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Genetic Polymorphisms and Arterial Thrombosis

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Recent Advances in Geriatrics

Abstract

In Western countries, acute myocardial infarction and stroke, are major causes of morbidity and mortality (1). An occlusive coronary thrombus on an ulcerated atherosclerotic plaque in the coronary arteries is the central event in more than 90% of patients with Q-wave myocardial infarction (2). The underlying abnormality in non-Q-wave infarctions is a ruptured atherosclerotic plaque, which acts as a nidus for the deposition and activation of platelets. Atherosclerotic changes in the carotid and vertebrobasilar arteries resemble those of coronary arteries (3). These lesions may progress to local occlusions, but most often do not become symptomatic until embolization to more distal arteries takes place (ischemic stroke). In the cerebral arteries, vessel wall and lumen may be normal until the artery is occluded by an embolus from a more proximal arterial lesion or from the heart (4). Rather than to emboli, occlusion of the small penetrating arteries is often due to degenerative changes of the vessels or to extracranial large-artery disease (5).

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References

  1. Fuster V, Badimon L, Badimon JJ, Chesebro JH. The pathogenesis of coronary artery disease and acute coronary syndromes. New Engl. J. Med. 1992;326, 242–250.

    Article  PubMed  CAS  Google Scholar 

  2. Mizuno K, Miyamoto A, Satomura K et al. Angioscopic coronary macromorphology in patients with acute coronary disorders. Lancet 1991;337, 809–12.

    Article  PubMed  CAS  Google Scholar 

  3. Jorgensen L, Torvik A. Ischemic cerebrovascular diseases in an autopsy series. Part 2: Prevalence, location, pathogenesis, and clinical course of cerebral infarct. J. Neurol. Science 1969; 9:285–320.

    Article  CAS  Google Scholar 

  4. Olsen TS, Skriver EB, Heming M. Cause of cerebral infarction in the carotid territori. Its relation to the size and the location of the infarct and to the underlying vascular lesion. Stroke 1985; 16:459–466.

    Article  PubMed  CAS  Google Scholar 

  5. Millikan C, Futrell N. The fallacy of the lacune hypothesis. Stroke 1990;21:1251–1257.

    Article  PubMed  CAS  Google Scholar 

  6. Parra HJ, Arveiler D, Evans AE, Cambou JP, Amouyel P, Bingham A, McMaster D, Schaffer P, Douste-Blazy P, Luc G, Richard JL, Ducimeti¸re P, Fruchart JC, Cambien F. A case-control study of lipoprotein particles in two populations at contrastino risk for coronary heart disease. Arterioscler Thromb 1992;12:701–707.

    Article  PubMed  CAS  Google Scholar 

  7. Sing CF, Moll PP. Genetics of variabilità of CHD risk. Int. J. Epidemiol. 1989;18 (suppl 1): S183–S195.

    Article  PubMed  CAS  Google Scholar 

  8. Kannell WB. Bishop lecture: Contribution of the Framingham study to preventive cardiology. J. Am. Coll. Cardiol. 1990; 15, 206–211.

    Article  Google Scholar 

  9. Ernst E., Resch KL. Fibrinogen as a cardiovascular risk factor: a meta-analysis and review of the literature. Ann Int Med 1993;118:956–963.

    Article  PubMed  CAS  Google Scholar 

  10. The WHO MONICA project. A worldwide monitoring system for cardiovascular disease. World Health Stat Annu. 1989;27.

    Google Scholar 

  11. Meade TW, Mellows S, Brozovic M, Miller GJ, Chakrabarti RR, North WRS, Haines AP, Stirling Y, Imeson JD, Thompson SG. Hemostatic function and ischemic heart disease: Principal results of the North-wick Park Study. Lancet 1986;2:533–7.

    Article  PubMed  CAS  Google Scholar 

  12. Ridker PM, Vaughan, DE, Stampfer MJ, Manson JE, Hennekens CH. Endogenous tissue-type Plasminogen activator and risk of myocardial infarction. Lancet 1993; 341: 1165–1168.

    Article  PubMed  CAS  Google Scholar 

  13. Hamsten A, De Faire U, Walldius G, Dahlen G, Szamosi A, Landou C, Blomback M, Wiman B: Plasminogen activator inhibitor in plasma: risk factor for recurrent myocardial infarction. Lancet 1987;2:3–9.

