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Brainstem pathology in amyotrophic lateral sclerosis and primary lateral sclerosis: A longitudinal neuroimaging study

机译:肌萎缩性侧索硬化和原发性侧索硬化的脑干病理学:一项纵向神经影像学研究

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BackgroundBrainstem pathology is a hallmark feature of ALS, yet most imaging studies focus on cortical grey matter alterations and internal capsule white matter pathology. Brainstem imaging in ALS provides a unique opportunity to appraise descending motor tract degeneration and bulbar lower motor neuron involvement.MethodsA prospective longitudinal imaging study has been undertaken with 100 patients with ALS, 33 patients with PLS, 30 patients with FTD and 100 healthy controls. Volumetric, vertex and morphometric analyses were conducted correcting for demographic factors to characterise disease-specific patterns of brainstem pathology. Using a Bayesian segmentation algorithm, the brainstem was segmented into the medulla, pons and mesencephalon to measure regional volume reductions, shape analyses were performed to ascertain the atrophy profile of each study group and region-of-interest morphometry was used to evaluate focal density alterations.ResultsALS and PLS patients exhibit considerable brainstem atrophy compared to both disease- and healthy controls. Volume reductions in ALS and PLS are dominated by medulla oblongata pathology, but pontine atrophy can also be detected. In ALS, vertex analyses confirm the flattening of the medullary pyramids bilaterally in comparison to healthy controls and widespread pontine shape deformations in contrast to PLS. The ALS cohort exhibit bilateral density reductions in the mesencephalic crura in contrast to healthy controls, central pontine atrophy compared to disease controls, peri-aqueduct mesencephalic and posterior pontine changes in comparison to PLS patients.Conclusions: Computational brainstem imaging captures the degeneration of both white and grey matter components in ALS. Our longitudinal data indicate progressive brainstem atrophy over time, underlining the biomarker potential of quantitative brainstem measures in ALS. At a time when a multitude of clinical trials are underway worldwide, there is an unprecedented need for accurate biomarkers to monitor disease progression and detect response to therapy. Brainstem imaging is a promising addition to candidate biomarkers of ALS and PLS.
机译:背景脑干病理学是ALS的标志性特征,但是大多数影像学研究集中于皮质灰质改变和内囊白质病理学。方法ALS的脑干成像为评估下降的运动系统变性和延髓下运动神经元受累提供了独特的机会。方法前瞻性纵向成像研究已对100例ALS患者,33例PLS患者,30例FTD患者和100名健康对照者进行了研究。进行了体积,顶点和形态分析,校正了人口统计学因素,以表征特定于脑干病理的疾病模式。使用贝叶斯分割算法,将脑干分为延髓,脑桥和中脑,以测量区域体积减少,进行形状分析以确定每个研究组的萎缩状况,并使用感兴趣区域形态来评估病灶密度变化结果与疾病和健康对照组相比,ALS和PLS患者表现出明显的脑干萎缩。 ALS和PLS的体积减少主要受延髓病理的影响,但也可检测到桥脑萎缩。在ALS中,与健康对照相比,顶点分析证实了双侧髓质锥体的扁平化,而与PLS相比,它证实了桥脑的广泛形变。与PLS患者相比,ALS队列与健康对照,与疾病对照相比,中脑桥中央萎缩,中导水管周围中脑和桥后后方改变相比,中脑小腿的双侧密度降低。结论:计算机脑干成像可捕捉到两个白人的变性和ALS中的灰质成分。我们的纵向数据显示随着时间的推移,进行性脑干萎缩,突显了ALS中定量脑干测量的生物标志物潜力。在全球范围内进行大量临床试验之际,前所未有的需要精确的生物标记物来监测疾病的进展并检测对治疗的反应。脑干成像是ALS和PLS候选生物标志物的有希望的补充。

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