Detection of TDP‐43 seeding activity in the olfactory mucosa from patients with frontotemporal dementia

Author:

Fontana Elena1,Bongianni Matilde1,Benussi Alberto23,Bronzato Erika1,Scialo Carlo4,Sacchetto Luca5,Cagnin Annachiara67,Castriciano Santina8,Buratti Emanuele9,Gardoni Fabrizio10,Italia Maria10,Schreiber Alberto11,Ferracin Chiara12,Fiorini Michele1,Newell Kathy L.13,Cracco Laura13,Garringer Holly J.13,Cecchini Maria Paola1,Polymenidou Magdalini4,Padovani Alessandro23,Monaco Salvatore1,Legname Giuseppe12,Ghetti Bernardino13,Borroni Barbara23,Zanusso Gianluigi1

Affiliation:

1. Department of Neuroscience, Biomedicine and Movement Sciences University of Verona Verona Italy

2. Department of Clinical and Experimental Sciences University of Brescia Brescia Italy

3. Department of Continuity of Care and Frailty ASST Spedali Civili Brescia Hospital Brescia Italy

4. Department of Quantitative Biomedicine University of Zurich Zurich Switzerland

5. Department of Surgery Dentistry Paediatrics and Gynaecology Otolaryngology Section University of Verona Verona Italy

6. Neurology Unit Department of Neuroscience University of Padova Padua Italy

7. Padova Neuroscience Center (PNC) University of Padova Padua Italy

8. Copan, S.P.A Brescia Italy

9. International Centre for Genetic Engineering and Biotechnology (ICGEB) Trieste Italy

10. Department of Pharmacological and Biomolecular Sciences (DiSFeB) “Rodolfo Paoletti,” University of Milan Milan Italy

11. Otorhinolaryngology Unit, Head and Neck Surgery ASST Spedali Civili University of Brescia Brescia Italy

12. Laboratory of Prion Biology Department of Neuroscience Scuola Internazionale Superiore Di Studi Avanzati (SISSA) Trieste Italy

13. Department of Pathology and Laboratory Medicine School of Medicine Indiana University Indianapolis Indiana USA

Abstract

AbstractINTRODUCTIONWe assessed TAR DNA‐binding protein 43 (TDP‐43) seeding activity and aggregates detection in olfactory mucosa of patients with frontotemporal lobar degeneration with TDP‐43‐immunoreactive pathology (FTLD‐TDP) by TDP‐43 seeding amplification assay (TDP43‐SAA) and immunocytochemical analysis.METHODSThe TDP43‐SAA was optimized using frontal cortex samples from 16 post mortem cases with FTLD‐TDP, FTLD with tau inclusions, and controls. Subsequently, olfactory mucosa samples were collected from 17 patients with FTLD‐TDP, 15 healthy controls, and three patients carrying MAPT variants.RESULTSTDP43‐SAA discriminated with 100% accuracy post mortem cases presenting or lacking TDP‐43 neuropathology. TDP‐43 seeding activity was detectable in the olfactory mucosa, and 82.4% of patients with FTLD‐TDP tested positive, whereas 86.7% of controls tested negative (P < 0.001). Two out of three patients with MAPT mutations tested negative. In TDP43‐SAA positive samples, cytoplasmatic deposits of phosphorylated TDP‐43 in the olfactory neural cells were detected.DISCUSSIONTDP‐43 aggregates can be detectable in olfactory mucosa, suggesting that TDP43‐SAA might be useful for identifying and monitoring FTLD‐TDP in living patients.

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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