Význam brain-derived neurotrophic factor (BDNF) genetického polymorfismu a hladin BDNF pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění
Alzheimer's disease (AD) is a slowly progressing neurodegenerative disease characterized by an extracellular accumulation of senile plaques and intracellular neurofibrillary tangles. Apart from these hallmarks, AD is very heterogeneous, especially at the age of onset and the rate of progression...
Main Author: | |
---|---|
Other Authors: | |
Format: | Doctoral Thesis |
Language: | Czech |
Published: |
2021
|
Online Access: | http://www.nusl.cz/ntk/nusl-439895 |
id |
ndltd-nusl.cz-oai-invenio.nusl.cz-439895 |
---|---|
record_format |
oai_dc |
spelling |
ndltd-nusl.cz-oai-invenio.nusl.cz-4398952021-05-31T05:11:07Z Význam brain-derived neurotrophic factor (BDNF) genetického polymorfismu a hladin BDNF pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění The impact of brain-derived neurotrophic factor (BDNF) gene polymorphism and BDNF levels for prediction, diagnosis and follow-up of cognitive deficit in neurodegenerative diseases Čechová, Kateřina Hort, Jakub Telenský, Petr Rektorová, Irena Alzheimer's disease (AD) is a slowly progressing neurodegenerative disease characterized by an extracellular accumulation of senile plaques and intracellular neurofibrillary tangles. Apart from these hallmarks, AD is very heterogeneous, especially at the age of onset and the rate of progression. Genetic polymorphisms are key modulators influencing these factors. One of them is a polymorphism for the Brain-derived neurotrophic factor (BDNF), a neurotrophin involved in the synaptic plasticity in the hippocampus and medial temporal lobe structures, areas primarily affected in AD. The thesis aimed to investigate the effect of BDNF Va66Met polymorphism together with the main genetic risk factor for sporadic AD, Apolipoprotein E (APOE) polymorphism, on cognitive functions and structural brain changes. We have shown that the combination of risk alleles BDNF Met and APOE ɛ4 is associated with more severe impairment in episodic memory, egocentric orientation and smaller volumes of medial temporal lobe structures in individuals with amnestic mild cognitive impairment (aMCI), and allocentric orientation in cognitively unimpaired individuals compared to non-carriers. These findings suggest that carriers of the combination of BDNF Met and APOE ɛ4 have a higher risk of progression to more severe disease stages,... 2021 info:eu-repo/semantics/doctoralThesis http://www.nusl.cz/ntk/nusl-439895 cze info:eu-repo/semantics/restrictedAccess |
collection |
NDLTD |
language |
Czech |
format |
Doctoral Thesis |
sources |
NDLTD |
description |
Alzheimer's disease (AD) is a slowly progressing neurodegenerative disease characterized by an extracellular accumulation of senile plaques and intracellular neurofibrillary tangles. Apart from these hallmarks, AD is very heterogeneous, especially at the age of onset and the rate of progression. Genetic polymorphisms are key modulators influencing these factors. One of them is a polymorphism for the Brain-derived neurotrophic factor (BDNF), a neurotrophin involved in the synaptic plasticity in the hippocampus and medial temporal lobe structures, areas primarily affected in AD. The thesis aimed to investigate the effect of BDNF Va66Met polymorphism together with the main genetic risk factor for sporadic AD, Apolipoprotein E (APOE) polymorphism, on cognitive functions and structural brain changes. We have shown that the combination of risk alleles BDNF Met and APOE ɛ4 is associated with more severe impairment in episodic memory, egocentric orientation and smaller volumes of medial temporal lobe structures in individuals with amnestic mild cognitive impairment (aMCI), and allocentric orientation in cognitively unimpaired individuals compared to non-carriers. These findings suggest that carriers of the combination of BDNF Met and APOE ɛ4 have a higher risk of progression to more severe disease stages,... |
author2 |
Hort, Jakub |
author_facet |
Hort, Jakub Čechová, Kateřina |
author |
Čechová, Kateřina |
spellingShingle |
Čechová, Kateřina Význam brain-derived neurotrophic factor (BDNF) genetického polymorfismu a hladin BDNF pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění |
author_sort |
Čechová, Kateřina |
title |
Význam brain-derived neurotrophic factor (BDNF) genetického polymorfismu a hladin BDNF pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění |
title_short |
Význam brain-derived neurotrophic factor (BDNF) genetického polymorfismu a hladin BDNF pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění |
title_full |
Význam brain-derived neurotrophic factor (BDNF) genetického polymorfismu a hladin BDNF pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění |
title_fullStr |
Význam brain-derived neurotrophic factor (BDNF) genetického polymorfismu a hladin BDNF pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění |
title_full_unstemmed |
Význam brain-derived neurotrophic factor (BDNF) genetického polymorfismu a hladin BDNF pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění |
title_sort |
význam brain-derived neurotrophic factor (bdnf) genetického polymorfismu a hladin bdnf pro predikci, diagnostiku a monitoraci kognitivního deficitu u neurodegenerativních onemocnění |
publishDate |
2021 |
url |
http://www.nusl.cz/ntk/nusl-439895 |
work_keys_str_mv |
AT cechovakaterina vyznambrainderivedneurotrophicfactorbdnfgenetickehopolymorfismuahladinbdnfpropredikcidiagnostikuamonitoracikognitivnihodeficituuneurodegenerativnichonemocneni AT cechovakaterina theimpactofbrainderivedneurotrophicfactorbdnfgenepolymorphismandbdnflevelsforpredictiondiagnosisandfollowupofcognitivedeficitinneurodegenerativediseases |
_version_ |
1719408224954744832 |