Distinct and shared therapeutic neural mechanisms of mindfulness-based and social support stress reduction groups in adults with autism spectrum disorder.

IF 4.1 2区 医学 Q2 NEUROSCIENCES
Journal of Psychiatry & Neuroscience Pub Date : 2023-03-29 Print Date: 2023-03-01 DOI:10.1503/jpn.220159
Broc A Pagni, Ethan Hill, Melissa J M Walsh, Shanna Delaney, Destiny Ogbeama, Leanna Monahan, James R Cook, Nicolas Guerithault, Maria V Dixon, Lisa Ballard, B Blair Braden
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引用次数: 0

Abstract

Background: Mindfulness-based stress reduction (MBSR) alleviates depression and anxiety in adults with autism spectrum disorder (ASD); however, underlying therapeutic neural mechanisms and mindfulness-specific effects have yet to be elucidated.

Methods: We randomly assigned adults with ASD to MBSR or social support/education (SE). They completed questionnaires that assessed depression, anxiety, mindfulness traits, autistic traits and executive functioning abilities as well as a self-reflection functional MRI task. We used repeated-measures analysis of covariance (ANCOVA) to evaluate behavioural changes. To identify task-specific connectivity changes, we performed a generalized psychophysiological interactions (gPPI) functional connectivity (FC) analysis on regions of interest (ROIs; insula, amygdala, cingulum and prefrontal cortex [PFC]). We used Pearson correlations to explore brain-behaviour relationships.

Results: Our final sample included 78 adults with ASD - 39 who received MBSR and 39 who received SE. Mindfulness-based stress reduction uniquely improved executive functioning abilities and increased mindfulness traits, whereas both MBSR and SE groups showed reductions in depression, anxiety and autistic traits. Decreases specific to MBSR in insula-thalamus FC were associated with anxiety reduction and increased mindfulness traits, including the trait "nonjudgment;" MBSR-specific decreases in PFC-posterior cingulate connectivity correlated with improved working memory. Both groups showed decreased amygdala-sensorimotor and medial-lateral PFC connectivity, which corresponded with reduced depression.

Limitations: Larger sample sizes and neuropsychological evaluations are needed to replicate and extend these findings.

Conclusion: Together, our findings suggest that MBSR and SE are similarly efficacious for depression, anxiety and autistic traits, whereas MBSR produced additional salutary effects related to executive functioning and mindfulness traits. Findings from gPPI identified shared and distinct therapeutic neural mechanisms, implicating the default mode and salience networks. Our results mark an early step toward the development of personalized medicine for psychiatric symptoms in ASD and offer novel neural targets for future neurostimulation research.

Clinical trial registration: ClinicalTrials.gov identifier NCT04017793.

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自闭症谱系障碍成人正念减压小组和社会支持减压小组的不同和共同治疗神经机制。
背景:正念减压疗法(MBSR)可减轻自闭症谱系障碍(ASD)成人的抑郁和焦虑;然而,其潜在的治疗神经机制和正念的特异性效果仍有待阐明:我们将患有自闭症谱系障碍的成年人随机分配到 MBSR 或社会支持/教育(SE)中。他们填写了评估抑郁、焦虑、正念特质、自闭症特质和执行功能能力的问卷,并完成了一项自我反省功能磁共振成像任务。我们使用重复测量协方差分析(ANCOVA)来评估行为变化。为了确定特定任务的连通性变化,我们对感兴趣区(ROIs;脑岛、杏仁核、脑嵴和前额叶皮层[PFC])进行了广义心理生理学交互作用(gPPI)功能连通性(FC)分析。我们使用皮尔逊相关性来探讨大脑与行为之间的关系:我们的最终样本包括 78 名患有 ASD 的成年人,其中 39 人接受了 MBSR,39 人接受了 SE。正念减压疗法独特地改善了执行功能能力并增加了正念特质,而MBSR和SE组都显示出抑郁、焦虑和自闭特质的减少。MBSR 特异性的丘脑胰岛功能下降与焦虑减少和正念特质(包括 "不判断 "特质)增加有关;MBSR 特异性的前额叶-后扣带回连通性下降与工作记忆改善有关。两组研究人员的杏仁核-感觉运动和内侧-外侧PFC连通性都有所下降,这与抑郁程度的降低相对应:局限性:需要更大的样本量和神经心理学评估来复制和扩展这些发现:总之,我们的研究结果表明,MBSR 和 SE 对抑郁、焦虑和自闭症特质具有相似的疗效,而 MBSR 则对执行功能和正念特质产生了额外的有益影响。gPPI 的研究结果发现了共同的和不同的治疗神经机制,这与默认模式和显著性网络有关。我们的研究结果标志着向针对 ASD 精神症状的个性化医学发展迈出了早期的一步,并为未来的神经刺激研究提供了新的神经靶点:临床试验注册:ClinicalTrials.gov 识别码 NCT04017793。
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来源期刊
CiteScore
6.80
自引率
2.30%
发文量
51
审稿时长
2 months
期刊介绍: The Journal of Psychiatry & Neuroscience publishes papers at the intersection of psychiatry and neuroscience that advance our understanding of the neural mechanisms involved in the etiology and treatment of psychiatric disorders. This includes studies on patients with psychiatric disorders, healthy humans, and experimental animals as well as studies in vitro. Original research articles, including clinical trials with a mechanistic component, and review papers will be considered.
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