Alexithymia may explain the genetic relationship between autism and sensory sensitivity.

IF 6.2 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2025-03-05 DOI:10.1038/s41398-025-03254-1
Isabel Yorke, Jennifer Murphy, Fruhling Rijsdijk, Emma Colvert, Stephanie Lietz, Francesca Happé, Geoffrey Bird
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Abstract

Sensory symptoms are highly prevalent amongst autistic individuals and are now considered in the diagnostic criteria. Whilst evidence suggests a genetic relationship between autism and sensory symptoms, sensory symptoms are neither universal within autism nor unique to autism. One explanation for the heterogeneity within autism and commonality across conditions with respect to sensory symptoms, is that it is alexithymia (a condition associated with difficulties identifying and describing one's own emotions) that has a genetic relationship with sensory symptoms, and that alexithymia commonly co-occurs with autism and with several other conditions. Using parent-reports of symptoms in a sample of adolescent twins, we sought to examine the genetic association between autism, alexithymia and sensory symptoms. Results showed that the genetic correlation between autism and sensory symptoms was not significant after controlling for alexithymia. In contrast, after controlling for variance in alexithymia explained by autism, the genetic correlation between alexithymia and sensory symptoms was significant (and the proportion of variance explained by genetic factors remained consistent after controlling for autism). These results suggest that 1) alexithymia and sensory symptoms share aetiology that is not accounted for by their association with autism and 2) that the genetic association between sensory symptoms and autism may be, in part or wholly, a product of alexithymia. Future research should seek to examine the contribution of alexithymia to sensory symptoms across other conditions.

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述情障碍可以解释自闭症和感觉敏感性之间的遗传关系。
感觉症状在自闭症患者中非常普遍,现在被纳入诊断标准。虽然有证据表明自闭症和感觉症状之间存在遗传关系,但感觉症状既不是自闭症中普遍存在的,也不是自闭症独有的。对于自闭症内部的异质性和感觉症状的共性的一种解释是,述情障碍(一种与难以识别和描述自己的情绪有关的疾病)与感觉症状有遗传关系,而且述情障碍通常与自闭症和其他几种疾病同时发生。利用父母对青春期双胞胎的症状报告,我们试图检验自闭症、述情障碍和感觉症状之间的遗传关联。结果显示,在控制述情障碍后,自闭症与感觉症状的遗传相关性不显著。相反,在控制了由自闭症解释的述情障碍的方差后,述情障碍与感觉症状之间的遗传相关性显著(在控制了自闭症后,由遗传因素解释的方差比例保持一致)。这些结果表明,1)述情障碍和感觉症状有共同的病因,而这并不能用它们与自闭症的联系来解释;2)感觉症状和自闭症之间的遗传联系可能部分或全部是述情障碍的产物。未来的研究应寻求检查述情障碍对其他条件下感觉症状的贡献。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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