Thromb Haemost 2000; 83(06): 826-832
DOI: 10.1055/s-0037-1613928
Commentary
Schattauer GmbH

Tissue Factor and Homocysteine Levels in Ischemic Heart Disease Are Associated with Angiographically Documented Clinical Recurrences after Coronary Angioplasty

Rossella Marcucci
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Domenico Prisco
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Tamara Brunelli
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Guglielmina Pepe
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Anna Maria Gori
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Sandra Fedi
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Monia Capanni
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Ignazio Simonetti
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Giorgio Federici
1   Dip. Medicina Interna, University “Tor Vergata”, Rome
,
Anna Pastore
2   Osp. Pediatrico Bambin Gesù, IRCCS, Rome, Italy
,
Rosanna Abbate
,
Gian Franco Gensini
› Author Affiliations
Further Information

Publication History

Received 03 August 1999

Accepted after resubmission 17 February 2000

Publication Date:
14 December 2017 (online)

Summary

Background In ischemic heart disease (IHD) patients high plasma levels of Tissue Factor (TF), the trigger of coagulation cascade, are present. Homocysteine (Hcy) is a risk factor for coronary artery disease, and several different pathophysiological mechanisms by which Hcy may play a role in thrombus formation have been postulated in “in vitro” studies. We investigated the “in vivo” role of Hcy in affecting plasma levels of TF, its inhibitor Tissue Factor Pathway Inhibitor (TFPI) and hypercoagulability. Methods and Results We investigated 119 IHD patients who underwent PTCA and compared them with 103 healthy subjects. TF, TFPI, Thrombin-Antithrombin complexes (TAT) and Hcy levels were significantly higher in the patients than in the controls. A positive correlation was found between Hcy and TF (r = 0.54; p < 0.0001), Hcy and TFPI (r = 0.26; p < 0.05) as well as Hcy and TAT (r = 0.33; p < 0.0001) levels. An inverse correlation existed between folate intake and Hcy levels (r = −0.28; p = 0.001). Hcy levels within the first quartile and in the highest quartile were associated with a lower (p < 0.001) and higher (p <0.0001) rate of clinical recurrences, respectively. Patients with TF values in the first quartile had a lower rate of angiographically documented clinical recurrences as compared to those in the fourth quartile (p < 0.01); those in the highest quartile of TF showed a higher rate of recurrences (p = 0.001). Multivariate analysis confirmed these results (first quartile of Hcy: OR 0.02, Cl 0.002–0.27; fourth quartile of Hcy: OR 36.5, Cl 3.6-365/first quartile of TF: OR 0.006, Cl 0.001–0.44; fourth quartile of TF: OR 16.4, Cl 3.0 – 90.0), also after adjustment for risk factors and Hcy and TF respectively. Conclusions In this study we show that TF, TFPI and TAT levels are correlated with Hcy plasma levels in IHD patients, providing evidence of an “in vivo” pathophysiological mechanism of hyperhomocysteinemia. The observed association between angiographically documented clinical recurrences and TF and Hcy values awaits confirmation in studies designated to evaluate this issue on a larger number of patients.

