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首页> 外文期刊>International Journal of Neuroscience >A longitudinal uncontrolled study of cerebral gray matter volume in patients receiving natalizumab for multiple sclerosis
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A longitudinal uncontrolled study of cerebral gray matter volume in patients receiving natalizumab for multiple sclerosis

机译:甲醛患者脑灰质体积的纵向不受控制的研究,Heary Saclizumab患者

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Objective: Brain atrophy in multiple sclerosis (MS) selectively affects gray matter (GM), which is highly relevant to disability and cognitive impairment. We assessed cerebral GM volume (GMV) during one year of natalizumab therapy. Design/methods: Patients with relapsing-remitting (n = 18) or progressive (n = 2) MS had MRI similar to 1 year apart during natalizumab treatment. At baseline, patients were on natalizumab for (mean +/- SD) 16.6 +/- 10.9 months with age 38.5 +/- 7.4 and disease duration 9.7 +/- 4.3 years. Results: At baseline, GMV was 664.0 +/- 56.4 ml, Expanded Disability Status Scale (EDSS) score was 2.3 +/- 2.0, timed 25-foot walk (T25FW) was 6.1+/-3.4 s; two patients (10%) had gadolinium (Gd)-enhancing lesions. At follow-up, GMV was 663.9 +/- 60.2 mL; EDSS was 2.6 +/- 2.1 and T25FW was 5.9 +/- 2.9 s. One patient had a mild clinical relapse during the observation period (0.052 annualized relapse rate for the entire cohort). No patients had Gd-enhancing lesions at follow-up. Linear mixed-effect models showed no significant change in annualized GMV [estimated mean change per year 0.338 mL, 95% confidence interval -9.66, 10.34, p = 0.94)], GM fraction (p = 0.92), whole brain parenchymal fraction (p = 0.64), T2 lesion load (p = 0.64), EDSS (p = 0.26) or T25FW (p = 0.79). Conclusions: This pilot study shows no GM atrophy during one year of natalizumab MS therapy. We also did not detect any loss of whole brain volume or progression of cerebral T2 hyperintense lesion volume during the observation period. These MRI results paralleled the lack of clinical worsening.
机译:目的:多发性硬化症(MS)的脑萎缩选择性地影响灰质(GM),这与残疾和认知障碍高度相关。我们评估了一年的Natalizumab疗法期间的脑甘型体积(GMV)。设计/方法:复发 - 延髓(n = 18)或渐进性(n = 2)MS的患者在Natalizumab治疗期间与1年相似的MRI。在基线时,患者在Natalizumab上(平均值+/-SD)16.6 +/- 10.9个月,58.5岁+/- 7.4和疾病期限9.7 +/- 4.3岁。结果:在基线,GMV为664.0 +/- 56.4 mL,扩大残疾状态规模(EDSS)得分为2.3 +/- 2.0,定时25英尺步行(T25FW)为6.1 +/- 3.4 s;两名患者(10%)有钆(GD) - 伤害病变。随访时,GMV为663.9 +/- 60.2毫升; EDSS为2.6 +/- 2.1,T25FW为5.9 +/- 2.9。一名患者在观察期间有轻度临床复发(整个队列的0.052年年度复发率)。没有患者在随访时患有GD增强病变。线性混合效应模型显示年化GMV的显着变化[每年估计平均变化0.338 mL,95%置信区间-9.66,10.34,p = 0.94)],GM分数(P = 0.92),全脑实质分数(P = 0.92)(P = 0.64),T2病变载荷(P = 0.64),EDS(P = 0.26)或T25FW(P = 0.79)。结论:该试点研究显示了在Natalizumab MS治疗的一年内没有转基因萎缩。在观察期间,我们还没有检测到任何全脑体积或脑T2超前病变体积的进展。这些MRI结果平行于缺乏临床恶化。

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