    Article  PubMed  CAS  Google Scholar 

  14. Kannel WB. Range of serum cholesterol values in the population developing coronary artery disease. Am. i. Cardiol. 1995;76:69C–77C.

    Article  CAS  Google Scholar 

  15. Schaefer EJ, Lamon-Fava S, Jenner JL, McNamara JL, Ordovas JM, Davis CE, Abolafia JM, Lippel K, Levy RI. Lipoprotein(a) levels and risk of coronary heart disease in men. The Lipid Research Clinics Coronary Primary Prevention Trial. JAMA 1994, 271: 999–1003

    Article  PubMed  CAS  Google Scholar 

  16. Tornvall P, Bavenholrn P, Landou C, de Faire U, Hamsten A. Relation of plasma levels and compogition of apolipoprotein B-containing lipoproteins to angiographically defined coronary artery disease in young patients with myocardial infarction. Circulation 1993;88(part 1):2180–2189.

    Article  PubMed  CAS  Google Scholar 

  17. Heinrich PC, Castell JV, Andus T. Interleukin 6 and the acute phase response. Biochem. J. 1990; 265:621–636.

    PubMed  CAS  Google Scholar 

  18. Schneiderman J, Loskutoff DJ. Plasminogen Activator inhibitors. Trends Cardiovasc. Med. 1991; 1:99–102.

    Article  PubMed  CAS  Google Scholar 

  19. Antiplatelet Trialists, Collaboration. Secondary prevention of vascular events by prolonged antiplatelet therapy. BMJ 1988;296:320–331

    Article  Google Scholar 

  20. Goldbourt U, Neufeld HN. Genetic aspect of arteriosclerosis. Arteriosclerosis 1986; 6:357–377.

    Article  PubMed  CAS  Google Scholar 

  21. Miletich JP, Prescott SM, White R, Majerus PW, Bovill EG. Inherited predisposition to thrombosis. Cell 1993; 72:477–480.

    Article  PubMed  CAS  Google Scholar 

  22. Hamsten A, Iselius L, Dahlen G, defaire U. Genetic and cultural inheritance of serum lipids, low and high density lipoprotein cholesterol and serum apoprotein A∼I, A-II, and B. Atherosclerosis 1986;60:199–208.

    Article  PubMed  CAS  Google Scholar 

  23. Humphries SE. The genetic contribution to the risk of thrombosis and cardiovascular disease. Trends Cardiovasc. Med. 1994;4:8–17.

    Article  PubMed  CAS  Google Scholar 

  24. Haverkate F, Samama M. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommitte on fibrinogen. Thromb. Haernost. 1995; 1e 73:151–161.

    Google Scholar 

  25. Deutscher S, Epstein F, Kjelsberg M. Familial aggregation of coronary heart disease. Circulation 1966;33:911–924.

    Article  PubMed  CAS  Google Scholar 

  26. Nora J, Lortscher R, Spangler R, Nora A, Kimberling W. Genetic-epidemiological study of early onset is-chemic heart disease. Circulation 1980;61:503–508.

    Article  PubMed  CAS  Google Scholar 

  27. de Faire U. Ischemic heart disease in death discordant twins. A study in 205 male and female pairs. Acta Med. Scand. Suppl. 1974;568:1–109.

    PubMed  Google Scholar 

  28. Berg K. Twin research in coronary heart disease. In Parisi GL, Nance WL. Twin research 3: Epidemiological and Clinical Studies. New York, Alan R Liss, 1981;pp. 117–130.

    Google Scholar 

  29. Khaw KT, Barrett CE. Family history of stroke as an independent predictor of ischemic heart disease in men and stroke in women. Am. J. Epidemiol. 1986;123:59–66.

    PubMed  CAS  Google Scholar 

  30. Welin L, Svardsudd K, Wilhelmsen L, Larsson B, Tibblin G. Analysis of risk factors for a stroke cohort of men born in 1913. N. Engl i. Med 1987;317:321–326.

    Article  Google Scholar 

  31. Boysen G, Nyboe J, Appleyard M, Sorensen PS, Boas J, Somnier F, Jensen J, schnohr P. stroke incidence and risk factors for stroke in Copenhagen, Denmark. Stroke 1988;19:1345–1353.

    Article  PubMed  CAS  Google Scholar 

  32. Kiely DK, Wolf PA, Cupples A, Beiser AS, Myers RH. Familial aggregation of stroke. The Framingham study. 1993;24:1366–1371.

