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Tau deposition patterns are associated with functional connectivity in primary tauopathies
Tau pathology is the main driver of neuronal dysfunction in 4-repeat tauopathies, including cortico-basal degeneration and progressive supranuclear palsy. Tau is assumed to spread prion-like across connected neurons, but the mechanisms of tau propagation are largely elusive in 4-repeat tauopathies,...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924216/ https://www.ncbi.nlm.nih.gov/pubmed/35292638 http://dx.doi.org/10.1038/s41467-022-28896-3 |
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author | Franzmeier, Nicolai Brendel, Matthias Beyer, Leonie Slemann, Luna Kovacs, Gabor G. Arzberger, Thomas Kurz, Carolin Respondek, Gesine Lukic, Milica J. Biel, Davina Rubinski, Anna Frontzkowski, Lukas Hummel, Selina Müller, Andre Finze, Anika Palleis, Carla Joseph, Emanuel Weidinger, Endy Katzdobler, Sabrina Song, Mengmeng Biechele, Gloria Kern, Maike Scheifele, Maximilian Rauchmann, Boris-Stephan Perneczky, Robert Rullman, Michael Patt, Marianne Schildan, Andreas Barthel, Henryk Sabri, Osama Rumpf, Jost J. Schroeter, Matthias L. Classen, Joseph Villemagne, Victor Seibyl, John Stephens, Andrew W. Lee, Edward B. Coughlin, David G. Giese, Armin Grossman, Murray McMillan, Corey T. Gelpi, Ellen Molina-Porcel, Laura Compta, Yaroslau van Swieten, John C. Laat, Laura Donker Troakes, Claire Al-Sarraj, Safa Robinson, John L. Xie, Sharon X. Irwin, David J. Roeber, Sigrun Herms, Jochen Simons, Mikael Bartenstein, Peter Lee, Virginia M. Trojanowski, John Q. Levin, Johannes Höglinger, Günter Ewers, Michael |
author_facet | Franzmeier, Nicolai Brendel, Matthias Beyer, Leonie Slemann, Luna Kovacs, Gabor G. Arzberger, Thomas Kurz, Carolin Respondek, Gesine Lukic, Milica J. Biel, Davina Rubinski, Anna Frontzkowski, Lukas Hummel, Selina Müller, Andre Finze, Anika Palleis, Carla Joseph, Emanuel Weidinger, Endy Katzdobler, Sabrina Song, Mengmeng Biechele, Gloria Kern, Maike Scheifele, Maximilian Rauchmann, Boris-Stephan Perneczky, Robert Rullman, Michael Patt, Marianne Schildan, Andreas Barthel, Henryk Sabri, Osama Rumpf, Jost J. Schroeter, Matthias L. Classen, Joseph Villemagne, Victor Seibyl, John Stephens, Andrew W. Lee, Edward B. Coughlin, David G. Giese, Armin Grossman, Murray McMillan, Corey T. Gelpi, Ellen Molina-Porcel, Laura Compta, Yaroslau van Swieten, John C. Laat, Laura Donker Troakes, Claire Al-Sarraj, Safa Robinson, John L. Xie, Sharon X. Irwin, David J. Roeber, Sigrun Herms, Jochen Simons, Mikael Bartenstein, Peter Lee, Virginia M. Trojanowski, John Q. Levin, Johannes Höglinger, Günter Ewers, Michael |
author_sort | Franzmeier, Nicolai |
collection | PubMed |
description | Tau pathology is the main driver of neuronal dysfunction in 4-repeat tauopathies, including cortico-basal degeneration and progressive supranuclear palsy. Tau is assumed to spread prion-like across connected neurons, but the mechanisms of tau propagation are largely elusive in 4-repeat tauopathies, characterized not only by neuronal but also by astroglial and oligodendroglial tau accumulation. Here, we assess whether connectivity is associated with 4R-tau deposition patterns by combining resting-state fMRI connectomics with both 2(nd) generation (18)F-PI-2620 tau-PET in 46 patients with clinically diagnosed 4-repeat tauopathies and post-mortem cell-type-specific regional tau assessments from two independent progressive supranuclear palsy patient samples (n = 97 and n = 96). We find that inter-regional connectivity is associated with higher inter-regional correlation of both tau-PET and post-mortem tau levels in 4-repeat tauopathies. In regional cell-type specific post-mortem tau assessments, this association is stronger for neuronal than for astroglial or oligodendroglial tau, suggesting that connectivity is primarily associated with neuronal tau accumulation. Using tau-PET we find further that patient-level tau patterns are associated with the connectivity of subcortical tau epicenters. Together, the current study provides combined in vivo tau-PET and histopathological evidence that brain connectivity is associated with tau deposition patterns in 4-repeat tauopathies. |
format | Online Article Text |
