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dc.contributor.authorSteinbart, D
dc.contributor.authorYaakub, SN
dc.contributor.authorSteinbrenner, M
dc.contributor.authorGuldin, LS
dc.contributor.authorHoltkamp, M
dc.contributor.authorKeller, SS
dc.contributor.authorWeber, B
dc.contributor.authorRüber, T
dc.contributor.authorHeckemann, RA
dc.contributor.authorIlyas‐Feldmann, M
dc.contributor.authorHammers, A
dc.date.accessioned2023-04-24T12:29:58Z
dc.date.available2023-04-24T12:29:58Z
dc.date.issued2023-04-13
dc.identifier.issn1065-9471
dc.identifier.issn1097-0193
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/20753
dc.description.abstract

The piriform cortex (PC) is located at the junction of the temporal and frontal lobes. It is involved physiologically in olfaction as well as memory and plays an important role in epilepsy. Its study at scale is held back by the absence of automatic segmentation methods on MRI. We devised a manual segmentation protocol for PC volumes, integrated those manually derived images into the Hammers Atlas Database (n = 30) and used an extensively validated method (multi-atlas propagation with enhanced registration, MAPER) for automatic PC segmentation. We applied automated PC volumetry to patients with unilateral temporal lobe epilepsy with hippocampal sclerosis (TLE; n = 174 including n = 58 controls) and to the Alzheimer's Disease Neuroimaging Initiative cohort (ADNI; n = 151, of whom with mild cognitive impairment (MCI), n = 71; Alzheimer's disease (AD), n = 33; controls, n = 47). In controls, mean PC volume was 485 mm3 on the right and 461 mm3 on the left. Automatic and manual segmentations overlapped with a Jaccard coefficient (intersection/union) of ~0.5 and a mean absolute volume difference of ~22 mm3 in healthy controls, ~0.40/ ~28 mm3 in patients with TLE, and ~ 0.34/~29 mm3 in patients with AD. In patients with TLE, PC atrophy lateralised to the side of hippocampal sclerosis (p < .001). In patients with MCI and AD, PC volumes were lower than those of controls bilaterally (p < .001). Overall, we have validated automatic PC volumetry in healthy controls and two types of pathology. The novel finding of early atrophy of PC at the stage of MCI possibly adds a novel biomarker. PC volumetry can now be applied at scale.

dc.format.extent3196-3209
dc.format.mediumPrint-Electronic
dc.languageen
dc.publisherWiley
dc.subjectHammers Atlas Database
dc.subjecthippocampal sclerosis
dc.subjectMAPER
dc.subjectmild cognitive impairment
dc.subjectmorphometry
dc.titleAutomatic and manual segmentation of the piriform cortex: Method development and validation in patients with temporal lobe epilepsy and Alzheimer's disease
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37052063
plymouth.issue8
plymouth.volume44
plymouth.publisher-urlhttp://dx.doi.org/10.1002/hbm.26274
plymouth.publication-statusPublished
plymouth.journalHuman Brain Mapping
dc.identifier.doi10.1002/hbm.26274
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|Faculty of Health|School of Psychology
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
dc.publisher.placeUnited States
dcterms.dateAccepted2023-02-24
dc.date.updated2023-04-24T12:29:38Z
dc.rights.embargodate2023-4-25
dc.identifier.eissn1097-0193
dc.rights.embargoperiodforever
rioxxterms.versionofrecord10.1002/hbm.26274


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