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Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study

BACKGROUND: The neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR) and systemic immune-inflammation index (SII) are readily available circulatory immunity markers that are associated with components of frailty. However, few studies have investigated the relationship between the...

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Autores principales: Zhang, Hui, Hao, Meng, Hu, Zixin, Li, Yi, Jiang, Xiaoyan, Wang, Jiucun, Jin, Li, Liu, Zuyun, Wang, Xiaofeng, Sun, Xuehui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722120/
https://www.ncbi.nlm.nih.gov/pubmed/34980175
http://dx.doi.org/10.1186/s12979-021-00257-6
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author Zhang, Hui
Hao, Meng
Hu, Zixin
Li, Yi
Jiang, Xiaoyan
Wang, Jiucun
Jin, Li
Liu, Zuyun
Wang, Xiaofeng
Sun, Xuehui
author_facet Zhang, Hui
Hao, Meng
Hu, Zixin
Li, Yi
Jiang, Xiaoyan
Wang, Jiucun
Jin, Li
Liu, Zuyun
Wang, Xiaofeng
Sun, Xuehui
author_sort Zhang, Hui
collection PubMed
description BACKGROUND: The neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR) and systemic immune-inflammation index (SII) are readily available circulatory immunity markers that are associated with components of frailty. However, few studies have investigated the relationship between these immunity markers and frailty, and it remains unknown whether they are predictive of incident frailty in older adults in general. Hence, we aimed to examine the association of these immunity markers with the risk of incident frailty. RESULTS: Overall, 1822 older adults (mean age was 78.03 ± 4.46 years) were included in the Rugao Longitudinal Aging Study. NLR, PLR and SII were calculated from blood cell counts. The frailty definition was based on the Fried phenotype. At baseline, 200 (10.98%) individuals were defined as frailty, and no significant associations of NLR, PLR and SII with frailty were found. During the 2-year follow-up, 180 (15.67%) individuals were new-onset frailty. After adjustment, an increased logNLR (odds ratio [OR] 2.92, 95% confidence interval [CI] 1.20–7.18), logPLR (OR 2.54, 95% CI: 1.01–6.53) and logSII (OR 2.34, 95% CI: 1.16–4.78) were significantly associated with a higher risk of incident frailty in all individuals. Additionally, the associations of logNLR (OR 4.21, 95% CI 1.54–11.62 logPLR (OR 3.38, 95% CI: 1.17–9.91) and logSII (OR 2.56, 95% CI: 1.15–5.72) with incident frailty were remained after excluding individuals with comorbidities. In further analyzed, individuals with higher levels of NLR and SII had higher risk of incident frailty when we stratified individuals by quartiles of these immunity markers. CONCLUSION: NLR and SII are easily obtained immunity markers that could be used to predict incident frailty in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-021-00257-6.
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spelling pubmed-87221202022-01-06 Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study Zhang, Hui Hao, Meng Hu, Zixin Li, Yi Jiang, Xiaoyan Wang, Jiucun Jin, Li Liu, Zuyun Wang, Xiaofeng Sun, Xuehui Immun Ageing Research BACKGROUND: The neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR) and systemic immune-inflammation index (SII) are readily available circulatory immunity markers that are associated with components of frailty. However, few studies have investigated the relationship between these immunity markers and frailty, and it remains unknown whether they are predictive of incident frailty in older adults in general. Hence, we aimed to examine the association of these immunity markers with the risk of incident frailty. RESULTS: Overall, 1822 older adults (mean age was 78.03 ± 4.46 years) were included in the Rugao Longitudinal Aging Study. NLR, PLR and SII were calculated from blood cell counts. The frailty definition was based on the Fried phenotype. At baseline, 200 (10.98%) individuals were defined as frailty, and no significant associations of NLR, PLR and SII with frailty were found. During the 2-year follow-up, 180 (15.67%) individuals were new-onset frailty. After adjustment, an increased logNLR (odds ratio [OR] 2.92, 95% confidence interval [CI] 1.20–7.18), logPLR (OR 2.54, 95% CI: 1.01–6.53) and logSII (OR 2.34, 95% CI: 1.16–4.78) were significantly associated with a higher risk of incident frailty in all individuals. Additionally, the associations of logNLR (OR 4.21, 95% CI 1.54–11.62 logPLR (OR 3.38, 95% CI: 1.17–9.91) and logSII (OR 2.56, 95% CI: 1.15–5.72) with incident frailty were remained after excluding individuals with comorbidities. In further analyzed, individuals with higher levels of NLR and SII had higher risk of incident frailty when we stratified individuals by quartiles of these immunity markers. CONCLUSION: NLR and SII are easily obtained immunity markers that could be used to predict incident frailty in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-021-00257-6. BioMed Central 2022-01-03 /pmc/articles/PMC8722120/ /pubmed/34980175 http://dx.doi.org/10.1186/s12979-021-00257-6 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
Zhang, Hui
Hao, Meng
Hu, Zixin
Li, Yi
Jiang, Xiaoyan
Wang, Jiucun
Jin, Li
Liu, Zuyun
Wang, Xiaofeng
Sun, Xuehui
Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study
title Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study
title_full Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study
title_fullStr Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study
title_full_unstemmed Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study
title_short Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study
title_sort association of immunity markers with the risk of incident frailty: the rugao longitudinal aging study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722120/
https://www.ncbi.nlm.nih.gov/pubmed/34980175
http://dx.doi.org/10.1186/s12979-021-00257-6
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