Abstract
Autism spectrum disorder (ASD) affects 1 in 68 children in the US and is distinguished by core deficits in social interactions. Developing pharmacologic treatments for ASD is complicated by clinical and genetic heterogeneity. Although pharmacological treatments have not been shown to be effective in treating the core symptoms of ASD (i.e., social deficits), there is evidence that the burden of emotional and behavioral problems can be reduced with pharmacotherapy. Numerous randomized clinical trials of treatments for the core ASD deficits have been conducted; however, most have provided inconclusive results due to the substantial variation in treatment response. Variation also exists in the considerable metabolic side effects of many of the current treatments. Some of this variation may be explained by differences in the underlying genetic pathways. Exploiting the link between genetic heterogeneity and clinical variation associated with behavioral problems may provide an opportunity for targeted treatment of ASD. In this review, we summarize the recent findings from pharmacogenomics studies of ASD and suggest further how understanding how genetic liability modifies the effect of drugs may present an opportunity to address the challenges of personalized medicine in autism.
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Acknowledgements
Drs. Bowers and Lin have no financial disclosures or conflicts of interest. Dr. Erickson: Equity in Confluence Pharmaceuticals, Consultant to the Roche Group and Alcobra Pharmaceuticals, Research Grant Support from the United States Department of Defense, The American Academy of Child and Adolescent Psychiatry, The John Merck Fund, Cincinnati Children’s Hospital Medical Center, The Simons Foundation, the Angelman Syndrome Foundation, and the National Fragile X Foundation/United States Centers for Disease Control. None of these conflicts relate to/funded the creation of this manuscript.
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Bowers, K., Lin, PI. & Erickson, C. Pharmacogenomic Medicine in Autism: Challenges and Opportunities. Pediatr Drugs 17, 115–124 (2015). https://doi.org/10.1007/s40272-014-0106-0
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DOI: https://doi.org/10.1007/s40272-014-0106-0