dc.contributor.author
Kovacs, Gabor G.
dc.contributor.author
Xie, Sharon X.
dc.contributor.author
Lee, Edward B.
dc.contributor.author
Robinson, John L.
dc.contributor.author
Caswell, Carrie
dc.contributor.author
Irwin, David J.
dc.contributor.author
Toledo, Jon B.
dc.contributor.author
Johnson. Victoria E.
dc.contributor.author
Smith, Douglas H.
dc.contributor.author
Alafuzoff, Irina
dc.contributor.author
Attems, Johannes
dc.contributor.author
Bencze, Janos
dc.contributor.author
Bieniek, Kevin F.
dc.contributor.author
Bigio, Eileen H.
dc.contributor.author
Bodi, Istvan
dc.contributor.author
Budka, Herbert
dc.contributor.author
Dickson, Dennis W.
dc.contributor.author
Dugger, Brittany N.
dc.contributor.author
Duyckaerts, Charles
dc.contributor.author
Ferrer, Isidro (Ferrer Abizanda)
dc.contributor.author
Forrest, Shelley L.
dc.contributor.author
Gelpi, Ellen
dc.contributor.author
Gentleman, Stephen M.
dc.contributor.author
Giaccone, Giorgio
dc.contributor.author
Grinberg, Lea T.
dc.contributor.author
Halliday, Glenda M.
dc.contributor.author
Hatanpaa, Kimmo J.
dc.contributor.author
Hof, Patrick R.
dc.contributor.author
Hofer, Monika
dc.contributor.author
Hortobágyi, Tibor
dc.contributor.author
Ironside, James W.
dc.contributor.author
King, Andrew
dc.contributor.author
Kofler, Julia
dc.contributor.author
Kövari, Enikö
dc.contributor.author
Kril, Jillian J.
dc.contributor.author
Love, Seth
dc.contributor.author
Mackenzie, Ian R.
dc.contributor.author
Mao, Qinwen
dc.contributor.author
Matej, Radoslav
dc.contributor.author
McLean, Catriona
dc.date.issued
2020-05-22T19:39:33Z
dc.date.issued
2020-05-22T19:39:33Z
dc.date.issued
2020-05-22T19:39:33Z
dc.identifier
https://hdl.handle.net/2445/162098
dc.description.abstract
Aging-related tau astrogliopathy (ARTAG) is a recently introduced terminology. To facilitate the consistent identification of ARTAG and to distinguish it from astroglial tau pathologies observed in the primary frontotemporal lobar degeneration tauopathies we evaluated how consistently neuropathologists recognize (1) different astroglial tau immunoreactivities, including those of ARTAG and those associated with primary tauopathies (Study 1); (2) ARTAG types (Study 2A); and (3) ARTAG severity (Study 2B). Microphotographs and scanned sections immunostained for phosphorylated tau (AT8) were made available for download and preview. Percentage of agreement and kappa values with 95% confidence interval (CI) were calculated for each evaluation. The overall agreement for Study 1 was>60% with a kappa value of 0.55 (95% CI 0.433-0.645). Moderate agreement (>90%, kappa 0.48, 95% CI 0.457-0.900) was reached in Study 2A for the identification of ARTAG pathology for each ARTAG subtype (kappa 0.37-0.72), whereas fair agreement (kappa 0.40, 95% CI 0.341-0.445) was reached for the evaluation of ARTAG severity. The overall assessment of ARTAG showed moderate agreement (kappa 0.60, 95% CI 0.534-0.653) among raters. Our study supports the application of the current harmonized evaluation strategy for ARTAG with a slight modification of the evaluation of its severity.
dc.format
application/pdf
dc.publisher
Lippincott, Williams & Wilkins. Wolters Kluwer Health
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1093/jnen/nlx041
dc.relation
Journal of Neuropathology and Experimental Neurology, 2017, vol. 76, p. 605-619
dc.relation
https://doi.org/10.1093/jnen/nlx041
dc.rights
(c) American Association of Neuropathologists, 2017
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Patologia i Terapèutica Experimental)
dc.subject
Envelliment cerebral
dc.subject
Malalties neurodegeneratives
dc.subject
Neurodegenerative Diseases
dc.title
Multisite Assessment of Aging-Related Tau Astrogliopathy (ARTAG)
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion