New developments of biofluid-based biomarkers for routine diagnosis and disease trajectories in frontotemporal dementia

Frontotemporal dementia (FTD) covers a spectrum of neurodegenerative disorders with different phenotypes, genetic backgrounds, and pathological states. Its clinicopathological diversity challenges the diagnostic process and the execution of clinical trials, calling for specific diagnostic biomarkers...

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Detalhes bibliográficos
Autores: Campo Milán, Marta del|||0000-0003-2808-3699, Zetterberg, Henrik|||0000-0003-3930-4354, Gandy, Sam, Onyike, Chiadi U., Oliveira, Fabricio, Udeh-Momoh, Chinedu|||0000-0002-7357-4692, Lleó, Alberto|||0000-0002-2568-5478, Teunissen, Charlotte E.|||0000-0002-4061-0837, Pijnenburg, Yolande|||0000-0003-2464-1905
Formato: artículo
Fecha de publicación:2022
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:277687
Acesso em linha:https://ddd.uab.cat/record/277687
https://dx.doi.org/urn:doi:10.1002/alz.12643
Access Level:acceso abierto
Palavra-chave:Biomarkers
Frontotemporal Dementia
Humans
Neurodegenerative Diseases
Descrição
Resumo:Frontotemporal dementia (FTD) covers a spectrum of neurodegenerative disorders with different phenotypes, genetic backgrounds, and pathological states. Its clinicopathological diversity challenges the diagnostic process and the execution of clinical trials, calling for specific diagnostic biomarkers of pathologic FTD types. There is also a need for biomarkers that facilitate disease staging, quantification of severity, monitoring in clinics and observational studies, and for evaluation of target engagement and treatment response in clinical trials. This review discusses current FTD biofluid-based biomarker knowledge taking into account the differing applications. The limitations, knowledge gaps, and challenges for the development and implementation of such markers are also examined. Strategies to overcome these hurdles are proposed, including the technologies available, patient cohorts, and collaborative research initiatives. Access to robust and reliable biomarkers that define the exact underlying pathophysiological FTD process will meet the needs for specific diagnosis, disease quantitation, clinical monitoring, and treatment development.