Loane Clare, Politis Marios, Kefalopoulou Zinovia, Valle-Guzman Natalie, Paul Gesine, Widner Hakan, Foltynie Thomas, Barker Roger A, Piccini Paola
Neurology Imaging Unit, Hammersmith Hospital, Imperial College London, London, UK.
Neurodegeneration Imaging Group, Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), King's College London, London, UK.
Mov Disord. 2016 Jul;31(7):1020-6. doi: 10.1002/mds.26606. Epub 2016 Apr 22.
Measuring microstructure alterations with diffusion tensor imaging in PD is potentially a valuable tool to use as a biomarker for early diagnosis and to track disease progression. Previous studies have reported a specific decrease of nigral fractional anisotropy in PD. However, to date the effect of disease progression on nigral or striatal diffusion indices has not been fully explored.
We have conducted a cross-sectional and longitudinal diffusion tensor imaging study in 18 early stage, treated PD patients and 14 age-matched controls. PD patients were scanned on 2 occasions OFF medication, 19.3 months apart (standard deviation = 3.1 months). Longitudinal change of regional nigral and striatal measures of fractional anisotropy and mean diffusivity were calculated using a region-of-interest approach.
Region-of-interest analysis demonstrated that at baseline, PD patients and controls did not differ in regard to diffusion indices in any region assessed. A significant difference of nigral fractional anisotropy and mean diffusivity between controls and PD patients at follow-up was detected and confirmed with longitudinal analysis within PD patients. Alterations in striatal regions were not detected in either group or over time.
Our findings indicate that nigral diffusion measure may be a valuable measure of disease progression. In the future, larger longitudinal studies will confirm whether diffusion indices may serve as sensitive and clinically meaningful measures of disease progression in PD. © 2016 International Parkinson and Movement Disorder Society.
利用扩散张量成像测量帕金森病(PD)患者的微观结构改变,可能是一种有价值的工具,可作为早期诊断的生物标志物并追踪疾病进展。先前的研究报道了PD患者黑质各向异性分数的特异性降低。然而,迄今为止,疾病进展对黑质或纹状体扩散指数的影响尚未得到充分研究。
我们对18例早期接受治疗的PD患者和14例年龄匹配的对照者进行了横断面和纵向扩散张量成像研究。PD患者在未服药状态下进行了2次扫描,间隔19.3个月(标准差=3.1个月)。采用感兴趣区域法计算黑质和纹状体区域各向异性分数和平均扩散率的纵向变化。
感兴趣区域分析表明,在基线时,PD患者和对照者在任何评估区域的扩散指数方面均无差异。随访时检测到对照者与PD患者之间黑质各向异性分数和平均扩散率存在显著差异,并通过对PD患者的纵向分析得到证实。两组在纹状体区域均未检测到随时间的变化。
我们的研究结果表明,黑质扩散测量可能是疾病进展的一项有价值的指标。未来,更大规模的纵向研究将证实扩散指数是否可作为PD疾病进展的敏感且具有临床意义的指标。©2016国际帕金森病和运动障碍协会。