Skip to main content
Top
Published in: Clinical Research in Cardiology 10/2012

Open Access 01-10-2012 | Original Paper

Green tea halts progression of cardiac transthyretin amyloidosis: an observational report

Authors: Arnt V. Kristen, Stephanie Lehrke, Sebastian Buss, Derliz Mereles, Henning Steen, Philipp Ehlermann, Stefan Hardt, Evangelos Giannitsis, Rupert Schreiner, Uwe Haberkorn, Philipp A. Schnabel, Reinhold P. Linke, Christoph Röcken, Erich E. Wanker, Thomas J. Dengler, Klaus Altland, Hugo A. Katus

Published in: Clinical Research in Cardiology | Issue 10/2012

Login to get access

Abstract

Background

Treatment options in patients with amyloidotic transthyretin (ATTR) cardiomyopathy are limited. Epigallocatechin-3-gallate (EGCG), the most abundant catechin in green tea (GT), inhibits fibril formation from several amyloidogenic proteins in vitro. Thus, it might also halt progression of TTR amyloidosis. This is a single-center observational report on the effects of GT consumption in patients with ATTR cardiomopathy.

Methods

19 patients with ATTR cardiomyopathy were evaluated by standard blood tests, echocardiography, and cardiac MRI (n = 9) before and after consumption of GT and/or green tea extracts (GTE) for 12 months.

Results

Five patients were not followed up for reasons of death (n = 2), discontinuation of GT/GTE consumption (n = 2), and heart transplantation (n = 1). After 12 months no increase of left ventricular (LV) wall thickness and LV myocardial mass was observed by echocardiography. In the subgroup of patients evaluated by cardiac MRI a mean decrease of LV myocardial mass (−12.5 %) was detected in all patients. This was accompanied by an increase of mean mitral annular systolic velocity of 9 % in all 14 patients. Total cholesterol (191.9 ± 8.9 vs. 172.7 ± 9.4 mg/dL; p < 0.01) and LDL cholesterol (105.8 ± 7.6 vs. 89.5 ± 8.0 mg/dL; p < 0.01) decreased significantly during the observational period. No serious adverse effects were reported by any of the participants.

