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  1. Article ; Online: TDP-43-associated atrophy in brains with and without frontotemporal lobar degeneration

    Marina Buciuc / Peter R. Martin / Nirubol Tosakulwong / Melissa E. Murray / Leonard Petrucelli / Matthew L. Senjem / Anthony J. Spychalla / David S. Knopman / Bradley F. Boeve / Ronald C. Petersen / Joseph E. Parisi / R. Ross Reichard / Dennis W. Dickson / Clifford R. Jack, Jr. / Jennifer L. Whitwell / Keith A. Josephs

    NeuroImage: Clinical, Vol 34, Iss , Pp 102954- (2022)

    2022  

    Abstract: Transactive response DNA-binding protein of ∼43 kDa (TDP-43), a primary pathologic substrate in tau-negative frontotemporal lobar degeneration (FTLD), is also often found in the brains of elderly individuals without FTLD and is a key player in the ... ...

    Abstract Transactive response DNA-binding protein of ∼43 kDa (TDP-43), a primary pathologic substrate in tau-negative frontotemporal lobar degeneration (FTLD), is also often found in the brains of elderly individuals without FTLD and is a key player in the process of neurodegeneration in brains with and without FTLD. It is unknown how rates and trajectories of TDP-43-associated brain atrophy compare between these two groups. Additionally, non-FTLD TDP-43 inclusions are not homogeneous and can be divided into two morphologic types: type-α and neurofibrillary tangle-associated type-β. Therefore, we explored whether neurodegeneration also varies due to the morphologic type. In this longitudinal retrospective study of 293 patients with 843 MRI scans spanning over ∼10 years, we used a Bayesian hierarchical linear model to quantify similarities and differences between the non-FTLD TDP-43 (type-α/type-β) and FTLD-TDP (n = 68) in both regional volume at various timepoints before death and annualized rate of atrophy. Since Alzheimer’s disease (AD) is a frequent co-pathology in non-FTLD TDP-43, we further divided types α/β based on presence/absence of intermediate-high likelihood AD: AD-TDP type-β (n = 90), AD-TDP type-α (n = 104), and Pure-TDP (n = 31, all type-α). FTLD-TDP was associated with faster atrophy rates in the inferior temporal lobe and temporal pole compared to all non-FTLD TDP-43 groups. The atrophy rate in the frontal lobe was modulated by age with younger FTLD-TDP having the fastest rates. Older FTLD-TDP showed a limbic predominant pattern of neurodegeneration. AD-TDP type-α showed faster rates of hippocampal atrophy and smaller volumes of amygdala, temporal pole, and inferior temporal lobe compared to AD-TDP type-β. Pure-TDP was associated with slowest rates and less atrophy in all brain regions. The results suggest that there are differences and similarities in longitudinal brain volume loss between FTLD-TDP and non-FTLD TDP-43. Within FTLD-TDP age plays a role in which brain regions are the most affected. ...
    Keywords Alzheimer’s disease ; TDP-43 ; MRI ; LATE ; Old age FTLD ; Computer applications to medicine. Medical informatics ; R858-859.7 ; Neurology. Diseases of the nervous system ; RC346-429
    Subject code 616
    Language English
    Publishing date 2022-01-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Longitudinal tau-PET uptake and atrophy in atypical Alzheimer's disease

    Irene Sintini / Peter R. Martin / Jonathan Graff-Radford / Matthew L. Senjem / Christopher G. Schwarz / Mary M. Machulda / Anthony J. Spychalla / Daniel A. Drubach / David S. Knopman / Ronald C. Petersen / Val J. Lowe / Clifford R. Jack, Jr / Keith A. Josephs / Jennifer L. Whitwell

    NeuroImage: Clinical, Vol 23, Iss , Pp - (2019)

    2019  

    Abstract: The aims of this study were: to examine regional rates of change in tau-PET uptake and grey matter volume in atypical Alzheimer's disease (AD); to investigate the role of age in such changes; to describe multimodal regional relationships between tau ... ...

    Abstract The aims of this study were: to examine regional rates of change in tau-PET uptake and grey matter volume in atypical Alzheimer's disease (AD); to investigate the role of age in such changes; to describe multimodal regional relationships between tau accumulation and atrophy. Thirty atypical AD patients underwent baseline and one-year follow-up MRI, [18F]AV-1451 PET and PiB PET. Region- and voxel-level rates of tau accumulation and grey matter atrophy relative to cognitively unimpaired individuals, and the influence of age on such rates, were assessed. Univariate and multivariate analyses were performed between baseline measurements and rates of change, between baseline tau and atrophy, and between the two rates of change. Regional patterns of change in tau and volume differed, with highest rates of tau accumulation in frontal lobe and highest rates of atrophy in temporoparietal regions. Age had a negative effect on disease progression, predominantly on tau, with younger patients having a more rapid accumulation. Baseline tau uptake and regions of tau accumulation were disconnected, with high baseline tau uptake across the cortex correlated with high rates of tau accumulation in frontal and sensorimotor regions. In contrast, baseline volume and atrophy were locally related in the occipitoparietal regions. Higher tau uptake at baseline was locally related to higher rates of atrophy in frontal and occipital lobes. Tau accumulation rates positively correlated with rates of atrophy. In summary, our study showed that tau accumulation and atrophy presented different regional patterns in atypical AD, with tau spreading into the frontal lobes while atrophy remains in temporoparietal and occipital cortex, suggesting a temporal disconnect between protein deposition and neurodegeneration. Keywords: Longitudinal tau-PET, Atrophy, Atypical AD, Multimodal imaging
    Keywords Computer applications to medicine. Medical informatics ; R858-859.7 ; Neurology. Diseases of the nervous system ; RC346-429
    Subject code 571
    Language English
    Publishing date 2019-01-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech

    Keith A. Josephs / Joseph R. Duffy / Heather M. Clark / Rene L. Utianski / Edythe A. Strand / Mary M. Machulda / Hugo Botha / Peter R. Martin / Nha Trang Thu Pham / Julie Stierwalt / Farwa Ali / Marina Buciuc / Matthew Baker / Cristhoper H. Fernandez De Castro / Anthony J. Spychalla / Christopher G. Schwarz / Robert I. Reid / Matthew L. Senjem / Clifford R. Jack /
    Val J. Lowe / Eileen H. Bigio / Ross R. Reichard / Eric. J. Polley / Nilufer Ertekin-Taner / Rosa Rademakers / Michael A. DeTure / Owen A. Ross / Dennis W. Dickson / Jennifer L. Whitwell

    Nature Communications, Vol 12, Iss 1, Pp 1-

    2021  Volume 17

    Abstract: Progressive apraxia of speech (PAOS) is a neurodegenerative syndrome of multiple etiologies which affects spoken communication. Here, the authors characterized the molecular pathology, biochemistry, genetics and longitudinal neuroimaging of 32 autopsy- ... ...

    Abstract Progressive apraxia of speech (PAOS) is a neurodegenerative syndrome of multiple etiologies which affects spoken communication. Here, the authors characterized the molecular pathology, biochemistry, genetics and longitudinal neuroimaging of 32 autopsy-confirmed patients with PAOS who were followed over 10 years.
    Keywords Science ; Q
    Language English
    Publishing date 2021-06-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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