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  1. Article ; Online: Paradigm Shift: Multiple Potential Pathways to Neurodegenerative Dementia.

    Perna, Amalia / Montine, Kathleen S / White, Lon R / Montine, Thomas J / Cholerton, Brenna A

    Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics

    2023  Volume 20, Issue 6, Page(s) 1641–1652

    Abstract: Neurodegenerative dementia can result from multiple underlying abnormalities, including neurotransmitter imbalances, protein aggregation, and other neurotoxic events. A major complication in identifying effective treatment targets is the frequent co- ... ...

    Abstract Neurodegenerative dementia can result from multiple underlying abnormalities, including neurotransmitter imbalances, protein aggregation, and other neurotoxic events. A major complication in identifying effective treatment targets is the frequent co-occurrence of multiple neurodegenerative processes, occurring either in parallel or sequentially. The path towards developing effective treatments for Alzheimer's disease (AD) and other dementias has been relatively slow and until recently has focused on disease symptoms. Aducanumab and lecanemab, recently approved by the FDA, are meant to target disease structures but have only modest benefit on symptom progression and remain unproven in reversing or preventing dementia. A third, donanemab, appears more promising but awaits FDA approval. Ongoing trials include potential cognition enhancers, new combinations of known drugs for synergistic effects, prodrugs with less toxicity, and increasing interest in drugs targeting neuroinflammation or microbiome. Scientific and technological advances offer the opportunity to move in new therapy directions, such as modifying microglia to prevent or suppress underlying disease. A major challenge, however, is that underlying comorbidities likely influence the effectiveness of therapies. Indeed, the full range of comorbidity, today only definitively identified postmortem, likely contributes to failed clinical trials and overmedication of older adults, since it is difficult to exclude (during life) people unlikely to respond. Our current knowledge thus signals that a paradigm shift towards individualized and multimodal treatments is necessary to effectively advance the field of dementia therapeutics.
    MeSH term(s) Humans ; Aged ; Alzheimer Disease/drug therapy ; Alzheimer Disease/metabolism ; Combined Modality Therapy
    Language English
    Publishing date 2023-09-21
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2316693-9
    ISSN 1878-7479 ; 1933-7213
    ISSN (online) 1878-7479
    ISSN 1933-7213
    DOI 10.1007/s13311-023-01441-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Understanding the molecular basis of resilience to Alzheimer's disease.

    Montine, Kathleen S / Berson, Eloïse / Phongpreecha, Thanaphong / Huang, Zhi / Aghaeepour, Nima / Zou, James Y / MacCoss, Michael J / Montine, Thomas J

    Frontiers in neuroscience

    2023  Volume 17, Page(s) 1311157

    Abstract: The cellular and molecular distinction between brain aging and neurodegenerative disease begins to blur in the oldest old. Approximately 15-25% of observations in humans do not fit predicted clinical manifestations, likely the result of suppressed damage ...

    Abstract The cellular and molecular distinction between brain aging and neurodegenerative disease begins to blur in the oldest old. Approximately 15-25% of observations in humans do not fit predicted clinical manifestations, likely the result of suppressed damage despite usually adequate stressors and of resilience, the suppression of neurological dysfunction despite usually adequate degeneration. Factors during life may predict the clinico-pathologic state of resilience: cardiovascular health and mental health, more so than educational attainment, are predictive of a continuous measure of resilience to Alzheimer's disease (AD) and AD-related dementias (ADRDs). In resilience to AD alone (RAD), core features include synaptic and axonal processes, especially in the hippocampus. Future focus on larger and more diverse cohorts and additional regions offer emerging opportunities to understand this counterforce to neurodegeneration. The focus of this review is the molecular basis of resilience to AD.
    Language English
    Publishing date 2023-12-19
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2411902-7
    ISSN 1662-453X ; 1662-4548
    ISSN (online) 1662-453X
    ISSN 1662-4548
    DOI 10.3389/fnins.2023.1311157
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Human cerebrospinal fluid single exosomes in Parkinson's and Alzheimer's diseases.

    Yakabi, Koya / Berson, Eloise / Montine, Kathleen S / Bendall, Sean C / MacCoss, Michael J / Poston, Kathleen L / Montine, Thomas J

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Exosomes are proposed to be important in the pathogenesis of prevalent neurodegenerative diseases. We report the first application of solid-state technology to perform multiplex analysis of single exosomes in human cerebrospinal fluid (CSF) obtained from ...

