Brain-Derived Neurotrophic Factor Polymorphism and Aphasia after Stroke

Stroke is one of the most deliberating causes of mortality and disability worldwide. Studies have implicated Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene as a genetic factor influencing stroke recovery. Still, the role of BDNF polymorphism in poststroke aphasia is relat...

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Main Authors: Nathan T. Lee, Fatimah Ahmedy, Natiara Mohamad Hashim, Khin Nyein Yin, Kai Ling Chin
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Behavioural Neurology
Online Access:http://dx.doi.org/10.1155/2021/8887012
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author Nathan T. Lee
Fatimah Ahmedy
Natiara Mohamad Hashim
Khin Nyein Yin
Kai Ling Chin
author_facet Nathan T. Lee
Fatimah Ahmedy
Natiara Mohamad Hashim
Khin Nyein Yin
Kai Ling Chin
author_sort Nathan T. Lee
collection DOAJ
description Stroke is one of the most deliberating causes of mortality and disability worldwide. Studies have implicated Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene as a genetic factor influencing stroke recovery. Still, the role of BDNF polymorphism in poststroke aphasia is relatively unclear. This review assesses the recent evidence on the association between the BDNF polymorphism and aphasia recovery in poststroke patients. The article highlights BNDF polymorphism characteristics, speech and language interventions delivered, and the influence of BNDF polymorphism on poststroke aphasia recovery. We conducted a literature search through PubMed and Google Scholar with the following terms: “brain derived-neurotrophic factor” and “aphasia” for original articles from January 2000 until June 2020. Out of 69 search results, a detailed selection process produced a total of 3 articles that met the eligibility criteria. All three studies included Val66Met polymorphism as the studied human BDNF gene. One of the studies demonstrated insufficient evidence to conclude that BDNF polymorphism plays a role in poststroke aphasia recovery. The remaining two studies have shown that Met allele genotype (either single or double nucleotides) was associated with poor aphasia recovery, in either acute or chronic stroke. Carriers of the Val66Met polymorphism of BDNF gave a poorer response to aphasia intervention and presented with more severe aphasia.
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spelling doaj-art-64e5ee97deea4ed1a6fd384a90bc3ec92025-02-03T01:27:00ZengWileyBehavioural Neurology0953-41801875-85842021-01-01202110.1155/2021/88870128887012Brain-Derived Neurotrophic Factor Polymorphism and Aphasia after StrokeNathan T. Lee0Fatimah Ahmedy1Natiara Mohamad Hashim2Khin Nyein Yin3Kai Ling Chin4Rehabilitation Medicine Unit, Faculty of Medicine & Health Sciences, Universiti Malaysia Sabah, Kota Kinabalu, MalaysiaRehabilitation Medicine Unit, Faculty of Medicine & Health Sciences, Universiti Malaysia Sabah, Kota Kinabalu, MalaysiaDepartment of Rehabilitation Medicine, Faculty of Medicine, Universiti Teknologi MARA, Sg. Buloh, MalaysiaDepartment of Surgery, Faculty of Medicine & Health Sciences, Universiti Malaysia Sabah, Kota Kinabalu, MalaysiaDepartment of Biomedical Sciences, Faculty of Medicine & Health Sciences, Universiti Malaysia Sabah, Kota Kinabalu, MalaysiaStroke is one of the most deliberating causes of mortality and disability worldwide. Studies have implicated Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene as a genetic factor influencing stroke recovery. Still, the role of BDNF polymorphism in poststroke aphasia is relatively unclear. This review assesses the recent evidence on the association between the BDNF polymorphism and aphasia recovery in poststroke patients. The article highlights BNDF polymorphism characteristics, speech and language interventions delivered, and the influence of BNDF polymorphism on poststroke aphasia recovery. We conducted a literature search through PubMed and Google Scholar with the following terms: “brain derived-neurotrophic factor” and “aphasia” for original articles from January 2000 until June 2020. Out of 69 search results, a detailed selection process produced a total of 3 articles that met the eligibility criteria. All three studies included Val66Met polymorphism as the studied human BDNF gene. One of the studies demonstrated insufficient evidence to conclude that BDNF polymorphism plays a role in poststroke aphasia recovery. The remaining two studies have shown that Met allele genotype (either single or double nucleotides) was associated with poor aphasia recovery, in either acute or chronic stroke. Carriers of the Val66Met polymorphism of BDNF gave a poorer response to aphasia intervention and presented with more severe aphasia.http://dx.doi.org/10.1155/2021/8887012
spellingShingle Nathan T. Lee
Fatimah Ahmedy
Natiara Mohamad Hashim
Khin Nyein Yin
Kai Ling Chin
Brain-Derived Neurotrophic Factor Polymorphism and Aphasia after Stroke
Behavioural Neurology
title Brain-Derived Neurotrophic Factor Polymorphism and Aphasia after Stroke
title_full Brain-Derived Neurotrophic Factor Polymorphism and Aphasia after Stroke
title_fullStr Brain-Derived Neurotrophic Factor Polymorphism and Aphasia after Stroke
title_full_unstemmed Brain-Derived Neurotrophic Factor Polymorphism and Aphasia after Stroke
title_short Brain-Derived Neurotrophic Factor Polymorphism and Aphasia after Stroke
title_sort brain derived neurotrophic factor polymorphism and aphasia after stroke
url http://dx.doi.org/10.1155/2021/8887012
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