 
  • References

  • 1 Graham M. The European Concerted Action Project. Plasma homocysteine as a risk factor for vascular disease. JAMA 1997; 277: 1775-89.
  • 2 Nygard O, Nordrehaug JE, Refsum H, Ueland PM, Farstad M, Vollset SE. Plasma homocysteine levels and mortality in patients with coronary artery disease. N Engl J Med 1997; 337: 230-6.
  • 3 Wald NJ, Watt HC, Law MR, Weir DG, McPartlin J, Scott JM. Homocysteine and ischemic heart disease. Results of a prospective study with implications regarding prevention. Arch Intern Med 1998; 158: 862-7.
  • 4 Clarke R, Daly L, Robinson K, Naughten E, Cahalane S, Fowler B. Graham Hyperhomocysteinemia: an independent risk factor for vascular disease. NEJM 1991; 324: 1149-55.
  • 5 Alfthan G, Pekkanen J, Janhianen M. Relations of serum homocysteine and lipoprotein (a) concentrations to atherosclerotic disease in a prospective Finnish population based study. Atherosclerosis 1994; 106: 9-19.
  • 6 Donner MG, Klein GK, Mathes PB, Schwandt P, Richter WO. Plasma total homocysteine levels in patients with early-onset coronary heart disease and a low cardiovascular risk profile. Metabolism 1998; 47: 273-9.
  • 7 Harpel PC, Zhang X, Borth W. Homocysteine and haemostasis: pathogenetic mechanisms predisposing to thrombosis. J Nutr 1996; 126: 1285S-9S.
  • 8 de Jong SC, Stehouwer CDA, van de Berg M, Vischer UM, Rauwerda JA, Emeis JJ. Endothelial marker proteins in hyperhomocysteinemia. Thromb Haemost 1997; 78: 1332-7.
  • 9 van de Berg M, Boers GHJ, Franken DG, Blom HJ, van Kamp GJ, Jakobs C, Rauwerda JA, Kluft C, Stehouwert CDA. Hyperhomocysteinaemia and endothelial dysfunction in young patients with peripheral arterial occlusive disease. Eur J Clin Invest 1995; 25: 176-81.
  • 10 Cattaneo M, Franchi F, Zighetti ML, Martinelli I, Asti D, Mannucci PM. Plasma levels of activated protein C in healthy subjects and patients with previous venous thromboembolism. Relationships with plasma homocysteine levels. Arterioscler Thromb Vasc Biol 1998; 18: 1371-5.
  • 11 Fryer RH, Wilson BD, Gubler DB, Fitzgerald LA, Rodgers GM. Homocysteine, a risk factor for premature vascular disease and thrombosis, induces tissue factor activity in endothelial cells. Arterioscler Thromb Vasc Biol 1993; 13: 1327-33.
  • 12 Durand P, Lussier-Cacan S, Blache D. Acute methionine load-induced hyperhomocysteinemia enhances platelet aggregation, thromboxane biosynthesis, and macrophage-derived tissue factor activity in rats. FASEB J 1997; 11: 1157-68.
  • 13 Falciani M, Gori AM, Fedi S, Chiarugi L, Simonetti I, Dabizzi RP, Prisco D, Pepe G, Abbate R, Gensini GF, Neri GGSerneri. Elevated tissue factor and tissue factor pathway inhibitor in ischaemic heart disease patients. Thromb Haemost 1998; 79: 495-9.
  • 14 Neri GGSerneri, Abbate R, Gori AM, Attanasio M, Martini F, Giusti B, Dabizzi P, Poggesi L, Modesti PA, Trotta F, Rostagno C, Boddi M, Gensini GF. Transient intermittent lymphocyte activation is responsible for the instability of angina. Circulation 1992; 86: 790-7.
  • 15 Ardissino D, Merlini PA, Ariens R, Coppola R, Bramucci E, Mannucci PM. Tissue factor antigen activity in human coronary atherosclerotic plaques. Lancet 1997; 349: 769-71.
  • 16 Brown BG, Bolson E, Frimer M, Dodge HT. Quantitative coronary angiography: estimation of dimensions hemodynamic resistance and atheroma mass of coronary artery lesions using arteriogram and digital computation. Circulation 1977; 55: 329-77.
  • 17 Simonetti I, De Caterina R, Marsilli M, de Nes M, L’Abbate A. Coronary vasodilatation by nitrates is not mediated by the prostaglandin system: an angiographic and hemodynamic study. Z Kardiol 1983; 72 3S 40-45.
