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Promise for finding brain biomarkers among infants at high familial risk for developing autism spectrum disorders

机译:在罹患自闭症谱系障碍的高家族风险婴儿中寻找脑生物标志物的承诺

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摘要

while it is widely accepted that early intervention is critical for achieving the best outcome among children with autism spectrum disorders (ASDs), the median age at earliest diagnosis is approximately 4.5 years, according to the Centers for Disease Control (1). One reason for this is that developmental trajectories in the core deficits seen in autism-language, social interaction, and stereotyped behaviors-are so variable in infants and toddlers. The diagnosis of ASDs is currently based on observations of behavior years after the complex interactions among genetic influences and environmental factors have taken their toll, potentially bypassing treatment or prevention opportunities during the critical first few years of life. Therefore, one of the key goals of the ASD research community has been to identify biomarkers that may predict future diagnosis.
机译:根据疾病控制中心的数据,尽管早期干预对于在自闭症谱系障碍(ASD)儿童中取得最佳结果至关重要,但最早诊断出的中位年龄约为4.5岁(1)。原因之一是自闭症-语言,社交互动和刻板行为中出现的核心缺陷的发展轨迹在婴儿和幼儿中变化很大。目前,ASD的诊断是基于对遗传影响和环境因素之间复杂的相互作用造成的损失数年后行为的观察,从而有可能在生命的最初几年中绕过治疗或预防的机会。因此,ASD研究社区的主要目标之一就是确定可以预测未来诊断的生物标志物。

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