Conclusions

Our observation suggests an inhibitory effect of GT and/or GTE on the progression of cardiac amyloidosis. We propose a randomized placebo-controlled investigation to confirm our observation.
Appendix
Available only for authorised users
Literature
1.
2.
go back to reference Suhr OB, Lindqvist P, Olofsson BO, Waldenstrom A, Backman C (2006) Myocardial hypertrophy and function are related to age at onset in familial amyloidotic polyneuropathy. Amyloid 13:154–159PubMedCrossRef Suhr OB, Lindqvist P, Olofsson BO, Waldenstrom A, Backman C (2006) Myocardial hypertrophy and function are related to age at onset in familial amyloidotic polyneuropathy. Amyloid 13:154–159PubMedCrossRef
3.
go back to reference Cornwell GG III, Murdoch WL, Kyle RA, Westermark P, Pitkanen P (1983) Frequency and distribution of senile cardiovascular amyloid. A clinicopathologic correlation. Am J Med 75:618–623PubMedCrossRef Cornwell GG III, Murdoch WL, Kyle RA, Westermark P, Pitkanen P (1983) Frequency and distribution of senile cardiovascular amyloid. A clinicopathologic correlation. Am J Med 75:618–623PubMedCrossRef
4.
go back to reference Puille M, Altland K, Linke RP, Klett R, Bauer R (2002) Tc99 m-DPD scintigraphy in transthyretin-type amyloidosis. Presented at the 5th Internat. Symposium on Familial Amyloidotic Polyneuropathy and Other Related Disorders, Sept 25–27, 2002 Matsumoto, Japan Puille M, Altland K, Linke RP, Klett R, Bauer R (2002) Tc99 m-DPD scintigraphy in transthyretin-type amyloidosis. Presented at the 5th Internat. Symposium on Familial Amyloidotic Polyneuropathy and Other Related Disorders, Sept 25–27, 2002 Matsumoto, Japan
5.
go back to reference Cibeira MT, Sanchorawala V, Seldin DC, Quillen K, Berk JL, Dember LM, Segal A, Ruberg F, Meier-Ewert H, Andrea NT, Sloan JM, Finn KT, Doros G, Blade J, Skinner M (2011) Outcome of AL amyloidosis after high-dose melphalan and autologous stem cell transplantation: long-term results in a series of 421 patients. Blood 118:4346–4352PubMedCrossRef Cibeira MT, Sanchorawala V, Seldin DC, Quillen K, Berk JL, Dember LM, Segal A, Ruberg F, Meier-Ewert H, Andrea NT, Sloan JM, Finn KT, Doros G, Blade J, Skinner M (2011) Outcome of AL amyloidosis after high-dose melphalan and autologous stem cell transplantation: long-term results in a series of 421 patients. Blood 118:4346–4352PubMedCrossRef
6.
go back to reference Okamoto S, Wixner J, Obayashi K, Ando Y, Ericzon BG, Friman S, Uchino M, Suhr OB (2009) Liver transplantation for familial amyloidotic polyneuropathy: impact on Swedish patients’ survival. Liver Transpl 15:1229–1235PubMedCrossRef Okamoto S, Wixner J, Obayashi K, Ando Y, Ericzon BG, Friman S, Uchino M, Suhr OB (2009) Liver transplantation for familial amyloidotic polyneuropathy: impact on Swedish patients’ survival. Liver Transpl 15:1229–1235PubMedCrossRef
7.
go back to reference Hornsten R, Wiklund U, Olofsson BO, Jensen SM, Suhr OB (2004) Liver transplantation does not prevent the development of life-threatening arrhythmia in familial amyloidotic polyneuropathy, Portuguese-type (ATTR Val30Met) patients. Transplantation 78:112–116PubMedCrossRef Hornsten R, Wiklund U, Olofsson BO, Jensen SM, Suhr OB (2004) Liver transplantation does not prevent the development of life-threatening arrhythmia in familial amyloidotic polyneuropathy, Portuguese-type (ATTR Val30Met) patients. Transplantation 78:112–116PubMedCrossRef
8.
go back to reference Benson MD, Kluve-Beckerman B, Zeldenrust SR, Siesky AM, Bodenmiller DM, Showalter AD, Sloop KW (2006) Targeted suppression of an amyloidogenic transthyretin with antisense oligonucleotides. Muscle Nerve 22:609–618CrossRef Benson MD, Kluve-Beckerman B, Zeldenrust SR, Siesky AM, Bodenmiller DM, Showalter AD, Sloop KW (2006) Targeted suppression of an amyloidogenic transthyretin with antisense oligonucleotides. Muscle Nerve 22:609–618CrossRef
9.
