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将精准医学原理转化为言语语言病理学:针对经典型半乳糖血症婴儿的前瞻性言语和语言干预临床试验。

Translating principles of precision medicine into speech-language pathology: Clinical trial of a proactive speech and language intervention for infants with classic galactosemia.

作者信息

Peter Beate, Davis Jennifer, Finestack Lizbeth, Stoel-Gammon Carol, VanDam Mark, Bruce Laurel, Kim Yookyung, Eng Linda, Cotter Sarah, Landis Emily, Beames Sam, Scherer Nancy, Knerr Ina, Williams Delaney, Schrock Claire, Potter Nancy

机构信息

College of Health Solutions, Arizona State University, Tempe, AZ, USA.

Speech-Language-Hearing Sciences, University of Minnesota, Minneapolis, MN, USA.

出版信息

HGG Adv. 2022 May 20;3(3):100119. doi: 10.1016/j.xhgg.2022.100119. eCollection 2022 Jul 14.

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.

摘要

精准医学是一种新兴的疾病管理方法,它通过考虑个体的基因和环境特征,实现改善疾病预防和个性化治疗效果这两个目标。该框架主要适用于传统上属于医学遗传学领域的疾病。在此,我们表明,同样改善治疗效果的方法也可应用于行为基因组学领域的疾病,特别是口语障碍。牙牙学语训练营(BBC)是首个全面且个性化的项目,旨在通过家长培训培养婴儿的语言前体和早期沟通技能,积极减轻有可预测风险的婴儿的言语和语言障碍。干预从孩子2至5个月大开始,到24个月大结束,并在30、42和54个月时进行随访测试。迄今为止,44名新生儿被诊断为经典型半乳糖血症(CG)的儿童参与了BBC的临床试验。CG是一种由遗传病因导致的先天性代谢缺陷,高达85%的患儿易患严重的言语和语言障碍。在13名完成干预及全部或部分随访测试的CG患儿中,只有1名存在言语障碍,且无人有语言技能障碍。对于完成了不止一次评估的接受治疗的儿童,其典型的言语和语言技能随时间推移得以保持。这表明,出生时的遗传风险知识可用于对行为表现出的疾病进行积极且个性化的管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ba9/9168611/812e5dbfa6fd/gr1.jpg

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