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The role of inflammatory and fibrogenic pathways in heart failure associated with aging

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Abstract

Heart failure is strongly associated with aging. Elderly patients with heart failure often have preserved systolic function exhibiting left ventricular hypertrophy accompanied by a decline in diastolic function. Experimental studies have demonstrated that age-related cardiac fibrosis plays an important role in the pathogenesis of diastolic heart failure in senescent hearts. Reactive oxygen species and angiotensin II are critically involved in fibrotic remodeling of the aging ventricle; their fibrogenic actions may be mediated, at least in part, through transforming growth factor (TGF)-β. The increased prevalence of heart failure in the elderly is also due to impaired responses of the senescent heart to cardiac injury. Aging is associated with suppressed inflammation, delayed phagocytosis of dead cardiomyocytes, and markedly diminished collagen deposition following myocardial infarction, due to a blunted response of fibroblasts to fibrogenic growth factors. Thus, in addition to a baseline activation of fibrogenic pathways, senescent hearts exhibit an impaired reparative reserve due to decreased responses of mesenchymal cells to stimulatory signals. Impaired scar formation in senescent hearts is associated with accentuated dilative remodeling and worse systolic dysfunction. Understanding the pathogenesis of interstitial fibrosis in the aging heart and dissecting the mechanisms responsible for age-associated healing defects following cardiac injury are critical in order to design new strategies for prevention of adverse remodeling and heart failure in elderly patients.

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References

  1. Chen MA (2009) Heart failure with preserved ejection fraction in older adults. Am J Med 122:713–723

    Article  PubMed  Google Scholar 

  2. Thomas S, Rich MW (2007) Epidemiology, pathophysiology, and prognosis of heart failure in the elderly. Clin Geriatr Med 23:1–10

    Article  PubMed  Google Scholar 

  3. DeFrances CJ, Cullen KA, Kozak LJ (2007) National hospital discharge survey: 2005 annual summary with detailed diagnosis and procedure data. Vital Health Stat 13:1–209

    Google Scholar 

  4. Lakatta EG, Levy D (2003) Arterial and cardiac aging: major shareholders in cardiovascular disease enterprises: part II: the aging heart in health: links to heart disease. Circulation 107:346–354

    Article  PubMed  Google Scholar 

  5. Kitzman DW, Gardin JM, Gottdiener JS, Arnold A, Boineau R, Aurigemma G, Marino EK, Lyles M, Cushman M, Enright PL (2001) Importance of heart failure with preserved systolic function in patients > or = 65 years of age. CHS research group. Cardiovascular health study. Am J Cardiol 87:413–419

    Article  CAS  PubMed  Google Scholar 

  6. Dannenberg AL, Levy D, Garrison RJ (1989) Impact of age on echocardiographic left ventricular mass in a healthy population (the Framingham Study). Am J Cardiol 64:1066–1068

    Article  CAS  PubMed  Google Scholar 

  7. Lakatta EG (2002) Age-associated cardiovascular changes in health: impact on cardiovascular disease in older persons. Heart Fail Rev 7:29–49

    Article  PubMed  Google Scholar 

  8. Lakatta EG, Wang M, Najjar SS (2009) Arterial aging and subclinical arterial disease are fundamentally intertwined at macroscopic and molecular levels. Med Clin North Am 93:583–604 Table of Contents

    Article  CAS  PubMed  Google Scholar 

  9. Lakatta EG, Levy D (2003) Arterial and cardiac aging: major shareholders in cardiovascular disease enterprises: part I: aging arteries: a “set up” for vascular disease. Circulation 107:139–146

    Article  PubMed  Google Scholar 

  10. Orlandi A, Marcellini M, Spagnoli LG (2000) Aging influences development and progression of early aortic atherosclerotic lesions in cholesterol-fed rabbits. Arterioscler Thromb Vasc Biol 20:1123–1136

    CAS  PubMed  Google Scholar 

  11. Anversa P, Palackal T, Sonnenblick EH, Olivetti G, Meggs LG, Capasso JM (1990) Myocyte cell loss and myocyte cellular hyperplasia in the hypertrophied aging rat heart. Circ Res 67:871–885

    CAS  PubMed  Google Scholar 

  12. Cheng W, Reiss K, Li P, Chun MJ, Kajstura J, Olivetti G, Anversa P (1996) Aging does not affect the activation of the myocyte insulin-like growth factor-1 autocrine system after infarction and ventricular failure in Fischer 344 rats. Circ Res 78:536–546

