Quantitative MRI of dorsal root ganglion alterations in neurofibromatosis type 1 patients with or without pain.

IF 3.7 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Magnus Schindehütte, Eva Meller, Thomas Kampf, Florian Hessenauer, Nurcan Üçeyler, György Homola, Heike L Rittner, Cordula Matthies, Mirko Pham, Simon Weiner
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引用次数: 0

Abstract

Background: Neurofibromatosis type 1 (NF1) is a genetic disorder characterised by skin and nervous system anomalies, primarily involving glial cells and nerve tumours. Pain, particularly chronic pain, is a significant but often overlooked symptom in NF1 patients, affecting their health-related quality of life. The dorsal root ganglion (DRG) is essential for pain signal transmission, yet in vivo studies of DRG in NF1 patients are lacking.

Methods: This prospective study included 20 NF1 patients (8 with neuropathic pain) and 28 healthy controls. Magnetic resonance imaging (MRI) scans of lumbosacral DRG (L5 + S1) were performed using a 3-T scanner. Quantitative MRI techniques were applied to assess DRG volume, T2 relaxation time, and proton density (PD). Statistical analyses compared NF1 patients and controls, and NF1 patients with and without pain.

Results: NF1 patients had a significantly larger DRG volume and higher quantitative T2 and PD values compared to controls. Furthermore, DRG PD was significantly higher in NF1 patients with neuropathic pain than in those without pain. Receiver operator characteristic curve analysis identified DRG PD as the best discriminator of pain in NF1 patients, with an area under the curve of 0.84, indicating relevant and useful discriminatory power.

Conclusion: NF1 patients showed objective macrostructural and microstructural DRG injury changes using dedicated DRG MRI, discriminating neuropathic pain status from non-pain status at the disease-symptom group level. These findings highlight the potential of DRG MRI to quantify DRG pathology in vivo and to determine the risk of functional pain status by imaging.

Relevance statement: The identification of structural and microstructural changes of the DRG by quantitative MRI provides a novel in vivo biomarker for understanding neuropathic pain mechanisms, pain risk assessment and treatment monitoring in NF1.

Key points: Dorsal root ganglia (DRG) in NF1 are enlarged by 176.3% in MRI. In quantitative MRI of DRG NF1, T2 relaxation time is increased by 22.9% and PD by 8.4%. DRG PD can distinguish a painful from a non-painful NF1 phenotype.

有或无疼痛的1型神经纤维瘤病患者背根神经节改变的定量MRI。
背景:1型神经纤维瘤病(NF1)是一种以皮肤和神经系统异常为特征的遗传性疾病,主要累及神经胶质细胞和神经肿瘤。疼痛,特别是慢性疼痛,是NF1患者的一个重要但经常被忽视的症状,影响他们与健康相关的生活质量。背根神经节(DRG)对疼痛信号传递至关重要,但缺乏NF1患者的体内研究。方法:本前瞻性研究纳入20例NF1患者(8例伴有神经性疼痛)和28例健康对照。使用3-T扫描仪对腰骶DRG (L5 + S1)进行磁共振成像(MRI)扫描。定量MRI技术评估DRG体积、T2弛豫时间和质子密度(PD)。统计分析比较NF1患者和对照组,NF1患者有和没有疼痛。结果:与对照组相比,NF1患者的DRG体积和定量T2和PD值显著增加。此外,伴有神经性疼痛的NF1患者的DRG PD显著高于无疼痛的NF1患者。受试者操作者特征曲线分析发现DRG PD是NF1患者疼痛的最佳鉴别指标,曲线下面积为0.84,表明鉴别能力相关且有用。结论:专用DRG MRI显示NF1患者DRG损伤的宏观结构和微观结构的客观改变,在疾病症状组水平上区分神经性疼痛状态和非疼痛状态。这些发现强调了DRG MRI在量化体内DRG病理和通过成像确定功能性疼痛状态风险方面的潜力。相关声明:通过定量MRI识别DRG的结构和微观结构变化,为了解NF1的神经性疼痛机制、疼痛风险评估和治疗监测提供了一种新的体内生物标志物。重点:NF1的背根神经节(Dorsal root ganglia, DRG) MRI增宽176.3%。DRG NF1定量MRI显示T2弛豫时间增加22.9%,PD增加8.4%。DRG PD可以区分疼痛型和非疼痛型NF1表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Radiology Experimental
European Radiology Experimental Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
6.70
自引率
2.60%
发文量
56
审稿时长
18 weeks
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