Antemortem volume loss mirrors TDP-43 staging in older adults with non-frontotemporal lobar degeneration

Author:

Bejanin Alexandre12ORCID,Murray Melissa E3,Martin Peter4,Botha Hugo1ORCID,Tosakulwong Nirubol4,Schwarz Christopher G5,Senjem Matthew L56,Chételat Gael2,Kantarci Kejal5,Jack Clifford R5,Boeve Bradley F1,Knopman David S1,Petersen Ronald C1,Giannini Caterina7,Parisi Joseph E7,Dickson Dennis W3ORCID,Whitwell Jennifer L5,Josephs Keith A1

Affiliation:

1. Department of Neurology, Mayo Clinic, Rochester, MN, USA

2. Inserm, Inserm UMR-S U1237, Université de Caen-Normandie, GIP Cyceron, Caen, France

3. Department of Neuroscience, Mayo Clinic, Florida, USA

4. Health Science Research, Mayo Clinic, Rochester, MN, USA

5. Department of Radiology, Mayo Clinic, Rochester, MN, USA

6. Department of Information Technology, Mayo Clinic, Rochester, MN, USA

7. Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA

Abstract

The specific effect of TDP-43 pathology on grey matter volume in individuals without frontotemporal lobar degeneration is unclear. Bejanin et al. reveal a major and independent contribution of TDP-43 to neurodegeneration and shed light on the regional distribution of TDP-43-related atrophy in older adults.

Funder

National Institutes of Health

Gerald and Henrietta Rauenhorst Foundation

Elsie and Marvin Dekelboum Family Foundation

Alexander Family Alzheimer’s Disease Research Professorship of the Mayo Clinic

Mayo Foundation for Medical Education and Research

Fondation Thérèse et René Planiol

Conseil Régional de Normandie

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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