    CAS  PubMed  Google Scholar 

  13. Burlew BS (2004) Diastolic dysfunction in the elderly–the interstitial issue. Am J Geriatr Cardiol 13:29–38

    Article  PubMed  Google Scholar 

  14. Cheitlin MD (2003) Cardiovascular physiology-changes with aging. Am J Geriatr Cardiol 12:9–13

    Article  PubMed  Google Scholar 

  15. Gazoti Debessa CR, Mesiano Maifrino LB, Rodrigues de Souza R (2001) Age related changes of the collagen network of the human heart. Mech Ageing Dev 122:1049–1058

    Article  CAS  PubMed  Google Scholar 

  16. de Souza RR (2002) Aging of myocardial collagen. Biogerontology 3:325–335

    Article  PubMed  Google Scholar 

  17. Eghbali M, Eghbali M, Robinson TF, Seifter S, Blumenfeld OO (1989) Collagen accumulation in heart ventricles as a function of growth and aging. Cardiovasc Res 23:723–729

    Article  CAS  PubMed  Google Scholar 

  18. Orlandi A, Francesconi A, Marcellini M, Ferlosio A, Spagnoli LG (2004) Role of ageing and coronary atherosclerosis in the development of cardiac fibrosis in the rabbit. Cardiovasc Res 64:544–552

    Article  CAS  PubMed  Google Scholar 

  19. Lin J, Lopez EF, Jin Y, Van Remmen H, Bauch T, Han HC, Lindsey ML (2008) Age-related cardiac muscle sarcopenia: combining experimental and mathematical modeling to identify mechanisms. Exp Gerontol 43:296–306

    Article  CAS  PubMed  Google Scholar 

  20. Thomas DP, Zimmerman SD, Hansen TR, Martin DT, McCormick RJ (2000) Collagen gene expression in rat left ventricle: interactive effect of age and exercise training. J Appl Physiol 89:1462–1468

    CAS  PubMed  Google Scholar 

  21. Iwanaga Y, Aoyama T, Kihara Y, Onozawa Y, Yoneda T, Sasayama S (2002) Excessive activation of matrix metalloproteinases coincides with left ventricular remodeling during transition from hypertrophy to heart failure in hypertensive rats. J Am Coll Cardiol 39:1384–1391

    Article  CAS  PubMed  Google Scholar 

  22. Janicki JS, Brower GL (2002) The role of myocardial fibrillar collagen in ventricular remodeling and function. J Card Fail 8:S319–S325

    Article  CAS  PubMed  Google Scholar 

  23. Baicu CF, Stroud JD, Livesay VA, Hapke E, Holder J, Spinale FG, Zile MR (2003) Changes in extracellular collagen matrix alter myocardial systolic performance. Am J Physiol Heart Circ Physiol 284:H122–H132

    CAS  PubMed  Google Scholar 

  24. Wang J, Hoshijima M, Lam J, Zhou Z, Jokiel A, Dalton ND, Hultenby K, Ruiz-Lozano P, Ross J Jr, Tryggvason K, Chien KR (2006) Cardiomyopathy associated with microcirculation dysfunction in laminin alpha4 chain-deficient mice. J Biol Chem 281:213–220

    Article  CAS  PubMed  Google Scholar 

  25. Beltrami CA, Finato N, Rocco M, Feruglio GA, Puricelli C, Cigola E, Quaini F, Sonnenblick EH, Olivetti G, Anversa P (1994) Structural basis of end-stage failure in ischemic cardiomyopathy in humans. Circulation 89:151–163

    CAS  PubMed  Google Scholar 

  26. Khan R, Sheppard R (2006) Fibrosis in heart disease: understanding the role of transforming growth factor-beta in cardiomyopathy, valvular disease and arrhythmia. Immunology 118:10–24

    Article  CAS  PubMed  Google Scholar 

  27. Dai DF, Santana LF, Vermulst M, Tomazela DM, Emond MJ, MacCoss MJ, Gollahon K, Martin GM, Loeb LA, Ladiges WC, Rabinovitch PS (2009) Overexpression of catalase targeted to mitochondria attenuates murine cardiac aging. Circulation 119:2789–2797

    Article  CAS  PubMed  Google Scholar 

  28. Basso N, Cini R, Pietrelli A, Ferder L, Terragno NA, Inserra F (2007) Protective effect of long-term angiotensin II inhibition. Am J Physiol Heart Circ Physiol 293:H1351–H1358

