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  4. BDNF as a Biomarker of Cognition in Schizophrenia/Psychosis: An Updated Review
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BDNF as a Biomarker of Cognition in Schizophrenia/Psychosis: An Updated Review

Journal
Frontiers in Psychiatry
ISSN
1664-0640
Date Issued
2021
Author(s)
Rodrigo R. Nieto
Andrea Carrasco
Sebastian Corral
Rolando Castillo
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Pablo A. Gaspar
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
M. Leonor Bustamante
Hernan Silva
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85113490700
WoS ID
WOS:000668127200001
DOI
10.3389/fpsyt.2021.662407
URL
https://investigadores.udd.cl/handle/123456789/5788
URL Institutional Repository
http://hdl.handle.net/11447/6598
Abstract
<jats:p>Brain Derived Neurotrophic Factor (BDNF) has been linked to cognitive symptoms of schizophrenia, which has been documented in previous reviews by several authors. However, a trend has recently emerged in this field moving from studying schizophrenia as a disease to studying psychosis as a group. This review article focuses on recent BDNF studies in relation to cognition in human subjects during different stages of the psychotic process, including subjects at high risk of developing psychosis, patients at their first episode of psychosis, and patients with chronic schizophrenia. We aim to provide an update of BDNF as a biomarker of cognitive function on human subjects with schizophrenia or earlier stages of psychosis, covering new trends, controversies, current research gaps, and suggest potential future developments in the field. We found that most of current research regarding BDNF and cognitive symptoms in psychosis is done around schizophrenia as a disease. Therefore, it is necessary to expand the study of the relationship between BDNF and cognitive symptoms to psychotic illnesses of different stages and origins.</jats:p>
Subjects
brain-derived neurotrophic factor

; 

neurotrophin

; 

neurocognition

; 

cognitive symptoms

; 

chronic schizophrenia

; 

first episode psychosis

; 

clinical high-risk for psychosis

; 

brain derived neurotrophic factor

; 

olanzapine

; 

cognition

; 

cognitive remediation therapy

; 

disease association

; 

drug effect

; 

executive function

; 

high risk patient

; 

human

; 

kinesiotherapy

; 

review

; 

risk assessment

; 

schizophrenia

; 

systematic review

; 

treatment outcome

; 

treatment planning
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