    CAS  Google Scholar 

  33. Brass LM, Isaacsohn I, Merikangas KR, Robinette CD. A study of twins and stroke. Stroke 1992;23:221–223.

    Article  PubMed  CAS  Google Scholar 

  34. Wannamethee SG, Shaper GA, Ebrahim S. History of parental death from stroke or heart trouble and the risk of stroke in middle-aged men. Stroke 1996;27:1492–1498.

    Article  PubMed  CAS  Google Scholar 

  35. Wright S. The shifting balance of evolution theory and macroevolution. Ann. Rev. Genet. 1982;16:1–19.

    Article  PubMed  CAS  Google Scholar 

  36. Humphries SE, Cook M, Dubovitz M, Stirling Y, Meade TW. Role of genetic variation at the fibrinogen locus in the determination of plasma fibrinogen concentrations. Lancet 1987;1:1452–5.

    Article  PubMed  CAS  Google Scholar 

  37. Green F, Kelleher C, Wilkes H, Temple A, Meade T, Humphries S. A common genetic polymorphism associate with lower coagulation factor VII levels in healthy individuale. Arterioscler. Thromb. 1991;11:540–546.

    Article  PubMed  CAS  Google Scholar 

  38. Dawson SJ, Wiman B, Hamsten A, Green F, Humphries S, Henney AM: The two allele sequences of a common polymorphism in the promoter of the Plasminogen activator inhibitor-1 (PAI-1) gene respond differently to interleukin-1 in HepG2 cells. J. Biol Chem 1993;268:10739–10745.

    PubMed  CAS  Google Scholar 

  39. Wade DP, Klarke JC, Lindahl GE, Liu AC Zysow BR, Meer K, Schwartz K, Lawn RM. 51 control regions of the apoprotein(a) gene and members of the related Plasminogen gene family. Proc. Natl. Acad. Sci. USA 1993;90:1369–1373.

    Article  PubMed  CAS  Google Scholar 

  40. Hansen PS, Gerdes LU, Klausen IC, Gregersen N, Faergeman O. Polymorphisms in the apoliprotein B-100 gene contributes to normal variation in plasma lipids in 464 Danish men born in 1948. Hum. Genet. 1993;91:45–50.

    Article  PubMed  CAS  Google Scholar 

  41. Cambien F, Poirier O, Lecerf L, Evans A, Cambou JP, Arveiler D, Luc G, Bara L, Ricard S, Tiret L, Amouyel P, Alhenc-Gelas F, Soubrier F. Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction. Nature 1992;359: 641–344.

    Article  PubMed  CAS  Google Scholar 

  42. Cumming AM, Robertson F. Polymorphism at the apo E locus in relation to risk of coronary disease. Clin. Genet. 1984;25:301–313.

    Google Scholar 

  43. Wahg XL, Sim AS, Badhenop RF, McCradie RM, Wilcken DEL. A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene. Nat. Med. 1996;2:41–45.

    Article  Google Scholar 

  44. de Franchis R, Mancini FP, D’Angelo A, Sebastio G, Fermo I, De Stefano V, Margaglione M, Mazzola G, Di Minno G, Andria G. Elevated total plasma homocysteine and 677C->T mutation of the 5, 10 Methyle-netetrahydrofolate reductase gene in thrombotic vascular disease. Am. J. Hum. Genet. 1996;59:262–264.

    PubMed  Google Scholar 

  45. Livshits G, Schettler G, Graff E, Bletter M, Wahrendorf J, Brunner D. Tel Aviv-Heidelberg three-generation offspring study: genetic determinants of plasma fibrinogen level. Am. J. Med. Genet. 1996;63:509–517.

    Article  PubMed  CAS  Google Scholar 

  46. Margaglione M, Grandone E, Mancini FP, Di Minno G. Genetic modulation of plasma fibrinogen concentrations: possible importance of interleukin-6. i. Thromb. Thrombolysis 1996;3:51–56.

    CAS  Google Scholar 

  47. Thomas AE, Green FR, Kelleher CH, et al. Variation in the promoter region of the b fibrinogen gene is associated with plasma fibrinogen levels in smokers and non-smokers. Thromb. Haemost. 1991;65: 487–490.

