13 Hypermobility and autonomic dysfunction: insights from bench to bedside

J. Eccles
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Abstract

Dr Jessica Eccles trained in medicine at University of Cambridge and University of Oxford, completing a BA in The History and Philosophy of Science, sparking a keen interest in philosophy of mind and brain-body interactions. Since graduation from medical school has pursued a combined academic clinical path at Brighton and Sussex Medical School. As an MRC Clinical Research Training Fellow she recently completed her PhD in the relationship between joint hypermobility, autonomic dysfunction and psychiatric symptoms and is now an NIHR Clinical Lecturer. She is currently working on an Academy of Medical Sciences grant to explore neural connectivity in hypermobility using leading edge Human Connectome Project techniques and has recently been awarded a MQ Arthritis Research UK Fellows Award to conduct a randomised clinical trial of a new targeted treatment for anxiety in hypermobility. Dr Eccles has also been awarded a grant from Dysautonomia International and will be working with Profs Critchley, Cercignani, Rowe, Murphy and Drs Nagai, Asslanni, Iodice and Giovanni to explore multi-modal correlates of ‘brain fog’ in Postural Tachycardia Syndrome. Dr Eccles is working with Profs Davies, Harrison, Cercignani, Critchley and Dr Tarzi to explore brain- body interactions in Fibromyalgia and ME/CFS. This involves autonomics, inflammatory and cytokine markers, brain imaging and genomics. This work is funded by Versus Arthritis and Action for ME Alongside clinical academic colleagues at BSMS, Prof Harrison and Dr Colasanti. Joint hypermobility is a common, yet poorly recognised variant of connective tissue affecting up to 20% of the population. Hypermobility is a cardinal feature of Hyermobility Spectrum Disorder (HSD) and hypermobile Ehlers Danlos Syndrome (hEDS), inherited disorders of connective tissue. Individuals with joint hypermobility are over represented in panic, anxiety and neurodevelopmental populations and are prone to dysautonomia, typically postural tachycardia syndrome (PoTS), in which there is a phenomenological overlap with anxiety disorder. Interestingly differences in brain structure and function have been described in hypermobility in regions associated with emotional processing, including amygdala and insula. Individuals with joint hypermobility are more likely to experience severe chronic widespread pain, and many have co-morbid rheumatic conditions. A data-driven theoretical model linking joint hypermobility to psychiatric disorder is proposed, characterised by aberrant autonomic control and central representation, grounded in current theoretical models that seek to frame emotion as interoceptive inference, using leading-edge predictive coding approaches. Ultimately this approach has considerable relevance to personalised psychiatric medicine in this disorder and greater understanding of brain-body mechanisms underpinning neuropsychiatric states.
过度活动和自主神经功能障碍:从实验到临床的见解
杰西卡·埃克尔斯博士曾在剑桥大学和牛津大学接受医学培训,获得了科学历史和哲学学士学位,引发了她对心灵和脑-体相互作用哲学的浓厚兴趣。从医学院毕业后,他在布莱顿和苏塞克斯医学院进行了综合学术临床研究。作为MRC临床研究培训研究员,她最近完成了关节过度活动,自主神经功能障碍和精神症状之间关系的博士学位,现在是NIHR临床讲师。她目前正在接受医学科学院的资助,利用尖端的人类连接组项目技术探索多动症的神经连通性,最近还获得了MQ关节炎研究英国研究员奖,进行了一项针对多动症焦虑的新靶向治疗的随机临床试验。Eccles博士还获得了国际自主神经异常协会的资助,他将与Critchley、Cercignani、Rowe、Murphy教授以及Nagai、Asslanni、Iodice和Giovanni博士合作,探索体位性心动过速综合征中“脑雾”的多模态相关性。埃克尔斯博士正在与戴维斯教授、哈里森教授、Cercignani教授、克里奇利教授和塔兹博士合作,探索纤维肌痛和ME/CFS的脑-体相互作用。这涉及到自主神经、炎症和细胞因子标记、脑成像和基因组学。这项工作是由抗关节炎和ME行动以及BSMS的临床学术同事Harrison教授和Colasanti博士资助的。关节过度活动是一种常见的结缔组织,但很少被认识到,影响到20%的人口。多动性是多动性谱系障碍(HSD)和多动性Ehlers Danlos综合征(hEDS)的主要特征,后者是遗传性结缔组织疾病。关节活动过度的个体在恐慌、焦虑和神经发育人群中被过度代表,并且容易出现自主神经异常,典型的体位性心动过速综合征(PoTS),在现象上与焦虑障碍有重叠。有趣的是,在与情绪处理相关的区域(包括杏仁核和脑岛)中,大脑结构和功能的差异被描述为多动症。关节活动过度的个体更有可能经历严重的慢性广泛性疼痛,许多人还伴有风湿病。提出了一个数据驱动的理论模型,将关节过度活动与精神障碍联系起来,其特征是异常的自主控制和中央表征,基于当前的理论模型,这些理论模型试图将情感框架化为内感受推理,使用领先的预测编码方法。最终,这种方法与针对这种疾病的个性化精神医学以及对支撑神经精神状态的脑-体机制的更深入理解具有相当大的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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