2010; Olfson et al. 2010, 2012]. In fact, within certain clinical groups, up to 4% of children are receiving an AP [Cooper et al. 2006; Crystal et al. 2009]. This widespread use likely reflects the increasing evidence supporting APs’ efficacy in a variety of psychiatric conditions, optimizing functioning, and possibly reducing the need for institutionalization [FDA, 2006, 2007, 2009; Zuddas Inhibitors,research,lifescience,medical et al. 2011]. However, concerns have been raised about the long-term safety of APs, particularly since many pediatric psychiatric conditions are chronic, often requiring extended treatment

[Vitiello et al. 2009]. In fact, across a variety of disorders, symptoms recur following the discontinuation of Inhibitors,research,lifescience,medical the AP or even despite continued therapy [Research Units on Pediatric Psychopharmacology Autism Network, 2005; Reyes et al. 2006a; Findling et al. 2010]. Much attention has been paid to AP-related weight gain and cardiometabolic abnormalities, particularly in children and adolescents [Calarge et al. 2009a;

Correll et al. 2009]. However, less research has explored other potential long-term side effects such as impaired skeletal development. This is of significance in light of accumulating evidence in adults implicating APs in suboptimal bone mineral density Inhibitors,research,lifescience,medical (BMD) [Bilici et al. 2002; Abraham et al. 2003; Becker et al. 2003; Meaney et al. 2004; Howes et al. 2005; Jung et al. 2006; Meaney and O’Keane, 2007; Kishimoto et al. 2008]. If AP treatment were to begin earlier in life, children and adolescents may be prevented from optimizing their peak bone mass and placed at a heightened risk for the later emergence of osteoporosis [NIH Consensus Development Panel on Osteoporosis Prevention, Diagnosis, and Therapy, 2001]. Osteoporosis is a taxing condition both financially, with costs estimated Inhibitors,research,lifescience,medical at US$10–15 billion annually in the USA for treatment of fractures alone, as well as personally due to reduced quality of life and increased morbidity and mortality [NIH Consensus Development Panel on Osteoporosis Prevention, Diagnosis, and

Therapy, 2001]. This paper briefly describes skeletal development to highlight Inhibitors,research,lifescience,medical the importance of optimizing peak bone mass, reviews the mechanisms through which APs might affect bone metabolism, summarizes the evidence Selleck MLN0128 linking APs to skeletal health in animals as well as in children and adolescents, and ends by underscoring the need for clinicians to be mindful of the potential Thymidine kinase long-term implications of the skeletal effects of psychotropics. Bone mineral density during development Peak bone mass achieved by early adulthood is a strong predictor of future BMD [NIH Consensus Development Panel on Osteoporosis Prevention, Diagnosis, and Therapy, 2001]. More than 85% of peak skeletal mass is accrued before age 18, making bone development during this phase critical for lifelong skeletal health [Theintz et al. 1992; Rauch and Schoenau, 2001]. Importantly, failure to achieve peak bone mass before young adulthood (e.g.