    PubMed  CAS  Google Scholar 

  48. Margaglione M, Di Minno G, Grandone E, Vecchione G, Celentano E, Cappucci G, Giordano M, Grilli M, Simone P, Fusilli S, Panico S, Mancini M. Raised plasma fibrinogen concentrations in subjects attendine a metabolic ward. Relation to family history and vascular risk factors. Thromb Haemost 1995;73:579–83.

    PubMed  CAS  Google Scholar 

  49. Humphries SE, Ye S, Talmud P, Bara L, Wilhelmsen L, Tiret L, on behalf of the European Atherosclerosis Research Study (EARS) group. European atherosclerosis research study: genotype at the fibrinogen locus (G-455-A b-gene) is associated with differences in plasma fibrinogen levels in young men and women from different regions in Europe. Evidence for gender-genotype-environment interaction. Arterioscler Thromb Vasc Biol 1995;15:96–104.

    Article  PubMed  CAS  Google Scholar 

  50. Fowkes FGR, Connor JM, Smith FB, Wood J, Donnan PT, Lowe GDO. Fibrinogen genotype and risk of peripheral atherosclerosis. Lancet 1992;339:693–696.

    Article  PubMed  CAS  Google Scholar 

  51. Behague I, Poirier O, Nicaud V, Evans A, Arveiler D, Luc G, Cambou JP, Scarabin PJ, Bara L, Green F, Cambien F. b-fibrinogen gene polymorphisms are associated with plasma fibrinogen and coronary artery disease in patients with myocardial infarction. The ECTIM study. Circulation 1996;93:440–9.

    Article  PubMed  CAS  Google Scholar 

  52. Lane A, Cruickshank JK, Mitchell J, Henderson A Humphries S, Green F. Genetic and environmental determinants of factor VII coagulant activity in ethnic groups at different risk of coronary heart disease. Atherosclerosis 1992;94:43–50.

    Article  PubMed  CAS  Google Scholar 

  53. Marchetti G, Petracchini P, Papacchini M, Ferrati M, Bernardi F. A polymorphism in the 51 region of coagulation factor VII gene (F7) due to an inserted decanucleotide. Hum Genet 1993;90:575–6.

    Article  PubMed  CAS  Google Scholar 

  54. Bernardi F, Marchetti G, Pinotti M, Arcieri P, Baroncini C, Papacchini M, Zepponi E, Ursicino N, Chiarotti F, Mariani G. Factor VII gene polymorphisms contributo about one third of the factor VII level variation in plasma. Arterioscler Thromb Vasc Biol 1996;16:72–6.

    PubMed  CAS  Google Scholar 

  55. Moor E, Silvera A, vanlt Hooft F, Suontaka AM, Eriksson P, Blomback M, Hamsten A. Coagulation factor VII mass and activity in young men with myocardial infarction at a young age. Role of plasma lipoproteins and factor VII genotype. Arterioscler Thromb Vasc Biol 1995;15:655–64.

    Article  PubMed  CAS  Google Scholar 

  56. Dawson S, Hamsten A, Wiman B, Hehney A, Humphries S. Genetic variation at the Plasminogen activator inhibitor-1 locus is associate with altered levels of plasma Plasminogen activator inhibitor-1 activity. Arterioscler. Thromb. 1991;11:183–190.

    Article  PubMed  CAS  Google Scholar 

  57. Panahloo A, Mohamed-Ali V, Lane A, Green F, Humphries SE, Yudkin JS. Determinants of Plasminogen activator inhibitor 1 activity in treated NIDDM and its relation to a polymorphism in the Plasminogen activator inhibitor 1 gene. Diabetes 1995;44: 37–42.

    Article  PubMed  CAS  Google Scholar 

  58. Eriksson P, Kallin B, van t’Hooft FM, Bavhenolm P, Hamsten A. Allelic-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associate with myocardial infarction. Proc. Natl. Acad. Sci. USA 1995;92:1851–1855.

    Article  PubMed  CAS  Google Scholar 

  59. Mansfield MW, Stickland MH, Grant PJ. Plasminogen activator inhibitor-1 (PAI-1) promoter polymorphism and coronary artery disease in non-insulin-dependent diabetes. Thromb. Haemost. 1995;74:1032–1034

    PubMed  CAS  Google Scholar 

  60. Margaglione M, Grandone E, Vecchione G, Cappucci G, Giuliani N, Colaizzo N, Celentano E, Panico S, Di Minno G. Plasminogen activator inhibitor-1 (PAI-1) antigen plasma levels in subjects attending a metabolic ward. Relation to polymorphisms of the PAI-1 and of the angiontensin converting enzyme (ACE) genes. Atrioscler. Thromb. Vasc. Biol. 1997 17: (in press).

