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The BDNF Val66Met polymorphism modulates resilience of neurological functioning to brain ageing and dementia: A narrative review

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F20%3A10410908" target="_blank" >RIV/00216208:11130/20:10410908 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00159816:_____/20:00072906 RIV/00064203:_____/20:10410908

  • Výsledek na webu

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=b8hmUnwhIW" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=b8hmUnwhIW</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/brainsci10040195" target="_blank" >10.3390/brainsci10040195</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    The BDNF Val66Met polymorphism modulates resilience of neurological functioning to brain ageing and dementia: A narrative review

  • Popis výsledku v původním jazyce

    Brain-derived neurotropic factor (BDNF) is an abundant and multi-function neurotrophin in the brain. It is released following neuronal activity and is believed to be particularly important in strengthening neural networks. A common variation in the BDNF gene, a valine to methionine substitution at codon 66 (Val66Met), has been linked to differential expression of BDNF associated with experience-dependent plasticity. The Met allele has been associated with reduced production of BDNF following neuronal stimulation, which suggests a potential role of this variation with respect to how the nervous system may respond to challenges, such as brain ageing and related neurodegenerative conditions (e.g., dementia and Alzheimer&apos;s disease). The current review examines the potential of the BDNF Val66Met variation to modulate an individual&apos;s susceptibility and trajectory through cognitive changes associated with ageing and dementia. On balance, research to date indicates that the BDNF Met allele at this codon is potentially associated with a detrimental influence on the level of cognitive functioning in older adults and may also impart increased risk of progression to dementia. Furthermore, recent studies also show that this genetic variation may modulate an individual&apos;s response to interventions targeted at building cognitive resilience to conditions that cause dementia. (C) 2020 by the authors. Licensee MDPI, Basel, Switzerland.

  • Název v anglickém jazyce

    The BDNF Val66Met polymorphism modulates resilience of neurological functioning to brain ageing and dementia: A narrative review

  • Popis výsledku anglicky

    Brain-derived neurotropic factor (BDNF) is an abundant and multi-function neurotrophin in the brain. It is released following neuronal activity and is believed to be particularly important in strengthening neural networks. A common variation in the BDNF gene, a valine to methionine substitution at codon 66 (Val66Met), has been linked to differential expression of BDNF associated with experience-dependent plasticity. The Met allele has been associated with reduced production of BDNF following neuronal stimulation, which suggests a potential role of this variation with respect to how the nervous system may respond to challenges, such as brain ageing and related neurodegenerative conditions (e.g., dementia and Alzheimer&apos;s disease). The current review examines the potential of the BDNF Val66Met variation to modulate an individual&apos;s susceptibility and trajectory through cognitive changes associated with ageing and dementia. On balance, research to date indicates that the BDNF Met allele at this codon is potentially associated with a detrimental influence on the level of cognitive functioning in older adults and may also impart increased risk of progression to dementia. Furthermore, recent studies also show that this genetic variation may modulate an individual&apos;s response to interventions targeted at building cognitive resilience to conditions that cause dementia. (C) 2020 by the authors. Licensee MDPI, Basel, Switzerland.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30103 - Neurosciences (including psychophysiology)

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2020

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Brain Sciences [online]

  • ISSN

    2076-3425

  • e-ISSN

  • Svazek periodika

    10

  • Číslo periodika v rámci svazku

    4

  • Stát vydavatele periodika

    CH - Švýcarská konfederace

  • Počet stran výsledku

    16

  • Strana od-do

    195

  • Kód UT WoS článku

    000534271500043

  • EID výsledku v databázi Scopus

    2-s2.0-85082853957