AI Article Synopsis

  • Precision medicine focuses on tailoring disease management based on individual genetic and environmental profiles, enhancing prevention and personalized treatment outcomes.
  • Babble Boot Camp (BBC) is a pioneering, personalized program aimed at reducing speech and language disorders in infants at risk, starting intervention as early as 2 months of age and concluding by 24 months, with follow-up assessments.
  • A clinical trial with 44 children diagnosed with classic galactosemia (CG) showed promising results, where most children who completed BBC intervention maintained typical speech and language skills, indicating the potential for early intervention based on genetic risk.

Article Abstract

Precision medicine is an emerging approach to managing disease by taking into consideration an individual's genetic and environmental profile toward two avenues to improved outcomes: prevention and personalized treatments. This framework is largely geared to conditions conventionally falling into the field of medical genetics. Here, we show that the same avenues to improving outcomes can be applied to conditions in the field of behavior genomics, specifically disorders of spoken language. Babble Boot Camp (BBC) is the first comprehensive and personalized program designed to proactively mitigate speech and language disorders in infants at predictable risk by fostering precursor and early communication skills via parent training. The intervention begins at child age 2 to 5 months and ends at age 24 months, with follow-up testing at 30, 42, and 54 months. To date, 44 children with a newborn diagnosis of classic galactosemia (CG) have participated in the clinical trial of BBC. CG is an inborn error of metabolism of genetic etiology that predisposes up to 85% of children to severe speech and language disorders. Of 13 children with CG who completed the intervention and all or part of the follow-up testing, only one had disordered speech and none had disordered language skills. For the treated children who completed more than one assessment, typical speech and language skills were maintained over time. This shows that knowledge of genetic risk at birth can be leveraged toward proactive and personalized management of a disorder that manifests behaviorally.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168611PMC
http://dx.doi.org/10.1016/j.xhgg.2022.100119DOI Listing

Publication Analysis

Top Keywords

speech language
16
precision medicine
8
clinical trial
8
classic galactosemia
8
language disorders
8
follow-up testing
8
children completed
8
language skills
8
language
6
speech
5

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!