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Inflammatory biomarkers, multi-morbidity, and biologic aging
OBJECTIVES: To study the association between multi-morbidity percentiles, which is a measure of clinical aging, and interleukin (IL)-6, IL-10, and tumor necrosis factor (TNF)-α. METHODS: Participants 50 to 95 years of age from the Mayo Clinic Study of Aging were assigned age- and sex-specific multi-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9274410/ https://www.ncbi.nlm.nih.gov/pubmed/35796512 http://dx.doi.org/10.1177/03000605221109393 |
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author | St. Sauver, Jennifer Rocca, Walter LeBrasseur, Nathan Chamberlain, Alanna Olson, Janet Jacobson, Debra McGree, Michaela Mielke, Michelle |
author_facet | St. Sauver, Jennifer Rocca, Walter LeBrasseur, Nathan Chamberlain, Alanna Olson, Janet Jacobson, Debra McGree, Michaela Mielke, Michelle |
author_sort | St. Sauver, Jennifer |
collection | PubMed |
description | OBJECTIVES: To study the association between multi-morbidity percentiles, which is a measure of clinical aging, and interleukin (IL)-6, IL-10, and tumor necrosis factor (TNF)-α. METHODS: Participants 50 to 95 years of age from the Mayo Clinic Study of Aging were assigned age- and sex-specific multi-morbidity percentiles using look-up tables that were reported previously (n = 1646). Percentiles were divided into quintiles for analysis. Plasma IL-6, IL-10, and TNF-α levels were measured in 1595 participants. Median inflammatory marker levels were compared across multi-morbidity quintiles using nonparametric tests. RESULTS: People with higher multi-morbidity percentiles had significantly higher IL-6 and TNF-α levels compared with those with lower multi-morbidity percentiles. Tests for trend across five multi-morbidity quintiles were significant among women for IL-6 and among participants 70 years of age or older for IL-6 and TNF-α. IL-10 was not associated with multi-morbidity percentiles. CONCLUSIONS: Multi-morbidity percentiles may be a useful clinical index of biological age for future studies, particularly in women and people 70 years of age and older. |
format | Online Article Text |
id | pubmed-9274410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-92744102022-07-13 Inflammatory biomarkers, multi-morbidity, and biologic aging St. Sauver, Jennifer Rocca, Walter LeBrasseur, Nathan Chamberlain, Alanna Olson, Janet Jacobson, Debra McGree, Michaela Mielke, Michelle J Int Med Res Retrospective Clinical Research Report OBJECTIVES: To study the association between multi-morbidity percentiles, which is a measure of clinical aging, and interleukin (IL)-6, IL-10, and tumor necrosis factor (TNF)-α. METHODS: Participants 50 to 95 years of age from the Mayo Clinic Study of Aging were assigned age- and sex-specific multi-morbidity percentiles using look-up tables that were reported previously (n = 1646). Percentiles were divided into quintiles for analysis. Plasma IL-6, IL-10, and TNF-α levels were measured in 1595 participants. Median inflammatory marker levels were compared across multi-morbidity quintiles using nonparametric tests. RESULTS: People with higher multi-morbidity percentiles had significantly higher IL-6 and TNF-α levels compared with those with lower multi-morbidity percentiles. Tests for trend across five multi-morbidity quintiles were significant among women for IL-6 and among participants 70 years of age or older for IL-6 and TNF-α. IL-10 was not associated with multi-morbidity percentiles. CONCLUSIONS: Multi-morbidity percentiles may be a useful clinical index of biological age for future studies, particularly in women and people 70 years of age and older. SAGE Publications 2022-07-07 /pmc/articles/PMC9274410/ /pubmed/35796512 http://dx.doi.org/10.1177/03000605221109393 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Retrospective Clinical Research Report St. Sauver, Jennifer Rocca, Walter LeBrasseur, Nathan Chamberlain, Alanna Olson, Janet Jacobson, Debra McGree, Michaela Mielke, Michelle Inflammatory biomarkers, multi-morbidity, and biologic aging |
title | Inflammatory biomarkers, multi-morbidity, and biologic
aging |
title_full | Inflammatory biomarkers, multi-morbidity, and biologic
aging |
title_fullStr | Inflammatory biomarkers, multi-morbidity, and biologic
aging |
title_full_unstemmed | Inflammatory biomarkers, multi-morbidity, and biologic
aging |
title_short | Inflammatory biomarkers, multi-morbidity, and biologic
aging |
title_sort | inflammatory biomarkers, multi-morbidity, and biologic
aging |
topic | Retrospective Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9274410/ https://www.ncbi.nlm.nih.gov/pubmed/35796512 http://dx.doi.org/10.1177/03000605221109393 |
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