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成人广泛性关节活动过度与自闭症谱系障碍之间的关系:一项大型横断面病例对照比较研究。

The Relationship Between Generalised Joint Hypermobility and Autism Spectrum Disorder in Adults: A Large, Cross-Sectional, Case Control Comparison.

作者信息

Glans Martin R, Thelin Nils, Humble Mats B, Elwin Marie, Bejerot Susanne

机构信息

School of Medical Sciences, Örebro University, Örebro, Sweden.

Division of Psychiatry, Linköping University Hospital, Linköping, Sweden.

出版信息

Front Psychiatry. 2022 Feb 8;12:803334. doi: 10.3389/fpsyt.2021.803334. eCollection 2021.

Abstract

Autism spectrum disorder (ASD) and generalised joint hypermobility (GJH) share a number of clinical manifestations including proprioceptive impairment, motor difficulties, sensory hypersensitivity, and autonomic dysfunction. Clinical observations suggest that GJH is overrepresented in ASD. However, there are currently few systematic studies available. Knowledge about comorbidities may unfold common aetiopathological pathways underlying the association and improve the clinical management. The aim of this large, cross-sectional comparative study is to evaluate the relationship between ASD and GJH in adults. Data on joint hypermobility, symptoms associated with both hypermobility spectrum disorders (HSD) and hypermobile Ehlers-Danlos syndrome (hEDS), lifetime psychiatric diagnoses, psychiatric rating scales for ASD and attention deficit hyperactivity disorder (ADHD), and socio-demographics was collected for 199 individuals with ASD and 419 non-ASD community controls. Logistic regression models adjusting for covariates (age, sex, ethnicity) revealed a significant relationship between ASD and GJH and between ASD and symptomatic GJH, with adjusted odds ratios of 3.1 (95% CI: 1.9, 5.2; < 0.001) and 4.9 (95% CI: 2.6, 9.0; < 0.001), respectively. However, the high prevalence of comorbid ADHD in the study sample reduces the generalizability of the results among individuals with ASD without comorbid ADHD. Possibly, an additional ADHD phenotype is the primary driver of the association between ASD and GJH. Furthermore, GJH with additional self-reported symptoms, suggestive of HSD/hEDS, showed a stronger association with ASD than did non-specified GJH, indicating that symptomatic GJH plays a greater role in the relationship than non-specified GJH does. Therefore, the current study underscores the need of careful sample subclassifications. ASD with GJH may represent a novel subgroup of ASD in terms of aetiopathology and clinical presentation. Future research should elucidate the aetiological factors behind the association between ASD and GJH and evaluate how the comorbidity of GJH affects ASD outcomes.

摘要

自闭症谱系障碍(ASD)和全身关节活动过度(GJH)有许多共同的临床表现,包括本体感觉障碍、运动困难、感觉过敏和自主神经功能障碍。临床观察表明,ASD患者中GJH的比例过高。然而,目前系统研究较少。了解共病情况可能会揭示两者关联背后共同的病因病理途径,并改善临床管理。这项大型横断面比较研究的目的是评估成人ASD与GJH之间的关系。收集了199名ASD患者和419名非ASD社区对照者的关节活动过度数据、与活动过度谱系障碍(HSD)和活动过度型埃勒斯-当洛综合征(hEDS)相关的症状、终生精神疾病诊断、ASD和注意力缺陷多动障碍(ADHD)的精神评定量表以及社会人口统计学数据。调整协变量(年龄、性别、种族)后的逻辑回归模型显示,ASD与GJH之间以及ASD与有症状的GJH之间存在显著关系,调整后的优势比分别为3.1(95%CI:1.9,5.2;P<0.001)和4.9(95%CI:2.6,9.0;P<0.001)。然而,研究样本中共病ADHD的高患病率降低了这些结果在无共病ADHD的ASD个体中的普遍性。可能,另一种ADHD表型是ASD与GJH之间关联的主要驱动因素。此外,伴有其他自我报告症状(提示HSD/hEDS)的GJH与ASD的关联比未明确的GJH更强,这表明有症状的GJH在两者关系中比未明确的GJH起更大作用。因此,本研究强调了仔细进行样本亚分类的必要性。伴有GJH的ASD在病因病理和临床表现方面可能代表ASD的一个新亚组。未来的研究应阐明ASD与GJH之间关联背后的病因因素,并评估GJH共病如何影响ASD的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7382/8861852/9967ea670182/fpsyt-12-803334-g0001.jpg

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