  • 18 Willett WC, Sampson L, Stampfer MJ, Rosner B, Bain C, Witschi J, Hennekens CH, Speizer FE. Reproducibility and validity of a semiquantitative food frequency questionnaire. Am J Epidemiol 1985; 122: 51-65.
  • 19 Willett WC, Sampson L, Browne ML, Stampfer MJ, Rosner B, Hennekens CH, Speizer FE. The use of a self-administered questionnaire to assess diet four years in the past. Am J Epidemiol 1988; 127: 188-99.
  • 20 Colditz GA, Willett WC, Stampfer MJ, Sampson L, Rosner B, Hennekens CH, Speizer FE. The influence of age, relative weight, smoking, and alcohol intake on the reproducibility of a dietary questionnaire. Inter J Epidemiol 1987; 16: 393-8.
  • 21 Nemerson Y. Tissue factor: Then and now. Thromb Haemost 1995; 07: 180-4.
  • 22 Nemerson Y. Tissue factor and haemostasis. Blood 1988; 71: 1-8.
  • 23 Soejima H, Ogawa H, Yasue H, Suefuji H, Kaikita K, Tsuji I, Kumeda K, Aoyama N. Effects of enalapril on tissue factor in patients with uncomplicated acute myocardial infarction. Am J Cardiol 1996; 78: 336-40.
  • 24 Jude B, Fontaine P. Modifications of monocyte procoagulant activity in diabetes mellitus. Semin Thromb Hemost 1991; 17: 445-7.
  • 25 Colli S, Elgini S, Lolli M, Camera M, Paoletti R, Tremoli E. Vastatins inhibit tissue factor in cultured human macrophages. A novel mechanism of protection against atherothrombosis. Arterioscler Thromb Vasc Biol 1997; 17: 265-72.
  • 26 Sutton-Tyrrell K, Bostom A, Selhub J, Zeigler-johnson C. High homocysteine levels are independently related to isolated systolic hypertension in older adults. Circulation 1997; 90: 1745-9.
  • 27 Nygard O, Refsum H, Ueland PM, Vollset SE. Major lifestyle determinants of plasma total Hcy distribution: the Hordaland Study. Am J Clin Nutr 1998; 67: 263-70.
  • 28 Jude B, Agraor B, McFadden EP, Susen S, Bauters C, Lepelley P, Vanhaesbracke C, Devos P, Cosson A, Asseman P. Evidence for time-dependent activation of monocytes in the systemic circulation in unstable angina but not in acute myocardial infarction or in stable angina. Circulation 1994; 90: 1662-8.
  • 29 Vaddi K, Nicolini FA, Mehta P, Mehta JL. Increased secretion of tumor necrosis factor-alpha and interferon-gamma by mononuclear leukocytes in patients with ischemic heart disease. Circulation 1994; 90: 694-9.
  • 30 Gori AM, Pepe G, Attanasio M, Falciani M, Abbate R, Prisco D, Fedi S, Giusti B, Brunelli T, Comeglio P, Gensini GF, Neri GGSerneri. Tissue factor reduction and tissue factor pathway inhibitor release after heparin administration. Thromb Haemost 1999; 81: 589-93.
  • 31 Egerton W, Silberberg J, Crooks R, Ray C, Xie L, Dudman N. Serial measures of plasma homocysteine after acute myocardial infarction. Am J Cardiol 1996; 77: 759-61.
  • 32 Lindgren A, Brattstrom L, Norrving B, Hultberg B, Andersson A, Johansson BB. Plasma homocysteine in the acute and convalescent phases after stroke. Stroke 1995; 26: 795-800.
  • 33 Neri GGSerneri, Prisco D, Martini F, Gori AM, Brunelli T, Poggesi L, Rostagno C, Gensini GF, Abbate R. Acute T-cell activation is detectable in unstable angina. Circulation 1997; 95: 1806-12.
  • 34 Liuzzo G, Biasucci LM, Gallimore JR, Griello RL, Rebuzzi AG, Pepys MB, Maseri A. The prognostic value of C-reactive protein and serum amyloid A protein in severe unstable angina. N Engl J Med 1994; 331: 417-24.
