Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/25701
Full metadata record
DC FieldValueLanguage
dc.contributor.authorParker, CS-
dc.contributor.authorVeale, T-
dc.contributor.authorBocchetta, M-
dc.contributor.authorSlattery, CF-
dc.contributor.authorMalone, IB-
dc.contributor.authorThomas, DL-
dc.contributor.authorSchott, JM-
dc.contributor.authorCash, DM-
dc.contributor.authorZhang, H-
dc.contributor.otherAlzheimer's Disease Neuroimaging Initiative-
dc.date.accessioned2023-01-03T18:09:28Z-
dc.date.available2023-01-03T18:09:28Z-
dc.date.issued2021-11-28-
dc.identifierORCID iD: Martina Bocchetta https://orcid.org/0000-0003-1814-5024-
dc.identifier118749-
dc.identifier.citationParker, C.S. et al. on behalf of the Alzheimer's Disease Neuroimaging Initiative (2021) 'Not all voxels are created equal: Reducing estimation bias in regional NODDI metrics using tissue-weighted means', NeuroImage, 245, 118749, pp. 1 - 11. doi: 10.1016/j.neuroimage.2021.118749.en_US
dc.identifier.issn1053-8119-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/25701-
dc.descriptionData and code availability: Code used in calculating the tissue-weighting mean is available here: https://github.com/tdveale/NODDI-tissue-weighting-tool. ROI data and other scripts used in this analysis are available on request and without restriction by contacting the corresponding author. Acquired or processed NIfTI images are not available due to patient confidentiality agreements.en_US
dc.descriptionData used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at: http://adni.loni.usc.edu/wp-content/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf-
dc.descriptionAppendix: Table A1 available at https://www.sciencedirect.com/science/article/pii/S1053811921010211?via%3Dihub#tbl0001 ; Appendix B. Supplementary materials available at https://ars.els-cdn.com/content/image/1-s2.0-S1053811921010211-mmc1.docx (Word document (3MB)).-
dc.description.abstractCopyright © 2021 The Authors. Neurite orientation dispersion and density imaging (NODDI) estimates microstructural properties of brain tissue relating to the organisation and processing capacity of neurites, which are essential elements for neuronal communication. Descriptive statistics of NODDI tissue metrics are commonly analyzed in regions-of-interest (ROI) to identify brain-phenotype associations. Here, the conventional method to calculate the ROI mean weights all voxels equally. However, this produces biased estimates in the presence of CSF partial volume. This study introduces the tissue-weighted mean, which calculates the mean NODDI metric across the tissue within an ROI, utilising the tissue fraction estimate from NODDI to reduce estimation bias. We demonstrate the proposed mean in a study of white matter abnormalities in young onset Alzheimer's disease (YOAD). Results show the conventional mean induces significant bias that correlates with CSF partial volume, primarily affecting periventricular regions and more so in YOAD subjects than in healthy controls. Due to the differential extent of bias between healthy controls and YOAD subjects, the conventional mean under- or over-estimated the effect size for group differences in many ROIs. This demonstrates the importance of using the correct estimation procedure when inferring group differences in studies where the extent of CSF partial volume differs between groups. These findings are robust across different acquisition and processing conditions. Bias persists in ROIs at higher image resolution, as demonstrated using data obtained from the third phase of the Alzheimer's disease neuroimaging initiative (ADNI); and when performing ROI analysis in template space. This suggests that conventional ROI means of NODDI metrics are biased estimates under most contemporary experimental conditions, the correction of which requires the proposed tissue-weighted mean. The tissue-weighted mean produces accurate estimates of ROI means and group differences when ROIs contain voxels with CSF partial volume. In addition to NODDI, the technique can be applied to other multi-compartment models that account for CSF partial volume, such as the free water elimination method. We expect the technique to help generate new insights into normal and abnormal variation in tissue microstructure of regions typically confounded by CSF partial volume, such as those in individuals with larger ventricles due to atrophy associated with neurodegenerative disease.en_US
dc.description.sponsorshipCP and GZ were funded by the Wellcome Trust (Collaborative Award 200181/Z/15/Z). TV was funded by an Alzheimer's Research UK PhD scholarship (ARUK-PhD2018–009). MB was supported by a Fellowship award from the Alzheimer's Society, UK (AS-JF-19a-004–517). MB's work was also supported by the UK Dementia Research Institute which receives its funding from DRI Ltd, funded by the UK Medical Research Council, Alzheimer's Society and Alzheimer's Research UK. IM was supported by Alzheimer's Research UK (ARUK-PG2014–1946, ARUK-PG2017–1946) and the Wolfson Foundation (PR/ylr/18575). DLT was supported by the UCL Leonard Wolfson Experimental Neurology Centre (PR/ylr/18575), UCLH NIHR Biomedical Research Centre and the Wellcome Trust (Centre award 539208). JMS acknowledges the support of the National Institute for Health Research University College London Hospitals Biomedical Research Centre, Wolfson Foundation, Alzheimer's Research UK, Brain Research UK, Weston Brain Institute, Medical Research Council, British Heart Foundation, UK Dementia Research Institute and Alzheimer's Association. DMC was supported by the UK Dementia Research Institute which receives its funding from DRI Ltd, funded by the UK Medical Research Council, Alzheimer's Society and Alzheimer's Research UK, as well as Alzheimer's Research UK (ARUK‐PG2017‐1946) and the UCL/UCLH NIHR Biomedical Research Centre. We would also like to acknowledge Prof. Nick Fox who is a senior NIHR investigator for his role in conceiving the initial YOAD study preceding this work. The authors would like to thank all research participants who made this study possible, as well as Alzheimer's Research UK and Iceland Foods Charitable Foundation for funding the Young-Onset Alzheimer's disease study. The Dementia Research Centre is supported by Alzheimer's Research UK, Brain Research Trust, and The Wolfson Foundation. They also thank Kirsty Lu, Amelia Carton, Timothy Shakespeare, Keir Yong, Aida Suarez Gonzalez and Silvia Primativo for assistance with neuropsychology assessments.en_US
dc.format.extent1 - 11-
dc.format.mediumPrint-Electronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.rightsCopyright © 2021 The Authors. Published by Elsevier Inc. under a Creative Commons license (https://creativecommons.org/licenses/by/4.0/).-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectdiffusion MRIen_US
dc.subjectmicrostructure imagingen_US
dc.subjectregion-of-interesten_US
dc.subjectarithmetic meanen_US
dc.subjecttissue-weighted meanen_US
dc.titleNot all voxels are created equal: Reducing estimation bias in regional NODDI metrics using tissue-weighted meansen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1016/j.neuroimage.2021.118749-
dc.relation.isPartOfNeuroImage-
pubs.publication-statusPublished-
pubs.volume245-
dc.identifier.eissn1095-9572-
dc.rights.holderThe Authors-
Appears in Collections:Dept of Life Sciences Research Papers

Files in This Item:
File Description SizeFormat 
FullText.pdfCopyright © 2021 The Authors. Published by Elsevier Inc. under a Creative Commons license (https://creativecommons.org/licenses/by/4.0/).2.63 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons