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CMV infection, CD19(+) B cell depletion, and Lymphopenia as predictors for unexpected admission in the institutionalized elderly
BACKGROUND: Chronic infections played a detrimental role on health outcomes in the aged population, and had complex associations with lymphocyte subsets distribution. Our study aimed to explore the predictive roles of chronic infections, lymphopenia, and lymphocyte subsets on unexpected admission an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094471/ https://www.ncbi.nlm.nih.gov/pubmed/33947427 http://dx.doi.org/10.1186/s12979-021-00233-0 |
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author | Chen, Liang-Yu Hwang, An-Chun Huang, Chung-Yu Chen, Liang-Kung Wang, Fu-Der Chan, Yu-Jiun |
author_facet | Chen, Liang-Yu Hwang, An-Chun Huang, Chung-Yu Chen, Liang-Kung Wang, Fu-Der Chan, Yu-Jiun |
author_sort | Chen, Liang-Yu |
collection | PubMed |
description | BACKGROUND: Chronic infections played a detrimental role on health outcomes in the aged population, and had complex associations with lymphocyte subsets distribution. Our study aimed to explore the predictive roles of chronic infections, lymphopenia, and lymphocyte subsets on unexpected admission and mortality in the institutionalized oldest-old during 3 year follow-up period. RESULTS: There were 163 participants enrolled prospectively with median age of 87.3 years (IQR: 83.1–90.2), male of 88.3%, and being followed for 156.4 weeks (IQR: 136.9–156.4 weeks). The unexpected admission and mortality rates were 55.2 and 24.5% respectively. The Cox proportional hazards models demonstrated the 3rd quartile of cytomegalovirus IgG (OR: 3.26, 95% CI: 1.55–6.84), lymphopenia (OR: 2.85, 95% CI: 1.2–6.74), and 1st quartile of CD19(+) B cell count (OR: 2.84, 95% CI: 1.29–6.25) predicted elevated risks of unexpected admission after adjusting for potential confounders; while the 3rd quartile of CD3(+) T cell indicated a reduced risk of mortality (OR: 0.19, 95% CI: 0.05–0.71). Negative association between CMV IgG and CD19(+) B cell count suggested that CMV infection might lead to B cell depletion via decreasing memory B cells repertoire. CONCLUSIONS: CMV infection, lymphopenia, and CD19(+) B cell depletion might predict greater risk of unexpected admission, while more CD3(+) T cell would suggest a reduced risk of mortality among the oldest-old population. A non-linear or U-shaped relationship was supposed between health outcomes and CMV infection, CD3(+) T cell, or CD19(+) B cell counts. Further prospective studies with more participants included would be needed to elucidate above findings. |
format | Online Article Text |
id | pubmed-8094471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80944712021-05-04 CMV infection, CD19(+) B cell depletion, and Lymphopenia as predictors for unexpected admission in the institutionalized elderly Chen, Liang-Yu Hwang, An-Chun Huang, Chung-Yu Chen, Liang-Kung Wang, Fu-Der Chan, Yu-Jiun Immun Ageing Research BACKGROUND: Chronic infections played a detrimental role on health outcomes in the aged population, and had complex associations with lymphocyte subsets distribution. Our study aimed to explore the predictive roles of chronic infections, lymphopenia, and lymphocyte subsets on unexpected admission and mortality in the institutionalized oldest-old during 3 year follow-up period. RESULTS: There were 163 participants enrolled prospectively with median age of 87.3 years (IQR: 83.1–90.2), male of 88.3%, and being followed for 156.4 weeks (IQR: 136.9–156.4 weeks). The unexpected admission and mortality rates were 55.2 and 24.5% respectively. The Cox proportional hazards models demonstrated the 3rd quartile of cytomegalovirus IgG (OR: 3.26, 95% CI: 1.55–6.84), lymphopenia (OR: 2.85, 95% CI: 1.2–6.74), and 1st quartile of CD19(+) B cell count (OR: 2.84, 95% CI: 1.29–6.25) predicted elevated risks of unexpected admission after adjusting for potential confounders; while the 3rd quartile of CD3(+) T cell indicated a reduced risk of mortality (OR: 0.19, 95% CI: 0.05–0.71). Negative association between CMV IgG and CD19(+) B cell count suggested that CMV infection might lead to B cell depletion via decreasing memory B cells repertoire. CONCLUSIONS: CMV infection, lymphopenia, and CD19(+) B cell depletion might predict greater risk of unexpected admission, while more CD3(+) T cell would suggest a reduced risk of mortality among the oldest-old population. A non-linear or U-shaped relationship was supposed between health outcomes and CMV infection, CD3(+) T cell, or CD19(+) B cell counts. Further prospective studies with more participants included would be needed to elucidate above findings. BioMed Central 2021-05-04 /pmc/articles/PMC8094471/ /pubmed/33947427 http://dx.doi.org/10.1186/s12979-021-00233-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 | Research Chen, Liang-Yu Hwang, An-Chun Huang, Chung-Yu Chen, Liang-Kung Wang, Fu-Der Chan, Yu-Jiun CMV infection, CD19(+) B cell depletion, and Lymphopenia as predictors for unexpected admission in the institutionalized elderly |
title | CMV infection, CD19(+) B cell depletion, and Lymphopenia as predictors for unexpected admission in the institutionalized elderly |
title_full | CMV infection, CD19(+) B cell depletion, and Lymphopenia as predictors for unexpected admission in the institutionalized elderly |
title_fullStr | CMV infection, CD19(+) B cell depletion, and Lymphopenia as predictors for unexpected admission in the institutionalized elderly |
title_full_unstemmed | CMV infection, CD19(+) B cell depletion, and Lymphopenia as predictors for unexpected admission in the institutionalized elderly |
title_short | CMV infection, CD19(+) B cell depletion, and Lymphopenia as predictors for unexpected admission in the institutionalized elderly |
title_sort | cmv infection, cd19(+) b cell depletion, and lymphopenia as predictors for unexpected admission in the institutionalized elderly |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094471/ https://www.ncbi.nlm.nih.gov/pubmed/33947427 http://dx.doi.org/10.1186/s12979-021-00233-0 |
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