Testud Benoit, Delacour Clara, El Ahmadi Ahmed Ali, Brun Gilles, Girard Nadine, Duhamel Guillaume, Heesen Christoph, Häußler Vivien, Thaler Christian, Has Silemek Arzu Ceylan, Stellmann Jan-Patrick
CEMEREM, APHM La Timone, Marseille, France.
Aix Marseille Univ, CNRS, CRMBM, Marseille, France, Marseille, France.
Eur J Neurol. 2022 Jun;29(6):1741-1752. doi: 10.1111/ene.15289. Epub 2022 Mar 1.
Extent and dynamic of neurodegeneration in progressive multiple sclerosis (MS) might be reflected by global and regional brain perfusion, an outcome at the intercept between structure and function. Here, we provide a first insight into the evolution of brain perfusion and its association with disability in primary progressive MS (PPMS) over several years.
Seventy-seven persons with PPMS were followed over up to 5 years. Visits included a 3-T magnetic resonance imaging with pulsed arterial spin labelling perfusion, the Timed 25-Foot Walk, 9-Hole Peg Test (NHPT), Symbol Digit Modalities Test (SDMT), and Expanded Disability Status Scale (EDSS). We extracted regional cerebral blood flow surrogates and compared them to 11 controls. Analyses focused on cortical and deep grey matter, the change over time, and associations with disability on the regional and global levels.
Baseline brain perfusion of patients and controls was comparable for the cortex (p = 0.716) and deep grey matter (p = 0.095). EDSS disability increased mildly (p = 0.023), whereas brain perfusion decreased during follow-up (p < 0.001) and with disease duration (p = 0.009). Lower global perfusion correlated with higher disability as indicated by EDSS, NHPT, and Timed 25-Foot Walk (p < 0.001). The motor task NHPT showed associations with 20 grey matter regions. In contrast, better SDMT performance correlated with lower perfusion (p < 0.001) in seven predominantly frontal regions, indicating a functional maladaptation.
Decreasing perfusion indicates a putative association with MS disease mechanisms such as neurodegeneration, reduced metabolism, and loss of resilience. A low alteration rate limits its use in clinical practice, but regional association patterns might provide a snapshot of adaptive and maladaptive functional reorganization.
进展性多发性硬化症(MS)中神经退行性变的程度和动态变化可能通过全脑和局部脑灌注反映出来,脑灌注是结构与功能相互作用的结果。在此,我们首次深入了解了原发性进展性MS(PPMS)患者脑灌注的演变及其与残疾的相关性,随访时间长达数年。
对77例PPMS患者进行了长达5年的随访。每次随访均包括3-T磁共振成像及动脉自旋标记脉冲灌注成像、25英尺计时步行测试、9孔插钉试验(NHPT)、符号数字模式测验(SDMT)以及扩展残疾状态量表(EDSS)评估。我们提取了局部脑血流量替代指标,并与11名对照者进行比较。分析重点在于皮质和深部灰质、随时间的变化以及局部和整体水平上与残疾的相关性。
患者和对照者的皮质(p = 0.716)和深部灰质(p = 0.095)基线脑灌注相当。随访期间EDSS残疾程度轻度增加(p = 0.023),而脑灌注下降(p < 0.001),且与病程相关(p = 0.009)。如EDSS、NHPT和25英尺计时步行测试所示,较低的全脑灌注与较高的残疾程度相关(p < 0.001)。运动任务NHPT显示与20个灰质区域存在关联。相比之下,SDMT表现较好与7个主要为额叶区域的较低灌注相关(p < 0.001),表明存在功能适应不良。
灌注降低表明可能与MS疾病机制如神经退行性变、代谢降低和恢复力丧失有关。较低的变化率限制了其在临床实践中的应用,但局部关联模式可能提供适应性和适应不良性功能重组的快照。