Deppe Michael, Krämer Julia, Tenberge Jan-Gerd, Marinell Jasmin, Schwindt Wolfram, Deppe Katja, Groppa Sergiu, Wiendl Heinz, Meuth Sven G
Department of Neurology, Westfälische Wilhelms University, Münster, Germany.
Department of Clinical Radiology, Westfälische Wilhelms University, Münster, Germany.
Hum Brain Mapp. 2016 May;37(5):1866-79. doi: 10.1002/hbm.23144. Epub 2016 Feb 27.
Recent studies on patients with clinically isolated syndrome (CIS) and multiple sclerosis (MS) demonstrated thalamic atrophy. Here we addressed the following question: Is early thalamic atrophy in patients with CIS and relapsing-remitting MS (RRMS) mainly a direct consequence of white matter (WM) lesions-as frequently claimed-or is the atrophy stronger correlated to "silent" (nonlesional) microstructural thalamic alterations? One-hundred and ten patients with RRMS, 12 with CIS, and 30 healthy controls were admitted to 3 T magnetic resonance imaging. Fractional anisotropy (FA) was computed from diffusion tensor imaging (DTI) to assess thalamic and WM microstructure. The relative thalamic volume (RTV) and thalamic FA were significantly reduced in patients with CIS and RRMS relative to healthy controls. Both measures were also correlated. The age, gender, WM lesion load, thalamic FA, and gray matter volume-corrected RTV were reduced even in the absence of thalamic and extensive white matter lesions-also in patients with short disease duration (≤24 months). A voxel-based correlation analysis revealed that the RTV reduction had a significant effect on local WM FA-in areas next to the thalamus and basal ganglia. These WM alterations could not be explained by WM lesions, which had a differing spatial distribution. Early thalamic atrophy is mainly driven by silent microstructural thalamic alterations. Lesions do not disclose the early damage of thalamocortical circuits, which seem to be much more affected in CIS and RRMS than expected. Thalamocortical damage can be detected by DTI in normal appearing brain tissue. Hum Brain Mapp 37:1866-1879, 2016. © 2016 Wiley Periodicals, Inc.
近期针对临床孤立综合征(CIS)和多发性硬化症(MS)患者的研究显示存在丘脑萎缩。在此我们探讨了以下问题:CIS和复发缓解型多发性硬化症(RRMS)患者早期出现的丘脑萎缩,主要是如人们常说的那样,是白质(WM)病变的直接后果,还是这种萎缩与“沉默”(无病变)的丘脑微观结构改变关联更强?110例RRMS患者、12例CIS患者和30名健康对照者接受了3T磁共振成像检查。通过扩散张量成像(DTI)计算分数各向异性(FA),以评估丘脑和白质的微观结构。与健康对照者相比,CIS和RRMS患者的相对丘脑体积(RTV)和丘脑FA显著降低。这两项指标也具有相关性。即使在没有丘脑和广泛白质病变的情况下,甚至在病程较短(≤24个月)的患者中,年龄、性别、白质病变负荷、丘脑FA和经灰质体积校正的RTV也有所降低。基于体素的相关性分析显示,RTV降低对丘脑和基底神经节旁区域的局部白质FA有显著影响。这些白质改变无法用具有不同空间分布的白质病变来解释。早期丘脑萎缩主要由沉默的丘脑微观结构改变驱动。病变并未揭示丘脑皮质回路的早期损伤,而在CIS和RRMS中,丘脑皮质回路似乎比预期受影响更大。通过DTI可在外观正常的脑组织中检测到丘脑皮质损伤。《人类大脑图谱》37:1866 - 1879, 2016。© 2016威利期刊公司。