    Google Scholar 

  61. Ye S, Greeh FR, Scarabin PY, Nicaud V, Bara L, Dawson Si, Humphries SE, Evans A, Luc G, Cambou JP Arveiler D, Henney AM, Cambien F. The 4G/5G genetic polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene is associate with differences in plasma PAI-1 activity but not with risk of myocardial infarction in the ECTIM study. Thromb. Haemost. 1995;74:837–841.

    PubMed  CAS  Google Scholar 

  62. Cambien F, Soubrier F. The angiotensin-converting enzyme: molecular biology and implication of the gene polymorphism in cardiovascular diseases. In Hypertension, pathophysiology and management. Second Edition. Raven Press LTD, New York, Larg JH, Brenner BM Eds, 1995;pp 1667-1682.

    Google Scholar 

  63. Cambien F, Poirier O, Lecerf L, Evans A, Cambou JP, Arveiler D, Luc G, Bara L, Ricard S, Tiret L, Amouyel P, Alhenc-Gelas F, Soubrier F. Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction. Nature 1992;359: 641–344.

    Article  PubMed  CAS  Google Scholar 

  64. Samani N, Thompson JR, O’Toole L, Channer K, Woods KL. A meta-analysis of the association of the deletion allele of the angiotensin-converting enzyme gene with myocardial infarction. Circulation 1996;94:708–712.

    Article  PubMed  CAS  Google Scholar 

  65. Reynolds MV, Bristow MR, Bush EW, Abraham WT, Lowes BD, Zisrnan LS, Taft CS, Perryman MB. Angiotensin-converting enzyme DD genotype in patients with ischaemic or dilated cardiomyopathy. Lancet 1993;342:1073–1075.

    Article  Google Scholar 

  66. Marian AJ, Yu QT, Workman R, Greve G, Roberts R. Angiotensin-converting enzyme polymorphism in hypertrophie cardiomyopathy and sudden cardiac death. Lancet 1993;342:1085–1086.

    Article  PubMed  CAS  Google Scholar 

  67. Samani NJ, Martin DS, Brack M, Cullen J, Chauhan A, Lodwick D, Harley A, Swales JD, de Bono DP, Gershlick AH. Insertion/deletion polymorphism in the angiotensin-converting enzyme gene and risk of restenosis after coronary angioplasty. Lancet 1995;345:1013–1016.

    Article  PubMed  CAS  Google Scholar 

  68. Margaglione M, Celentano E, Grandone E, Vecchione G, Cappucci G, Giuliani N, Colaizzo D, Panico S, Mancini FP, Di Minno G. Deletion Polymorphism of the angiotensin convertine enzyme gene in patients with a history of ischemic stroke. Arterioscl. Thrombos Vasc. Biol. 1996;16: 304–309.

    Article  CAS  Google Scholar 

  69. Kario K, Kanai N, Saito K, Nago N, Matsuo T, Shimada K. Ischemic stroke and the gene for angiotensin-converting enzyme in Japanese hypertensives. Circulation 1996;93:1630–1633.

    Article  PubMed  CAS  Google Scholar 

  70. Maeda Y, Ikeda U, Ebata H, Hojo Y, Scino Y, Hayashi Y, Kuroki S, Shimada. Angiotensin-converting enzyme gene in hypertensive individuate with parental history of stroke. Stroke 1996;27:1521–1523.

    Article  PubMed  CAS  Google Scholar 

  71. Bonh, Berge KE, Bakkan A, Erikssen J, Berg K. Insertion/deletion (I/D) polymorphism at the locus for angiotensin I-converting enzyme and myocardial infarction. Clin. Genetics, 1993;44:298–301.

    Google Scholar 

  72. Catto A, Carter AM, Barrett JH, Stickland M, Bamford J, Davis JA, Grant PJ. Angiotensin-converting enzyme insertion/deletion polymorphism and cerebrovascular disease. Stroke 1996;27:435–440.

