Literature DB >> 34095977

Clinical and neuropathological diversity of tauopathy in MAPT duplication carriers.

David Wallon1, Susana Boluda2,3, Anne Rovelet-Lecrux4, Manon Thierry2,3, Julien Lagarde5,6,7, Laetitia Miguel4, Magalie Lecourtois4, Antoine Bonnevalle8, Marie Sarazin5,6,7, Michel Bottlaender7,9, Mathieu Mula3, Serge Marty2, Natsuko Nakamura2, Catherine Schramm4, François Sellal10, Thérèse Jonveaux11, Camille Heitz12, Isabelle Le Ber13,14, Stéphane Epelbaum15,16, Eloi Magnin15,16, Aline Zarea8, Stéphane Rousseau4, Olivier Quenez4, Didier Hannequin8, Florence Clavaguera2, Dominique Campion4, Charles Duyckaerts2,3, Gaël Nicolas17.   

Abstract

Microduplications of the 17q21.31 chromosomal region encompassing the MAPT gene, which encodes the Tau protein, were identified in patients with a progressive disorder initially characterized by severe memory impairment with or without behavioral changes that can clinically mimic Alzheimer disease. The unique neuropathological report showed a primary tauopathy, which could not be unanimously classified in a given known subtype, showing both 4R- and 3R-tau inclusions, mainly within temporal cortical subregions and basal ganglia, without amyloid deposits. Recently, two subjects harboring the same duplication were reported with an atypical extrapyramidal syndrome and gait disorder. To decipher the phenotypic spectrum associated with MAPT duplications, we studied ten carriers from nine families, including two novel unrelated probands, gathering clinical (n = 10), cerebrospinal fluid (n = 6), MRI (n = 8), dopamine transporter scan (n = 4), functional (n = 5), amyloid (n = 3) and Tau-tracer (n = 2) PET imaging data as well as neuropathological examination (n = 4). Ages at onset ranged from 37 to 57 years, with prominent episodic memory impairment in 8/10 patients, associated with behavioral changes in four, while two patients showed atypical extrapyramidal syndrome with gait disorder at presentation, including one with associated cognitive deficits. Amyloid imaging was negative but Tau imaging showed significant deposits mainly in both mesiotemporal cortex. Dopaminergic denervation was found in 4/4 patients, including three without extrapyramidal symptoms. Neuropathological examination exclusively showed Tau-immunoreactive lesions. Distribution, aspect and 4R/3R tau aggregates composition suggested a spectrum from predominantly 3R, mainly cortical deposits well correlating with cognitive and behavioral changes, to predominantly 4R deposits, mainly in the basal ganglia and midbrain, in patients with prominent extrapyramidal syndrome. Finally, we performed in vitro seeding experiments in HEK-biosensor cells. Morphological features of aggregates induced by homogenates of three MAPT duplication carriers showed dense/granular ratios graduating between those induced by homogenates of a Pick disease and a progressive supranuclear palsy cases. These results suggest that MAPT duplication causes a primary tauopathy associated with diverse clinical and neuropathological features.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Keywords:  MAPT duplication; Pick disease; Progressive supranuclear palsy; Tau; Tau seeding

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Year:  2021        PMID: 34095977     DOI: 10.1007/s00401-021-02320-4

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  1 in total

1.  Sensitive Detection of Proteopathic Seeding Activity with FRET Flow Cytometry.

Authors:  Jennifer L Furman; Brandon B Holmes; Marc I Diamond
Journal:  J Vis Exp       Date:  2015-12-08       Impact factor: 1.355

  1 in total

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