先天性中枢通气不足综合征年轻患者的自闭症谱系障碍:自主神经系统功能障碍的作用。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Benjamin Dudoignon, Anna Maruani, Richard Delorme, Maxime Patout, Mylene Fefeu, Pierre Ellul, Plamen Bokov, Christophe Delclaux
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引用次数: 0

摘要

背景:先天性中枢通气不足综合征(CCHS)是一种罕见疾病,其特点是肺泡通气不足和自主神经系统(ANS)功能障碍,需要长期通气。先天性中枢通气不足综合征可能是自闭症谱系障碍(ASD)的一个危险因素,原因是与呼吸衰竭有关的产伤,这一点仍有待确定。自闭症谱系障碍中也有自律神经系统功能障碍的描述,有迹象表明自律神经系统与中枢神经系统在处理社会信息时的相互作用发生了改变;因此,基于病理生理学背景,CCHS 也可能是自闭症谱系障碍的一个危险因素。我们的研究旨在确定CCHS患者中ASD的患病率,识别风险因素,并探讨通过心率变异性指数评估的自律神经系统与适应功能之间的关系:我们的回顾性研究基于对法国一家国家中心 20 岁以下 CCHS 患者记录的分析,结果发现 ASD(由精神科医生根据 DSM-4 或 DSM-5 标准诊断)的发病率为 6/69 例患者,占 8.7%(95% 置信区间:3.3-18.0%)。在一项性别匹配的病例(患有自闭症的儿童保健中心,n = 6)-对照(不患有自闭症的儿童保健中心,n = 12)研究中,新生儿住院时间延长和血糖功能障碍与自闭症有关。采用文兰适应行为量表(VABS)对适应功能进行评估,并从当天进行的心电图 Holter 中获得心率变异性指数(包括作为副交感神经调节指数的日间 RMSSD)。在 19 名同时具有心电图 Holter 和 VABS 的 CCHS 年轻受试者中,观察到 RMSSD 与 VABS 四个子域中的三个子域之间存在显著的正相关性(交流:R=0.50,p=0.028;日常生活技能:R=0.60,p=0.006;社会化:结论:我们的研究表明,CCHS 患者中 ASD 的发病率很高。结论:我们的研究表明,CCHS 患者中 ASD 的发病率很高。副交感神经调节功能的缺陷与适应功能较差有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autism spectrum disorder in young patients with congenital central hypoventilation syndrome: role of the autonomic nervous system dysfunction.

Background: Congenital central hypoventilation syndrome (CCHS) is a rare condition characterized by alveolar hypoventilation and autonomic nervous system (ANS) dysfunction requiring long-term ventilation. CCHS could constitute a risk factor of autism spectrum disorder (ASD) due to birth injury related to respiratory failure, which remains to be determined. ANS dysfunction has also been described in ASD and there are indications for altered contribution of ANS-central nervous system interaction in processing of social information; thus, CCHS could be a risk factor for ASD based on pathophysiological background also. Our study aimed to determine the prevalence of ASD among CCHS patients, identify risk factors, and explore the relationship between the ANS, evaluated by heart rate variability indices, and adaptative functioning.

Results: Our retrospective study, based on the analysis of records of a French national center of patients with CCHS under 20 years of age, determined that the prevalence of ASD (diagnosed by a psychiatrist, following the criteria of DSM-4 or DSM-5) was 6/69 patients, 8.7% (95% confidence interval: 3.3-18.0%). In a case (CCHS with ASD, n = 6) - control (CCHS without ASD, n = 12) study with matching on sex, longer neonatal hospitalization stay and glycemic dysfunction were associated with ASD. Adaptative functioning was assessed using Vineland Adaptative behavioral scales (VABS) and heart rate variability indices (including daytime RMSSD as an index of parasympathetic modulation) were obtained from ECG Holter performed the same day. In 19 young subjects with CCHS who had both ECG Holter and VABS, significant positive correlations were observed between RMSSD and three of four sub-domains of the VABS (communication: R = 0.50, p = 0.028; daily living skills: R = 0.60, p = 0.006; socialization: R = 0.52, p = 0.021).

Conclusion: Our study suggests a high prevalence of ASD in patients with CCHS. Glycemic dysfunction and longer initial hospitalization stays were associated with ASD development. A defect in parasympathetic modulation was associated with worse adaptative functioning.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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