  • 35 Kyrle PA, Stumpflen A, Hirschl M, Bialonczyk C, Herkner K, Spelser W, Weltermann A, Kaider A, Pabinger I, Lechner K, Elchinger S. Levels of prothrombin fragment F1+2 in patients with hyperhomocysteinemia and a history of venous thromboembolism. Thromb Haemost 1997; 78: 1327-31.
  • 36 Schwartz SM, Siscovick DS, Malinow MR, Rosendaal FR, Beverly RK, Hess DL, Psaty BM, Longstreth WT, Koepsell TD, Raghunathan TE, Reitsma PH. Myocardial infarction in young women in relation to plasma total homocysteine, folate, and a common variant in the methylenetetrahydrofolate reductase gene. Circulation 1997; 96: 412-7.
  • 37 Selhub J, Jacques P, Bostom AG, D’Agostino RB, Wilson PWF, Belanger AJ, O’Leary DH, Wolf PA, Schaefer EJ, Rosenberg IH. Association between plasma homocysteine concentrations and extracranial carotidartery stenosis. N Engl J Med 1995; 332: 286-91.
  • 38 Abbate R, Sardi I, Pepe G, Marcucci R, Brunelli T, Prisco D, Fatini C, Capanni M, Simonetti I, Gensini GF. The high prevalence of thermolabile 5-10 methylenetetrahydrofolate reductase (MTHFR) in Italians is not associated to an increased risk for coronary artery disease. Thromb Haemost 1998; 79: 727-30.
  • 39 Tsai J, Perrella MA, Yoshizumi M, Hsieh C, Haber E, Schlegel R, Lee M. Promotion of vascular smooth muscle cell growth by homocysteine: a link to atherosclerosis. Proc Natl Acad Sci USA 1994; 91: 6369-73.
  • 40 Grech ED, Dodd NJF, Jackson MJ, Morrison WL, Faragher EB, Ramsdale DR. Evidence for free radical generation after primary percutaneous transluminal coronary angioplasty recanalization in acute myocardial infarction. Am J Cardiol 1996; 77: 122-7.
  • 41 Tardif JC, Cote G, Lesperance J, Bourassa M, Lambert J, Doucet S, Bilodeau L, Nattel S, De Guise P. for the Multivitamins and Probucol Study Group. Probucol and multivitamins in the prevention of restenosis after coronary angioplasty. NEJM 1997; 337: 365-72.
  • 42 Ragni M, Cirillo P, Pascucci I, Scognamiglio A, D’Andrea D, Eramo N, Ezekowitz MD, Pawashe AB, Chiariello M, Golino P. Monoclonal antibody against tissue factor shortens tissue plasminogen activator lysis time and prevents reocclusion in a rabbit model of carotid artery thrombosis. Circulation 1996; 93: 1913-8.
  • 43 Jang Y, Guzman LA, Lincoff AM, Gottsauner-Wolf M, forudi F, Hart CE, Courtman DW, Ezban M, Ellis SG, Topol EJ. Influence of blockade at specific levels of the coagulation cascade on restenosis in a rabbit atherosclerotic femoral artery injury model. Circulation 1995; 92: 3041-50.
  • 44 Pietersma A, Kofflard M, de Wit LEA, Stijnen T, Koster JF, Serruys PW, Sluiter W. Late lumen loss after coronary angioplasty is associated with the activation status of circulating phagocytes before treatment. Circulation 1995; 91: 1320-5.
  • 45 Jovinge S, Hultgardh-Nilsson A, Regnstrom J, Nilsson J. Tumor necrosis factor-alpha activates smooth muscle cell migration in culture and is expressed in the balloon-injured rat aorta. Arterioscler Thromb Vasc Biol 1997; 17: 490-7.
  • 46 Barron MK, Lake RS, Buda AJ, Tenaglia AN. Intimal hyperplasia after balloon injury is attenuated by blocking selectins. Circulation 1997; 96: 3587-92.
  • 47 Desmarais RL, Sarembock IJ, Ayers CR, Vernon SM, Powers ER, Gimple LW. Elevated serum lipoprotein (a) is a risk factor for clinical recurrence after coronary angioplasty. Circulation 1995; 91: 1403-9.
  • 48 Gordon PC, Friederich SP, Piana RN. Is 40% to 70% diameter narrowing at the site of previous stenting or directional coronary aterectomy clinically significant?. Am J Cardiol 1994; 74: 26-32.
  • 49 Malinow MR, Bostom AG, Krauss RM. Homocysteine, diet and cardiovascular disease. Circulation 1999; 99: 178-82.