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  1. Article ; Online: Comparison of histological delineations of medial temporal lobe cortices by four independent neuroanatomy laboratories.

    Wuestefeld, Anika / Baumeister, Hannah / Adams, Jenna N / de Flores, Robin / Hodgetts, Carl J / Mazloum-Farzaghi, Negar / Olsen, Rosanna K / Puliyadi, Vyash / Tran, Tammy T / Bakker, Arnold / Canada, Kelsey L / Dalton, Marshall A / Daugherty, Ana M / La Joie, Renaud / Wang, Lei / Bedard, Madigan L / Buendia, Esther / Chung, Eunice / Denning, Amanda /
    Del Mar Arroyo-Jiménez, María / Artacho-Pérula, Emilio / Irwin, David J / Ittyerah, Ranjit / Lee, Edward B / Lim, Sydney / Del Pilar Marcos-Rabal, María / Iñiguez de Onzoño Martin, Maria Mercedes / Lopez, Monica Munoz / de la Rosa Prieto, Carlos / Schuck, Theresa / Trotman, Winifred / Vela, Alicia / Yushkevich, Paul / Amunts, Katrin / Augustinack, Jean C / Ding, Song-Lin / Insausti, Ricardo / Kedo, Olga / Berron, David / Wisse, Laura E M

    Hippocampus

    2024  Volume 34, Issue 5, Page(s) 241–260

    Abstract: The medial temporal lobe (MTL) cortex, located adjacent to the hippocampus, is crucial for memory and prone to the accumulation of certain neuropathologies such as Alzheimer's disease neurofibrillary tau tangles. The MTL cortex is composed of several ... ...

    Abstract The medial temporal lobe (MTL) cortex, located adjacent to the hippocampus, is crucial for memory and prone to the accumulation of certain neuropathologies such as Alzheimer's disease neurofibrillary tau tangles. The MTL cortex is composed of several subregions which differ in their functional and cytoarchitectonic features. As neuroanatomical schools rely on different cytoarchitectonic definitions of these subregions, it is unclear to what extent their delineations of MTL cortex subregions overlap. Here, we provide an overview of cytoarchitectonic definitions of the entorhinal and parahippocampal cortices as well as Brodmann areas (BA) 35 and 36, as provided by four neuroanatomists from different laboratories, aiming to identify the rationale for overlapping and diverging delineations. Nissl-stained series were acquired from the temporal lobes of three human specimens (two right and one left hemisphere). Slices (50 μm thick) were prepared perpendicular to the long axis of the hippocampus spanning the entire longitudinal extent of the MTL cortex. Four neuroanatomists annotated MTL cortex subregions on digitized slices spaced 5 mm apart (pixel size 0.4 μm at 20× magnification). Parcellations, terminology, and border placement were compared among neuroanatomists. Cytoarchitectonic features of each subregion are described in detail. Qualitative analysis of the annotations showed higher agreement in the definitions of the entorhinal cortex and BA35, while the definitions of BA36 and the parahippocampal cortex exhibited less overlap among neuroanatomists. The degree of overlap of cytoarchitectonic definitions was partially reflected in the neuroanatomists' agreement on the respective delineations. Lower agreement in annotations was observed in transitional zones between structures where seminal cytoarchitectonic features are expressed less saliently. The results highlight that definitions and parcellations of the MTL cortex differ among neuroanatomical schools and thereby increase understanding of why these differences may arise. This work sets a crucial foundation to further advance anatomically-informed neuroimaging research on the human MTL cortex.
    MeSH term(s) Humans ; Temporal Lobe/pathology ; Neuroanatomy/methods ; Male ; Parahippocampal Gyrus/pathology ; Parahippocampal Gyrus/diagnostic imaging ; Female ; Aged ; Entorhinal Cortex/pathology ; Entorhinal Cortex/anatomy & histology ; Laboratories ; Aged, 80 and over
    Language English
    Publishing date 2024-02-28
    Publishing country United States
    Document type Journal Article ; Comparative Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 1074352-2
    ISSN 1098-1063 ; 1050-9631
    ISSN (online) 1098-1063
    ISSN 1050-9631
    DOI 10.1002/hipo.23602
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Three-dimensional mapping of neurofibrillary tangle burden in the human medial temporal lobe.

