Giovannoni G, Thorpe J W, Kidd D, Kendall B E, Moseley I F, Thompson A J, Keir G, Miller D H, Feldmann M, Thompson E J
Institute of Neurology, Department of Neuroimmunology, London, UK.
J Neurol Neurosurg Psychiatry. 1996 Jan;60(1):20-6. doi: 10.1136/jnnp.60.1.20.
To determine whether concentrations of soluble E-selectin (sE-selectin), an immunological marker of endothelial activation, were correlated with gadolinium-DPTA enhancement on MRI in patients with multiple sclerosis.
Serial sE-selectin concentrations were measured in 28 patients with multiple sclerosis undergoing monthly gadolinium (Gd) enhanced MRI of the brain and spinal cord, and in 10 control subjects. C reactive protein (CRP), von Willebrand factor (vWF), and tumour necrosis factor-alpha (TNF alpha) were also determined.
Primary progressive patients had significantly increased sE-selectin concentrations compared with the relapsing remitting and secondary progressive patients who had normal sE-selectin concentrations (22.2 (SD1 6.1) ng/ml v 9.8 (SD2.1) ng/ml and 7.7 (SD2.7) ng/ml, respectively, P = 0.03). This difference was attributable to five of the 10 primary progressive patients who had persistently raised sE-selectin concentrations, with relatively inactive MRI studies. No correlation could be found between sE-selectin concentrations and Gd enhancement on MRI, but a close correlation existed between mean concentrations of sE-selectin and TNF alpha (r = 0.71, P < 0.001). Despite raised sE-selectin and TNF alpha concentrations, primary progressive patients had normal CRP concentrations (1.03 (SD1.14) mg/l), which were significantly lower than the relapsing remitting (3.16 (SD2.54) mg/l) and secondary progressive patients (2.28 (SD2.1) mg/l, P = 0.03). Raised CRP concentrations did correlate with infectious episodes, clinical relapse, and Gd enhancement, and were significantly raised when no MRI activity was found. Concentrations of vWF were normal in all patient groups.
The results further high-light the differences between patients with primary progressive and those with relapsing remitting/secondary progressive multiple sclerosis.
确定可溶性E选择素(sE选择素)(一种内皮细胞活化的免疫标志物)的浓度与多发性硬化症患者MRI钆-二乙三胺五醋酸(Gd-DPTA)增强是否相关。
对28例接受脑部和脊髓每月一次钆(Gd)增强MRI检查的多发性硬化症患者以及10名对照者进行系列sE选择素浓度测定。同时还测定了C反应蛋白(CRP)、血管性血友病因子(vWF)和肿瘤坏死因子-α(TNFα)。
与复发缓解型和继发进展型患者(其sE选择素浓度正常,分别为9.8(标准差2.1)ng/ml和7.7(标准差2.7)ng/ml)相比,原发进展型患者的sE选择素浓度显著升高(22.2(标准差6.1)ng/ml,P = 0.03)。这种差异归因于10例原发进展型患者中的5例,其sE选择素浓度持续升高,而MRI检查相对不活跃。sE选择素浓度与MRI的Gd增强之间未发现相关性,但sE选择素平均浓度与TNFα之间存在密切相关性(r = 0.71,P < 0.001)。尽管原发进展型患者的sE选择素和TNFα浓度升高,但其CRP浓度正常(1.03(标准差1.14)mg/l),显著低于复发缓解型患者(3.16(标准差2.54)mg/l)和继发进展型患者(2.28(标准差2.1)mg/l,P = 0.03)。CRP浓度升高确实与感染发作、临床复发和Gd增强相关,且在未发现MRI活动时显著升高。所有患者组的vWF浓度均正常。
结果进一步凸显了原发进展型多发性硬化症患者与复发缓解型/继发进展型多发性硬化症患者之间的差异。