    Article  CAS  PubMed  Google Scholar 

  29. Benigni A, Corna D, Zoja C, Sonzogni A, Latini R, Salio M, Conti S, Rottoli D, Longaretti L et al (2009) Disruption of the Ang II type 1 receptor promotes longevity in mice. J Clin Invest 119:524–530

    Article  CAS  PubMed  Google Scholar 

  30. Billet S, Bardin S, Verp S, Baudrie V, Michaud A, Conchon S, Muffat-Joly M, Escoubet B, Souil E et al (2007) Gain-of-function mutant of angiotensin II receptor, type 1A, causes hypertension and cardiovascular fibrosis in mice. J Clin Invest 117:1914–1925

    Article  CAS  PubMed  Google Scholar 

  31. Sawada M, Carlson JC (1987) Changes in superoxide radical and lipid peroxide formation in the brain, heart and liver during the lifetime of the rat. Mech Ageing Dev 41:125–137

    Article  CAS  PubMed  Google Scholar 

  32. Siwik DA, Pagano PJ, Colucci WS (2001) Oxidative stress regulates collagen synthesis and matrix metalloproteinase activity in cardiac fibroblasts. Am J Physiol Cell Physiol 280:C53–C60

    CAS  PubMed  Google Scholar 

  33. Cheng TH, Cheng PY, Shih NL, Chen IB, Wang DL, Chen JJ (2003) Involvement of reactive oxygen species in angiotensin II-induced endothelin-1 gene expression in rat cardiac fibroblasts. J Am Coll Cardiol 42:1845–1854

    Article  CAS  PubMed  Google Scholar 

  34. Frangogiannis NG (2004) Chemokines in the ischemic myocardium: from inflammation to fibrosis. Inflamm Res 53:585–595

    Article  CAS  PubMed  Google Scholar 

  35. Frangogiannis NG (2007) Chemokines in ischemia and reperfusion. Thromb Haemost 97:738–747

    CAS  PubMed  Google Scholar 

  36. Frangogiannis NG, Dewald O, Xia Y, Ren G, Haudek S, Leucker T, Kraemer D, Taffet G, Rollins BJ, Entman ML (2007) Critical role of monocyte chemoattractant protein-1/CC chemokine ligand 2 in the pathogenesis of ischemic cardiomyopathy. Circulation 115:584–592

    Article  CAS  PubMed  Google Scholar 

  37. Dewald O, Zymek P, Winkelmann K, Koerting A, Ren G, Abou-Khamis T, Michael LH, Rollins BJ, Entman ML, Frangogiannis NG (2005) CCL2/Monocyte chemoattractant protein-1 regulates inflammatory responses critical to healing myocardial infarcts. Circ Res 96:881–889

    Article  CAS  PubMed  Google Scholar 

  38. Desmouliere A, Geinoz A, Gabbiani F, Gabbiani G (1993) Transforming growth factor-beta 1 induces alpha-smooth muscle actin expression in granulation tissue myofibroblasts and in quiescent and growing cultured fibroblasts. J Cell Biol 122:103–111

    Article  CAS  PubMed  Google Scholar 

  39. Bujak M, Frangogiannis NG (2007) The role of TGF-beta signaling in myocardial infarction and cardiac remodeling. Cardiovasc Res 74:184–195

    Article  CAS  PubMed  Google Scholar 

  40. Brooks WW, Conrad CH (2000) Myocardial fibrosis in transforming growth factor beta(1)heterozygous mice. J Mol Cell Cardiol 32:187–195

    Article  CAS  PubMed  Google Scholar 

  41. Barcellos-Hoff MH, Dix TA (1996) Redox-mediated activation of latent transforming growth factor-beta 1. Mol Endocrinol 10:1077–1083

    Article  CAS  PubMed  Google Scholar 

  42. Park SK, Kim J, Seomun Y, Choi J, Kim DH, Han IO, Lee EH, Chung SK, Joo CK (2001) Hydrogen peroxide is a novel inducer of connective tissue growth factor. Biochem Biophys Res Commun 284:966–971

    Article  CAS  PubMed  Google Scholar 

  43. Lee AA, Dillmann WH, McCulloch AD, Villarreal FJ (1995) Angiotensin II stimulates the autocrine production of transforming growth factor-beta 1 in adult rat cardiac fibroblasts. J Mol Cell Cardiol 27:2347–2357

    Article  CAS  PubMed  Google Scholar 

  44. Campbell SE, Katwa LC (1997) Angiotensin II stimulated expression of transforming growth factor-beta1 in cardiac fibroblasts and myofibroblasts. J Mol Cell Cardiol 29:1947–1958

