Rovaris M, Viti B, Ciboddo G, Gerevini S, Capra R, Iannucci G, Comi G, Filippi M
Neuroimaging Research Unit, Department of Neuroscience, Hopital San Raffaele, Milan, Italy.
J Neurol Neurosurg Psychiatry. 2000 Feb;68(2):170-7. doi: 10.1136/jnnp.68.2.170.
Magnetisation transfer imaging (MTI) provides information about brain damage with increased pathological specificity over conventional MRI and detects subtle abnormalities in the normal appearing brain tissue, which go undetected with conventional scanning. Brain MRI and MTI findings were compared in patients with multiple sclerosis (MS) and systemic immune mediated diseases (SIDs) affecting the CNS to investigate their roles in understanding the nature of brain damage in these diseases.
Brain dual echo, T1 weighted and MTI scans were obtained in patients affected by systemic lupus erithematosus (SLE) with (NSLE, n=9) and without clinical CNS involvement (n=15), Behçet's disease (BD) (n=5), Wegener's granulomatosis (WG) (n=9), and antiphospholipid antibody syndrome (APLAS) (n=6). Ten patients with clinically definite MS and 15 healthy controls also underwent the same scanning protocol. Brain MRI and MT ratio (MTR) images of the same subject were coregistered and postprocessed to obtain MTR histograms of the whole brain and of the NABT.
Brain hyperintense lesions were found in all patients with MS and with NSLE and in 5/15 patients with SLE, 5/9 with WG, 1/5 with BD, and 3/6 with APLAS. The lesion burden in the brain was significantly higher in patients with MS compared with all the other disease groups. All MTR histogram parameters were significantly different among patient subgroups. Patients with MS had significantly lower average MTR than all except patients with NSLE and significantly lower peak height and location than patients with SLE. patients with NSLE had significantly lower average MTR than patients with SLE.
Microscopic brain tissue damage is relevant in patients with MS, but, apart from patients with NSLE, it seems to be absent in systemic immune mediated diseases, even in the presence of macroscopic MRI lesions or clinical evidence of CNS involvement.
与传统磁共振成像(MRI)相比,磁化传递成像(MTI)能提供关于脑损伤的信息,且具有更高的病理特异性,可检测出常规扫描未发现的正常脑组织中的细微异常。对患有多发性硬化症(MS)和影响中枢神经系统(CNS)的系统性免疫介导疾病(SIDs)的患者进行脑MRI和MTI检查结果的比较,以研究它们在理解这些疾病中脑损伤本质方面的作用。
对患有系统性红斑狼疮(SLE)且有(神经精神性狼疮,n = 9)和无临床CNS受累(n = 15)、白塞病(BD)(n = 5)、韦格纳肉芽肿病(WG)(n = 9)以及抗磷脂抗体综合征(APLAS)(n = 6)的患者进行脑双回波、T1加权和MTI扫描。10例临床确诊的MS患者和15名健康对照者也接受相同的扫描方案。对同一受试者的脑MRI和MT比率(MTR)图像进行配准和后处理,以获得全脑和正常表观脑白质(NABT)的MTR直方图。
在所有MS患者、神经精神性狼疮患者以及15例SLE患者中的5例、9例WG患者中的5例、5例BD患者中的1例、6例APLAS患者中的3例中发现脑高信号病变。与所有其他疾病组相比,MS患者的脑内病变负荷显著更高。患者亚组间所有MTR直方图参数均有显著差异。除神经精神性狼疮患者外,MS患者的平均MTR显著低于所有其他患者,且其峰值高度和位置显著低于SLE患者。神经精神性狼疮患者的平均MTR显著低于SLE患者。
微观脑组织损伤在MS患者中较为常见,但除神经精神性狼疮患者外,在系统性免疫介导疾病中似乎不存在,即使存在宏观MRI病变或CNS受累的临床证据。