dc.contributor.author | Bede, Peter | |
dc.contributor.author | Hardiman, Orla | |
dc.contributor.author | Finegan, Eoin | |
dc.contributor.author | Omer, Taha | |
dc.contributor.author | Iyer, Parameswaran M. | |
dc.date.accessioned | 2020-03-09T17:18:09Z | |
dc.date.available | 2020-03-09T17:18:09Z | |
dc.date.issued | 2017 | |
dc.date.submitted | 2017 | en |
dc.identifier.citation | Bede, P., Iyer, P.M., Finegan, E., Omer, T. & Hardiman, O., Virtual brain biopsies in amyotrophic lateral sclerosis: diagnostic classification based on in vivo pathological patterns, Neuroimage Clinical, 15, 2017, 653-658 | en |
dc.identifier.other | Y | |
dc.description.abstract | Background:
Diagnostic uncertainty in ALS has serious management implications and delays recruitment into clinical trials. Emerging evidence of presymptomatic disease-burden provides the rationale to develop diagnostic applications based on the evaluation of in-vivo pathological patterns early in the disease.
Objectives:
To outline and test a diagnostic classification approach based on an array of complementary imaging metrics in key disease-associated anatomical structures.
Methods:
Data from 75 ALS patients and 75 healthy controls were randomly allocated in a ‘training’ and ‘validation’ cohort. Spatial masks were created for anatomical foci which best discriminate patients from controls in the ‘training sample’. In a virtual ‘brain biopsy’, data was then retrieved from these key disease-associated brain regions. White matter diffusivity indices, grey matter T1-signal intensity values and basal ganglia volumes were evaluated as predictor variables in a canonical discriminant function.
Results:
Following predictor variable selection, a classification specificity of 85.5% and sensitivity of 89.1% was achieved in the training sample and 90% specificity and 90% sensitivity in the validation sample.
Discussion:
This study evaluates disease-associated imaging measures in a dummy diagnostic application. Although larger samples will be required for robust validation, the study confirms the potential of multimodal quantitative imaging in future clinical applications. | en |
dc.format.extent | 653-658 | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Neuroimage Clinical; | |
dc.relation.ispartofseries | 15; | |
dc.rights | Y | en |
dc.subject | Magnetic resonance imaging | en |
dc.subject | Neuroimaging | en |
dc.subject | Diagnosis | en |
dc.subject | Neurodegeneration | en |
dc.subject | Amyotrophic lateral sclerosis (ALS) | en |
dc.subject | Motor neuron disease | en |
dc.title | Virtual brain biopsies in amyotrophic lateral sclerosis: diagnostic classification based on in vivo pathological patterns | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/pbede | |
dc.identifier.peoplefinderurl | http://people.tcd.ie/hardimao | |
dc.identifier.rssinternalid | 175182 | |
dc.identifier.doi | http://dx.doi.org/10.1016/j.nicl.2017.06.010 | |
dc.rights.ecaccessrights | openAccess | |
dc.subject.TCDTheme | Neuroscience | en |
dc.identifier.orcid_id | 0000-0003-2610-1291 | |
dc.status.accessible | N | en |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S2213158217301420?via%3Dihub | |
dc.identifier.uri | http://hdl.handle.net/2262/91747 | |