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Macro- and micro-structural insights into primary dystonia: a UK Biobank study
Journal of Neurology, Volume: 271, Issue: 3, Pages: 1416 - 1427
Swansea University Author: Grace Bailey
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DOI (Published version): 10.1007/s00415-023-12086-2
Abstract
BackgroundDystonia is a hyperkinetic movement disorder with key motor network dysfunction implicated in pathophysiology. The UK Biobank encompasses > 500,000 participants, of whom 42,565 underwent brain MRI scanning. This study applied an optimized pre-processing pipeline, aimed at better account...
Published in: | Journal of Neurology |
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ISSN: | 0340-5354 1432-1459 |
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Springer Science and Business Media LLC
2024
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URI: | https://cronfa.swan.ac.uk/Record/cronfa66534 |
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This study applied an optimized pre-processing pipeline, aimed at better accounting for artifact and improving data reliability, to assess for grey and white matter structural MRI changes between individuals diagnosed with primary dystonia and an unaffected control cohort.MethodsIndividuals with dystonia (n = 76) were identified from the UK Biobank using published algorithms, alongside an age- and sex-matched unaffected control cohort (n = 311). Grey matter morphometric and diffusion measures were assessed, together with white matter diffusion tensor and diffusion kurtosis metrics using tractography and tractometry. Post-hoc Neurite Orientation and Density Distribution Imaging (NODDI) was also undertaken for tracts in which significant differences were observed.ResultsGrey matter tremor-specific striatal differences were observed, with higher radial kurtosis. Tractography identified no white matter differences, however segmental tractometry identified localised differences, particularly in the superior cerebellar peduncles and anterior thalamic radiations, including higher fractional anisotropy and lower orientation distribution index in dystonia, compared to controls. Additional tremor-specific changes included lower neurite density index in the anterior thalamic radiations.ConclusionsAnalysis of imaging data from one of the largest dystonia cohorts to date demonstrates microstructural differences in cerebellar and thalamic white matter connections, with architectural differences such as less orientation dispersion potentially being a component of the morphological structural changes implicated in dystonia. Distinct tremor-related imaging features are also implicated in both grey and white matter.</abstract><type>Journal Article</type><journal>Journal of Neurology</journal><volume>271</volume><journalNumber>3</journalNumber><paginationStart>1416</paginationStart><paginationEnd>1427</paginationEnd><publisher>Springer Science and Business Media LLC</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint>0340-5354</issnPrint><issnElectronic>1432-1459</issnElectronic><keywords>Dystonia; MRI; Diffusion MRI; Structural MRI</keywords><publishedDay>1</publishedDay><publishedMonth>3</publishedMonth><publishedYear>2024</publishedYear><publishedDate>2024-03-01</publishedDate><doi>10.1007/s00415-023-12086-2</doi><url/><notes/><college>COLLEGE NANME</college><department>Medical School</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>MEDS</DepartmentCode><institution>Swansea University</institution><apcterm>Another institution paid the OA fee</apcterm><funders>This work was supported by an ABN/Guarantors of Brain Clinical Research Training Fellowship (520,286) and a Wellcome Trust Translation of Concept Scheme (Institutional Translational Partnership Award) (520,958). KJP is funded by an MRC Clinician-Scientist Fellowship & Transition Award (MR/P008593/1, MR/V036084/1). CMWT is supported by a Sir Henry Wellcome Fellowship (215,944/Z/19/Z) and a Veni grant from the Dutch Research Council (NWO) (17,331). 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2024-06-19T12:50:57.4548870 v2 66534 2024-05-29 Macro- and micro-structural insights into primary dystonia: a UK Biobank study 1e09a407fca9e8047e7738b18d381130 0000-0003-4646-3134 Grace Bailey Grace Bailey true false 2024-05-29 MEDS BackgroundDystonia is a hyperkinetic movement disorder with key motor network dysfunction implicated in pathophysiology. The UK Biobank encompasses > 500,000 participants, of whom 42,565 underwent brain MRI scanning. This study applied an optimized pre-processing pipeline, aimed at better accounting for artifact and improving data reliability, to assess for grey and white matter structural MRI changes between individuals diagnosed with primary dystonia and an unaffected control cohort.MethodsIndividuals with dystonia (n = 76) were identified from the UK Biobank using published algorithms, alongside an age- and sex-matched unaffected control cohort (n = 311). Grey matter morphometric and diffusion measures were assessed, together with white matter diffusion tensor and diffusion kurtosis metrics using tractography and tractometry. Post-hoc Neurite Orientation and Density Distribution Imaging (NODDI) was also undertaken for tracts in which significant differences were observed.ResultsGrey matter tremor-specific striatal differences were observed, with higher radial kurtosis. Tractography identified no white matter differences, however segmental tractometry identified localised differences, particularly in the superior cerebellar