Characterization of the relative thrombogenicity of atherosclerotic plaque components: implications for consequences of plaque rupture
A Fernandez-Ortiz,
JJ Badimon,
E Falk,
V Fuster,
B Meyer,
A Mailhac,
D Weng,
PK Shah,
and
L Badimon
Cardiovascular Biology Laboratory, Massachusetts General Hospital, Boston.
OBJECTIVES. The purpose of this study was to determine whether different components of human atherosclerotic plaques exposed to flowing blood resulted in different degrees of thrombus formation. BACKGROUND. It is likely that the nature of the substrate exposed after spontaneous or angioplasty-induced plaque rupture is one factor determining whether an unstable plaque proceeds rapidly to an occlusive thrombus or persists as a nonocclusive mural thrombus. Although observational data show that plaque rupture is a potent stimulus for thrombosis, and exposed collagen is suggested to have a predominant role in thrombosis, the relative thrombogenicity of different components of human atherosclerotic plaques is not well established. METHODS. We investigated thrombus formation on foam cell-rich matrix (obtained from fatty streaks), collagen-rich matrix (from sclerotic plaques), collagen-poor matrix without cholesterol crystals (from fibrolipid plaques), atheromatous core with abundant cholesterol crystals (from atheromatous plaques) and segments of normal intima derived from human aortas at necropsy. Specimens were mounted in a tubular chamber placed within an ex vivo extracorporeal perfusion system and exposed to heparinized porcine blood (mean [+/- SEM] activated partial thromboplastin time ratio 1.5 +/- 0.04) for 5 min under high shear rate conditions (1,690 s-1). Thrombus was quantitated by measurement of indium-labeled platelets and morphometric analysis. Under similar conditions, substrates were perfused with heparinized human blood (2 IU/ml) in an in vitro system, and thrombus formation was similarly evaluated. RESULTS. Thrombus formation on atheromatous core was up to sixfold greater than that on other substrates, including collagen-rich matrix (p = 0.0001) in both heterologous and homologous systems. Although the atheromatous core had a more irregular exposed surface and thrombus formation tended to increase with increasing roughness, the atheromatous core remained the most thrombogenic substrate when the substrates were normalized by the degree of irregularity as defined by the roughness index (p = 0.002). CONCLUSIONS. The atheromatous core is the most thrombogenic component of human atherosclerotic plaques. Therefore, plaques with a large atheromatous core content are at high risk of leading to acute coronary syndromes after spontaneous or mechanically induced rupture because of the increased thrombogenicity of their content.
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Sequential Injury of the Rabbit Abdominal Aorta Induces Intramural Coagulation and Luminal Narrowing Independent of Intimal Mass : Extrinsic Pathway Inhibition Eliminates Luminal Narrowing
Circ. Res.,
May 19, 1998;
82(9):
996 - 1006.
[Abstract]
[Full Text]
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R. Gallo, A. Padurean, V. Toschi, J. Bichler, J. T. Fallon, J. H. Chesebro, V. Fuster, and J. J. Badimon
Prolonged Thrombin Inhibition Reduces Restenosis After Balloon Angioplasty in Porcine Coronary Arteries
Circulation,
February 17, 1998;
97(6):
581 - 588.
[Abstract]
[Full Text]
[PDF]
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S. Rota, N. A. McWilliam, T. P. Baglin, and C. D. Byrne
Atherogenic Lipoproteins Support Assembly of the Prothrombinase Complex and Thrombin Generation: Modulation by Oxidation and Vitamin E
Blood,
January 15, 1998;
91(2):
508 - 515.
[Abstract]
[Full Text]
[PDF]
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A. D. Schecter, B. J. Rollins, Y. J. Zhang, I. F. Charo, J. T. Fallon, M. Rossikhina, P. L. A. Giesen, Y. Nemerson, and M. B. Taubman
Tissue Factor Is Induced by Monocyte Chemoattractant Protein-1 in Human Aortic Smooth Muscle and THP-1 Cells
J. Biol. Chem.,
November 7, 1997;
272(45):
28568 - 28573.
[Abstract]
[Full Text]
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R. T. Lee and P. Libby
The Unstable Atheroma
Arterioscler Thromb Vasc Biol,
October 1, 1997;
17(10):
1859 - 1867.
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K. Kaikita, H. Ogawa, H. Yasue, M. Takeya, K. Takahashi, T. Saito, K. Hayasaki, K. Horiuchi, A. Takizawa, Y. Kamikubo, et al.
Tissue Factor Expression on Macrophages in Coronary Plaques in Patients with Unstable Angina
Arterioscler Thromb Vasc Biol,
October 1, 1997;
17(10):
2232 - 2237.
[Abstract]
[Full Text]
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T. Laperche, C. Laurian, R. Roudaut, P. G. Steg, and f. t. F. E. d. l. S. F. de Cardiologie
Mobile Thromboses of the Aortic Arch Without Aortic Debris : A Transesophageal Echocardiographic Finding Associated With Unexplained Arterial Embolism
Circulation,
July 1, 1997;
96(1):
288 - 294.
[Abstract]
[Full Text]
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V. Toschi, R. Gallo, M. Lettino, J. T. Fallon, S. D. Gertz, A. Fernandez-Ortiz, J. H. Chesebro, L. Badimon, Y. Nemerson, V. Fuster, et al.
