儿童特纳综合征患者神经发育和心理健康诊断的人群评估:一项PEDSnet研究

Christa Hutaff-Lee, Morgan Jolliffe, Karli S Swenson, Holly Wakeman, Deanna Swain, Anna Furniss, Natalie Nokoff, Jen Hansen-Moore, Chijioke Ikomi, Vaneeta Bamba, Rachel E Lean, Skyler Leonard, Shanlee M Davis
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引用次数: 0

摘要

众所周知,特纳综合征(TS)患者患神经发育障碍(NDD)和精神健康(MH)疾病的风险增加,但来自大型、基于人群的儿科样本的数据仍然有限。我们检查了美国六个儿科卫生系统中患有TS的青少年(N = 2145)中NDD和MH诊断的患病率,并与匹配的女性对照组(N = 8580)进行了比较。比值比(OR)和95%置信区间(CI)使用广义估计方程计算。患有TS的青少年被诊断为NDD的几率明显更高(24.2% vs 11.9%;OR 2.37, 95% CI 2.11-2.67),尤其是言语、运动、学习和注意力障碍。自闭症谱系障碍(ASD)和智力发育障碍(IDD)的几率也有所增加,尽管这些相对来说仍然不常见。相比之下,MH诊断,如焦虑和情绪障碍,在TS中并不比对照组更普遍(17.3%比18.5%;或0.92,95% ci 0.81-1.05)。这些发现支持了在TS中进行主动神经发育筛查的必要性,并提出了在该人群中识别和记录MH状况的重要问题。有必要进行进一步的研究,以了解青少年TS患者的MH症状是否未被充分诊断,或在发展后期才出现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Population-based assessment of neurodevelopmental and mental health diagnoses among pediatric patients with Turner Syndrome: A PEDSnet study.

Individuals with Turner syndrome (TS) are known to be at increased risk for neurodevelopmental disorders (NDD) and mental health (MH) conditions, but data from large, population-based pediatric samples remain limited. We examined the prevalence of NDD and MH diagnoses among youth with TS (N = 2,145) compared to matched female controls (N = 8,580) across six U.S. pediatric health systems. Odds ratios (OR) and 95% confidence intervals (CI) were calculated using generalized estimating equations. Youth with TS had significantly higher odds of an NDD diagnosis (24.2% vs. 11.9%; OR 2.37, 95% CI 2.11-2.67), particularly for speech-language, motor, learning, and attentional disorders. Increased odds were also observed for autism spectrum disorder (ASD) and intellectual developmental disorder (IDD), though these remained relatively uncommon. In contrast, MH diagnoses, such as anxiety and mood disorders, were not more prevalent in TS compared to controls (17.3% vs. 18.5%; OR 0.92, 95% CI 0.81-1.05). These findings support the need for proactive neurodevelopmental screening in TS and raise important questions about the recognition and documentation of MH conditions in this population. Additional research is warranted to understand whether MH symptoms are underdiagnosed in youth with TS or emerge later in development.

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