    Abstract Exosomes are proposed to be important in the pathogenesis of prevalent neurodegenerative diseases. We report the first application of solid-state technology to perform multiplex analysis of single exosomes in human cerebrospinal fluid (CSF) obtained from the lumbar sac of people diagnosed with Alzheimer's disease dementia (ADD, n=30) or Parkinson's disease dementia (PDD, n=30), as well as age-matched health controls (HCN, n=30). Single events were captured with mouse monoclonal antibodies to one of three different tetraspanins (CD9, CD63, or CD81) or with mouse (M) IgG control, and then probed with fluorescently labeled antibodies to prion protein (PrP) or CD47 to mark neuronal or presynaptic origin, as well as ADD- and PDD-related proteins: amyloid beta (Aβ), tau, α-synuclein, and Apolipoprotein (Apo) E. Data were collected only from captured events that were within the size range of 50 to 200 nm. Exosomes were present at approximately 100 billion per mL human CSF and were similarly abundant for CD9+ and CD81+ events, but CD63+ were only 22% to 25% of CD9+ (P<0.0001) or CD81+ (P<0.0001) events. Approximately 24% of CSF exosomes were PrP+, while only 2% were CD47+. The vast majority of exosomes were surface ApoE+, and the number of PrP-ApoE+ (P<0.001) and PrP+ApoE+ (P<0.01) exosomes were significantly reduced in ADD vs. HCN for CD9+ events only. Aβ, tau, and α-synuclein were not detected on the exosome surface or in permeabilized cargo. These data provide new insights into single exosome molecular features and highlight reduction in the CSF concentration of ApoE+ exosomes in patients with ADD.
    Language English
    Publishing date 2023-12-23
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.12.22.573124
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Book: Comparative anatomy and histology

    Dintzis, Suzanne M / Montine, Kathleen S / Treuting, Piper M

    a mouse, rat, and human Atlas

    2018  

    Author's details edited by Piper M. Treuting, DVM, MS, Diplomate, ACVP, Associate Professor, Chief of Comparative Pathology, Department of Comparative Medicine, adjunct Associate Professor, Department of Pathology, University of Washington School of Medicine, Seattle, WA, United States; Suzanne M. Dintzis, MD, PhD, Associate Professor, Department of Anatomic Pathology, University of Washington School of Medicine, Seattle, WA, United States; Kathleen S. Montine, PhD, ELS, Senior Principal Research Scientist, Department of Pathology, University of Washington School of Medicine, Seattle, WA, United States
    Language English
    Size XVIII, 552 Seiten, Illustrationen
    Edition Second edition
    Document type Book
    ISBN 9780128029008 ; 0128029005
    Database Friedrich Loeffler-Institute, Federal Research Institute for Animal Health

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  5. Article ; Online: Mass Synaptometry: Applying Mass Cytometry to Single Synapse Analysis.

    Gajera, Chandresh R / Fernandez, Rosemary / Postupna, Nadia / Montine, Kathleen S / Keene, C Dirk / Bendall, Sean C / Montine, Thomas J

    Methods in molecular biology (Clifton, N.J.)

    2022  Volume 2417, Page(s) 69–88

    Abstract: Synaptic degeneration is one of the earliest and phenotypically most significant features associated with numerous neurodegenerative conditions, including Alzheimer's and Parkinson's diseases. Synaptic changes are also known to be important in ... ...

    Abstract Synaptic degeneration is one of the earliest and phenotypically most significant features associated with numerous neurodegenerative conditions, including Alzheimer's and Parkinson's diseases. Synaptic changes are also known to be important in neurocognitive disorders such as schizophrenia and autism spectrum disorders. Several labs, including ours, have demonstrated that conventional (fluorescence-based) flow cytometry of individual synaptosomes is a robust and reproducible method. However, the repertoire of probes needed to assess comprehensively the type of synapse, pathologic proteins (including protein products of risk genes discovered in GWAS), and markers of stress and injury far exceeds what is achievable with conventional flow cytometry. We recently developed a method that applies CyTOF (Cytometry by Time-Of-Flight mass spectrometry) to high-dimensional analysis of individual human synaptosomes, overcoming many of the multiplexing limitations of conventional flow cytometry. We call this new method Mass Synaptometry. Here we describe the preparation of synaptosomes from human and mouse brain, the generation and quality control of the "SynTOF" (Synapse by Time-Of-Flight mass spectrometry) antibody panel, the staining protocol, and CyTOF parameter setup for acquisition, post-acquisition processing, and analysis.
    MeSH term(s) Animals ; Flow Cytometry ; Mass Spectrometry ; Mice ; Synapses ; Synaptosomes
    Language English
    Publishing date 2022-01-18
    Publishing country United States
    Document type Journal Article
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-0716-1916-2_6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Precision medicine: Clarity for the clinical and biological complexity of Alzheimer's and Parkinson's diseases.

    Montine, Thomas J / Montine, Kathleen S

    The Journal of experimental medicine

    2015  Volume 212, Issue 5, Page(s) 601–605

    Abstract: The goal of precision medicine is to deliver optimally targeted and timed interventions tailored to an individual's molecular drivers of disease. This concept has wide currency in cancer care and in some diseases caused by monogenetic mutations, such as ... ...