go back to reference Baures PW, Oza VB, Peterson SA, Kelly JW (1999) Synthesis and evaluation of inhibitors of transthyretin amyloid formation based on the non-steroidal anti-inflammatory drug, flufenamic acid. Bioorg Med Chem 7:1339–1347PubMedCrossRef Baures PW, Oza VB, Peterson SA, Kelly JW (1999) Synthesis and evaluation of inhibitors of transthyretin amyloid formation based on the non-steroidal anti-inflammatory drug, flufenamic acid. Bioorg Med Chem 7:1339–1347PubMedCrossRef
10.
go back to reference Lueprasitsakul W, Alex S, Fang SL, Pino S, Irmscher K, Kohrle J, Braverman LE (1990) Flavonoid administration immediately displaces thyroxine (T4) from serum transthyretin, increases serum free T4, and decreases serum thyrotropin in the rat. Endocrinology 126:2890–2895PubMedCrossRef Lueprasitsakul W, Alex S, Fang SL, Pino S, Irmscher K, Kohrle J, Braverman LE (1990) Flavonoid administration immediately displaces thyroxine (T4) from serum transthyretin, increases serum free T4, and decreases serum thyrotropin in the rat. Endocrinology 126:2890–2895PubMedCrossRef
11.
go back to reference Maia F, Almeida MR, Gales L, Kijjoa A, Pinto MM, Saraiva MJ, Damas AM (2005) The binding of xanthone derivatives to transthyretin. Biochem Pharmacol 70:1861–1869PubMedCrossRef Maia F, Almeida MR, Gales L, Kijjoa A, Pinto MM, Saraiva MJ, Damas AM (2005) The binding of xanthone derivatives to transthyretin. Biochem Pharmacol 70:1861–1869PubMedCrossRef
12.
go back to reference Altland K, Winter P, Saraiva MJ, Suhr O (2004) Sulfite and base for the treatment of familial amyloidotic polyneuropathy: two additive approaches to stabilize the conformation of human amyloidogenic transthyretin. Neurogenetics 5:61–67PubMedCrossRef Altland K, Winter P, Saraiva MJ, Suhr O (2004) Sulfite and base for the treatment of familial amyloidotic polyneuropathy: two additive approaches to stabilize the conformation of human amyloidogenic transthyretin. Neurogenetics 5:61–67PubMedCrossRef
13.
go back to reference Altland K, Richardson SJ (2009) Histidine 31: The Achilles’ Heel of human transthyretin. Microheterogeneity is not enough to understand the molecular causes of amyloidgenicity. In: Richardson SJ, Cody V (eds) Recent advances in transthyretin evolution, structure and biological function. Springer, Berlin-Heidelberg, pp 201–214CrossRef Altland K, Richardson SJ (2009) Histidine 31: The Achilles’ Heel of human transthyretin. Microheterogeneity is not enough to understand the molecular causes of amyloidgenicity. In: Richardson SJ, Cody V (eds) Recent advances in transthyretin evolution, structure and biological function. Springer, Berlin-Heidelberg, pp 201–214CrossRef
14.
go back to reference Ehrnhoefer DE, Bieschke J, Boeddrich A, Herbst M, Masino L, Lurz R, Engemann S, Pastore A, Wanker EE (2008) EGCG redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers. Nat Struct Mol Biol 15:558–566PubMedCrossRef Ehrnhoefer DE, Bieschke J, Boeddrich A, Herbst M, Masino L, Lurz R, Engemann S, Pastore A, Wanker EE (2008) EGCG redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers. Nat Struct Mol Biol 15:558–566PubMedCrossRef
15.
go back to reference Ferreira N, Cardoso I, Domingues MR, Vitorino R, Bastos M, Bai G, Saraiva MJ, Almeida MR (2009) Binding of epigallocatechin-3-gallate to transthyretin modulates its amyloidogenicity. FEBS Lett 19 583:3569–3576CrossRef Ferreira N, Cardoso I, Domingues MR, Vitorino R, Bastos M, Bai G, Saraiva MJ, Almeida MR (2009) Binding of epigallocatechin-3-gallate to transthyretin modulates its amyloidogenicity. FEBS Lett 19 583:3569–3576CrossRef
16.
go back to reference Bieschke J, Russ J, Friedrich RP, Ehrnhoefer DE, Wobst H, Neugebauer K, Wanker EE (2010) EGCG remodels mature alpha-synuclein and amyloid-beta fibrils and reduces cellular toxicity. Proc Natl Acad Sci USA 107:7710–7715PubMedCrossRef Bieschke J, Russ J, Friedrich RP, Ehrnhoefer DE, Wobst H, Neugebauer K, Wanker EE (2010) EGCG remodels mature alpha-synuclein and amyloid-beta fibrils and reduces cellular toxicity. Proc Natl Acad Sci USA 107:7710–7715PubMedCrossRef
17.
