Elevated autistic features in Parkinson's disease and other motor disorders.

IF 5.6 2区 心理学 Q1 PSYCHOLOGY, DEVELOPMENTAL
Autism Pub Date : 2025-08-26 DOI:10.1177/13623613251362267
Ipsita Dey, Swarnima Pathak, Sreerupa Chakrabarty, Matthew K Belmonte, Supriyo Choudhury, Hrishikesh Kumar, Bhismadev Chakrabarti
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引用次数: 0

Abstract

Biological accounts have suggested an overlap between Parkinson's disease and autism despite their being studied largely at opposite ends of the life course. Characterising this overlap can identify potentially shared aetiologies and care pathways for these conditions. However, this overlap has so far only been tested in older autistic adults who show greater Parkinson's disease traits. The converse has not been directly assayed, that is, if adults with Parkinson's disease have higher autistic features. This preregistered study addressed this gap in the literature by asking whether adults with Parkinson's disease manifest elevated autistic traits. To test whether any such overlap might be unique to Parkinson's disease, we included two control groups: (1) people without any parkinsonism but with motor disability of neurological or neurovascular origin (other motor disorders), and (2) typically ageing controls with no motor disorders. We tested N = 330 participants (equal numbers of Parkinson's disease, other motor disorders and typically ageing controls) on their autistic traits and cognitive abilities. Clinical diagnoses were verified through a tertiary neurology clinic. Higher autistic traits were noted in both Parkinson's disease and other motor disorder groups compared to the typically ageing controls, suggesting an association between motor disorders and dimensional autistic traits. Exploratory analyses revealed a clear pattern of results in males, where Parkinson's disease was associated with the highest autistic traits, followed by the other motor disorders, and then by the typically ageing group. No such pattern was observed in females. These results are not explained by differences in language or age or reporter effects. This new evidence suggests a sex-specific overlap between these conditions and highlights the need for accounting for elevated autistic features in planning support for males with Parkinson's disease and other movement disorders.Lay AbstractPeople with autism are three times more likely than non-autistic people to develop Parkinson's disease in later life, and some of the same genetic variants contribute to risks for both these conditions. Although Parkinson's disease is more common in people with autism, is autism correspondingly more common in people with Parkinson's disease? Or what about autistic patterns of thought and behaviour, even in Parkinson's patients who are not also diagnosed, or diagnosable, with autism itself? We surveyed such autistic traits in three groups of older people: Parkinson's patients, patients with other neurological disorders of movement and those without any neurological or movement disorder or condition. Men with Parkinson's disease and men with non-parkinsonian motor disorders had more autistic traits than normal. Women with Parkinson's or other motor disorders, on the other hand, did not differ from women without any motor disorder. This was true no matter in which of the three languages surveys were given, and no matter whether it was patients themselves or their caregivers who completed the survey. Some underlying genetic or other biological shared factors might increase autistic traits not only in Parkinson's disease but also in some of the other motor disorders represented in this study's comparison group, for example, essential tremor. Conversely, Parkinson's disease might not be the only motor disorder to which people with autism stand at heightened risk. Assessment of autistic traits should be considered as part of care planning for people with Parkinson's disease or other motor disorders.

帕金森病和其他运动障碍中自闭症特征升高。
生物学研究表明,帕金森病和自闭症之间存在重叠,尽管它们主要是在生命历程的两端进行研究。表征这种重叠可以确定这些疾病的潜在共同病因和护理途径。然而,到目前为止,这种重叠只在老年自闭症成年人中进行了测试,他们表现出更大的帕金森病特征。相反的情况还没有被直接分析,也就是说,患有帕金森氏症的成年人是否有更高的自闭症特征。这项预先注册的研究通过询问患有帕金森病的成年人是否表现出更高的自闭症特征来解决文献中的这一空白。为了测试这种重叠是否可能是帕金森病独有的,我们纳入了两个对照组:(1)没有任何帕金森病,但有神经或神经血管起源的运动障碍(其他运动障碍)的人;(2)没有运动障碍的典型老年对照组。我们测试了330名参与者(帕金森氏症患者、其他运动障碍患者和典型的衰老对照组)的自闭症特征和认知能力。临床诊断通过三级神经病学诊所进行验证。与典型的衰老对照组相比,帕金森病患者和其他运动障碍组的自闭症特征都更高,这表明运动障碍和维度自闭症特征之间存在关联。探索性分析在男性中揭示了一个清晰的结果模式,帕金森病与最高的自闭症特征相关,其次是其他运动障碍,然后是典型的老年人。在女性中没有观察到这种模式。这些结果不能用语言、年龄或报告者效应的差异来解释。这一新的证据表明,这些疾病之间存在性别特异性重叠,并强调在为患有帕金森病和其他运动障碍的男性制定支持计划时,需要考虑到自闭症特征的增加。【摘要】自闭症患者在晚年患帕金森病的可能性是非自闭症患者的三倍,一些相同的基因变异会增加患这两种疾病的风险。虽然帕金森氏症在自闭症患者中更常见,但自闭症是否相应地在帕金森氏症患者中更常见?或者自闭症患者的思维和行为模式如何,即使是那些没有被诊断或可诊断为自闭症的帕金森患者?我们调查了三组老年人的自闭症特征:帕金森氏症患者、患有其他运动神经障碍的患者和没有任何神经或运动障碍或疾病的患者。患有帕金森氏症和非帕金森氏运动障碍的男性比正常人有更多的自闭症特征。另一方面,患有帕金森氏症或其他运动障碍的女性与没有任何运动障碍的女性没有什么不同。无论用三种语言中的哪一种进行调查,也无论完成调查的是病人自己还是他们的护理人员,都是如此。一些潜在的遗传或其他生物共享因素可能会增加自闭症特征,不仅在帕金森氏症中,而且在本研究的对照组中代表的其他一些运动障碍中,例如特发性震颤。相反,帕金森氏症可能不是自闭症患者面临高风险的唯一一种运动障碍。对自闭症特征的评估应被视为帕金森病或其他运动障碍患者护理计划的一部分。
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来源期刊
Autism
Autism PSYCHOLOGY, DEVELOPMENTAL-
CiteScore
9.80
自引率
11.50%
发文量
160
期刊介绍: Autism is a major, peer-reviewed, international journal, published 8 times a year, publishing research of direct and practical relevance to help improve the quality of life for individuals with autism or autism-related disorders. It is interdisciplinary in nature, focusing on research in many areas, including: intervention; diagnosis; training; education; translational issues related to neuroscience, medical and genetic issues of practical import; psychological processes; evaluation of particular therapies; quality of life; family needs; and epidemiological research. Autism provides a major international forum for peer-reviewed research of direct and practical relevance to improving the quality of life for individuals with autism or autism-related disorders. The journal''s success and popularity reflect the recent worldwide growth in the research and understanding of autistic spectrum disorders, and the consequent impact on the provision of treatment and care. Autism is interdisciplinary in nature, focusing on evaluative research in all areas, including: intervention, diagnosis, training, education, neuroscience, psychological processes, evaluation of particular therapies, quality of life issues, family issues and family services, medical and genetic issues, epidemiological research.
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