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Detecting Primary Progressive Aphasia Atrophy Patterns: A Comparison of Visual Assessment and Quantitative Neuroimaging Techniques

BACKGROUND: There are now clinically available automated MRI analysis software programs that compare brain volumes of patients to a normative sample and provide z-score data for various brain regions. These programs have yet to be validated in primary progressive aphasia (PPA). OBJECTIVE: To address...

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Detalles Bibliográficos
Autores principales: Franczak, Stephanie, Pommy, Jessica, Minor, Greta, Zolliecoffer, Chandler, Bhalla, Manav, Agarwal, Mohit, Nencka, Andrew, Wang, Yang, Klein, Andrew, O’Neill, Darren, Henry, Jude, Umfleet, Glass
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484148/
https://www.ncbi.nlm.nih.gov/pubmed/36186726
http://dx.doi.org/10.3233/ADR-220036
Descripción
Sumario:BACKGROUND: There are now clinically available automated MRI analysis software programs that compare brain volumes of patients to a normative sample and provide z-score data for various brain regions. These programs have yet to be validated in primary progressive aphasia (PPA). OBJECTIVE: To address this gap in the literature, we examined Neuroreader(™) z-scores in PPA, relative to visual MRI assessment. We predicted that Neuroreader(™) 1) would be more sensitive for detecting left > right atrophy in the cortical lobar regions in logopenic variant PPA clinical phenotype (lvPPA), and 2) would distinguish lvPPA (n = 11) from amnestic mild cognitive impairment (aMCI; n = 12). METHODS: lvPPA or aMCI patients who underwent MRI with Neuroreader(™) were included in this study. Two neuroradiologists rated 10 regions. Neuroreader(™) lobar z-scores for those 10 regions, as well as a hippocampal asymmetry metric, were included in analyses. RESULTS: Cohen’s Kappa coefficients were significant in 10 of the 28 computations (k = 0.351 to 0.593, p≤0.029). Neuroradiologists agreed 0% of the time that left asymmetry was present across regions. No significant differences emerged between aMCI and lvPPA in Neuroreader(™) z-scores across left or right frontal, temporal, or parietal regions (ps > 0.10). There were significantly lower z-scores in the left compared to right for the hippocampus, as well as parietal, occipital, and temporal cortices in lvPPA. CONCLUSION: Overall, our results indicated moderate to low interrater reliability, and raters never agreed that left asymmetry was present. While lower z-scores in the left hemisphere regions emerged in lvPPA, Neuroreader(™) failed to differentiate lvPPA from aMCI.