    Article  CAS  PubMed  Google Scholar 

  45. Saito K, Ishizaka N, Aizawa T, Sata M, Iso-o N, Noiri E, Mori I, Ohno M, Nagai R (2005) Iron chelation and a free radical scavenger suppress angiotensin II-induced upregulation of TGF-beta1 in the heart. Am J Physiol Heart Circ Physiol 288:H1836–H1843

    Article  CAS  PubMed  Google Scholar 

  46. Rosenkranz S (2004) TGF-beta1 and angiotensin networking in cardiac remodeling. Cardiovasc Res 63:423–432

    Article  CAS  PubMed  Google Scholar 

  47. Asif M, Egan J, Vasan S, Jyothirmayi GN, Masurekar MR, Lopez S, Williams C, Torres RL, Wagle D et al (2000) An advanced glycation endproduct cross-link breaker can reverse age-related increases in myocardial stiffness. Proc Natl Acad Sci USA 97:2809–2813

    Article  CAS  PubMed  Google Scholar 

  48. Shapiro BP, Owan TE, Mohammed SF, Meyer DM, Mills LD, Schalkwijk CG, Redfield MM (2008) Advanced glycation end products accumulate in vascular smooth muscle and modify vascular but not ventricular properties in elderly hypertensive canines. Circulation 118:1002–1010

    Article  CAS  PubMed  Google Scholar 

  49. Maggioni AP, Maseri A, Fresco C, Franzosi MG, Mauri F, Santoro E, Tognoni G (1993) Age-related increase in mortality among patients with first myocardial infarctions treated with thrombolysis. The investigators of the Gruppo Italiano per lo Studio della Sopravvivenza nell’Infarto Miocardico (GISSI-2). N Engl J Med 329:1442–1448

    Article  CAS  PubMed  Google Scholar 

  50. St John Sutton M, Pfeffer MA, Moye L, Plappert T, Rouleau JL, Lamas G, Rouleau J, Parker JO, Arnold MO, Sussex B, Braunwald E (1997) Cardiovascular death and left ventricular remodeling two years after myocardial infarction: baseline predictors and impact of long-term use of captopril: information from the survival and ventricular enlargement (SAVE) trial. Circulation 96:3294–3299

    CAS  PubMed  Google Scholar 

  51. Frangogiannis NG (2008) The immune system and cardiac repair. Pharmacol Res 58:88–111

    Article  CAS  PubMed  Google Scholar 

  52. Bujak M, Dobaczewski M, Gonzalez-Quesada C, Xia Y, Leucker T, Zymek P, Veeranna V, Tager AM, Luster AD, Frangogiannis NG (2009) Induction of the CXC chemokine interferon-gamma-inducible protein 10 regulates the reparative response following myocardial infarction. Circ Res 105:973–983

    Article  CAS  PubMed  Google Scholar 

  53. Dobaczewski M, Gonzalez-Quesada C, Frangogiannis NG (2009) The extracellular matrix as a modulator of the inflammatory and reparative response following myocardial infarction. J Mol Cell Cardiol 48(3):504–511

    Article  PubMed  Google Scholar 

  54. Jugdutt BI (2003) Ventricular remodeling after infarction and the extracellular collagen matrix: when is enough enough? Circulation 108:1395–1403

    Article  PubMed  Google Scholar 

  55. Frangogiannis NG (2006) The mechanistic basis of infarct healing. Antioxid Redox Signal 8:1907–1939

    Article  CAS  PubMed  Google Scholar 

  56. Frangogiannis NG, Ren G, Dewald O, Zymek P, Haudek S, Koerting A, Winkelmann K, Michael LH, Lawler J, Entman ML (2005) The critical role of endogenous Thrombospondin (TSP)-1 in preventing expansion of healing myocardial infarcts. Circulation 111:2935–2942

    Article  CAS  PubMed  Google Scholar 

  57. Cohn JN, Ferrari R, Sharpe N (2000) Cardiac remodeling–concepts and clinical implications: a consensus paper from an international forum on cardiac remodeling. Behalf of an international forum on cardiac remodeling. J Am Coll Cardiol 35:569–582

    Article  CAS  PubMed  Google Scholar 

  58. Bujak M, Kweon HJ, Chatila K, Li N, Taffet G, Frangogiannis NG (2008) Aging-related defects are associated with adverse cardiac remodeling in a mouse model of reperfused myocardial infarction. J Am Coll Cardiol 51:1384–1392

    Article  PubMed  Google Scholar 

  59. Swift ME, Burns AL, Gray KL, DiPietro LA (2001) Age-related alterations in the inflammatory response to dermal injury. J Invest Dermatol 117:1027–1035

