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Association of baseline inflammatory biomarkers with cancer mortality in the REGARDS cohort
This study examines the association between inflammatory biomarkers and risk of cancer mortality by race. Data were obtained from 1,856 participants in the prospective REGARDS cohort who were cancer-free at baseline, and analyzed in relation to cancer mortality prospectively. Biomarkers were log-tra...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690671/ https://www.ncbi.nlm.nih.gov/pubmed/31448052 http://dx.doi.org/10.18632/oncotarget.27108 |
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author | Akinyemiju, Tomi Moore, Justin X. Pisu, Maria Goodman, Michael Howard, Virginia J. Safford, Monika Gilchrist, Susan C. Cushman, Mary Long, LeAnn Judd, Suzanne E. |
author_facet | Akinyemiju, Tomi Moore, Justin X. Pisu, Maria Goodman, Michael Howard, Virginia J. Safford, Monika Gilchrist, Susan C. Cushman, Mary Long, LeAnn Judd, Suzanne E. |
author_sort | Akinyemiju, Tomi |
collection | PubMed |
description | This study examines the association between inflammatory biomarkers and risk of cancer mortality by race. Data were obtained from 1,856 participants in the prospective REGARDS cohort who were cancer-free at baseline, and analyzed in relation to cancer mortality prospectively. Biomarkers were log-transformed and categorized into tertiles due to non-normal distributions, and Cox proportional hazard regression models were utilized to compute hazard ratios with 95% confidence intervals using robust sandwich methods. Individuals in the highest tertile of IL-6 had over a 12-fold increased risk of cancer mortality (HR: 12.97, 95% CI: 3.46–48.63); those in the highest tertile of IL-8 had over a 2-fold increased risk of cancer mortality (HR: 2.21, 95% CI: 0.86–5.71), while those in the highest tertile of IL-10 had over a 3-fold increased risk of cancer mortality (HR: 3.06, 95% CI: 1.35–6.89). In race-stratified analysis, each unit increase in IL-6 was associated with increased risk of cancer mortality among African-Americans (HR: 3.88, 95% CI: 1.17–12.88) and Whites (5.25, 95% CI: 1.24–22.31). If replicated in larger, racially diverse prospective cohorts, these results suggest that cancer patients may benefit from clinical or lifestyle approaches to regulate systemic inflammation as a cancer prevention strategy. |
format | Online Article Text |
id | pubmed-6690671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-66906712019-08-23 Association of baseline inflammatory biomarkers with cancer mortality in the REGARDS cohort Akinyemiju, Tomi Moore, Justin X. Pisu, Maria Goodman, Michael Howard, Virginia J. Safford, Monika Gilchrist, Susan C. Cushman, Mary Long, LeAnn Judd, Suzanne E. Oncotarget Research Paper This study examines the association between inflammatory biomarkers and risk of cancer mortality by race. Data were obtained from 1,856 participants in the prospective REGARDS cohort who were cancer-free at baseline, and analyzed in relation to cancer mortality prospectively. Biomarkers were log-transformed and categorized into tertiles due to non-normal distributions, and Cox proportional hazard regression models were utilized to compute hazard ratios with 95% confidence intervals using robust sandwich methods. Individuals in the highest tertile of IL-6 had over a 12-fold increased risk of cancer mortality (HR: 12.97, 95% CI: 3.46–48.63); those in the highest tertile of IL-8 had over a 2-fold increased risk of cancer mortality (HR: 2.21, 95% CI: 0.86–5.71), while those in the highest tertile of IL-10 had over a 3-fold increased risk of cancer mortality (HR: 3.06, 95% CI: 1.35–6.89). In race-stratified analysis, each unit increase in IL-6 was associated with increased risk of cancer mortality among African-Americans (HR: 3.88, 95% CI: 1.17–12.88) and Whites (5.25, 95% CI: 1.24–22.31). If replicated in larger, racially diverse prospective cohorts, these results suggest that cancer patients may benefit from clinical or lifestyle approaches to regulate systemic inflammation as a cancer prevention strategy. Impact Journals LLC 2019-08-06 /pmc/articles/PMC6690671/ /pubmed/31448052 http://dx.doi.org/10.18632/oncotarget.27108 Text en Copyright: © 2019 Akinyemiju et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Akinyemiju, Tomi Moore, Justin X. Pisu, Maria Goodman, Michael Howard, Virginia J. Safford, Monika Gilchrist, Susan C. Cushman, Mary Long, LeAnn Judd, Suzanne E. Association of baseline inflammatory biomarkers with cancer mortality in the REGARDS cohort |
title | Association of baseline inflammatory biomarkers with cancer mortality in the REGARDS cohort |
title_full | Association of baseline inflammatory biomarkers with cancer mortality in the REGARDS cohort |
title_fullStr | Association of baseline inflammatory biomarkers with cancer mortality in the REGARDS cohort |
title_full_unstemmed | Association of baseline inflammatory biomarkers with cancer mortality in the REGARDS cohort |
title_short | Association of baseline inflammatory biomarkers with cancer mortality in the REGARDS cohort |
title_sort | association of baseline inflammatory biomarkers with cancer mortality in the regards cohort |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690671/ https://www.ncbi.nlm.nih.gov/pubmed/31448052 http://dx.doi.org/10.18632/oncotarget.27108 |
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