    Abstract The goal of precision medicine is to deliver optimally targeted and timed interventions tailored to an individual's molecular drivers of disease. This concept has wide currency in cancer care and in some diseases caused by monogenetic mutations, such as cystic fibrosis, and recently has been endorsed by the White House Office of Science and Technology for more widespread application in medicine. Here we describe our vision of how precision medicine can bring greater clarity to the clinical and biological complexity of the two most common neurodegenerative diseases, Alzheimer's disease and Parkinson's disease.
    MeSH term(s) Alzheimer Disease/genetics ; Alzheimer Disease/pathology ; Alzheimer Disease/therapy ; Humans ; Mutation ; Parkinson Disease/genetics ; Parkinson Disease/pathology ; Parkinson Disease/therapy
    Language English
    Publishing date 2015-05-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 218343-2
    ISSN 1540-9538 ; 0022-1007
    ISSN (online) 1540-9538
    ISSN 0022-1007
    DOI 10.1084/jem.20150656
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Unveiling Resilience to Alzheimer's Disease: Insights From Brain Regional Proteomic Markers.

    Huang, Zhi / Merrihew, Gennifer E / Larson, Eric B / Park, Jea / Plubell, Deanna / Fox, Edward J / Montine, Kathleen S / Keene, C Dirk / Latimer, Caitlin S / Zou, James Y / MacCoss, Michael J / Montine, Thomas J

    Neuroscience insights

    2023  Volume 18, Page(s) 26331055231201600

    Abstract: Studying proteomics data of the human brain could offer numerous insights into unraveling the signature of resilience to Alzheimer's disease. In our previous study with rigorous cohort selection criteria that excluded 4 common comorbidities, we harnessed ...

    Abstract Studying proteomics data of the human brain could offer numerous insights into unraveling the signature of resilience to Alzheimer's disease. In our previous study with rigorous cohort selection criteria that excluded 4 common comorbidities, we harnessed multiple brain regions from 43 research participants with 12 of them displaying cognitive resilience to Alzheimer's disease. Based on the previous findings, this work focuses on 6 proteins out of the 33 differentially expressed proteins associated with resilience to Alzheimer's disease. These proteins are used to construct a decision tree classifier, enabling the differentiation of 3 groups: (i) healthy control, (ii) resilience to Alzheimer's disease, and (iii) Alzheimer's disease with dementia. Our analysis unveiled 2 important regional proteomic markers: Aβ peptides in the hippocampus and PA1B3 in the inferior parietal lobule. These findings underscore the potential of using distinct regional proteomic markers as signatures in characterizing the resilience to Alzheimer's disease.
    Language English
    Publishing date 2023-10-05
    Publishing country United States
    Document type Journal Article ; Comment
    ISSN 2633-1055
    ISSN (online) 2633-1055
    DOI 10.1177/26331055231201600
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Brain proteomic analysis implicates actin filament processes and injury response in resilience to Alzheimer's disease.

    Huang, Zhi / Merrihew, Gennifer E / Larson, Eric B / Park, Jea / Plubell, Deanna / Fox, Edward J / Montine, Kathleen S / Latimer, Caitlin S / Dirk Keene, C / Zou, James Y / MacCoss, Michael J / Montine, Thomas J

    Nature communications

    2023  Volume 14, Issue 1, Page(s) 2747

    Abstract: Resilience to Alzheimer's disease is an uncommon combination of high disease burden without dementia that offers valuable insights into limiting clinical impact. Here we assessed 43 research participants meeting stringent criteria, 11 healthy controls, ... ...

    Abstract Resilience to Alzheimer's disease is an uncommon combination of high disease burden without dementia that offers valuable insights into limiting clinical impact. Here we assessed 43 research participants meeting stringent criteria, 11 healthy controls, 12 resilience to Alzheimer's disease and 20 Alzheimer's disease with dementia and analyzed matched isocortical regions, hippocampus, and caudate nucleus by mass spectrometry-based proteomics. Of 7115 differentially expressed soluble proteins, lower isocortical and hippocampal soluble Aβ levels is a significant feature of resilience when compared to healthy control and Alzheimer's disease dementia groups. Protein co-expression analysis reveals 181 densely-interacting proteins significantly associated with resilience that were enriched for actin filament-based processes, cellular detoxification, and wound healing in isocortex and hippocampus, further supported by four validation cohorts. Our results suggest that lowering soluble Aβ concentration may suppress severe cognitive impairment along the Alzheimer's disease continuum. The molecular basis of resilience likely holds important therapeutic insights.
    MeSH term(s) Humans ; Alzheimer Disease/metabolism ; Proteomics ; Brain/metabolism ; Cognitive Dysfunction/metabolism ; Hippocampus/metabolism ; Neocortex/metabolism
    Language English
    Publishing date 2023-05-12
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-38376-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Anatomic and clinical pathology of cognitive impairment and dementia.