    Article  CAS  PubMed  Google Scholar 

  60. Ding A, Hwang S, Schwab R (1994) Effect of aging on murine macrophages. Diminished response to IFN-gamma for enhanced oxidative metabolism. J Immunol 153:2146–2152

    CAS  PubMed  Google Scholar 

  61. Flanders KC (2004) Smad3 as a mediator of the fibrotic response. Int J Exp Pathol 85:47–64

    Article  CAS  PubMed  Google Scholar 

  62. Bujak M, Ren G, Kweon HJ, Dobaczewski M, Reddy A, Taffet G, Wang XF, Frangogiannis NG (2007) Essential role of Smad3 in infarct healing and in the pathogenesis of cardiac remodeling. Circulation 116:2127–2138

    Article  CAS  PubMed  Google Scholar 

  63. Shivakumar K, Dostal DE, Boheler K, Baker KM, Lakatta EG (2003) Differential response of cardiac fibroblasts from young adult and senescent rats to ANG II. Am J Physiol Heart Circ Physiol 284:H1454–H1459

    CAS  PubMed  Google Scholar 

  64. Wynn TA (2008) Cellular and molecular mechanisms of fibrosis. J Pathol 214:199–210

    Article  CAS  PubMed  Google Scholar 

  65. Jugdutt BI, Jelani A (2008) Aging and defective healing, adverse remodeling, and blunted post-conditioning in the reperfused wounded heart. J Am Coll Cardiol 51:1399–1403

    Article  PubMed  Google Scholar 

  66. Jugdutt BI (2008) Pleiotropic effects of cardiac drugs on healing post-MI. The good, bad, and ugly. Heart Fail Rev 13:439–452

    Article  PubMed  Google Scholar 

  67. Simpson PJ, Todd RF 3rd, Fantone JC, Mickelson JK, Griffin JD, Lucchesi BR (1988) Reduction of experimental canine myocardial reperfusion injury by a monoclonal antibody (anti-Mo1, anti-CD11b) that inhibits leukocyte adhesion. J Clin Invest 81:624–629

    Article  CAS  PubMed  Google Scholar 

  68. Frangogiannis NG (2006) Targeting the inflammatory response in healing myocardial infarcts. Curr Med Chem 13:1877–1893

    Article  CAS  PubMed  Google Scholar 

  69. Baran KW, Nguyen M, McKendall GR, Lambrew CT, Dykstra G, Palmeri ST, Gibbons RJ, Borzak S, Sobel BE, et al. (2001) Double-blind, randomized trial of an anti-CD18 antibody in conjunction with recombinant tissue plasminogen activator for acute myocardial infarction: limitation of myocardial infarction following thrombolysis in acute myocardial infarction (LIMIT AMI) study. Circulation 104:2778–2783

    Google Scholar 

  70. Cai D, Xaymardan M, Holm JM, Zheng J, Kizer JR, Edelberg JM (2003) Age-associated impairment in TNF-alpha cardioprotection from myocardial infarction. Am J Physiol Heart Circ Physiol 285:H463–H469

    CAS  PubMed  Google Scholar 

  71. Xaymardan M, Zheng J, Duignan I, Chin A, Holm JM, Ballard VL, Edelberg JM (2004) Senescent impairment in synergistic cytokine pathways that provide rapid cardioprotection in the rat heart. J Exp Med 199:797–804

    Article  CAS  PubMed  Google Scholar 

  72. Lehrke S, Mazhari R, Durand DJ, Zheng M, Bedja D, Zimmet JM, Schuleri KH, Chi AS, Gabrielson KL, Hare JM (2006) Aging impairs the beneficial effect of granulocyte colony-stimulating factor and stem cell factor on post-myocardial infarction remodeling. Circ Res 99:553–560

    Article  CAS  PubMed  Google Scholar 

  73. Davis ME, Hsieh PC, Grodzinsky AJ, Lee RT (2005) Custom design of the cardiac microenvironment with biomaterials. Circ Res 97:8–15

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

Dr Frangogiannis’ laboratory is supported by NIH R01 HL-76246 and R01 HL-85440, the Alkek endowment and the Medallion Foundation.

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Correspondence to Nikolaos G. Frangogiannis.

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Chen, W., Frangogiannis, N.G. The role of inflammatory and fibrogenic pathways in heart failure associated with aging. Heart Fail Rev 15, 415–422 (2010). https://doi.org/10.1007/s10741-010-9161-y

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