Behavioral Sciences, Academic College of Tel Aviv-Yaffo, Tel Aviv, Israel..
Department of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, MB, Canada.
Biochim Biophys Acta Mol Basis Dis. 2025 Jan;1871(1):167564. doi: 10.1016/j.bbadis.2024.167564. Epub 2024 Nov 8.
Fibromyalgia (FM) is a chronic condition marked by widespread pain, fatigue, sleep problems, cognitive decline, and other symptoms. Despite extensive research, the pathophysiology of FM remains poorly understood, complicating diagnosis and treatment, which often relies on self-report questionnaires. This study explored structural and functional brain changes in women with FM, identified potential biomarkers, and examined their relationship with FM severity. MRI data from 33 female FM patients and 33 matched healthy controls were utilized, focusing on T1-weighted MRI and resting-state fMRI scans. Functional connectivity (FC) analysis was performed using a machine learning framework to differentiate FM patients from healthy controls and predict FM symptom severity. No significant differences were found in brain structural features, such as gray matter volume, white matter volume, deformation-based morphometry, and cortical thickness. However, significant differences in FC were observed between FM patients and healthy controls, particularly in the default mode network (DMN), somatomotor network (SMN), visual network (VIS), and dorsal attention network (DAN). The FC metrics were significantly associated with FM severity. Our prediction model differentiated FM patients from healthy controls with an area under the curve of 0.65. FC measures accurately estimated FM symptom severities with a significant correlation (r = 0.45, p = 0.007). Functional connections in the DMN, VIS, and DAN were crucial in determining FM severity. These findings suggest that integrating brain FC measurements could serve as valuable biomarkers for identifying FM patients from healthy individuals and predicting FM symptom severity, improving diagnostic accuracy and facilitating the development of targeted therapeutic strategies.
纤维肌痛症 (FM) 是一种慢性疾病,其特征是广泛疼痛、疲劳、睡眠问题、认知能力下降和其他症状。尽管进行了广泛的研究,但 FM 的病理生理学仍未得到很好的理解,这使得诊断和治疗变得复杂,而这些往往依赖于自我报告问卷。本研究探讨了女性纤维肌痛症患者的大脑结构和功能变化,确定了潜在的生物标志物,并研究了它们与纤维肌痛症严重程度的关系。使用来自 33 名女性纤维肌痛症患者和 33 名匹配的健康对照者的 MRI 数据,重点是 T1 加权 MRI 和静息态 fMRI 扫描。使用机器学习框架对功能连接(FC)进行分析,以区分纤维肌痛症患者和健康对照者,并预测纤维肌痛症症状的严重程度。在大脑结构特征方面,如灰质体积、白质体积、基于变形的形态测量和皮质厚度,没有发现显著差异。然而,在纤维肌痛症患者和健康对照者之间观察到功能连接的显著差异,特别是在默认模式网络(DMN)、躯体运动网络(SMN)、视觉网络(VIS)和背侧注意网络(DAN)中。FC 指标与纤维肌痛症的严重程度显著相关。我们的预测模型以 0.65 的曲线下面积区分纤维肌痛症患者和健康对照者。FC 测量值与纤维肌痛症症状严重程度的相关性显著(r=0.45,p=0.007)。DMN、VIS 和 DAN 中的功能连接对于确定纤维肌痛症的严重程度至关重要。这些发现表明,整合大脑 FC 测量值可能成为从健康个体中识别纤维肌痛症患者和预测纤维肌痛症症状严重程度的有价值的生物标志物,提高诊断准确性并促进靶向治疗策略的发展。