School of Health Sciences, Faculty of Health and Medicine, University of Newcastle, Callaghan, NSW, 2308, Australia; Hunter Medical Research Institute, 1 Kookaburra Circuit, New Lambton, NSW, 2305, Australia.
The Russell H. Morgan Department of Radiology and Radiological Science, the Johns Hopkins University School of Medicine, Baltimore, MD, USA; F. M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore MD, USA.
Eur J Radiol. 2021 Apr;137:109610. doi: 10.1016/j.ejrad.2021.109610. Epub 2021 Feb 24.
Fatigue is a common symptom in patients with multiple sclerosis (MS) with unknown pathophysiology. Dysfunction of the GABAergic/glutamatergic pathways involving inhibitory and excitatory neurotransmitters such as γ-aminobutyric acid (GABA) and glutamine + glutamate pool (Glx) have been implicated in several neurological disorders. This study is aimed to evaluate the potential role of GABA and Glx in the origin of central fatigue in relapse remitting MS (RRMS) patients.
24 RRMS patients and 16 age- and sex-matched healthy controls (HC) were scanned using Mescher-Garwood point resolved spectroscopy (MEGA-PRESS) with a 3 T system to quantify GABA+ and Glx from prefrontal (PFC) and sensorimotor (SMC) cortices. Self-reported fatigue status was measured on all participants using the Modified Fatigue Impact Scale (MFIS).
RRMS patients had higher fatigue scores relative to HC (p ≤ 0.05). Compared to HC, Glx levels in RRMS patients were significantly decreased in SMC (p = 0.04). Significant correlations were found between fatigue scores and GABA+ (r = -0.531, p = 0.008) and Glx (r = 0.511, p = 0.018) in PFC. Physical fatigue was negatively correlated with GABA+ in SMC and PFC (r = -0.428 and -0.472 respectively, p ≤ 0.04) and positively with PFC Glx (r = 0.480, p = 0.028).
The associations between fatigue and GABA + and Glx suggest that there might be dysregulation of GABAergic/glutamatergic neurotransmission in the pathophysiological mechanism of central fatigue in MS.
疲劳是多发性硬化症(MS)患者的常见症状,但病因的病理生理学机制尚不清楚。涉及抑制性和兴奋性神经递质(如γ-氨基丁酸(GABA)和谷氨酰胺+谷氨酸池(Glx))的 GABA 能/谷氨酸能通路功能障碍与几种神经疾病有关。本研究旨在评估 GABA 和 Glx 在复发缓解型多发性硬化症(RRMS)患者中枢疲劳发生中的潜在作用。
使用 3T 系统的 Mescher-Garwood 点分辨波谱(MEGA-PRESS)对 24 名 RRMS 患者和 16 名年龄和性别匹配的健康对照者(HC)进行扫描,以从前额叶(PFC)和感觉运动(SMC)皮质定量测量 GABA+和 Glx。所有参与者均使用改良疲劳影响量表(MFIS)评估疲劳状况。
RRMS 患者的疲劳评分高于 HC(p≤0.05)。与 HC 相比,RRMS 患者 SMC 中的 Glx 水平明显降低(p=0.04)。在 PFC 中,疲劳评分与 GABA+(r=-0.531,p=0.008)和 Glx(r=0.511,p=0.018)呈显著相关。在 SMC 和 PFC 中,躯体疲劳与 GABA+呈负相关(r=-0.428 和 -0.472,分别为 p≤0.04),与 PFC Glx 呈正相关(r=0.480,p=0.028)。
疲劳与 GABA+和 Glx 之间的相关性表明,在 MS 中枢疲劳的病理生理机制中,可能存在 GABA 能/谷氨酸能神经传递的失调。