Thromb Haemost 2011; 105(04): 605-609
DOI: 10.1160/TH10-09-0626
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Association between γ′ fibrinogen levels and inflammation

Kristine S. Alexander
1   Department of Molecular and Medical Genetics, School of Medicine, Oregon Health & Science University, Portland, Oregon, USA
,
Theresa E. Madden
2   Dr. Theresa E. Madden & Associates, PLLC, Olympia, Washington, USA
,
David H. Farrell
3   Division of Cardiovascular Medicine, Department of Medicine, School of Medicine, Oregon Health & Science University, Portland, Oregon, USA
› Author Affiliations
Financial support: This study was supported by the National Heart, Lung, and Blood Institute (R21HL097298 to D.H.F.) and by the Oregon Clinical and Translational Research Institute TL1 grant (1TL1RR024159 to K.S.A.) from the National Center for Research Resources, a component of the National Institutes of Health, and the NIH Roadmap for Medical Research.
Further Information

Publication History

Received: 29 September 2010

Accepted after major revision: 11 December 2010

Publication Date:
28 November 2017 (online)

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Summary

The γ’ fibrinogen isoform produces clots that are stiffer and more resistant to breakdown than the more common fibrinogen isoform, γA. Increased levels of γ’ fibrinogen are associated with several forms of cardiovascular disease. The purpose of this cross-sectional study was to investigate the relationship between γ’ fibrinogen, an emerging risk factor for cardiovascular disease, and inflammatory markers in subjects with a chronic inflammatory state. The 284 subjects for this study came from the Periodontitis And Vascular Events (PAVE) study, and γ’ fibrinogen and total fibrinogen in plasma were measured by ELISA. Information on patient demographics and health status, as well as levels of C-reactive protein (CRP), an inflammatory marker, have previously been collected for this study. The mean (SE) γ’ fibrinogen level in the subjects was 0.622 (0.017) mg/ml. Levels of γ’ fibrinogen were correlated with CRP (p = 0.006), with a one unit increase in CRP associated with a 1.9% increase in γ’ fibrinogen, after adjustment for potential confounders. Total fibrinogen was not correlated with γ’ fibrinogen in these subjects. The number of dental sites with evidence of tissue inflammation was also significantly associated with γ’ fibrinogen levels. These results provide an important step in the evolution of γ’ fibrinogen not only as a general risk factor for cardiovascular disease, but as a potentially useful biomarker for assessing a patient’s inflammatory state and associated cardiovascular disease risk.