Tissue Factor Modulates the Thrombogenicity of Human Atherosclerotic Plaques
Circulation,
February 4, 1997;
95(3):
594 - 599.
[Abstract]
[Full Text]
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S. Kaul, T. Z. Naqvi, M. C. Fishbein, B. Cercek, J. J. Badimon, T. C. Hutsell, S. Thomas, M. Molloy, and P. K. Shah
Local Delivery of an Ultra-short-acting Nitric Oxide- releasing Compound, DMHD/NO, Is Highly Effective in Inhibiting Acute Platelet-Thrombus Formation on Injured Arterial Strips
Journal of Cardiovascular Pharmacology and Therapeutics,
January 1, 1997;
2(3):
181 - 193.
[Abstract]
[PDF]
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P. R. Moreno, V. H. Bernardi, J. Lopez-Cuellar, A. M. Murcia, I. F. Palacios, H. K. Gold, R. Mehran, S. K. Sharma, Y. Nemerson, V. Fuster, et al.
Macrophages, Smooth Muscle Cells, and Tissue Factor in Unstable Angina: Implications for Cell-Mediated Thrombogenicity in Acute Coronary Syndromes
Circulation,
December 15, 1996;
94(12):
3090 - 3097.
[Abstract]
[Full Text]
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J. A. Bittl
Advances in Coronary Angioplasty
N. Engl. J. Med.,
October 24, 1996;
335(17):
1290 - 1302.
[Full Text]
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M. J. Davies
Stability and Instability: Two Faces of Coronary Atherosclerosis: The Paul Dudley White Lecture 1995
Circulation,
October 15, 1996;
94(8):
2013 - 2020.
[Full Text]
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J. D. Marmur, S. V. Thiruvikraman, B. S. Fyfe, A. Guha, S. K. Sharma, J. A. Ambrose, J. T. Fallon, Y. Nemerson, and M. B. Taubman
Identification of Active Tissue Factor in Human Coronary Atheroma
Circulation,
September 15, 1996;
94(6):
1226 - 1232.
[Abstract]
[Full Text]
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J. M. Mann and M. J. Davies
Vulnerable Plaque: Relation of Characteristics to Degree of Stenosis in Human Coronary Arteries
Circulation,
September 1, 1996;
94(5):
928 - 931.
[Abstract]
[Full Text]
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J.-F. Toussaint, G. M. LaMuraglia, J. F. Southern, V. Fuster, and H. L. Kantor
Magnetic Resonance Images Lipid, Fibrous, Calcified, Hemorrhagic, and Thrombotic Components of Human Atherosclerosis In Vivo
Circulation,
September 1, 1996;
94(5):
932 - 938.
[Abstract]
[Full Text]
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S. Waxman, M. A. Sassower, M. A. Mittleman, S. Zarich, A. Miyamoto, K. S. Manzo, J. E. Muller, G. S. Abela, and R. W. Nesto
Angioscopic Predictors of Early Adverse Outcome After Coronary Angioplasty in Patients With Unstable Angina and Non–Q-Wave Myocardial Infarction
Circulation,
June 15, 1996;
93(12):
2106 - 2113.
[Abstract]
[Full Text]
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P. K. Shah
New Antithrombotic Drugs for Coronary Artery Disease
Journal of Cardiovascular Pharmacology and Therapeutics,
April 1, 1996;
1(2):
165 - 176.
[PDF]
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E. Falk, P. K. Shah, and V. Fuster
Coronary Plaque Disruption
Circulation,
August 1, 1995;
92(3):
657 - 671.
[Full Text]
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J. S. Mruk, P. Zoldhelyi, M. W.I. Webster, M. Heras, D. E. Grill, D. R. Holmes Jr, V. Fuster, and J. H. Chesebro
Does Antithrombotic Therapy Influence Residual Thrombus After Thrombolysis of Platelet-Rich Thrombus? : Effects of Recombinant Hirudin, Heparin, or Aspirin
Circulation,
February 15, 1995;
93(4):
792 - 799.
[Abstract]
[Full Text]
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E. A. Weinstein, H. Li, J. A. Lawson, J. Rokach, G. A. FitzGerald, and P. H. Axelsen
Prothrombinase Acceleration by Oxidatively Damaged Phospholipids
J. Biol. Chem.,
July 21, 2000;
275(30):
22925 - 22930.
[Abstract]
[Full Text]
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P. Maschberger, M. Bauer, J. Baumann-Siemons, K. J. Zangl, E. V. Negrescu, A. J. Reininger, and W. Siess
Mildly Oxidized Low Density Lipoprotein Rapidly Stimulates via Activation of the Lysophosphatidic Acid Receptor Src Family and Syk Tyrosine Kinases and Ca2+ Influx in Human Platelets
J. Biol. Chem.,
June 16, 2000;
275(25):
19159 - 19166.
[Abstract]
[Full Text]
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G. Helft, S. G. Worthley, V. Fuster, Z. A. Fayad, A. G. Zaman, R. Corti, J. T. Fallon, and J. J. Badimon
Progression and Regression of Atherosclerotic Lesions: Monitoring With Serial Noninvasive Magnetic Resonance Imaging
Circulation,
February 26, 2002;
105(8):
993 - 998.
[Abstract]
[Full Text]
[PDF]
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