4.7 Review

Structural magnetic resonance imaging in dystonia: A systematic review of methodological approaches and findings

期刊

EUROPEAN JOURNAL OF NEUROLOGY
卷 29, 期 11, 页码 3418-3448

出版社

WILEY
DOI: 10.1111/ene.15483

关键词

diffusion MRI; dystonia; movement disorders; MRI; systematic review

资金

  1. ABN/Guarantors of Brain Clinical Research Training Fellowship [520286]
  2. Wellcome Trust translation of concept scheme [520958]

向作者/读者索取更多资源

This review summarizes the methodological approaches used in structural brain imaging studies of dystonia cohorts and identifies commonly implicated pathways, networks, or regions in pathogenesis. The findings suggest microstructural brain changes in individuals diagnosed with dystonia, although the underlying nature of these changes remains unknown. The use of techniques such as multiple diffusion weightings or multi-exponential relaxometry has the potential to enhance understanding of these differences.
Background and purpose Structural magnetic resonance techniques have been widely applied in neurological disorders to better understand tissue changes, probing characteristics such as volume, iron deposition and diffusion. Dystonia is a hyperkinetic movement disorder, resulting in abnormal postures and pain. Its pathophysiology is poorly understood, with normal routine clinical imaging in idiopathic forms. More advanced tools provide an opportunity to identify smaller scale structural changes which may underpin pathophysiology. This review aims to provide an overview of methodological approaches undertaken in structural brain imaging of dystonia cohorts, and to identify commonly identified pathways, networks or regions that are implicated in pathogenesis. Methods Structural magnetic resonance imaging studies of idiopathic and genetic forms of dystonia were systematically reviewed. Adhering to strict inclusion and exclusion criteria, PubMed and Embase databases were searched up to January 2022, with studies reviewed for methodological quality and key findings. Results Seventy-seven studies were included, involving 1945 participants. The majority of studies employed diffusion tensor imaging (DTI) (n = 45) or volumetric analyses (n = 37), with frequently implicated areas of abnormality in the brainstem, cerebellum, basal ganglia and sensorimotor cortex and their interconnecting white matter pathways. Genotypic and motor phenotypic variation emerged, for example fewer cerebello-thalamic tractography streamlines in genetic forms than idiopathic and higher grey matter volumes in task-specific than non-task-specific dystonias. Discussion Work to date suggests microstructural brain changes in those diagnosed with dystonia, although the underlying nature of these changes remains undetermined. Employment of techniques such as multiple diffusion weightings or multi-exponential relaxometry has the potential to enhance understanding of these differences.

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