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Simultaneous consideration of multiple candidate protein biomarkers for long-term risk for cardiovascular events.

Publication ,  Journal Article
Halim, SA; Neely, ML; Pieper, KS; Shah, SH; Kraus, WE; Hauser, ER; Califf, RM; Granger, CB; Newby, LK
Published in: Circ Cardiovasc Genet
February 2015

BACKGROUND: Although individual protein biomarkers are associated with cardiovascular risk, rarely have multiple proteins been considered simultaneously to identify which set of proteins best predicts risk. METHODS AND RESULTS: In a nested case-control study of 273 death/myocardial infarction (MI) cases and 273 age- (within 10 years), sex-, and race-matched and event-free controls from among 2023 consecutive patients (median follow-up 2.5 years) with suspected coronary disease, plasma levels of 53 previously reported biomarkers of cardiovascular risk were determined in a core laboratory. Three penalized logistic regression models were fit using the elastic net to identify panels of proteins independently associated with death/MI: proteins alone (Model 1); proteins in a model constrained to retain clinical variables (Model 2); and proteins and clinical variables available for selection (Model 3). Model 1 identified 6 biomarkers strongly associated with death/MI: intercellular adhesion molecule-1, matrix metalloproteinase-3, N-terminal pro-B-type natriuretic peptide, interleukin-6, soluble CD40 ligand, and insulin-like growth factor binding protein-2. In Model 2, only soluble CD40 ligand remained strongly associated with death/MI when all clinical risk predictors were retained. Model 3 identified a set of 6 biomarkers (intercellular adhesion molecule-1, matrix metalloproteinase-3, N-terminal pro-B-type natriuretic peptide, interleukin-6, soluble CD40 ligand, and insulin-like growth factor binding protein-2) and 5 clinical variables (age, red-cell distribution width, diabetes mellitus, hemoglobin, and New York Heart Association class) strongly associated with death/MI. CONCLUSIONS: Simultaneously assessing the association between multiple putative protein biomarkers of cardiovascular risk and clinical outcomes is useful in identifying relevant biomarker panels for further assessment.

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Published In

Circ Cardiovasc Genet

DOI

EISSN

1942-3268

Publication Date

February 2015

Volume

8

Issue

1

Start / End Page

168 / 177

Location

United States

Related Subject Headings

  • Myocardial Infarction
  • Models, Genetic
  • Middle Aged
  • Male
  • Humans
  • Genetic Markers
  • Female
  • Cardiovascular System & Hematology
  • Aged
  • 3201 Cardiovascular medicine and haematology
 

Citation

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Halim, S. A., Neely, M. L., Pieper, K. S., Shah, S. H., Kraus, W. E., Hauser, E. R., … Newby, L. K. (2015). Simultaneous consideration of multiple candidate protein biomarkers for long-term risk for cardiovascular events. Circ Cardiovasc Genet, 8(1), 168–177. https://doi.org/10.1161/CIRCGENETICS.113.000490
Halim, Sharif A., Megan L. Neely, Karen S. Pieper, Svati H. Shah, William E. Kraus, Elizabeth R. Hauser, Robert M. Califf, Christopher B. Granger, and L Kristin Newby. “Simultaneous consideration of multiple candidate protein biomarkers for long-term risk for cardiovascular events.Circ Cardiovasc Genet 8, no. 1 (February 2015): 168–77. https://doi.org/10.1161/CIRCGENETICS.113.000490.
Halim SA, Neely ML, Pieper KS, Shah SH, Kraus WE, Hauser ER, et al. Simultaneous consideration of multiple candidate protein biomarkers for long-term risk for cardiovascular events. Circ Cardiovasc Genet. 2015 Feb;8(1):168–77.
Halim, Sharif A., et al. “Simultaneous consideration of multiple candidate protein biomarkers for long-term risk for cardiovascular events.Circ Cardiovasc Genet, vol. 8, no. 1, Feb. 2015, pp. 168–77. Pubmed, doi:10.1161/CIRCGENETICS.113.000490.
Halim SA, Neely ML, Pieper KS, Shah SH, Kraus WE, Hauser ER, Califf RM, Granger CB, Newby LK. Simultaneous consideration of multiple candidate protein biomarkers for long-term risk for cardiovascular events. Circ Cardiovasc Genet. 2015 Feb;8(1):168–177.

Published In

Circ Cardiovasc Genet

DOI

EISSN

1942-3268

Publication Date

February 2015

Volume

8

Issue

1

Start / End Page

168 / 177

Location

United States

Related Subject Headings

  • Myocardial Infarction
  • Models, Genetic
  • Middle Aged
  • Male
  • Humans
  • Genetic Markers
  • Female
  • Cardiovascular System & Hematology
  • Aged
  • 3201 Cardiovascular medicine and haematology