Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Van Hemelrijck, Mieke, Eichholzer, Monika, Faeh, David, Rohrmann, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
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
_version_ 1782256471457660928
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
work_keys_str_mv AT vanhemelrijckmieke abilityofabiomarkerbasedscoretopredictdeathfromcirculatorydiseaseandcancerinnhanesiii
AT eichholzermonika abilityofabiomarkerbasedscoretopredictdeathfromcirculatorydiseaseandcancerinnhanesiii
AT faehdavid abilityofabiomarkerbasedscoretopredictdeathfromcirculatorydiseaseandcancerinnhanesiii
AT rohrmannsabine abilityofabiomarkerbasedscoretopredictdeathfromcirculatorydiseaseandcancerinnhanesiii