Cargando…
A longitudinal study of the post-stroke immune response and cognitive functioning: the StrokeCog study protocol
BACKGROUND: Stroke increases the risk of cognitive impairment even several years after the stroke event. The exact mechanisms of post-stroke cognitive decline are unclear, but the immunological response to stroke might play a role. The aims of the StrokeCog study are to examine the associations betw...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448308/ https://www.ncbi.nlm.nih.gov/pubmed/32847540 http://dx.doi.org/10.1186/s12883-020-01897-9 |
_version_ | 1783574473936470016 |
---|---|
author | Drag, Lauren L. Mlynash, Michael Nassar, Huda Osborn, Elizabeth Kim, Da E. Angst, Martin S. Aghaeepour, Nima Buckwalter, Marion Lansberg, Maarten G. |
author_facet | Drag, Lauren L. Mlynash, Michael Nassar, Huda Osborn, Elizabeth Kim, Da E. Angst, Martin S. Aghaeepour, Nima Buckwalter, Marion Lansberg, Maarten G. |
author_sort | Drag, Lauren L. |
collection | PubMed |
description | BACKGROUND: Stroke increases the risk of cognitive impairment even several years after the stroke event. The exact mechanisms of post-stroke cognitive decline are unclear, but the immunological response to stroke might play a role. The aims of the StrokeCog study are to examine the associations between immunological responses and long-term post-stroke cognitive trajectories in individuals with ischemic stroke. METHODS: StrokeCog is a single-center, prospective, observational, cohort study. Starting 6–12 months after stroke, comprehensive neuropsychological assessment, plasma and serum, and psychosocial variables will be collected at up to 4 annual visits. Single cell sequencing of peripheral blood monocytes and plasma proteomics will be conducted. The primary outcome will be the change in global and domain-specific neuropsychological performance across annual evaluations. To explain the differences in cognitive change amongst participants, we will examine the relationships between comprehensive immunological measures and these cognitive trajectories. It is anticipated that 210 participants will be enrolled during the first 3 years of this 4-year study. Accounting for attrition, an anticipated final sample size of 158 participants with an average of 3 annual study visits will be available at the completion of the study. Power analyses indicate that this sample size will provide 90% power to detect an average cognitive change of at least 0.23 standard deviations in either direction. DISCUSSION: StrokeCog will provide novel insight into the relationships between immune events and cognitive change late after stroke. |
format | Online Article Text |
id | pubmed-7448308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74483082020-08-27 A longitudinal study of the post-stroke immune response and cognitive functioning: the StrokeCog study protocol Drag, Lauren L. Mlynash, Michael Nassar, Huda Osborn, Elizabeth Kim, Da E. Angst, Martin S. Aghaeepour, Nima Buckwalter, Marion Lansberg, Maarten G. BMC Neurol Study Protocol BACKGROUND: Stroke increases the risk of cognitive impairment even several years after the stroke event. The exact mechanisms of post-stroke cognitive decline are unclear, but the immunological response to stroke might play a role. The aims of the StrokeCog study are to examine the associations between immunological responses and long-term post-stroke cognitive trajectories in individuals with ischemic stroke. METHODS: StrokeCog is a single-center, prospective, observational, cohort study. Starting 6–12 months after stroke, comprehensive neuropsychological assessment, plasma and serum, and psychosocial variables will be collected at up to 4 annual visits. Single cell sequencing of peripheral blood monocytes and plasma proteomics will be conducted. The primary outcome will be the change in global and domain-specific neuropsychological performance across annual evaluations. To explain the differences in cognitive change amongst participants, we will examine the relationships between comprehensive immunological measures and these cognitive trajectories. It is anticipated that 210 participants will be enrolled during the first 3 years of this 4-year study. Accounting for attrition, an anticipated final sample size of 158 participants with an average of 3 annual study visits will be available at the completion of the study. Power analyses indicate that this sample size will provide 90% power to detect an average cognitive change of at least 0.23 standard deviations in either direction. DISCUSSION: StrokeCog will provide novel insight into the relationships between immune events and cognitive change late after stroke. BioMed Central 2020-08-26 /pmc/articles/PMC7448308/ /pubmed/32847540 http://dx.doi.org/10.1186/s12883-020-01897-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol Drag, Lauren L. Mlynash, Michael Nassar, Huda Osborn, Elizabeth Kim, Da E. Angst, Martin S. Aghaeepour, Nima Buckwalter, Marion Lansberg, Maarten G. A longitudinal study of the post-stroke immune response and cognitive functioning: the StrokeCog study protocol |
title | A longitudinal study of the post-stroke immune response and cognitive functioning: the StrokeCog study protocol |
title_full | A longitudinal study of the post-stroke immune response and cognitive functioning: the StrokeCog study protocol |
title_fullStr | A longitudinal study of the post-stroke immune response and cognitive functioning: the StrokeCog study protocol |
title_full_unstemmed | A longitudinal study of the post-stroke immune response and cognitive functioning: the StrokeCog study protocol |
title_short | A longitudinal study of the post-stroke immune response and cognitive functioning: the StrokeCog study protocol |
title_sort | longitudinal study of the post-stroke immune response and cognitive functioning: the strokecog study protocol |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448308/ https://www.ncbi.nlm.nih.gov/pubmed/32847540 http://dx.doi.org/10.1186/s12883-020-01897-9 |
work_keys_str_mv | AT draglaurenl alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT mlynashmichael alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT nassarhuda alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT osbornelizabeth alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT kimdae alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT angstmartins alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT aghaeepournima alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT buckwaltermarion alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT lansbergmaarteng alongitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT draglaurenl longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT mlynashmichael longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT nassarhuda longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT osbornelizabeth longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT kimdae longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT angstmartins longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT aghaeepournima longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT buckwaltermarion longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol AT lansbergmaarteng longitudinalstudyofthepoststrokeimmuneresponseandcognitivefunctioningthestrokecogstudyprotocol |