Dissecting the heterogeneity of autism spectrum disorder with sensory behavior, brain, and epigenetic factors.

IF 6.2 1区 医学 Q1 PSYCHIATRY
Yongjeon Cheong, Jihyun Bae, Seonkyoung Lee, Jihyeong Ro, Hidehiko Okazawa, Hirotaka Kosaka, Minyoung Jung
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Abstract

Autism spectrum disorder (ASD), a disorder with heterogeneous etiology, is characterized by abnormal behavioral responses to sensory inputs. However, there is still limited understanding of how brain and epigenetic factors, along with behavioral abnormality, contribute to ASD. After completing Adolescent-Adult Sensory Profile, a self-report questinnaire, 34 individuals with ASD and 72 controls underwent neuroimaging scans to measure brain structural (cortical and subcortical volume) and functional (thalamo-cortical resting-state functional connectivity) characteristics. For epigenetic measures, we computed DNA methylation values of the oxytocin receptor and arginine vasopressin receptor (AVPR) genes from the participants' saliva. When sensory-related behavior was the default baseline, a machine learning algorithm demonstrated that the neuroimaging-epigenetic model outperformed the neuroimaging model or the epigenetic model. Thalamo-cortical hyperconnectivity and AVPR 1A epigenetic modification were found to be significant contributing factors in these models. By integrating neuroimaging and epigenetic biomarkers with behaviors, a more precise diagnosis of ASD can be achieved.

Abstract Image

Abstract Image

Abstract Image

从感觉行为、大脑和表观遗传因素剖析自闭症谱系障碍的异质性。
自闭症谱系障碍(ASD)是一种异质性病因障碍,其特征是对感觉输入的异常行为反应。然而,对于大脑和表观遗传因素以及行为异常如何导致ASD,人们的理解仍然有限。在完成一份自我报告问卷“青少年-成人感觉档案”后,34名ASD患者和72名对照者接受了神经成像扫描,以测量大脑结构(皮层和皮层下体积)和功能(丘脑-皮层静息状态功能连接)特征。对于表观遗传测量,我们计算了参与者唾液中催产素受体和精氨酸抗利尿激素受体(AVPR)基因的DNA甲基化值。当感觉相关行为作为默认基线时,机器学习算法证明神经成像-表观遗传模型优于神经成像模型或表观遗传模型。在这些模型中发现丘脑-皮质超连通性和AVPR 1A表观遗传修饰是重要的影响因素。通过将神经影像学和表观遗传生物标志物与行为相结合,可以实现更精确的ASD诊断。
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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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