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Consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients
Acute ischemic stroke (AIS) is a primary cause of mortality and morbidity worldwide. Currently, no clinically approved immune intervention is available for AIS treatment, partly due to the lack of relevant patient classification based on the peripheral immunity status of patients with AIS. In this s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388856/ https://www.ncbi.nlm.nih.gov/pubmed/35989931 http://dx.doi.org/10.3389/fneur.2022.937501 |
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author | Yang, Zhiyong Wang, Guanghui Luo, Nan Tsang, Chi Kwan Huang, Li'an |
author_facet | Yang, Zhiyong Wang, Guanghui Luo, Nan Tsang, Chi Kwan Huang, Li'an |
author_sort | Yang, Zhiyong |
collection | PubMed |
description | Acute ischemic stroke (AIS) is a primary cause of mortality and morbidity worldwide. Currently, no clinically approved immune intervention is available for AIS treatment, partly due to the lack of relevant patient classification based on the peripheral immunity status of patients with AIS. In this study, we adopted the consensus clustering approach to classify patients with AIS into molecular subgroups based on the transcriptomic profiles of peripheral blood, and we identified three distinct AIS molecular subgroups and 8 modules in each subgroup by the weighted gene co-expression network analysis. Remarkably, the pre-ranked gene set enrichment analysis revealed that the co-expression modules with subgroup I-specific signature genes significantly overlapped with the differentially expressed genes in AIS patients with hemorrhagic transformation (HT). With respect to subgroup II, exclusively male patients with decreased proteasome activity were identified. Intriguingly, the majority of subgroup III was composed of female patients who showed a comparatively lower level of AIS-induced immunosuppression (AIIS). In addition, we discovered a non-linear relationship between female age and subgroup-specific gene expression, suggesting a gender- and age-dependent alteration of peripheral immunity. Taken together, our novel AIS classification approach could facilitate immunomodulatory therapies, including the administration of gender-specific therapeutics, and attenuation of the risk of HT and AIIS after ischemic stroke. |
format | Online Article Text |
id | pubmed-9388856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93888562022-08-20 Consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients Yang, Zhiyong Wang, Guanghui Luo, Nan Tsang, Chi Kwan Huang, Li'an Front Neurol Neurology Acute ischemic stroke (AIS) is a primary cause of mortality and morbidity worldwide. Currently, no clinically approved immune intervention is available for AIS treatment, partly due to the lack of relevant patient classification based on the peripheral immunity status of patients with AIS. In this study, we adopted the consensus clustering approach to classify patients with AIS into molecular subgroups based on the transcriptomic profiles of peripheral blood, and we identified three distinct AIS molecular subgroups and 8 modules in each subgroup by the weighted gene co-expression network analysis. Remarkably, the pre-ranked gene set enrichment analysis revealed that the co-expression modules with subgroup I-specific signature genes significantly overlapped with the differentially expressed genes in AIS patients with hemorrhagic transformation (HT). With respect to subgroup II, exclusively male patients with decreased proteasome activity were identified. Intriguingly, the majority of subgroup III was composed of female patients who showed a comparatively lower level of AIS-induced immunosuppression (AIIS). In addition, we discovered a non-linear relationship between female age and subgroup-specific gene expression, suggesting a gender- and age-dependent alteration of peripheral immunity. Taken together, our novel AIS classification approach could facilitate immunomodulatory therapies, including the administration of gender-specific therapeutics, and attenuation of the risk of HT and AIIS after ischemic stroke. Frontiers Media S.A. 2022-08-05 /pmc/articles/PMC9388856/ /pubmed/35989931 http://dx.doi.org/10.3389/fneur.2022.937501 Text en Copyright © 2022 Yang, Wang, Luo, Tsang and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Yang, Zhiyong Wang, Guanghui Luo, Nan Tsang, Chi Kwan Huang, Li'an Consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients |
title | Consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients |
title_full | Consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients |
title_fullStr | Consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients |
title_full_unstemmed | Consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients |
title_short | Consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients |
title_sort | consensus clustering of gene expression profiles in peripheral blood of acute ischemic stroke patients |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388856/ https://www.ncbi.nlm.nih.gov/pubmed/35989931 http://dx.doi.org/10.3389/fneur.2022.937501 |
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