    Montine, Kathleen S / Montine, Thomas J

    Journal of Alzheimer's disease : JAD

    2012  Volume 33 Suppl 1, Page(s) S181–4

    Abstract: Progressive cognitive impairment and its clinical culmination in dementia loom as a major public health problem in the coming generation of older adults, and this fact compels investigation to develop interventions that prevent, delay, or cure. The tools ...

    Abstract Progressive cognitive impairment and its clinical culmination in dementia loom as a major public health problem in the coming generation of older adults, and this fact compels investigation to develop interventions that prevent, delay, or cure. The tools of anatomic pathology have provided key insights into the complex convergence of multiple diseases that commonly contribute to the dementia syndrome and its prodrome in the community setting, and they have suggested some exposures that may modulate disease burden. The tools of clinical pathology, in combination with neuroimaging, have revolutionized the approach to clinical investigation of Alzheimer's disease and are now doing the same with Lewy body disease and vascular brain injury. The tools of anatomic and clinical pathology will continue to contribute to our understanding of these diseases as we advance toward effective interventions for the diseases that commonly cause cognitive impairment and dementia in older adults.
    MeSH term(s) Brain/pathology ; Cognition Disorders/pathology ; Dementia/pathology ; Humans
    Language English
    Publishing date 2012-06-15
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1440127-7
    ISSN 1875-8908 ; 1387-2877
    ISSN (online) 1875-8908
    ISSN 1387-2877
    DOI 10.3233/JAD-2012-129032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Quantitative estimate of cognitive resilience and its medical and genetic associations.

    Phongpreecha, Thanaphong / Godrich, Dana / Berson, Eloise / Espinosa, Camilo / Kim, Yeasul / Cholerton, Brenna / Chang, Alan L / Mataraso, Samson / Bukhari, Syed A / Perna, Amalia / Yakabi, Koya / Montine, Kathleen S / Poston, Kathleen L / Mormino, Elizabeth / White, Lon / Beecham, Gary / Aghaeepour, Nima / Montine, Thomas J

    Alzheimer's research & therapy

    2023  Volume 15, Issue 1, Page(s) 192

    Abstract: Background: We have proposed that cognitive resilience (CR) counteracts brain damage from Alzheimer's disease (AD) or AD-related dementias such that older individuals who harbor neurodegenerative disease burden sufficient to cause dementia remain ... ...

    Abstract Background: We have proposed that cognitive resilience (CR) counteracts brain damage from Alzheimer's disease (AD) or AD-related dementias such that older individuals who harbor neurodegenerative disease burden sufficient to cause dementia remain cognitively normal. However, CR traditionally is considered a binary trait, capturing only the most extreme examples, and is often inconsistently defined.
    Methods: This study addressed existing discrepancies and shortcomings of the current CR definition by proposing a framework for defining CR as a continuous variable for each neuropsychological test. The linear equations clarified CR's relationship to closely related terms, including cognitive function, reserve, compensation, and damage. Primarily, resilience is defined as a function of cognitive performance and damage from neuropathologic damage. As such, the study utilized data from 844 individuals (age = 79 ± 12, 44% female) in the National Alzheimer's Coordinating Center cohort that met our inclusion criteria of comprehensive lesion rankings for 17 neuropathologic features and complete neuropsychological test results. Machine learning models and GWAS then were used to identify medical and genetic factors that are associated with CR.
    Results: CR varied across five cognitive assessments and was greater in female participants, associated with longer survival, and weakly associated with educational attainment or APOE ε4 allele. In contrast, damage was strongly associated with APOE ε4 allele (P value < 0.0001). Major predictors of CR were cardiovascular health and social interactions, as well as the absence of behavioral symptoms.
    Conclusions: Our framework explicitly decoupled the effects of CR from neuropathologic damage. Characterizations and genetic association study of these two components suggest that the underlying CR mechanism has minimal overlap with the disease mechanism. Moreover, the identified medical features associated with CR suggest modifiable features to counteract clinical expression of damage and maintain cognitive function in older individuals.
    MeSH term(s) Humans ; Female ; Aged ; Aged, 80 and over ; Male ; Cognitive Dysfunction/diagnosis ; Apolipoprotein E4/genetics ; Neurodegenerative Diseases ; Alzheimer Disease/pathology ; Cognition
    Chemical Substances Apolipoprotein E4
    Language English
    Publishing date 2023-11-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 2506521-X
    ISSN 1758-9193 ; 1758-9193
    ISSN (online) 1758-9193
    ISSN 1758-9193
    DOI 10.1186/s13195-023-01329-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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