Association between brain metabolism and clinical course of motor functional neurological disorders.

I. Conejero, L. Collombier, J. López-Castromán, T. Mura, S. Alonso, E. Olié, V. Boudousq, Fabrice Boulet, C. Arquizan, Charlotte Boulet, A. Wacongne, C. Heitz, C. Castelli, S. Mouchabac, P. Courtet, M. Abbar, E. Thouvenot
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引用次数: 5

Abstract

Features of resting brain metabolism in motor functional neurological disorder are poorly characterized. This study aimed to investigate the alterations of resting brain metabolism in a cohort of patients experiencing a first episode of motor functional neurological disorder with recent symptom onset, and their association with persistent disability after 3 months. Patients eligible for inclusion were diagnosed with first episode of motor functional neurological disorder, were free from bipolar disorder, substance use disorder, schizophrenia, psychogenic non-epileptic seizure or any chronic or acute organic neurological disorder. Exclusion criteria included current suicidal ideation, antipsychotic intake and previous history of functional neurological disorder. Nineteen patients were recruited in Psychiatry and Neurology departments from 2 hospitals. Resting brain metabolism measured with 18F-fluorodeoxyglucose positron emission computed tomography at baseline and 3 months was compared to 23 controls without neurological impairment. Disability was scored using Expanded Disability Status Scale and National Institutes of Health Stroke Scale score at baseline and 3 months. Correlations were calculated with Spearman correlation coefficient. Hypometabolism was found at baseline in bilateral frontal regions in patients versus controls, disappearing by 3 months. The patients with Expanded Disability Status Scale score improvement showed greater resting state activity of prefrontal dorsolateral cortex, right orbito-frontal cortex and bilateral frontopolar metabolism at 3 months versus other patients. The resting state metabolism of the right subgenual anterior cingular cortex at baseline was negatively correlated with improvement of motor disability (measured with Expanded Disability Status Scale) between inclusion and 3 months (r=-0.75, p = 0.0018) and with change in motor symptoms assessed with the National Institutes of Health Stroke Scale (r=-0.81, p= 0.0005). The resting state metabolism of the left subgenual anterior cingular cortex at baseline was negatively correlated with improvement in Expanded Disability Status Scale and National Institutes of Health Stroke Scale scores between inclusion and 3 months (r= -0.65, p = 0.01 and r= -0.75, p = 0.0021, respectively). The negative association between the brain metabolism of the right subgenual anterior cingular cortex at baseline and change in National Institutes of Health Stroke Scale score remained significant (r=-0.81, p= 0.0414) after correction for multiple comparisons. Our findings suggest the existence of metabolic "state markers" associated with motor disability and that brain markers are associated with motor recovery in functional neurological disorder patients.
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脑代谢与运动功能神经障碍临床病程的关系。
运动功能性神经障碍的静息脑代谢特征尚不清楚。本研究旨在探讨一组新近出现症状的首发运动功能神经障碍患者静息脑代谢的变化及其与3个月后持续性残疾的关系。符合纳入条件的患者被诊断为首次发作的运动功能神经障碍,无双相情感障碍、物质使用障碍、精神分裂症、心因性非癫痫性发作或任何慢性或急性器质性神经障碍。排除标准包括目前有自杀意念、服用抗精神病药物和既往功能性神经障碍史。从两家医院的精神科和神经科招募了19名患者。在基线和3个月时,用18f -氟脱氧葡萄糖正电子发射计算机断层扫描测量静息脑代谢,并与23名无神经损伤的对照组进行比较。在基线和3个月时使用扩展残疾状态量表和美国国立卫生研究院卒中量表对残疾进行评分。用Spearman相关系数计算相关性。与对照组相比,患者双侧额叶区基线代谢降低,3个月后消失。与其他患者相比,扩展残疾状态量表评分改善的患者在3个月时前额叶背外侧皮层、右眶额叶皮层和双侧额极代谢的静息状态活动更高。基线时右侧膝下前扣带皮层的静息状态代谢与纳入组至3个月期间运动障碍的改善(用扩展残疾状态量表测量)呈负相关(r=-0.75, p= 0.0018),与美国国立卫生研究院卒中量表评估的运动症状的改变呈负相关(r=-0.81, p= 0.0005)。基线时左侧亚属前扣带皮层的静息状态代谢与纳入组至3个月间扩展残疾状态量表和美国国立卫生研究院卒中量表评分的改善呈负相关(r= -0.65, p = 0.01和r= -0.75, p = 0.0021)。在多重比较校正后,基线时右侧亚属前扣带皮层脑代谢与美国国立卫生研究院卒中量表评分变化之间的负相关仍然显著(r=-0.81, p= 0.0414)。我们的研究结果表明,存在与运动障碍相关的代谢“状态标记”,以及与功能性神经障碍患者的运动恢复相关的脑标记。
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