Systematic review: genetic, neuroimaging, and fluids biomarkers for frontotemporal dementia across Latin America countries
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Durán Aniotz, Claudia Andrea
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Systematic review: genetic, neuroimaging, and fluids biomarkers for frontotemporal dementia across Latin America countries
Author
- Durán Aniotz, Claudia Andrea;
- Orellana, Paulina;
- Rodríguez, Tomas León;
- Henríquez, Fernando;
- Cabello, Victoria;
- Aguirre Pinto, María Francisca;
- Escobedo, Tamara;
- Takada, Leonel T.;
- Pina Escudero, Stefanie D.;
- López, Oscar;
- Yokoyama, Jennifer S.;
- Ibáñez, Agustín;
- Parra, Mario A.;
- Slachevsky Chonchol, Andrea Maria;
Abstract
Frontotemporal dementia (FTD) includes a group of clinically, genetically,
and pathologically heterogeneous neurodegenerative disorders, affecting the
fronto-insular-temporal regions of the brain. Clinically, FTD is characterized by
progressive deficits in behavior, executive function, and language and its diagnosis
relies mainly on the clinical expertise of the physician/consensus group and the use of
neuropsychological tests and/or structural/functional neuroimaging, depending on local
availability. The modest correlation between clinical findings and FTD neuropathology
makes the diagnosis difficult using clinical criteria and often leads to underdiagnosis
or misdiagnosis, primarily due to lack of recognition or awareness of FTD as a
disease and symptom overlap with psychiatric disorders. Despite advances in
understanding the underlying neuropathology of FTD, accurate and sensitive diagnosis
for this disease is still lacking. One of the major challenges is to improve diagnosis
in FTD patients as early as possible. In this context, biomarkers have emerged as
useful methods to provide and/or complement clinical diagnosis for this complex
syndrome, although more evidence is needed to incorporate most of them into
clinical practice. However, most biomarker studies have been performed using North
American or European populations, with little representation of the Latin American
and the Caribbean (LAC) region. In the LAC region, there are additional challenges, particularly the lack of awareness and knowledge about FTD, even in specialists.
Also, LAC genetic heritage and cultures are complex, and both likely influence clinical
presentations and may modify baseline biomarker levels. Even more, due to diagnostic
delay, the clinical presentation might be further complicated by both neurological and
psychiatric comorbidity, such as vascular brain damage, substance abuse, mood
disorders, among others. This systematic review provides a brief update and an overview
of the current knowledge on genetic, neuroimaging, and fluid biomarkers for FTD in
LAC countries. Our review highlights the need for extensive research on biomarkers in
FTD in LAC to contribute to a more comprehensive understanding of the disease and
its associated biomarkers. Dementia research is certainly reduced in the LAC region,
highlighting an urgent need for harmonized, innovative, and cross-regional studies with
a global perspective across multiple areas of dementia knowledge.
Patrocinador
Alzheimer Disease Association 2018-AARG-591107
GBHI ALZ UK-20-639295
ANID/FONDEF ID20I10152
18I10113
ANID/FONDECYT 1210622
Takeda Pharmaceutical Company Ltd CW2680521
Sistema General de Regalias BPIN2018000100059
National Institutes of Health, National Institutes of Aging R01 AG057234
Alzheimer's Association SG-20-725707
Tau Consortium
Global Brain Health Institute
ANID/FONDAP/15150012
ANID/Fondecyt/1191726
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Frontiers in Neurology June 2021 Volume 12 Article 663407
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