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MRI 脑白质消融性白质营养不良自然史

MRI Natural History of the Leukodystrophy Vanishing White Matter.

机构信息

From the Department of Child Neurology, Emma Children's Hospital, Amsterdam University Medical Centers, Vrije Universiteit and Amsterdam Neuroscience, De Boelelaan 1117, Amsterdam 1081 HV, the Netherlands (M.D.S., M.L.A., M.S.v.d.K.); Department of Epidemiology and Data Science, Amsterdam University Medical Centers, Amsterdam, the Netherlands (T.v.d.B.); Department of Radiology and Nuclear Medicine, Amsterdam University Medical Center, Vrije Universiteit and Amsterdam Neuroscience, Amsterdam, the Netherlands (F.B., P.J.W.P.); Institutes of Neurology and Health Care Engineering, University College London, London, England (F.B.); and Department of Functional Genomics, Center for Neurogenomics and Cognitive Research, VU University, Amsterdam, the Netherlands (M.S.v.d.K.).

出版信息

Radiology. 2021 Sep;300(3):671-680. doi: 10.1148/radiol.2021210110. Epub 2021 Jun 29.

Abstract

Background In vanishing white matter (VWM), a form of leukodystrophy, earlier onset is associated with faster clinical progression. MRI typically shows rarefaction and cystic destruction of the cerebral white matter. Information on the evolution of VWM according to age at onset is lacking. Purpose To determine whether nature and progression of cerebral white matter abnormalities in VWM differ according to age at onset. Materials and Methods Patients with genetically confirmed VWM were stratified into six groups according to age at onset: younger than 1 year, 1 year to younger than 2 years, 2 years to younger than 4 years, 4 years to younger than 8 years, 8 years to younger than 18 years, and 18 years or older. With institutional review board approval, all available MRI scans obtained between 1985 and 2019 were retrospectively analyzed with three methods: ratio of the width of the lateral ventricles over the skull (ventricle-to-skull ratio [VSR]) was measured to estimate brain atrophy; cerebral white matter was visually scored as percentage normal, hyperintense, rarefied, or cystic on fluid-attenuated inversion recovery (FLAIR) images and converted into a white matter decay score; and the intracranial volume was segmented into normal-appearing white and gray matter, abnormal but structurally present (FLAIR-hyperintense) and rarefied or cystic (FLAIR-hypointense) white matter, and ventricular and extracerebral cerebrospinal fluid (CSF). Multilevel regression analyses with patient as a clustering variable were performed to account for the nested data structure. Results A total of 461 examinations in 270 patients (median age, 7 years [interquartile range, 3-18 years]; 144 female patients) were evaluated; 112 patients had undergone serial imaging. Patients with later onset had higher VSR [F(5) = 8.42; < .001] and CSF volume [F(5) = 21.7; < .001] and lower white matter decay score [F(5) = 4.68; < .001] and rarefied or cystic white matter volume [F(5) = 13.3; < .001]. Rate of progression of white matter decay scores [b = -1.6, t(109) = -3.9; < .001] and VSRs [b = -0.05, t (109) = -3.7; < .001] were lower with later onset. Conclusion A radiologic spectrum based on age at onset exists in vanishing white matter. The earlier the onset, the faster and more cystic the white matter decay, whereas with later onset, white matter atrophy and gliosis predominate. © RSNA, 2021.

摘要

背景 在脑白质消失症(VWM)中,一种白质营养不良,发病年龄越早,临床进展越快。MRI 通常显示脑白质稀疏和囊性破坏。关于发病年龄与 VWM 病变演变之间关系的信息尚缺乏。

目的 确定 VWM 患者的发病年龄不同时,脑白质异常的性质和进展是否存在差异。

材料与方法 经基因证实的 VWM 患者根据发病年龄分为 6 组:小于 1 岁、1 岁至小于 2 岁、2 岁至小于 4 岁、4 岁至小于 8 岁、8 岁至小于 18 岁、以及 18 岁及以上。本研究经机构审查委员会批准,回顾性分析了 1985 年至 2019 年间所有可用的 MRI 扫描,采用 3 种方法:通过测量侧脑室与颅骨的宽度比(脑室-颅骨比[VSR])评估脑萎缩;通过液体衰减反转恢复(FLAIR)图像将脑白质视觉评分转化为正常、高信号、稀疏或囊性的百分比,以转化为白质衰减评分;以及对颅内容积进行分割,分为正常外观的白质和灰质、异常但结构存在(FLAIR 高信号)、稀疏或囊性(FLAIR 低信号)白质、脑室和脑外脑脊液(CSF)。采用患者为聚类变量的多水平回归分析来解释嵌套数据结构。

结果 共评估了 270 例患者的 461 次检查(中位年龄为 7 岁[四分位数范围,3-18 岁];144 例为女性患者);112 例患者进行了连续影像学检查。发病年龄较晚的患者 VSR[F(5)=8.42;<.001]和 CSF 容积[F(5)=21.7;<.001]更高,白质衰减评分[F(5)=4.68;<.001]和稀疏或囊性白质容积[F(5)=13.3;<.001]更低。白质衰减评分的进展速度[b=-1.6,t(109)=-3.9;<.001]和 VSR [b=-0.05,t(109)=-3.7;<.001]也随着发病年龄的延迟而降低。

结论 在 VWM 中,存在基于发病年龄的影像学谱。发病年龄越早,脑白质的破坏就越快,囊性成分越多,而发病年龄较晚的患者则以脑白质萎缩和神经胶质增生为主。

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