id | pubmed-8924216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89242162022-04-01 Tau deposition patterns are associated with functional connectivity in primary tauopathies Franzmeier, Nicolai Brendel, Matthias Beyer, Leonie Slemann, Luna Kovacs, Gabor G. Arzberger, Thomas Kurz, Carolin Respondek, Gesine Lukic, Milica J. Biel, Davina Rubinski, Anna Frontzkowski, Lukas Hummel, Selina Müller, Andre Finze, Anika Palleis, Carla Joseph, Emanuel Weidinger, Endy Katzdobler, Sabrina Song, Mengmeng Biechele, Gloria Kern, Maike Scheifele, Maximilian Rauchmann, Boris-Stephan Perneczky, Robert Rullman, Michael Patt, Marianne Schildan, Andreas Barthel, Henryk Sabri, Osama Rumpf, Jost J. Schroeter, Matthias L. Classen, Joseph Villemagne, Victor Seibyl, John Stephens, Andrew W. Lee, Edward B. Coughlin, David G. Giese, Armin Grossman, Murray McMillan, Corey T. Gelpi, Ellen Molina-Porcel, Laura Compta, Yaroslau van Swieten, John C. Laat, Laura Donker Troakes, Claire Al-Sarraj, Safa Robinson, John L. Xie, Sharon X. Irwin, David J. Roeber, Sigrun Herms, Jochen Simons, Mikael Bartenstein, Peter Lee, Virginia M. Trojanowski, John Q. Levin, Johannes Höglinger, Günter Ewers, Michael Nat Commun Article Tau pathology is the main driver of neuronal dysfunction in 4-repeat tauopathies, including cortico-basal degeneration and progressive supranuclear palsy. Tau is assumed to spread prion-like across connected neurons, but the mechanisms of tau propagation are largely elusive in 4-repeat tauopathies, characterized not only by neuronal but also by astroglial and oligodendroglial tau accumulation. Here, we assess whether connectivity is associated with 4R-tau deposition patterns by combining resting-state fMRI connectomics with both 2(nd) generation (18)F-PI-2620 tau-PET in 46 patients with clinically diagnosed 4-repeat tauopathies and post-mortem cell-type-specific regional tau assessments from two independent progressive supranuclear palsy patient samples (n = 97 and n = 96). We find that inter-regional connectivity is associated with higher inter-regional correlation of both tau-PET and post-mortem tau levels in 4-repeat tauopathies. In regional cell-type specific post-mortem tau assessments, this association is stronger for neuronal than for astroglial or oligodendroglial tau, suggesting that connectivity is primarily associated with neuronal tau accumulation. Using tau-PET we find further that patient-level tau patterns are associated with the connectivity of subcortical tau epicenters. Together, the current study provides combined in vivo tau-PET and histopathological evidence that brain connectivity is associated with tau deposition patterns in 4-repeat tauopathies. Nature Publishing Group UK 2022-03-15 /pmc/articles/PMC8924216/ /pubmed/35292638 http://dx.doi.org/10.1038/s41467-022-28896-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Franzmeier, Nicolai Brendel, Matthias Beyer, Leonie Slemann, Luna Kovacs, Gabor G. Arzberger, Thomas Kurz, Carolin Respondek, Gesine Lukic, Milica J. Biel, Davina Rubinski, Anna Frontzkowski, Lukas Hummel, Selina Müller, Andre Finze, Anika Palleis, Carla Joseph, Emanuel Weidinger, Endy Katzdobler, Sabrina Song, Mengmeng Biechele, Gloria Kern, Maike Scheifele, Maximilian Rauchmann, Boris-Stephan Perneczky, Robert Rullman, Michael Patt, Marianne Schildan, Andreas Barthel, Henryk Sabri, Osama Rumpf, Jost J. Schroeter, Matthias L. Classen, Joseph Villemagne, Victor Seibyl, John Stephens, Andrew W. Lee, Edward B. Coughlin, David G. Giese, Armin Grossman, Murray McMillan, Corey T. Gelpi, Ellen Molina-Porcel, Laura Compta, Yaroslau van Swieten, John C. Laat, Laura Donker Troakes, Claire Al-Sarraj, Safa Robinson, John L. Xie, Sharon X. Irwin, David J. Roeber, Sigrun Herms, Jochen Simons, Mikael Bartenstein, Peter Lee, Virginia M. Trojanowski, John Q. Levin, Johannes Höglinger, Günter Ewers, Michael Tau deposition patterns are associated with functional connectivity in primary tauopathies |
title | Tau deposition patterns are associated with functional connectivity in primary tauopathies |
title_full | Tau deposition patterns are associated with functional connectivity in primary tauopathies |
title_fullStr | Tau deposition patterns are associated with functional connectivity in primary tauopathies |
title_full_unstemmed | Tau deposition patterns are associated with functional connectivity in primary tauopathies |
title_short | Tau deposition patterns are associated with functional connectivity in primary tauopathies |
title_sort | tau deposition patterns are associated with functional connectivity in primary tauopathies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924216/ https://www.ncbi.nlm.nih.gov/pubmed/35292638 http://dx.doi.org/10.1038/s41467-022-28896-3 |
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