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Higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults

BACKGROUND: The complex physiology underpinning the frailty syndrome is responsible for the absence of robust biomarkers that can be used for screening, diagnostic and/or prognostic purposes and has made clinical implementation difficult. Considering socially vulnerable populations, who have poor he...

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Autores principales: Nascimento, Carla M. C., Zazzetta, Marisa S., Gomes, Grace A. O., Orlandi, Fabiana S., Gramani-Say, Karina, Vasilceac, Fernando A., Gratão, Aline C. M., Pavarini, Sofia C. I., Cominetti, Marcia R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219095/
https://www.ncbi.nlm.nih.gov/pubmed/30400833
http://dx.doi.org/10.1186/s12877-018-0961-6
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author Nascimento, Carla M. C.
Zazzetta, Marisa S.
Gomes, Grace A. O.
Orlandi, Fabiana S.
Gramani-Say, Karina
Vasilceac, Fernando A.
Gratão, Aline C. M.
Pavarini, Sofia C. I.
Cominetti, Marcia R.
author_facet Nascimento, Carla M. C.
Zazzetta, Marisa S.
Gomes, Grace A. O.
Orlandi, Fabiana S.
Gramani-Say, Karina
Vasilceac, Fernando A.
Gratão, Aline C. M.
Pavarini, Sofia C. I.
Cominetti, Marcia R.
author_sort Nascimento, Carla M. C.
collection PubMed
description BACKGROUND: The complex physiology underpinning the frailty syndrome is responsible for the absence of robust biomarkers that can be used for screening, diagnostic and/or prognostic purposes and has made clinical implementation difficult. Considering socially vulnerable populations, who have poor health status and increased morbidity and mortality, this scenario is even more complex. However, to the best of our knowledge, there are no studies available to investigate frailty biomarkers in socially vulnerable populations. Thus, the aim of this cross-sectional study was to identify potential blood-based biomarkers of frailty in a socially vulnerable population. METHODS: A sample consisting of 347 community-dwelling older people living in a context of high social vulnerability was divided into non-frail (robust), pre-frail and frail groups, according to modified Fried frailty phenotype criteria. Blood samples were collected and analyzed for basic metabolic parameters and for inflammatory cytokines. RESULTS: Levels of Interleukin-1α (IL-1α) and Tumor Necrosis Factor α (TNF-α) were significantly higher in pre-frail subjects, compared to non-frail ones. Tumor Necrosis Factor β (TNF-β) levels presented higher values in the frail compared to non-frail individuals. Interleukin-6 (IL-6) levels in pre-frail and frail subjects were significantly higher compared to the levels of non-frail subjects. Using an ordinal regression analysis, we observed that socially vulnerable older people at higher risk of developing frailty were subjects above 80 years old (OR: 2.5; 95% CI: 1.1–5.6) and who presented higher levels of TNF-β (≥0.81 pg/mL, OR: 2.53; 95% CI: 1.3–4.9). CONCLUSION: As vulnerable populations continue to age, it is imperative to have a greater understanding of the frailty condition, identifying novel potential blood-based biomarkers. The results presented here could help to implement preventive healthcare strategies by evaluating frailty and at the same time measuring a set of inflammatory biomarkers, paying special attention to TNF-β plasmatic levels. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12877-018-0961-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-62190952018-11-16 Higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults Nascimento, Carla M. C. Zazzetta, Marisa S. Gomes, Grace A. O. Orlandi, Fabiana S. Gramani-Say, Karina Vasilceac, Fernando A. Gratão, Aline C. M. Pavarini, Sofia C. I. Cominetti, Marcia R. BMC Geriatr Research Article BACKGROUND: The complex physiology underpinning the frailty syndrome is responsible for the absence of robust biomarkers that can be used for screening, diagnostic and/or prognostic purposes and has made clinical implementation difficult. Considering socially vulnerable populations, who have poor health status and increased morbidity and mortality, this scenario is even more complex. However, to the best of our knowledge, there are no studies available to investigate frailty biomarkers in socially vulnerable populations. Thus, the aim of this cross-sectional study was to identify potential blood-based biomarkers of frailty in a socially vulnerable population. METHODS: A sample consisting of 347 community-dwelling older people living in a context of high social vulnerability was divided into non-frail (robust), pre-frail and frail groups, according to modified Fried frailty phenotype criteria. Blood samples were collected and analyzed for basic metabolic parameters and for inflammatory cytokines. RESULTS: Levels of Interleukin-1α (IL-1α) and Tumor Necrosis Factor α (TNF-α) were significantly higher in pre-frail subjects, compared to non-frail ones. Tumor Necrosis Factor β (TNF-β) levels presented higher values in the frail compared to non-frail individuals. Interleukin-6 (IL-6) levels in pre-frail and frail subjects were significantly higher compared to the levels of non-frail subjects. Using an ordinal regression analysis, we observed that socially vulnerable older people at higher risk of developing frailty were subjects above 80 years old (OR: 2.5; 95% CI: 1.1–5.6) and who presented higher levels of TNF-β (≥0.81 pg/mL, OR: 2.53; 95% CI: 1.3–4.9). CONCLUSION: As vulnerable populations continue to age, it is imperative to have a greater understanding of the frailty condition, identifying novel potential blood-based biomarkers. The results presented here could help to implement preventive healthcare strategies by evaluating frailty and at the same time measuring a set of inflammatory biomarkers, paying special attention to TNF-β plasmatic levels. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12877-018-0961-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-06 /pmc/articles/PMC6219095/ /pubmed/30400833 http://dx.doi.org/10.1186/s12877-018-0961-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Nascimento, Carla M. C.
Zazzetta, Marisa S.
Gomes, Grace A. O.
Orlandi, Fabiana S.
Gramani-Say, Karina
Vasilceac, Fernando A.
Gratão, Aline C. M.
Pavarini, Sofia C. I.
Cominetti, Marcia R.
Higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults
title Higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults
title_full Higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults
title_fullStr Higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults
title_full_unstemmed Higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults
title_short Higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults
title_sort higher levels of tumor necrosis factor β are associated with frailty in socially vulnerable community-dwelling older adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219095/
https://www.ncbi.nlm.nih.gov/pubmed/30400833
http://dx.doi.org/10.1186/s12877-018-0961-6
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