Review of the Long-Term Effect of the Atypical Antipsychotic Medication on the Bone Mineral Density of the Pediatric Patient with Consideration of Autism Spectrum Disorder. Issue 1 (March 2022)

• Record Type: Journal Article
• Authors: Jumaili, Wisam Al; Muzwagi, Ashraf
• Is Part Of: Journal of pharmacology and pharmacotherapeutics. Volume 13:Issue 1(2022)
• Page Start: 24
• Page End: 30
• Publication Date: 2022-03
• Subjects: Antipsychotic -- Bone mineral density -- Children -- Autism spectrum disorder; 615.1
• DOI: 10.1177/0976500X221080296
• Languages: English
• ISSNs: 0976-500X

Abstract

Objectives: To shed some light on the understudied complication of chronic prolonged exposure to antipsychotics (AP) in children with consideration to with autism spectrum disorder (ASD). Methods: We electronically searched PubMed, Google Scholar, clinical trial.gov, and Medline Database of clinical studies up to June 2021. We used the following keywords: "bone mineral density, osteoporosis, osteopenia, bone loss, bone changes" AND "antipsychotics, SGAs, atypical antipsychotics" AND "pediatric, adolescent, young, youth, children." We used [Mesh] Term for "antipsychotics agent" and "bone mineral density" and "autism spectrum disorder" and "child." We retrieved relevant observational studies, reviews, case series, and randomized clinical trials. Results: Yvette Roke et al., in 2012, reported in a retrospective observational study that lumbar spine bone mineral density (BMD) and the biochemical bone marker were lower in the AP-treated boy with hyperprolactinemia in comparison to the non-AP-treated group, while a retrospective observational study of institutional adolescents with a psychiatric condition, carried out by Bonnot et al. in 2011, found significant vitamin D deficiency in psychiatric inpatient adolescents that is unrelated to the specific APs. Third, Calarge et al. in a 2010 retrospective observational study have reported a significant reduction in BMD in adolescents with risperidone-induced hyperprolactinemia and selective serotonin reuptake inhibitor (SSRI) compared to another group with risperidone-induced hyperprolactinemia without SSRI. On the other hand, Nivin A. Nagiub et al. (2019) in the cross-sectional study found no correlation between BMD and AP use in children with ASD. Houghton et al., in 2021, found a high fracture prevalence of 38% with aripiprazole compared to risperidone in children with ASD. Conclusion: Clinicians should be aware of the potential negative effects of APs on BMD, considerably in children with ASD that has additional risk factors for osteoporosis and bone disease. A provider needs to utilize more sensitive screening and diagnostic tools; the pediatric physician should evaluate other risk factors to prevent early osteopenia and bone fracture in children with ASD who are on chronic psychotropic medication, before adjusting to the AP medication.