go back to reference Ferreira N, Saraiva MJ, Almeida MR (2012) Epigallocatechin-3-gallate as a potential therapeutic drug for TTR-related amyloidosis: “in vivo” evidence from FAP mice models. PLoS ONE 7:e29933PubMedCrossRef Ferreira N, Saraiva MJ, Almeida MR (2012) Epigallocatechin-3-gallate as a potential therapeutic drug for TTR-related amyloidosis: “in vivo” evidence from FAP mice models. PLoS ONE 7:e29933PubMedCrossRef
18.
go back to reference Hunstein W (2007) Epigallocathechin-3-gallate in AL amyloidosis: a new therapeutic option? Blood 110:2216PubMedCrossRef Hunstein W (2007) Epigallocathechin-3-gallate in AL amyloidosis: a new therapeutic option? Blood 110:2216PubMedCrossRef
19.
go back to reference Mereles D, Wanker EE, Katus HA (2008) Therapy effects of green tea in a patient with systemic light-chain amyloidosis. Clin Res Cardiol 97:341–344PubMedCrossRef Mereles D, Wanker EE, Katus HA (2008) Therapy effects of green tea in a patient with systemic light-chain amyloidosis. Clin Res Cardiol 97:341–344PubMedCrossRef
20.
go back to reference Mereles D, Buss SJ, Hardt SE, Hunstein W, Katus HA (2010) Effects of the main green tea polyphenol epigallocatechin-3-gallate on cardiac involvement in patients with AL amyloidosis. Clin Res Cardiol 99:483–490PubMedCrossRef Mereles D, Buss SJ, Hardt SE, Hunstein W, Katus HA (2010) Effects of the main green tea polyphenol epigallocatechin-3-gallate on cardiac involvement in patients with AL amyloidosis. Clin Res Cardiol 99:483–490PubMedCrossRef
21.
go back to reference Declaration of Helsinki (1967) Recommendations guiding doctors in clinical research. Adopted by the World Medical Association in 1964. Wiss Med J 66:25–26 Declaration of Helsinki (1967) Recommendations guiding doctors in clinical research. Adopted by the World Medical Association in 1964. Wiss Med J 66:25–26
22.
go back to reference Eriksson M, Buttner J, Todorov T, Yumlu S, Schonland S, Hegenbart U, Kristen AV, Dengler T, Lohse P, Helmke B, Schmidt H, Rocken C (2009) Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid. Am J Surg Pathol 33:58–65PubMedCrossRef Eriksson M, Buttner J, Todorov T, Yumlu S, Schonland S, Hegenbart U, Kristen AV, Dengler T, Lohse P, Helmke B, Schmidt H, Rocken C (2009) Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid. Am J Surg Pathol 33:58–65PubMedCrossRef
23.
go back to reference Schroder R, Deckert M, Linke RP (2009) Novel isolated cerebral ALlambda amyloid angiopathy with widespread subcortical distribution and leukoencephalopathy due to atypical monoclonal plasma cell proliferation, and terminal systemic gammopathy. J Neuropathol Exp Neurol 68:286–299PubMedCrossRef Schroder R, Deckert M, Linke RP (2009) Novel isolated cerebral ALlambda amyloid angiopathy with widespread subcortical distribution and leukoencephalopathy due to atypical monoclonal plasma cell proliferation, and terminal systemic gammopathy. J Neuropathol Exp Neurol 68:286–299PubMedCrossRef
24.
go back to reference Altland K, Benson MD, Costello CE, Ferlini A, Hazenberg BP, Hund E, Kristen AV, Linke RP, Merlini G, Salvi F, Saraiva MJ, Singer R, Skinner M, Winter P (2007) Genetic microheterogeneity of human transthyretin detected by IEF. Electrophoresis 28:2053–2064PubMedCrossRef Altland K, Benson MD, Costello CE, Ferlini A, Hazenberg BP, Hund E, Kristen AV, Linke RP, Merlini G, Salvi F, Saraiva MJ, Singer R, Skinner M, Winter P (2007) Genetic microheterogeneity of human transthyretin detected by IEF. Electrophoresis 28:2053–2064PubMedCrossRef
25.
go back to reference Puille M, Altland K, Linke RP, Steen Muller MK, Kiett R, Steiner D, Bauer R (2002) 99mTc-DPD scintigraphy in transthyretin-related familial amyloidotic polyneuropathy. Eur J Nucl Med Mol Imaging 29:376–379PubMedCrossRef Puille M, Altland K, Linke RP, Steen Muller MK, Kiett R, Steiner D, Bauer R (2002) 99mTc-DPD scintigraphy in transthyretin-related familial amyloidotic polyneuropathy. Eur J Nucl Med Mol Imaging 29:376–379PubMedCrossRef
26.
