Understanding the mechanisms of fatigue in multiple sclerosis: linking interoception, metacognition and white matter dysconnectivity.

IF 4.1 Q1 CLINICAL NEUROLOGY Brain communications Pub Date : 2024-09-11 eCollection Date: 2024-01-01 DOI:10.1093/braincomms/fcae292
Iulia Danciut, Charlotte L Rae, Waqar Rashid, James Scott, Marco Bozzali, Mihaela Iancu, Sarah N Garfinkel, Samira Bouyagoub, Nicholas G Dowell, Dawn Langdon, Mara Cercignani
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Abstract

One of the most prominent symptoms in multiple sclerosis is pathological fatigue, often described by sufferers as one of the most debilitating symptoms, affecting quality of life and employment. However, the mechanisms of both, physical and cognitive fatigue in multiple sclerosis remain elusive. Here, we use behavioural tasks and quantitative MRI to investigate the neural correlates of interoception (the ability to sense internal bodily signals) and metacognition (the ability of the brain to assess its own performance), in modulating cognitive fatigue. Assuming that structural damage caused by multiple sclerosis pathology might impair the neural pathways subtending interoception and/or metacognition, we considered three alternative hypotheses to explain fatigue as a consequence of, respectively: (i) reduced interoceptive accuracy, (ii) reduced interoceptive insight or (iii) reduced global metacognition. We then explored associations between these behavioural measures and white matter microstructure, assessed by diffusion and magnetisation transfer MRI. Seventy-one relapsing-remitting multiple sclerosis patients participated in this cross-sectional study (mean age 43, 62% female). Patient outcomes relevant for fatigue were measured, including disability, disease duration, depression, anxiety, sleepiness, cognitive function, disease modifying treatment and quality of life. Interoceptive and metacognitive parameters were measured using heartbeat tracking and discrimination tasks, and metacognitive visual and memory tasks. MRI was performed in 69 participants, including diffusion tensor MRI, neurite orientation dispersion and density imaging and quantitative magnetisation transfer. Associations between interoception and metacognition and the odds of high cognitive fatigue were tested by unconditional binomial logistic regression. The odds of cognitive fatigue were higher in the people with low interoceptive insight (P = 0.03), while no significant relationships were found between fatigue and other interoceptive or metacognitive parameters, suggesting a specific impairment in interoceptive metacognition, rather than interoception generally, or metacognition generally. Diffusion MRI-derived fractional anisotropy and neurite density index showed significant (P < 0.05) negative associations with cognitive fatigue in a widespread bilateral white matter network. Moreover, there was a significant (P < 0.05) interaction between cognitive fatigue and interoceptive insight, suggesting that the poorer the white matter structure, the lower the interoceptive insight, and the worse the fatigue. The results point towards metacognitive impairment confined to the interoceptive domain, in relapsing-remitting patients with cognitive fatigue. The neural basis of this impairment is supported by a widespread white matter network in which loss of neurite density plays a role.

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了解多发性硬化症的疲劳机制:将内感知、元认知和白质连接障碍联系起来。
病理性疲劳是多发性硬化症最突出的症状之一,患者常把它描述为最令人衰弱的症状之一,影响生活质量和就业。然而,多发性硬化症患者的生理疲劳和认知疲劳的机制仍然难以捉摸。在这里,我们使用行为任务和定量核磁共振成像技术来研究互感(感知身体内部信号的能力)和元认知(大脑评估自身表现的能力)在调节认知疲劳方面的神经相关性。假设多发性硬化症病理造成的结构性损伤可能会损害支配内感知和/或元认知的神经通路,我们考虑了三种假设,分别将疲劳解释为:(i) 内感知准确性降低,(ii) 内感知洞察力降低或 (iii) 全局元认知降低的结果。然后,我们探讨了这些行为测量与白质微结构之间的关联,并通过弥散和磁化转移核磁共振成像进行了评估。71名复发缓解型多发性硬化症患者参与了这项横断面研究(平均年龄43岁,62%为女性)。研究测量了与疲劳相关的患者结果,包括残疾、病程、抑郁、焦虑、嗜睡、认知功能、疾病调整治疗和生活质量。使用心跳跟踪和辨别任务以及元认视觉和记忆任务测量了感知间参数和元认知参数。对 69 名参与者进行了核磁共振成像,包括弥散张量核磁共振成像、神经元取向弥散和密度成像以及定量磁化转移。通过无条件二项式逻辑回归测试了内感知和元认知与高度认知疲劳几率之间的关系。内感知洞察力低的人出现认知疲劳的几率更高(P = 0.03),而疲劳与其他内感知或元认知参数之间没有发现显著的关系,这表明内感知元认知存在特定的损伤,而不是一般的内感知或一般的元认知。弥散核磁共振成像衍生的分数各向异性和神经元密度指数显示,在广泛的双侧白质网络中,认知疲劳与分数各向异性和神经元密度指数呈显著负相关(P < 0.05)。此外,认知疲劳与感知间洞察力之间存在明显的交互作用(P < 0.05),这表明白质结构越差,感知间洞察力越低,疲劳程度越严重。研究结果表明,在认知疲劳的复发缓解型患者中,元认知障碍仅限于感知间领域。这种损伤的神经基础得到了广泛的白质网络的支持,神经元密度的损失在其中发挥了作用。
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审稿时长
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