Association of sICAM-1 and MCP-1 with coronary artery calcification in families enriched for coronary heart disease or hypertension: the NHLBI Family Heart Study
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Tang, Weihong, et al. Association of Sicam-1 and Mcp-1 with Coronary Artery Calcification In Families Enriched for Coronary Heart Disease Or Hypertension: the Nhlbi Family Heart Study. BioMed Central Ltd, 2007. https://doi.org/10.17615/14xq-br42APA
Tang, W., Pankow, J., Carr, J., Tracy, R., Bielinski, S., North, K., Hopkins, P., Kraja, A., & Arnett, D. (2007). Association of sICAM-1 and MCP-1 with coronary artery calcification in families enriched for coronary heart disease or hypertension: the NHLBI Family Heart Study. BioMed Central Ltd. https://doi.org/10.17615/14xq-br42Chicago
Tang, Weihong, James S Pankow, J Jeffrey Carr, Russell P Tracy, Suzette J Bielinski, Kari North, Paul N Hopkins et al. 2007. Association of Sicam-1 and Mcp-1 with Coronary Artery Calcification In Families Enriched for Coronary Heart Disease Or Hypertension: the Nhlbi Family Heart Study. BioMed Central Ltd. https://doi.org/10.17615/14xq-br42- Creator
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Tang, Weihong
- Other Affiliation: Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, USA
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Pankow, James S
- Other Affiliation: Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, USA
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Carr, J Jeffrey
- Other Affiliation: Department of Radiology, Wake Forest University School of Medicine, Winston-Salem, NC, USA
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Tracy, Russell P
- Other Affiliation: Department of Pathology and Biochemistry, University of Vermont, Burlington, VT, USA
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Bielinski, Suzette J
- Other Affiliation: Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, USA
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North, Kari
- Affiliation: Gillings School of Global Public Health, Department of Epidemiology
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Hopkins, Paul N
- Other Affiliation: Cardiovascular Genetics, University of Utah School of Medicine, Salt Lake City, UT, USA
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Kraja, Aldi T
- Other Affiliation: Division of Statistical Genomics, Washington University School of Medicine, Saint Louis, MO, USA
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Arnett, Donna K
- Other Affiliation: Department of Epidemiology, School of Public Health, University of Alabama- Birmingham, Birmingham, AL, USA
- Abstract
- Background: Data accumulated from mouse studies and in vitro studies of human arteries support the notion that soluble intercellular adhesion molecule-1 (sICAM-1) and monocyte chemoattractant protein-1 (MCP-1) play important roles in the inflammation process involved in atherosclerosis. However, at the population level, the utility of sICAM-1 and MCP-1 as biomarkers for subclinical atherosclerosis is less clear. In the follow-up exam of the NHLBI Family Heart Study, we evaluated whether plasma levels of sICAM-1 and MCP-1 were associated with coronary artery calcification (CAC), a measure of the burden of coronary atherosclerosis. Methods: CAC was measured using the Agatston score with multidetector computed tomography. Information on CAC and MCP-1 was obtained in 2246 whites and 470 African Americans (mean age 55 years) without a history of coronary heart disease (CHD). Information on sICAM-1 was obtained for white participants only. Results: In whites, after adjustment for age and gender, the odds ratios (ORs) of CAC (CAC > 0) associated with the second, third, fourth, and fifth quintiles of sICAM-1 compared to the first quintile were 1.22 (95% confidence interval [CI]: 0.91–1.63), 1.15 (0.84–1.58), 1.49 (1.09–2.05), and 1.72 (1.26–2.36) (p = 0.0005 for trend test), respectively. The corresponding ORs for the second to fifth quintiles of MCP-1 were 1.26 (0.92–1.73), 0.99 (0.73–1.34), 1.42 (1.03–1.96), and 2.00 (1.43–2.79) (p < 0.0001 for trend test), respectively. In multivariable analysis that additionally adjusted for other CHD risk factors, the association of CAC with sICAM-1 and MCP-1 was attenuated and no longer statistically significant. In African Americans, the age and gender-adjusted ORs of CAC associated with the second and third tertiles of MCP-1 compared to the first tertile were 1.16 (0.64–2.08) and 1.25 (0.70–2.23) (p = 0.44 for trend test), respectively. This result did not change materially after additional adjustment for other CHD risk factors. Test of race interaction showed that the magnitude of association between MCP-1 and CAC did not differ significantly between African Americans and whites. Similar results were obtained when CAC ≥ 10 was analyzed as an outcome for both MCP-1 and sICAM-1. Conclusion: This study suggests that sICAM-1 and MCP-1 are biomarkers of coronary atherosclerotic burden and their association with CAC was mainly driven by established CHD risk factors.
- Date of publication
- October 26, 2007
- DOI
- Identifier
- 17963506
- doi:10.1186/1471-2261-7-30
- Resource type
- Article
- Rights statement
- In Copyright
- Rights holder
- Weihong Tang et al.; licensee BioMed Central Ltd.
- License
- Journal title
- BMC Cardiovascular Disorders
- Journal volume
- 7
- Journal issue
- 1
- Page start
- 30
- Language
- English
- Is the article or chapter peer-reviewed?
- Yes
- ISSN
- 1471-2261
- Bibliographic citation
- BMC Cardiovascular Disorders. 2007 Oct 26;7(1):30
- Publisher
- BioMed Central Ltd
- Access right
- Open Access
- Date uploaded
- August 24, 2012
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