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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...

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Autores principales: Akinyemiju, Tomi, Moore, Justin X., Pisu, Maria, Goodman, Michael, Howard, Virginia J., Safford, Monika, Gilchrist, Susan C., Cushman, Mary, Long, LeAnn, Judd, Suzanne E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
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.
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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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