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Ability of a biomarker-based score to predict death from circulatory disease and cancer in NHANES III
BACKGROUND: A score based on serum concentrations of C-reactive protein (CRP), albumin, gamma-glutamyl transferase (GGT), and HDL cholesterol was positively associated with death from cancer, circulatory disease, and all-cause mortality. We replicated this in the third National Health and Nutrition...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549794/ https://www.ncbi.nlm.nih.gov/pubmed/23092358 http://dx.doi.org/10.1186/1471-2458-12-895 |
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author | Van Hemelrijck, Mieke Eichholzer, Monika Faeh, David Rohrmann, Sabine |
author_facet | Van Hemelrijck, Mieke Eichholzer, Monika Faeh, David Rohrmann, Sabine |
author_sort | Van Hemelrijck, Mieke |
collection | PubMed |
description | BACKGROUND: A score based on serum concentrations of C-reactive protein (CRP), albumin, gamma-glutamyl transferase (GGT), and HDL cholesterol was positively associated with death from cancer, circulatory disease, and all-cause mortality. We replicated this in the third National Health and Nutrition Examination Survey (NHANES III), a US nationally representative survey conducted between 1988–1994. METHODS: Baseline measurements of CRP, albumin, GGT, and HDL were available for participants with mortality follow-up (n=13,056). A biomarker score, ranging 0–4, was created by adding number of markers with abnormal values (cut-off: CRP>10mg/L, albumin<35mg/L, GGT>36U/L, HDL<1.04mmol/L). Its association with mortality was analyzed with multivariate Cox proportional hazards models. RESULTS: The score was positively associated with death from all causes, cancer and circulatory disease [e.g. HR all-cause mortality: 1.21 (95% CI: 1.09, 1.35), 1.92 (1.67, 2.20), 3.38 (2.62, 4.36), and 7.93 (5.77, 10.89), for score 1, 2, 3, 4 vs.0]. These patterns were found across the Charlson Comorbidity Index (CCI). Where CCI =3, risk of cancer death was 1.09 (0.93, 1.28), 1.81 (1.43, 2.29), 4.67 (3.05, 7.14), and 6.97 (5.32, 9.14) for score 1, 2, 3, 4 vs. 0. No effect-modification by sex or race/ethnicity was observed. CONCLUSIONS: These findings correlate with results from a Swedish study. This biomarker-based score could help clinicians make decisions in prevention and disease management. |
format | Online Article Text |
id | pubmed-3549794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35497942013-01-23 Ability of a biomarker-based score to predict death from circulatory disease and cancer in NHANES III Van Hemelrijck, Mieke Eichholzer, Monika Faeh, David Rohrmann, Sabine BMC Public Health Research Article BACKGROUND: A score based on serum concentrations of C-reactive protein (CRP), albumin, gamma-glutamyl transferase (GGT), and HDL cholesterol was positively associated with death from cancer, circulatory disease, and all-cause mortality. We replicated this in the third National Health and Nutrition Examination Survey (NHANES III), a US nationally representative survey conducted between 1988–1994. METHODS: Baseline measurements of CRP, albumin, GGT, and HDL were available for participants with mortality follow-up (n=13,056). A biomarker score, ranging 0–4, was created by adding number of markers with abnormal values (cut-off: CRP>10mg/L, albumin<35mg/L, GGT>36U/L, HDL<1.04mmol/L). Its association with mortality was analyzed with multivariate Cox proportional hazards models. RESULTS: The score was positively associated with death from all causes, cancer and circulatory disease [e.g. HR all-cause mortality: 1.21 (95% CI: 1.09, 1.35), 1.92 (1.67, 2.20), 3.38 (2.62, 4.36), and 7.93 (5.77, 10.89), for score 1, 2, 3, 4 vs.0]. These patterns were found across the Charlson Comorbidity Index (CCI). Where CCI =3, risk of cancer death was 1.09 (0.93, 1.28), 1.81 (1.43, 2.29), 4.67 (3.05, 7.14), and 6.97 (5.32, 9.14) for score 1, 2, 3, 4 vs. 0. No effect-modification by sex or race/ethnicity was observed. CONCLUSIONS: These findings correlate with results from a Swedish study. This biomarker-based score could help clinicians make decisions in prevention and disease management. BioMed Central 2012-10-23 /pmc/articles/PMC3549794/ /pubmed/23092358 http://dx.doi.org/10.1186/1471-2458-12-895 Text en Copyright ©2012 Van Hemelrijck et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Van Hemelrijck, Mieke Eichholzer, Monika Faeh, David Rohrmann, Sabine Ability of a biomarker-based score to predict death from circulatory disease and cancer in NHANES III |
title | Ability of a biomarker-based score to predict death from circulatory disease and cancer in NHANES III |
title_full | Ability of a biomarker-based score to predict death from circulatory disease and cancer in NHANES III |
title_fullStr | Ability of a biomarker-based score to predict death from circulatory disease and cancer in NHANES III |
title_full_unstemmed | Ability of a biomarker-based score to predict death from circulatory disease and cancer in NHANES III |
title_short | Ability of a biomarker-based score to predict death from circulatory disease and cancer in NHANES III |
title_sort | ability of a biomarker-based score to predict death from circulatory disease and cancer in nhanes iii |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549794/ https://www.ncbi.nlm.nih.gov/pubmed/23092358 http://dx.doi.org/10.1186/1471-2458-12-895 |
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