go back to reference Rapezzi C, Quarta CC, Guidalotti PL, Pettinato C, Fanti S, Leone O, Ferlini A, Longhi S, Lorenzini M, Reggiani LB, Gagliardi C, Gallo P, Villani C, Salvi F (2011) Role of (99m)Tc-DPD scintigraphy in diagnosis and prognosis of hereditary transthyretin-related cardiac amyloidosis. JACC Cardiovasc Imaging 4:659–670PubMedCrossRef Rapezzi C, Quarta CC, Guidalotti PL, Pettinato C, Fanti S, Leone O, Ferlini A, Longhi S, Lorenzini M, Reggiani LB, Gagliardi C, Gallo P, Villani C, Salvi F (2011) Role of (99m)Tc-DPD scintigraphy in diagnosis and prognosis of hereditary transthyretin-related cardiac amyloidosis. JACC Cardiovasc Imaging 4:659–670PubMedCrossRef
27.
go back to reference Gertz MA, Comenzo R, Falk RH, Fermand JP, Hazenberg BP, Hawkins PN, Merlini G, Moreau P, Ronco P, Sanchorawala V, Sezer O, Solomon A, Grateau G (2005) Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10(th) International Symposium on Amyloid and Amyloidosis. Am J Hematol 79:319–328PubMedCrossRef Gertz MA, Comenzo R, Falk RH, Fermand JP, Hazenberg BP, Hawkins PN, Merlini G, Moreau P, Ronco P, Sanchorawala V, Sezer O, Solomon A, Grateau G (2005) Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10(th) International Symposium on Amyloid and Amyloidosis. Am J Hematol 79:319–328PubMedCrossRef
28.
go back to reference Devereux RB, Alonso DR, Lutas EM, Gottlieb GJ, Campo E, Sachs I, Reichek N (1986) Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol 57:450–458PubMedCrossRef Devereux RB, Alonso DR, Lutas EM, Gottlieb GJ, Campo E, Sachs I, Reichek N (1986) Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol 57:450–458PubMedCrossRef
29.
go back to reference Zile MR, Brutsaert DL (2002) New concepts in diastolic dysfunction and diastolic heart failure: Part I: diagnosis, prognosis, and measurements of diastolic function. Circulation 105:1387–1393PubMedCrossRef Zile MR, Brutsaert DL (2002) New concepts in diastolic dysfunction and diastolic heart failure: Part I: diagnosis, prognosis, and measurements of diastolic function. Circulation 105:1387–1393PubMedCrossRef
30.
go back to reference Lehrke S, Steen H, Kristen AV, Merten C, Lossnitzer D, Dengler TJ, Katus HA, Giannitsis E (2009) Serum levels of NT-proBNP as surrogate for cardiac amyloid burden: new evidence from gadolinium-enhanced cardiac magnetic resonance imaging in patients with amyloidosis. Amyloid 16:187–195PubMedCrossRef Lehrke S, Steen H, Kristen AV, Merten C, Lossnitzer D, Dengler TJ, Katus HA, Giannitsis E (2009) Serum levels of NT-proBNP as surrogate for cardiac amyloid burden: new evidence from gadolinium-enhanced cardiac magnetic resonance imaging in patients with amyloidosis. Amyloid 16:187–195PubMedCrossRef
31.
go back to reference Henning SM, Niu Y, Liu Y, Lee NH, Hara Y, Thames GD, Minutti RR, Carpenter CL, Wang H, Heber D (2005) Bioavailability and antioxidant effect of epigallocatechin gallate administered in purified form versus as green tea extract in healthy individuals. J Nutr Biochem 16:610–616PubMedCrossRef Henning SM, Niu Y, Liu Y, Lee NH, Hara Y, Thames GD, Minutti RR, Carpenter CL, Wang H, Heber D (2005) Bioavailability and antioxidant effect of epigallocatechin gallate administered in purified form versus as green tea extract in healthy individuals. J Nutr Biochem 16:610–616PubMedCrossRef
32.
go back to reference Tanabe N, Suzuki H, Aizawa Y, Seki N (2008) Consumption of green and roasted teas and the risk of stroke incidence: results from the Tokamachi-Nakasato cohort study in Japan. Int J Epidemiol 37:1030–1040PubMedCrossRef Tanabe N, Suzuki H, Aizawa Y, Seki N (2008) Consumption of green and roasted teas and the risk of stroke incidence: results from the Tokamachi-Nakasato cohort study in Japan. Int J Epidemiol 37:1030–1040PubMedCrossRef
33.
go back to reference Lee SM, Kim CW, Kim JK, Shin HJ, Baik JH (2008) GCG-rich tea catechins are effective in lowering cholesterol and triglyceride concentrations in hyperlipidemic rats. Lipids 43:419–429PubMedCrossRef Lee SM, Kim CW, Kim JK, Shin HJ, Baik JH (2008) GCG-rich tea catechins are effective in lowering cholesterol and triglyceride concentrations in hyperlipidemic rats. Lipids 43:419–429PubMedCrossRef