    Article  PubMed  CAS  Google Scholar 

  73. Lindpaintner K, Pfeffer MA, Kreutz R, Stampfer MJ, Grodstein F, LaMotte F, Burig J, Hennekens CH. A prospective evaluation of angiotensin-converting enzyme gene polymorphism and the risk of ischemic heart disease. N. Engl. J Med 1995, 332, 706–711.

    Article  PubMed  CAS  Google Scholar 

  74. Lindpainter K, Lee M, larson M, Rao VR, Pfeffer MA, Ordovas JM, Schaefer EJ, Wilson AF, Wilson PWF, Vasan RS, Myers RH, Levy D. Absence of association or genetic linkage between the angiotensin-converting enzyme gene and left ventricular mass. N. Engl. J. Med 1996;334:1023–1028.

    Article  Google Scholar 

  75. Bloem LJ, Manatunga AK, Pratt JH. Racial différente in the relationship of an angiotensin-converting enzyme gene polymorphism to serum angiotensin Iconverting enzyme activity. Hypertension 1996;27:62–66.

    Article  PubMed  CAS  Google Scholar 

  76. Davignon J. Apolipoprotein E polymorphism and atherosclerosis. In: Born GVR, Schwartz CJ, eds. New horizons in coronary heart disease. London UK: Science Press Ltd. 1993:5.1–5.21.

    Google Scholar 

  77. Dallongeville J, Lussier-Cacan S, Davignon J. Modulation of plasma triglyceride levels by apo E pheno-type: a meta-analysis. J. Lipid Res. 1992;33:447–454.

    PubMed  CAS  Google Scholar 

  78. Hixson JE, Pathobiological Determinants of Atherosclerosis in Youth (PDAY) research group. Apolipoprotein E polymorphisms affect atherosclerosis in young males. Arterioscler. Thromb. 1991;11:1237–1244.

    Article  PubMed  CAS  Google Scholar 

  79. Pedro-Botet J, Senti M, Nogues X, Rubi¸s-Prat J, Roquer J, D’Olhaberriague L, Olivéj. Lipoprotein and apolipoprotein profile in men with ischemic stroke. Role of lipoprotein(a), triglyceride-rich lipoproteins, and apolipoprotein E polymorphism. Stroke 1992;23:1556–1562.

    Article  PubMed  CAS  Google Scholar 

  80. Schachter F, Faure-Delanef L, Guenot F, Rouger H, Froguel R, Lesueur-Ginot L and Cohen D. Genetic associations with human longevitc at the Apo E and ACE loci. Nat Genet 1994;6: 29–32

    Article  PubMed  CAS  Google Scholar 

  81. Utermann G, Hardewig A, Zimmer F. Apo E phenotypes in patients with myocardial infarction. Hum. Genet. 1984;65:237–241.

    Article  PubMed  CAS  Google Scholar 

  82. Wilson PWF, myers RH, larson MG, Ordovas JM, Wolf PA, Schaefer EJ. Apolipoprotein E alleles, dyslipidemia, and coronary heart disease. The Framingham Offspring Study. JAMA 1994;272:1666–1671.

    Article  PubMed  CAS  Google Scholar 

  83. Stengard JH, Zerba KE, Pekkanen J, Ehnholm C, Nissinen A, Sing CF. Apolipoprotein E polymorphism predicts death from coronary heart disease in a longitudinal study of elderly Finnish men. Circulation 1995;91:265–269.

    Article  PubMed  CAS  Google Scholar 

  84. Wilson PWF, Schaefer EJ, Larson MG, Ordovas JM. Apolipoprotein E alleles and risk of coronary disease. A meta-analysis. Arterioscler. Thromb. Vasc. Biol. 1996;16:1250–1255.

    Article  PubMed  CAS  Google Scholar 

  85. Couderc R, Mahieux F, Bailleul S, Fenelon G, Mary R, Fermianan J. Prevalence of apolipoprotein E phenotypes in ischemic cerebrovascular disease. A case-control study. Stroke 1993;24:661–664.

    CAS  Google Scholar 

  86. Basun H, Corder EH, Guo Z, Lannfelt L, Corder LS, Manton KG, Winblad B, Viitanen N. Apolipoprotein E polymorphism and stroke in a population aged 75 years or more. Stroke 1996;27:1310–1315.

