儿童早期ADHD症状的稳定性

Meghan Miller,Monica Orme,Antonia Piergies,Ana-Maria Iosif,Sally Ozonoff
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引用次数: 0

摘要

目的:我们在一个丰富了各种神经发育风险的样本中评估从幼儿(24个月)到学龄前(36-64个月)注意力缺陷/多动(ADHD)症状的稳定性,以确保ADHD症状的范围。方法参与者(n = 256)包括有ADHD家族史(n = 66)、自闭症家族史(n = 115)或无自闭症家族史(n = 75)的婴儿,这些婴儿在出生后几年进行前瞻性随访。在24个月和36-64个月大时,父母完成了学龄前ADHD评定量表。在学龄前访问中,儿童被分为三个相互排斥的结果组之一:ADHD关注组(即症状升高,临床医生关注组),自闭症组或比较组。评估ADHD症状从幼儿期到学龄前时期的稳定性,以及早期症状的可变性和学龄前临床表现随时间的变化。结果患者症状稳定,总评分相关性为0.56 ~ 0.60。在24个月时,那些后来被诊断为多动症或自闭症的人的总分明显更高,随着时间的推移,这两组的总分都有所增加,但对照组的总分则有所下降。结论2岁时的症状测量可能有助于识别幼儿后期行为挑战的高风险,并对早期筛查具有指导意义。在这一领域的未来工作可以帮助划定发育典型与非典型的界限,评估早期症状升高对长期结果的特异性,并确定从学步期开始的症状稳定模式,这可能有助于识别儿童面临持续/增加挑战的最大风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brief Report: Stability of ADHD Symptoms in Early Childhood.
OBJECTIVE We evaluated the stability of attention-deficit/hyperactivity (ADHD) symptoms from the toddler (24 months of age) to the preschool period (36-64 months of age) in a sample enriched for varied neurodevelopmental risk to ensure a range of ADHD symptoms. METHOD Participants (n = 256) included infants with a family history of ADHD (n = 66), autism (n = 115), or neither (n = 75) who were prospectively followed over the first several years of life. At 24 and 36-64 months of age, parents completed the Preschool ADHD Rating Scale. At the preschool visit, children were classified into one of three mutually exclusive outcome groups: ADHD Concerns (i.e. elevated symptoms, clinician concern), Autism, or Comparison. ADHD symptom stability from the toddler to the preschool period was assessed, along with variability in early symptoms and change over time by preschool clinical presentation. RESULTS Symptoms were moderately stable, with summary score correlations of 0.56-0.60. Total scores were significantly higher at 24 months among those with later concerns for ADHD or diagnoses of autism, and increased in these two groups over time, but decreased in the Comparison group. CONCLUSIONS Symptom measurement at age 2 may be useful for identifying toddlers at higher risk for later behavioral challenges, with implications for early screening. Future work in this area can help delineate boundaries of developmental typicality versus atypicality, evaluate the specificity of early symptom elevations to longer-term outcomes, and identify patterns of symptom stability from the toddler period over time that may aid in identifying children at greatest risk for persistent/increasing challenges.
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