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...

Descripción completa

Detalles Bibliográficos
Autores principales: Drag, Lauren L., Mlynash, Michael, Nassar, Huda, Osborn, Elizabeth, Kim, Da E., Angst, Martin S., Aghaeepour, Nima, Buckwalter, Marion, Lansberg, Maarten G.
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