2020-05-22T19:39:33Z
2020-05-22T19:39:33Z
2017
2020-05-22T19:39:33Z
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.
Article
Versió acceptada
Anglès
Envelliment cerebral; Astròcits; Malalties neurodegeneratives; Aging brain; Astrocytes; Neurodegenerative Diseases
Lippincott, Williams & Wilkins. Wolters Kluwer Health
Versió postprint del document publicat a: https://doi.org/10.1093/jnen/nlx041
Journal of Neuropathology and Experimental Neurology, 2017, vol. 76, p. 605-619
https://doi.org/10.1093/jnen/nlx041
(c) American Association of Neuropathologists, 2017