peduncles and anterior thalamic radiations, including higher fractional anisotropy and lower orientation distribution index in dystonia, compared to controls. Additional tremor-specific changes included lower neurite density index in the anterior thalamic radiations.ConclusionsAnalysis of imaging data from one of the largest dystonia cohorts to date demonstrates microstructural differences in cerebellar and thalamic white matter connections, with architectural differences such as less orientation dispersion potentially being a component of the morphological structural changes implicated in dystonia. Distinct tremor-related imaging features are also implicated in both grey and white matter. Journal Article Journal of Neurology 271 3 1416 1427 Springer Science and Business Media LLC 0340-5354 1432-1459 Dystonia; MRI; Diffusion MRI; Structural MRI 1 3 2024 2024-03-01 10.1007/s00415-023-12086-2 COLLEGE NANME Medical School COLLEGE CODE MEDS Swansea University Another institution paid the OA fee This work was supported by an ABN/Guarantors of Brain Clinical Research Training Fellowship (520,286) and a Wellcome Trust Translation of Concept Scheme (Institutional Translational Partnership Award) (520,958). KJP is funded by an MRC Clinician-Scientist Fellowship & Transition Award (MR/P008593/1, MR/V036084/1). CMWT is supported by a Sir Henry Wellcome Fellowship (215,944/Z/19/Z) and a Veni grant from the Dutch Research Council (NWO) (17,331). DKJ is supported by Wellcome Trust grants (096646/Z/11/Z and 104,943/Z/14/Z). 2024-06-19T12:50:57.4548870 2024-05-29T20:05:18.3167171 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Health Data Science Claire L. MacIver 0000-0002-5040-3487 1 Grace Bailey 0000-0003-4646-3134 2 Pedro Luque Laguna 3 Megan E. Wadon 4 Ann-Kathrin Schalkamp 5 Cynthia Sandor 6 Derek K. Jones 7 Chantal M. W. Tax 8 Kathryn J. Peall 9 66534__30574__9ae08b3c0eb644cb95d9a5cccc3874a8.pdf 65534.pdf 2024-06-07T15:18:50.9250166 Output 3960317 application/pdf Version of Record true This article is licensed under a Creative Commons Attribution 4.0 International License. true eng https://creativecommons.org/licenses/by/4.0/ |
title |
Macro- and micro-structural insights into primary dystonia: a UK Biobank study |
spellingShingle |
Macro- and micro-structural insights into primary dystonia: a UK Biobank study Grace Bailey |
title_short |
Macro- and micro-structural insights into primary dystonia: a UK Biobank study |
title_full |
Macro- and micro-structural insights into primary dystonia: a UK Biobank study |
title_fullStr |
Macro- and micro-structural insights into primary dystonia: a UK Biobank study |
title_full_unstemmed |
Macro- and micro-structural insights into primary dystonia: a UK Biobank study |
title_sort |
Macro- and micro-structural insights into primary dystonia: a UK Biobank study |
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1e09a407fca9e8047e7738b18d381130 |
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1e09a407fca9e8047e7738b18d381130_***_Grace Bailey |
author |
Grace Bailey |
author2 |
Claire L. MacIver Grace Bailey Pedro Luque Laguna Megan E. Wadon Ann-Kathrin Schalkamp Cynthia Sandor Derek K. Jones Chantal M. W. Tax Kathryn J. Peall |
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Journal of Neurology |
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10.1007/s00415-023-12086-2 |
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Springer Science and Business Media LLC |
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BackgroundDystonia is a hyperkinetic movement disorder with key motor network dysfunction implicated in pathophysiology. The UK Biobank encompasses > 500,000 participants, of whom 42,565 underwent brain MRI scanning. This study applied an optimized pre-processing pipeline, aimed at better accounting for artifact and improving data reliability, to assess for grey and white matter structural MRI changes between individuals diagnosed with primary dystonia and an unaffected control cohort.MethodsIndividuals with dystonia (n = 76) were identified from the UK Biobank using published algorithms, alongside an age- and sex-matched unaffected control cohort (n = 311). Grey matter morphometric and diffusion measures were assessed, together with white matter diffusion tensor and diffusion kurtosis metrics using tractography and tractometry. Post-hoc Neurite Orientation and Density Distribution Imaging (NODDI) was also undertaken for tracts in which significant differences were observed.ResultsGrey matter tremor-specific striatal differences were observed, with higher radial kurtosis. Tractography identified no white matter differences, however segmental tractometry identified localised differences, particularly in the superior cerebellar peduncles and anterior thalamic radiations, including higher fractional anisotropy and lower orientation distribution index in dystonia, compared to controls. Additional tremor-specific changes included lower neurite density index in the anterior thalamic radiations.ConclusionsAnalysis of imaging data from one of the largest dystonia cohorts to date demonstrates microstructural differences in cerebellar and thalamic white matter connections, with architectural differences such as less orientation dispersion potentially being a component of the morphological structural changes implicated in dystonia. Distinct tremor-related imaging features are also implicated in both grey and white matter. |
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2024-03-01T14:33:38Z |
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