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Adapting UK Biobank imaging for use in a routine memory clinic setting: The Oxford Brain Health Clinic
The Oxford Brain Health Clinic (BHC) is a joint clinical-research service that provides memory clinic patients and clinicians access to high-quality assessments not routinely available, including brain MRI aligned with the UK Biobank imaging study (UKB). In this work we present how we 1) adapted the...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723313/ https://www.ncbi.nlm.nih.gov/pubmed/36451375 http://dx.doi.org/10.1016/j.nicl.2022.103273 |
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author | Griffanti, Ludovica Gillis, Grace O'Donoghue, M. Clare Blane, Jasmine Pretorius, Pieter M. Mitchell, Robert Aikin, Nicola Lindsay, Karen Campbell, Jon Semple, Juliet Alfaro-Almagro, Fidel Smith, Stephen M. Miller, Karla L. Martos, Lola Raymont, Vanessa Mackay, Clare E. |
author_facet | Griffanti, Ludovica Gillis, Grace O'Donoghue, M. Clare Blane, Jasmine Pretorius, Pieter M. Mitchell, Robert Aikin, Nicola Lindsay, Karen Campbell, Jon Semple, Juliet Alfaro-Almagro, Fidel Smith, Stephen M. Miller, Karla L. Martos, Lola Raymont, Vanessa Mackay, Clare E. |
author_sort | Griffanti, Ludovica |
collection | PubMed |
description | The Oxford Brain Health Clinic (BHC) is a joint clinical-research service that provides memory clinic patients and clinicians access to high-quality assessments not routinely available, including brain MRI aligned with the UK Biobank imaging study (UKB). In this work we present how we 1) adapted the UKB MRI acquisition protocol to be suitable for memory clinic patients, 2) modified the imaging analysis pipeline to extract measures that are in line with radiology reports and 3) explored the alignment of measures from BHC patients to the largest brain MRI study in the world (ultimately 100,000 participants). Adaptations of the UKB acquisition protocol for BHC patients include dividing the scan into core and optional sequences (i.e., additional imaging modalities) to improve patients’ tolerance for the MRI assessment. We adapted the UKB structural MRI analysis pipeline to take into account the characteristics of a memory clinic population (e.g., high amount of white matter hyperintensities and hippocampal atrophy). We then compared the imaging derived phenotypes (IDPs) extracted from the structural scans to visual ratings from radiology reports, non-imaging factors (age, cognition) and to reference distributions derived from UKB data. Of the first 108 BHC attendees (August 2020-November 2021), 92.5 % completed the clinical scans, 88.0 % consented to use of data for research, and 43.5 % completed the additional research sequences, demonstrating that the protocol is well tolerated. The high rates of consent to research makes this a valuable real-world quality research dataset routinely captured in a clinical service. Modified tissue-type segmentation with lesion masking greatly improved grey matter volume estimation. CSF-masking marginally improved hippocampal segmentation. The IDPs were in line with radiology reports and showed significant associations with age and cognitive performance, in line with the literature. Due to the age difference between memory clinic patients of the BHC (age range 65–101 years, average 78.3 years) and UKB participants (44–82 years, average 64 years), additional scans on elderly healthy controls are needed to improve reference distributions. Current and future work aims to integrate automated quantitative measures in the radiology reports and evaluate their clinical utility. |
format | Online Article Text |
id | pubmed-9723313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97233132022-12-07 Adapting UK Biobank imaging for use in a routine memory clinic setting: The Oxford Brain Health Clinic Griffanti, Ludovica Gillis, Grace O'Donoghue, M. Clare Blane, Jasmine Pretorius, Pieter M. Mitchell, Robert Aikin, Nicola Lindsay, Karen Campbell, Jon Semple, Juliet Alfaro-Almagro, Fidel Smith, Stephen M. Miller, Karla L. Martos, Lola Raymont, Vanessa Mackay, Clare E. Neuroimage Clin Regular Article The Oxford Brain Health Clinic (BHC) is a joint clinical-research service that provides memory clinic patients and clinicians access to high-quality assessments not routinely available, including brain MRI aligned with the UK Biobank imaging study (UKB). In this work we present how we 1) adapted the UKB MRI acquisition protocol to be suitable for memory clinic patients, 2) modified the imaging analysis pipeline to extract measures that are in line with radiology reports and 3) explored the alignment of measures from BHC patients to the largest brain MRI study in the world (ultimately 100,000 participants). Adaptations of the UKB acquisition protocol for BHC patients include dividing the scan into core and optional sequences (i.e., additional imaging modalities) to improve patients’ tolerance for the MRI assessment. We adapted the UKB structural MRI analysis pipeline to take into account the characteristics of a memory clinic population (e.g., high amount of white matter hyperintensities and hippocampal atrophy). We then compared the imaging derived phenotypes (IDPs) extracted from the structural scans to visual ratings from radiology reports, non-imaging factors (age, cognition) and to reference distributions derived from UKB data. Of the first 108 BHC attendees (August 2020-November 2021), 92.5 % completed the clinical scans, 88.0 % consented to use of data for research, and 43.5 % completed the additional research sequences, demonstrating that the protocol is well tolerated. The high rates of consent to research makes this a valuable real-world quality research dataset routinely captured in a clinical service. Modified tissue-type segmentation with lesion masking greatly improved grey matter volume estimation. CSF-masking marginally improved hippocampal segmentation. The IDPs were in line with radiology reports and showed significant associations with age and cognitive performance, in line with the literature. Due to the age difference between memory clinic patients of the BHC (age range 65–101 years, average 78.3 years) and UKB participants (44–82 years, average 64 years), additional scans on elderly healthy controls are needed to improve reference distributions. Current and future work aims to integrate automated quantitative measures in the radiology reports and evaluate their clinical utility. Elsevier 2022-11-21 /pmc/articles/PMC9723313/ /pubmed/36451375 http://dx.doi.org/10.1016/j.nicl.2022.103273 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Regular Article Griffanti, Ludovica Gillis, Grace O'Donoghue, M. Clare Blane, Jasmine Pretorius, Pieter M. Mitchell, Robert Aikin, Nicola Lindsay, Karen Campbell, Jon Semple, Juliet Alfaro-Almagro, Fidel Smith, Stephen M. Miller, Karla L. Martos, Lola Raymont, Vanessa Mackay, Clare E. Adapting UK Biobank imaging for use in a routine memory clinic setting: The Oxford Brain Health Clinic |
title | Adapting UK Biobank imaging for use in a routine memory clinic setting: The Oxford Brain Health Clinic |
title_full | Adapting UK Biobank imaging for use in a routine memory clinic setting: The Oxford Brain Health Clinic |
title_fullStr | Adapting UK Biobank imaging for use in a routine memory clinic setting: The Oxford Brain Health Clinic |
title_full_unstemmed | Adapting UK Biobank imaging for use in a routine memory clinic setting: The Oxford Brain Health Clinic |
title_short | Adapting UK Biobank imaging for use in a routine memory clinic setting: The Oxford Brain Health Clinic |
title_sort | adapting uk biobank imaging for use in a routine memory clinic setting: the oxford brain health clinic |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723313/ https://www.ncbi.nlm.nih.gov/pubmed/36451375 http://dx.doi.org/10.1016/j.nicl.2022.103273 |
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