4.5 Article

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

期刊

NEUROIMAGE-CLINICAL
卷 24, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2019.102054

关键词

Motor neuron disease; Amyotrophic lateral sclerosis; Primary lateral sclerosis; Longitudinal study; Brainstem; Medulla; Pons; Mesencephalon; Neuroimaging

资金

  1. Health Research Board [HRB EIA-2017-019]
  2. Andrew Lydon scholarship
  3. Irish Institute of Clinical Neuroscience (IICN)
  4. Iris O'Brien Foundation
  5. Research Motor Neuron (RMN-Ireland) Foundation
  6. Irish Motor Neuron Disease Association (IMNDA)
  7. Motor Neurone Disease Association [957-799]
  8. Science Foundation Ireland [17/CDA/4737, 15/SPP/3244]
  9. Science Foundation Ireland (SFI) [15/SPP/3244] Funding Source: Science Foundation Ireland (SFI)

向作者/读者索取更多资源

Background: Brainstem 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. Methods: A 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. Results: ALS 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 PIS patients. Conclus: ions: 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.

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