et al., Chapter 15 of this book). With pharmacological and behavioral clinical trials coming to fruition in the next few years, there is an immediate need for valid and reliable clinical endpoints in DS. These trials will only be meaningful if they include a battery of measurements that are well suited for this population and sensitive enough to detect change. Our group has been involved in the development of such a battery, the Arizona Cognitive Test Battery (ACTB) (Figure 3.1), which serves as a foundation for assessing characteristics of the phenotype of DS. The history of pharmacological and dietary interventions for the cognitive deficits in humans with DS is largely one of disappointment (Salman, 2002). A number of drugs [e.g. Drugs used in Alzheimer's disease, such as donepezil (Prasher et al., 2002)] or dietary supplements currently on the market have been tested for use in individuals with DS, with little effect on the whole.

Original languageEnglish (US)
Title of host publicationNeurocognitive Rehabilitation of Down Syndrome
Subtitle of host publicationThe Early Years
PublisherCambridge University Press
Number of pages16
ISBN (Electronic)9780511919299
ISBN (Print)9781107400436
StatePublished - Jan 1 2011

ASJC Scopus subject areas

  • General Psychology


Dive into the research topics of 'Advances in clinical endpoints for neurocognitive rehabilitation in down syndrome'. Together they form a unique fingerprint.

Cite this