Infratentorial pathology in frontotemporal dementia: cerebellar grey and white matter alterations in FTD phenotypes

التفاصيل البيبلوغرافية
العنوان: Infratentorial pathology in frontotemporal dementia: cerebellar grey and white matter alterations in FTD phenotypes
المؤلفون: Foteini Christidi, Jasmin Lope, Jennifer C. Hengeveld, Peter Bede, Stacey Li Hi Shing, Siobhan Hutchinson, Mary Clare McKenna, Mark A. Doherty, Orla Hardiman, Russell L. McLaughlin, Rangariroyashe H. Chipika, Alice Vajda
المصدر: Journal of Neurology
بيانات النشر: Springer Science and Business Media LLC, 2021.
سنة النشر: 2021
مصطلحات موضوعية: 0301 basic medicine, Cerebellum, Pathology, medicine.medical_specialty, Biology, Cortical thickness, Primary progressive aphasia, White matter, 03 medical and health sciences, 0302 clinical medicine, Atrophy, Fractional anisotropy, medicine, Humans, Behaviour, Prospective Studies, Original Communication, Amyotrophic Lateral Sclerosis, medicine.disease, Magnetic Resonance Imaging, White Matter, Phenotype, 030104 developmental biology, medicine.anatomical_structure, Neurology, Frontotemporal Dementia, Cerebellar atrophy, Neurology (clinical), PPA, 030217 neurology & neurosurgery, MRI, Diffusion MRI, Frontotemporal dementia
الوصف: The contribution of cerebellar pathology to cognitive and behavioural manifestations is increasingly recognised, but the cerebellar profiles of FTD phenotypes are relatively poorly characterised. A prospective, single-centre imaging study has been undertaken with a high-resolution structural and diffusion tensor protocol to systematically evaluate cerebellar grey and white matter alterations in behavioural-variant FTD(bvFTD), non-fluent variant primary progressive aphasia(nfvPPA), semantic-variant primary progressive aphasia(svPPA), C9orf72-positive ALS-FTD(C9 + ALSFTD) and C9orf72-negative ALS-FTD(C9-ALSFTD). Cerebellar cortical thickness and complementary morphometric analyses were carried out to appraise atrophy patterns controlling for demographic variables. White matter integrity was assessed in a study-specific white matter skeleton, evaluating three diffusivity metrics: fractional anisotropy (FA), axial diffusivity (AD) and radial diffusivity (RD). Significant cortical thickness reductions were identified in: lobule VII and crus I in bvFTD; lobule VI VII, crus I and II in nfvPPA; and lobule VII, crus I and II in svPPA; lobule IV, VI, VII and Crus I and II in C9 + ALSFTD. Morphometry revealed volume reductions in lobule V in all groups; in addition to lobule VIII in C9 + ALSFTD; lobule VI, VIII and vermis in C9-ALSFTD; lobule V, VII and vermis in bvFTD; and lobule V, VI, VIII and vermis in nfvPPA. Widespread white matter alterations were demonstrated by significant fractional anisotropy, axial diffusivity and radial diffusivity changes in each FTD phenotype that were more focal in those with C9 + ALSFTD and svPPA. Our findings indicate that FTD subtypes are associated with phenotype-specific cerebellar signatures with the selective involvement of specific lobules instead of global cerebellar atrophy.
تدمد: 1432-1459
0340-5354
DOI: 10.1007/s00415-021-10575-w
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e7b68f8fce6980f7388e369468859d6
https://doi.org/10.1007/s00415-021-10575-w
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....0e7b68f8fce6980f7388e369468859d6
قاعدة البيانات: OpenAIRE
الوصف
تدمد:14321459
03405354
DOI:10.1007/s00415-021-10575-w