Genetic and Pathological Characteristics of Frontotemporal Dementia with Right Anterior Temporal Predominance: A Multicenter Retrospective Cohort Study

While FTD with RATL atrophy primarily appears sporadic, a significant proportion of cases exhibit genetic variants. These sporadic and genetic subtypes display distinct neuropathological features and clinical manifestations. Given the implications for therapeutic strategies, precise clinical and molecular subtyping is critical for enhancing patient management and ensuring appropriate enrollment in clinical trials.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70857_103987
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
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article

Genetic and Pathological Characteristics of Frontotemporal Dementia with Right Anterior Temporal Predominance: A Multicenter Retrospective Cohort Study

Elisa Canu, Hakan Gürvit, Kyan Younes, Bedia Samancı et al.
Alzheimer s & Dementia
Amyotrophic Lateral Sclerosis Research
article

Genetic and Pathological Characteristics of Frontotemporal Dementia with Right Anterior Temporal Predominance: A Multicenter Retrospective Cohort Study

Elisa Canu, Hakan Gürvit, Kyan Younes, Bedia Samancı, Giorgio Fumagalli, Alexandre Morin, Hülya Ulugut, Ignacio Illán‐Gala, Toji Miyagawa, Lina Riedl, Katherine Rankin, Maxime Montembeault, Virginia E. Sturm, Jason D. Warren, Maxime Bertoux, Alma Ghirelli, J. C. Thompson, Janine Diehl‐Schmid, Thibaud Lebouvier, Alexander Santillo, Julie S. Snowden, So Young Moon, Peter Pressman, Yolande A.L. Pijnenburg, Carmela M. Tartaglia, Simon Ducharme, Elisabet Englund, Federica Agosta, Maria Luisa Gorno Tempini, Jan Van den Stock, Massimo Filippi, Brad F Boeve, Leonel Tadao Takada, Na‐Yeon Jung, Mathieu Vandenbulcke, Bruce L. Miller, Rik Vandenberghe, Jennifer L. Whitwell, Robert Laforce, Daniela Galimberti, Matthias L Schroeter, Edoardo G. Spinelli, María Landqvist Waldö, Leonardo Cruz de Souza, International rtvFTD Working Group, Eun‐Joo Kim, Keith A. Josephs, Jonathan D. Rohrer
article en

Abstract

While FTD with RATL atrophy primarily appears sporadic, a significant proportion of cases exhibit genetic variants. These sporadic and genetic subtypes display distinct neuropathological features and clinical manifestations. Given the implications for therapeutic strategies, precise clinical and molecular subtyping is critical for enhancing patient management and ensuring appropriate enrollment in clinical trials.

Alzheimer s & DementiaVol. 21(S3)
Universidade Federal de Minas Gerais (BR), Universitat Autònoma de Barcelona (ES), Montreal Neurological Institute and Hospital (CA), Vita-Salute San Raffaele University (IT), Inserm (FR), University of California, San Francisco (US), University of Toronto (CA), Lund University (SE), University of Milan (IT), University of Trento (IT), Université de Lille (FR), Douglas Mental Health University Institute (CA), Hospital de Sant Pau (ES), University of Manchester (GB), Centre Hospitalier Universitaire de Lille (FR), Kidney Foundation of Canada (CA), University Memory and Aging Center (US), Alzheimer’s Disease Neuroimaging Initiative (US), Amsterdam Neuroscience (NL), Inn-Salzach-Klinikum (DE), Mayo Clinic in Arizona (US), UK Dementia Research Institute (GB), Max Planck Institute for Human Cognitive and Brain Sciences (DE), Skåne University Hospital (SE), NIHR Queen Square Dementia Biomedical Research Unit (GB), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (BR), Pusan National University Yangsan Hospital (KR), Istituti di Ricovero e Cura a Carattere Scientifico (IT), VIB-KU Leuven Center for Brain & Disease Research (BE), Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele (IT), University College London (GB), Pusan National University (KR), McGill University (CA), Ajou University (KR), Université de Rouen Normandie (FR), Technical University of Munich (DE), Istanbul University (TR), Stanford University (US), KU Leuven (BE)
Partnerships for the goals
Openalex Percentile: Top 31%
Amyotrophic Lateral Sclerosis Research
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