Inflammation, C-Reactive Protein, and Atherothrombosis

被引:186
|
作者
Ridker, Paul M. [1 ,2 ]
Silvertown, Josh D. [3 ]
机构
[1] Brigham & Womens Hosp, Ctr Cardiovasc Dis Prevent, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[3] Axon Med Commun Grp, Toronto, ON, Canada
关键词
Cardiovascular disease; cholesterol; myocardial infarction; periodontal disease; Reynolds Risk Score; statin;
D O I
10.1902/jop.2008.080249
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Atherothrombosis of the coronary and cerebral vessels is understood to be a disorder of inflammation and innate immunity, as well as a disorder of lipid accumulation. From a vascular biology perspective, the processes of cellular adhesion, monocyte and macrophage attachment, and transmigration of immune cells across the endothelium are crucial steps in early atherogenesis and in the later stages of mature plaque rupture, particularly the transition of unstable plaque at the time of acute thrombosis. There is abundant clinical evidence demonstrating that many biomarkers of inflammation are elevated years in advance of first ever myocardial infarction (MI) or thrombotic stroke and that these same biomarkers are highly predictive of recurrent MI, recurrent stroke, diabetes, and cardiovascular death. In daily practice, the inflammatory biomarker in widest use is high-sensitivity C-reactive protein (hsCRP); when interpreted within the context of usual risk factors, levels of hsCRP <1, 1 to 3, and >3 mg/I denote lower, average, and higher relative risk for future vascular events. Risk-prediction models that incorporate hsCRP, such as the Reynolds Risk Score, have been developed that improve risk classification and the accuracy for global risk prediction, particularly for those deemed at "intermediate risk" by usual algorithms, such as the Framingham Risk Score. With regard to cerebral vessels, increased biomarkers of inflammation, including hsCRP, have been associated with increased stroke risk as well as an increased rate of atherosclerosis progression in the carotid vessels. Although the proportion of variation in hsCRP explained by genetic factors may be as large as 20% to 40%, diet, exercise, and smoking cessation remain critical tools for risk reduction and CRP reduction. Statin therapy reduces hsCRP in a largely low-density lipoprotein (LDL)-independent manner, and the "anti-inflammatory" properties of these agents have been suggested as a potential mechanism beyond LDL reduction for the efficacy of these agents. The ongoing multinational Justification for the Use of statins in Primary prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial of 17,802 initially healthy men and women with low levels of LDL cholesterol but increased levels of hsCRP will help to define whether vascular protection can be achieved with statin therapy, even in the absence of hyperlipidemia. Targeted anti-inflammatory therapies are being developed that may provide a direct method of translating the biology of inflammation into new clinical treatments across multiple vascular beds. This article summarizes data supporting a role for inflammation in cardiovascular disease and offers the possibility that other disorders characterized by inflammation, such as periodontal disease, may have an indirect role by influencing the risk, manifestation, and progression of vascular events. J Periodontol 2008;79:1544-7551.
引用
收藏
页码:1544 / 1551
页数:8
相关论文
共 50 条
  • [21] Current Position on the Role of Monomeric C-reactive Protein in Vascular Pathology and Atherothrombosis
    Melnikov, Ivan S.
    Kozlov, Sergey G.
    Saburova, Olga S.
    Avtaeva, Yulia N.
    Prokofieva, Lyudmila, V
    Gabbasov, Zufar A.
    CURRENT PHARMACEUTICAL DESIGN, 2020, 26 (01) : 37 - 43
  • [22] C-reactive protein as a risk factor for atherothrombosis: a post-mortem study
    Burke, AP
    Tracy, R
    Virmani, R
    MODERN PATHOLOGY, 2001, 14 (01) : 43A - 43A
  • [23] C-reactive protein as a risk factor for atherothrombosis: a post-mortem study
    Burke, AP
    Tracy, R
    Virmani, R
    LABORATORY INVESTIGATION, 2001, 81 (01) : 43A - 43A
  • [24] Lipoprotein(a) is linked to atherothrombosis and aortic valve stenosis independent of C-reactive protein
    Thomas, Peter E.
    Vedel-Krogh, Signe
    Kamstrup, Pia R.
    Nordestgaard, Borge G.
    EUROPEAN HEART JOURNAL, 2023, 44 (16) : 1449 - 1460
  • [25] C-reactive protein and atherothrombosis - Beyond a biomarker: an actual partaker of lesion formation
    Verma, S
    Yeh, ETH
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2003, 285 (05) : R1253 - R1256
  • [26] DOES C-REACTIVE PROTEIN PROMOTE INFLAMMATION IN POLYARTHRITIS
    HIGHTON, J
    HESSIAN, P
    MYERS, DB
    PROCEEDINGS OF THE UNIVERSITY OF OTAGO MEDICAL SCHOOL, 1983, 61 (03): : 71 - 73
  • [27] The functional role of C-Reactive Protein in allergic inflammation
    Fujita, M.
    Ito, W.
    Takeda, M.
    Yamaguchi, K.
    Ueki, S.
    Kayaba, H.
    Chihara, J.
    ALLERGY, 2008, 63 : 578 - 578
  • [28] C-reactive protein, cytokines and inflammation in cardiovascular diseases
    Bucova, M.
    Bernadic, M.
    Buckingham, T.
    BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY, 2008, 109 (08): : 333 - 340
  • [29] Linking inflammation and thrombosis: Role of C-reactive protein
    Fay, William P.
    WORLD JOURNAL OF CARDIOLOGY, 2010, 2 (11): : 365 - 369
  • [30] C-reactive protein, inflammation and coronary heart disease
    Shrivastava, Amit Kumar
    Singh, Harsh Vardhan
    Raizada, Arun
    Singh, Sanjeev Kumar
    EGYPTIAN HEART JOURNAL, 2015, 67 (02): : 89 - 97