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亨廷顿病患者脑白质结构损伤的区域分布与临床相关性:基于束路径的空间统计学研究。

Regional distribution and clinical correlates of white matter structural damage in Huntington disease: a tract-based spatial statistics study.

机构信息

Radiodiagnostic Unit, San Giuseppe Hospital, Empoli, Italy.

出版信息

AJNR Am J Neuroradiol. 2010 Oct;31(9):1675-81. doi: 10.3174/ajnr.A2128. Epub 2010 May 20.

DOI:10.3174/ajnr.A2128
PMID:20488902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7964981/
Abstract

BACKGROUND AND PURPOSE

HD entails damage of the WM. Our aim was to explore in vivo the regional volume and microstructure of the brain WM in HD and to correlate such findings with clinical status of the patients.

MATERIALS AND METHODS

Fifteen HD gene carriers in different clinical stages of the disease and 15 healthy controls were studied with T1-weighted images for VBM and DTI for TBSS. Maps of FA, MD, and λ∥ and λ⊥ were reconstructed.

RESULTS

Compared with controls, in addition to neostriatum and cortical GM volume loss, individuals with HD showed volume loss in the genu of the internal capsule and subcortical frontal WM bilaterally, the right splenium of the corpus callosum, and the left corona radiata. TBSS revealed symmetrically decreased FA in the corpus callosum, fornix, external/extreme capsule, inferior fronto-occipital fasciculus, and inferior longitudinal fasciculus. Areas of increased MD were more extensive and included arciform fibers of the cerebral hemispheres and cerebral peduncles. Increase of the λ∥ and a comparatively more pronounced increase of the λ⊥ underlay the decreased FA of the WM in HD. Areas of WM atrophy, decreased FA, and increased MD correlated with the severity of the motor and cognitive dysfunction, whereas only the areas with increased MD correlated with disease duration.

CONCLUSIONS

Microstructural damage accompanies volume decrease of the WM in HD and is correlated with the clinical deficits and disease duration. MR imaging-based measures could be considered as a biomarker of neurodegeneration in HD gene carriers.

摘要

背景与目的

HD 会导致 WM 损伤。我们的目的是在体内探索 HD 患者大脑 WM 的局部体积和微观结构,并将这些发现与患者的临床状况相关联。

材料与方法

对 15 名处于不同疾病临床阶段的 HD 基因携带者和 15 名健康对照者进行 T1 加权成像 VBM 和 DTI 用于 TBSS 分析。重建 FA、MD、λ∥和 λ⊥图。

结果

与对照组相比,HD 患者除了新纹状体和皮质 GM 体积损失外,还表现出内囊体部和双侧皮质下额 WM、右侧胼胝体体部和左侧放射冠的体积损失。TBSS 显示胼胝体、穹窿、外/极部、下额枕束和下纵束的 FA 对称性降低。MD 增加的区域更为广泛,包括大脑半球和脑干的弓状纤维。WM 中 FA 的降低伴随着 λ∥的增加和 λ⊥的相对更明显增加。WM 萎缩、FA 降低和 MD 增加的区域与运动和认知功能障碍的严重程度相关,而只有 MD 增加的区域与疾病持续时间相关。

结论

HD 患者 WM 的微观结构损伤伴随着体积减少,与临床缺陷和疾病持续时间相关。基于磁共振成像的测量可被视为 HD 基因携带者神经退行性变的生物标志物。

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