    Yushkevich, Paul A / Muñoz López, Mónica / Iñiguez de Onzoño Martin, María Mercedes / Ittyerah, Ranjit / Lim, Sydney / Ravikumar, Sadhana / Bedard, Madigan L / Pickup, Stephen / Liu, Weixia / Wang, Jiancong / Hung, Ling Yu / Lasserve, Jade / Vergnet, Nicolas / Xie, Long / Dong, Mengjin / Cui, Salena / McCollum, Lauren / Robinson, John L / Schuck, Theresa /
    de Flores, Robin / Grossman, Murray / Tisdall, M Dylan / Prabhakaran, Karthik / Mizsei, Gabor / Das, Sandhitsu R / Artacho-Pérula, Emilio / Arroyo Jiménez, Marı'a Del Mar / Marcos Raba, Marı'a Pilar / Molina Romero, Francisco Javier / Cebada Sánchez, Sandra / Delgado González, José Carlos / de la Rosa-Prieto, Carlos / Córcoles Parada, Marta / Lee, Edward B / Trojanowski, John Q / Ohm, Daniel T / Wisse, Laura E M / Wolk, David A / Irwin, David J / Insausti, Ricardo

    Brain : a journal of neurology

    2021  Volume 144, Issue 9, Page(s) 2784–2797

    Abstract: Tau protein neurofibrillary tangles are closely linked to neuronal/synaptic loss and cognitive decline in Alzheimer's disease and related dementias. Our knowledge of the pattern of neurofibrillary tangle progression in the human brain, critical to the ... ...

    Abstract Tau protein neurofibrillary tangles are closely linked to neuronal/synaptic loss and cognitive decline in Alzheimer's disease and related dementias. Our knowledge of the pattern of neurofibrillary tangle progression in the human brain, critical to the development of imaging biomarkers and interpretation of in vivo imaging studies in Alzheimer's disease, is based on conventional two-dimensional histology studies that only sample the brain sparsely. To address this limitation, ex vivo MRI and dense serial histological imaging in 18 human medial temporal lobe specimens (age 75.3 ± 11.4 years, range 45 to 93) were used to construct three-dimensional quantitative maps of neurofibrillary tangle burden in the medial temporal lobe at individual and group levels. Group-level maps were obtained in the space of an in vivo brain template, and neurofibrillary tangles were measured in specific anatomical regions defined in this template. Three-dimensional maps of neurofibrillary tangle burden revealed significant variation along the anterior-posterior axis. While early neurofibrillary tangle pathology is thought to be confined to the transentorhinal region, we found similar levels of burden in this region and other medial temporal lobe subregions, including amygdala, temporopolar cortex, and subiculum/cornu ammonis 1 hippocampal subfields. Overall, the three-dimensional maps of neurofibrillary tangle burden presented here provide more complete information about the distribution of this neurodegenerative pathology in the region of the cortex where it first emerges in Alzheimer's disease, and may help inform the field about the patterns of pathology spread, as well as support development and validation of neuroimaging biomarkers.
    MeSH term(s) Aged ; Aged, 80 and over ; Brain Mapping/methods ; Cohort Studies ; Female ; Humans ; Imaging, Three-Dimensional/methods ; Magnetic Resonance Imaging/methods ; Male ; Middle Aged ; Neurofibrillary Tangles/pathology ; Temporal Lobe/diagnostic imaging ; Temporal Lobe/pathology
    Language English
    Publishing date 2021-07-08
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 80072-7
    ISSN 1460-2156 ; 0006-8950
    ISSN (online) 1460-2156
    ISSN 0006-8950
    DOI 10.1093/brain/awab262
    Database MEDical Literature Analysis and Retrieval System OnLINE

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