Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/25702
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dc.contributor.authorHarper, L-
dc.contributor.authorLindberg, O-
dc.contributor.authorBocchetta, M-
dc.contributor.authorTodd, EG-
dc.contributor.authorStrandberg, O-
dc.contributor.authorvan Westen, D-
dc.contributor.authorStomrud, E-
dc.contributor.authorLandqvist Waldö, M-
dc.contributor.authorWahlund, L-O-
dc.contributor.authorHansson, O-
dc.contributor.authorRohrer, JD-
dc.contributor.authorSantillo, A-
dc.date.accessioned2023-01-03T18:34:53Z-
dc.date.available2023-01-03T18:34:53Z-
dc.date.issued2022-01-17-
dc.identifier.citationHarper, L. et al. (2022) 'Prenatal gyrification pattern affects age at onset in frontotemporal dementia', Cerebral Cortex, 32 (18), pp. 3937 - 3944. doi: 10.1093/cercor/bhab457.-
dc.identifier.issn1047-3211-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/25702-
dc.descriptionSupplementary data: Harper_et_al_Supplementary_211111_bhab457 (docx file) - available online at https://doi.org/10.1093/cercor/bhab457 .-
dc.description.abstractCopyright © The Author(s) 2022. The paracingulate sulcus is a tertiary sulcus formed during the third trimester. In healthy individuals paracingulate sulcation is more prevalent in the left hemisphere. The anterior cingulate and paracingulate gyri are focal points of neurodegeneration in behavioral variant frontotemporal dementia (bvFTD). This study aims to determine the prevalence and impact of paracingulate sulcation in bvFTD. Structural magnetic resonance images of individuals with bvFTD (n = 105, mean age 66.9 years), Alzheimer’s disease (n = 92, 73.3), and healthy controls (n = 110, 62.4) were evaluated using standard protocol for hemispheric paracingulate sulcal presence. No difference in left hemisphere paracingulate sulcal frequency was observed between groups; 0.72, 0.79, and 0.70, respectively, in the bvFTD, Alzheimer’s disease, and healthy control groups, (P = 0.3). A significant impact of right (but not left) hemispheric paracingulate sulcation on age at disease onset was identified in bvFTD (mean 60.4 years where absent vs. 63.8 where present [P = 0.04, Cohen’s d = 0.42]). This relationship was not observed in Alzheimer’s disease. These findings demonstrate a relationship between prenatal neuronal development and the expression of a neurodegenerative disease providing a gross morphological example of brain reserve.-
dc.description.sponsorshipWork at the Clinical Memory Research Unit Lund University was supported by the Swedish Research Council (2016–00906); the Knut and Alice Wallenberg foundation (2017–0383); the Marianne and Marcus Wallenberg foundation (2015.0125); the Strategic Research Area MultiPark (Multidisciplinary Research in Parkinson’s disease) at Lund University, the Swedish Alzheimer Foundation (AF-939932); the Swedish Brain Foundation (FO2019–0326); The Parkinson foundation of Sweden (1280/20); the Skåne University Hospital Foundation (2020-O000028); Regionalt Forskningsstöd (2020–0314); and the Swedish Federal Government under the ALF Agreement (2018-Projekt0279). Additional funding to A.F.S. was provided by the Swedish Society for Medical Research and the Bente Rexed Gersteds Foundation for Brain Research. L.H., A.F.S., and O.L. are all supported by the Schörling foundation. The UCL Dementia Research Centre is supported by Alzheimer’s Research UK, Alzheimer’s Society, Brain Research UK, and The Wolfson Foundation. This work was supported by the National Institute of Health Research UCL/H Biomedical Research Centre and the UK Dementia Research Institute, which receives its funding from UK DRI Ltd, funded by the UK Medical Research Council, Alzheimer’s Society and Alzheimer’s Research UK. J.D.R. is supported by the Miriam Marks Brain Research UK Senior Fellowship and has received funding from an Medical Research Council Clinician Scientist Fellowship (MR/M008525/1) and the NIHR Rare Disease Translational Research Collaboration (BRC149/NS/MH); the Alzheimer’s Society, UK (AS-JF-19a-004-517 to M.B.). The funding sources had no role in the design and conduct of the study; in the collection, analysis, interpretation of the data; or in the preparation, review, or approval of the manuscript.-
dc.format.extent3937 - 3944-
dc.format.mediumPrint-Electronic-
dc.languageEnglish-
dc.publisherOxford University Press-
dc.rightsCopyright © The Author(s) 2022. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.titlePrenatal gyrification pattern affects age at onset in frontotemporal dementia-
dc.typeJournal Article-
dc.identifier.doihttps://doi.org/10.1093/cercor/bhab457-
dc.relation.isPartOfCerebral Cortex-
pubs.issue18-
pubs.publication-statusPublished-
pubs.volume32-
dc.identifier.eissn1460-2199-
dc.rights.holderThe Author(s)-
Appears in Collections:Dept of Life Sciences Research Papers

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