Abstract
Experimental research over just the past decade has raised the possibility that learning deficits connected to Down syndrome (DS) might be effectively managed by medication. In the current chapter, we touch on some of the work that paved the way for these advances and discuss the challenges associated with translating them. In particular, we highlight sources of phenotypic variability in the DS population that are likely to impact performance assessments. Throughout, suggestions are made on how to detect meaningful changes in cognitive–adaptive function in people with DS during drug treatment. The importance of within-subjects evaluation is emphasized.
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Acknowledgements
We acknowledge Ms. Lucy Han for her assistance in preparing the manuscript. Special thanks are extended to the LuMind Foundation, the Anna and John J. Sie Foundation, and Research Down syndrome for their tireless support. This work was also funded under R01 HD38384 from the National Institute of Child Health and Human Development. F.F. is indebted to J.O. Edgin for her wellspring of enthusiasm, inspiration, and strength.
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Fernandez, F., Reeves, R.H. (2015). Assessing Cognitive Improvement in People with Down Syndrome: Important Considerations for Drug-Efficacy Trials. In: Kantak, K., Wettstein, J. (eds) Cognitive Enhancement. Handbook of Experimental Pharmacology, vol 228. Springer, Cham. https://doi.org/10.1007/978-3-319-16522-6_12
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