    Article  PubMed  CAS  Google Scholar 

  87. Weiss EJ, Bray PF, Tayback M, Schulman SP, Kickler TS, Becker LC, Weiss JL, Gerstenblith G, Goldschmidt-Clermont PJ. A polymorphism of a platelet glycoprotein receptor as an inserite risk factor for coronary thrombosis. N. Engl. J. Med. 1996;334:1090–1094.

    Article  PubMed  CAS  Google Scholar 

  88. Ye S, Eriksson P, Hamsten A, Kurkinen M, Humphries SE, Henney AM. Progression of coronary atherosclerosis is associate with a common genetic variant of the human stromelysin-1 promoter which results in reduced gene expression. Biol. Chem. 1996;271:13055–13060.

    Article  CAS  Google Scholar 

  89. Castelli WP, Garrison RJ, Wilson PWF, Abbott RD, Kalousdian F, Kannell WB. Incidence of coronary heart disease and lipoprotein cholesterol levels in the Framingham Study. JAMA 1986;256:2835–2838.

    Article  PubMed  CAS  Google Scholar 

  90. Alberts MJ. Genetic aspects of cerebrovascular disease. Stroke 1991;22:277–280.

    Article  Google Scholar 

  91. Hamilton PJ, Allardyce PJM, ogston D, Dawson AA, Douglas AS. The effect of age upon the coagulation system. J. Clin. Pathol. 1974;27:980–989.

    Article  PubMed  CAS  Google Scholar 

  92. Meade TW, North WRS, Chakrabarti R, Haines AP, Stirling Y. Population-based distribution of hemostatic variables. Br. Med. Bull. 1977;33:283–288.

    PubMed  CAS  Google Scholar 

  93. Meade TW, Chakrabarti R, Haines AP, North WRS, Stirling Y. Characteristics affecting fibrinolytic activity and plasma fibrinogen concentrations. Br. Med. 1979;1:153–156.

    Article  CAS  Google Scholar 

  94. Bauer KA, Wiess LM, Sparrow D, Vokonas PS, Rosenberg RD. Aging-associated changes in indices of thrombin generation and protein C activation in humans. Normative aging study. J. Clin. Invest. 1987;80:1527–1533.

    Article  PubMed  CAS  Google Scholar 

  95. Bauer KA, Kass BL, ten Cate H, Bednareck MA Hawiger JJ, Rosenberg RD. Detection of Factor X in humans. Blood 1989;74:2007–2012.

    PubMed  CAS  Google Scholar 

  96. Mari D, Mannucci PM, Coppola R, Bottasso B, Bauer KA, Rosenberg RD. Hypercoagulability in centenarians: the paradox of successful aging. Blood 1995;85:3144–3149.

    PubMed  CAS  Google Scholar 

  97. Yoshida H, Mitarai T, Kawamura T, Kitajima T, Miyazaki Y, Nagasawa R, Kawaguchi Y, Kubo H, Ichikawa I, Sakai O. Role of the deletion polymorphism of the angiotensin convertine enzyme gene in the progression and therapeutic responsiveness of IgA nephropathy. J. Clin. Invest. 1995;96:2162–2169.

    Article  PubMed  CAS  Google Scholar 

  98. van Essen GG, Rensma P, de Zeeuw D, Sliter WJ, Apperloo AJ, de Jong PE. Association between angiotensin-converting-enzyme gene polymorphism and failure of renoprotective therapy. Lancet 1996;347:94–95.

    Article  PubMed  Google Scholar 

  99. Cobb MM, Teitlebaum H, Risch N, iekel J, Ostfeld A. Influence of dietary fat, apolipoprotein E phenotype, and sex on plasma lipoprotein levels. Circulation 1992;86:849–857.

    Article  PubMed  CAS  Google Scholar 

  100. Carmena R, Roederer G, Mailloux H, Lussier-Cacan S, Davignon J. The response to lovastatin treatment in patients with heterozygous familial hypercholesterolemia is modulate by apolipoprotein E polymorphism. Metabolism 1993;42:895–901.

    Article  PubMed  CAS  Google Scholar 

  101. Harrap SB. Genetics and coronary disease: beginning the long journey. Lancet 1994;344: 901–902

    Article  PubMed  CAS  Google Scholar 

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Margaglione, M., Grandone, E., Mancini, F.P., Di Minno, G. (1998). Genetic Polymorphisms and Arterial Thrombosis. In: Barbagallo, M., Licata, G., Sowers, J.R. (eds) Recent Advances in Geriatrics. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-1483-5_22

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