Robayo Linda E, Govind Varan, Salan Teddy, Cherup Nicholas P, Sheriff Sulaiman, Maudsley Andrew A, Widerström-Noga Eva
The Miami Project to Cure Paralysis, University of Miami, Miami, FL, United States.
Neuroscience Graduate Program, University of Miami, Miami, FL, United States.
Front Neurosci. 2023 Feb 23;17:1125128. doi: 10.3389/fnins.2023.1125128. eCollection 2023.
Traumatic brain injury (TBI) can lead to a variety of comorbidities, including chronic pain. Although brain tissue metabolite alterations have been extensively examined in several chronic pain populations, it has received less attention in people with TBI. Thus, the primary aim of this study was to compare brain tissue metabolite levels in people with TBI and chronic pain ( = 16), TBI without chronic pain ( = 17), and pain-free healthy controls ( = 31). The metabolite data were obtained from participants using whole-brain proton magnetic resonance spectroscopic imaging (H-MRSI) at 3 Tesla. The metabolite data included -acetylaspartate, -inositol, total choline, glutamate plus glutamine, and total creatine. Associations between -acetylaspartate levels and pain severity, neuropathic pain symptom severity, and psychological variables, including anxiety, depression, post-traumatic stress disorder (PTSD), and post-concussive symptoms, were also explored. Our results demonstrate -acetylaspartate, -inositol, total choline, and total creatine alterations in pain-related brain regions such as the frontal region, cingulum, postcentral gyrus, and thalamus in individuals with TBI with and without chronic pain. Additionally, NAA levels in the left and right frontal lobe regions were positively correlated with post-concussive symptoms; and NAA levels within the left frontal region were also positively correlated with neuropathic pain symptom severity, depression, and PTSD symptoms in the TBI with chronic pain group. These results suggest that neuronal integrity or density in the prefrontal cortex, a critical region for nociception and pain modulation, is associated with the severity of neuropathic pain symptoms and psychological comorbidities following TBI. Our data suggest that a combination of neuronal loss or dysfunction and maladaptive neuroplasticity may contribute to the development of persistent pain following TBI, although no causal relationship can be determined based on these data.
创伤性脑损伤(TBI)可导致多种合并症,包括慢性疼痛。尽管在多个慢性疼痛人群中已对脑组织代谢物改变进行了广泛研究,但在创伤性脑损伤患者中却较少受到关注。因此,本研究的主要目的是比较创伤性脑损伤伴慢性疼痛患者(n = 16)、创伤性脑损伤不伴慢性疼痛患者(n = 17)和无疼痛的健康对照者(n = 31)的脑组织代谢物水平。代谢物数据通过在3特斯拉条件下对参与者进行全脑质子磁共振波谱成像(H-MRSI)获得。代谢物数据包括N-乙酰天门冬氨酸、肌醇、总胆碱、谷氨酸加谷氨酰胺以及总肌酸。还探讨了N-乙酰天门冬氨酸水平与疼痛严重程度、神经性疼痛症状严重程度以及心理变量(包括焦虑、抑郁、创伤后应激障碍(PTSD)和脑震荡后症状)之间的关联。我们的结果表明,在有和没有慢性疼痛的创伤性脑损伤个体中,额叶、扣带回、中央后回和丘脑等与疼痛相关的脑区存在N-乙酰天门冬氨酸、肌醇、总胆碱和总肌酸的改变。此外,左右额叶区域的NAA水平与脑震荡后症状呈正相关;在伴有慢性疼痛的创伤性脑损伤组中,左侧额叶区域内的NAA水平还与神经性疼痛症状严重程度、抑郁和PTSD症状呈正相关。这些结果表明,前额叶皮质作为伤害感受和疼痛调节的关键区域,其神经元完整性或密度与创伤性脑损伤后神经性疼痛症状的严重程度和心理合并症有关。我们的数据表明,神经元丢失或功能障碍与适应性不良的神经可塑性相结合可能导致创伤性脑损伤后持续性疼痛的发生,尽管基于这些数据无法确定因果关系。