34.
go back to reference Sarma DN, Barrett ML, Chavez ML, Gardiner P, Ko R, Mahady GB, Marles RJ, Pellicore LS, Giancaspro GI, Low DT (2008) Safety of green tea extracts : a systematic review by the US Pharmacopeia. Drug Saf 31:469–484PubMedCrossRef Sarma DN, Barrett ML, Chavez ML, Gardiner P, Ko R, Mahady GB, Marles RJ, Pellicore LS, Giancaspro GI, Low DT (2008) Safety of green tea extracts : a systematic review by the US Pharmacopeia. Drug Saf 31:469–484PubMedCrossRef
35.
go back to reference Herlenius G, Wilczek HE, Larsson M, Ericzon BG (2004) Ten years of international experience with liver transplantation for familial amyloidotic polyneuropathy: results from the Familial Amyloidotic Polyneuropathy World Transplant Registry. Transplantation 77:64–71PubMedCrossRef Herlenius G, Wilczek HE, Larsson M, Ericzon BG (2004) Ten years of international experience with liver transplantation for familial amyloidotic polyneuropathy: results from the Familial Amyloidotic Polyneuropathy World Transplant Registry. Transplantation 77:64–71PubMedCrossRef
36.
go back to reference Haagsma EB, Van Gameren II, Bijzet J, Posthumus MD, Hazenberg BP (2007) Familial amyloidotic polyneuropathy: long-term follow-up of abdominal fat tissue aspirate in patients with and without liver transplantation. Amyloid 14:221–226PubMedCrossRef Haagsma EB, Van Gameren II, Bijzet J, Posthumus MD, Hazenberg BP (2007) Familial amyloidotic polyneuropathy: long-term follow-up of abdominal fat tissue aspirate in patients with and without liver transplantation. Amyloid 14:221–226PubMedCrossRef
37.
go back to reference Okamoto S, Yamashita T, Ando Y, Ueda M, Misumi Y, Obayashi K, Horibata Y, Uchino M (2008) Evaluation of myocardial changes in familial amyloid polyneuropathy after liver transplantation. Intern Med 47:2133–2137PubMedCrossRef Okamoto S, Yamashita T, Ando Y, Ueda M, Misumi Y, Obayashi K, Horibata Y, Uchino M (2008) Evaluation of myocardial changes in familial amyloid polyneuropathy after liver transplantation. Intern Med 47:2133–2137PubMedCrossRef
38.
go back to reference Garcia-Herola A, Prieto M, Pascual S, Berenguer M, Lopez-Viedma B, Mir J, Vilchez JJ, Berenguer J (1999) Progression of cardiomyopathy and neuropathy after liver transplantation in a patient with familial amyloidotic polyneuropathy caused by tyrosine-77 transthyretin variant. Liver Transpl Surg 5:246–248PubMedCrossRef Garcia-Herola A, Prieto M, Pascual S, Berenguer M, Lopez-Viedma B, Mir J, Vilchez JJ, Berenguer J (1999) Progression of cardiomyopathy and neuropathy after liver transplantation in a patient with familial amyloidotic polyneuropathy caused by tyrosine-77 transthyretin variant. Liver Transpl Surg 5:246–248PubMedCrossRef
39.
go back to reference Liepnieks JJ, Benson MD (2007) Progression of cardiac amyloid deposition in hereditary transthyretin amyloidosis patients after liver transplantation. Amyloid 14:277–282PubMedCrossRef Liepnieks JJ, Benson MD (2007) Progression of cardiac amyloid deposition in hereditary transthyretin amyloidosis patients after liver transplantation. Amyloid 14:277–282PubMedCrossRef
40.
go back to reference Miyata M, Sato T, Kugimiya M, Sho M, Nakamura T, Ikemizu S, Chirifu M, Mizuguchi M, Nabeshima Y, Suwa Y, Morioka H, Arimori T, Suico MA, Shuto T, Sako Y, Momohara M, Koga T, Morino-Koga S, Yamagata Y, Kai H (2010) The crystal structure of the green tea polyphenol (−)-epigallocatechin gallate-transthyretin complex reveals a novel binding site distinct from the thyroxine binding site. Biochemistry 49:6104–6114PubMedCrossRef Miyata M, Sato T, Kugimiya M, Sho M, Nakamura T, Ikemizu S, Chirifu M, Mizuguchi M, Nabeshima Y, Suwa Y, Morioka H, Arimori T, Suico MA, Shuto T, Sako Y, Momohara M, Koga T, Morino-Koga S, Yamagata Y, Kai H (2010) The crystal structure of the green tea polyphenol (−)-epigallocatechin gallate-transthyretin complex reveals a novel binding site distinct from the thyroxine binding site. Biochemistry 49:6104–6114PubMedCrossRef
41.
go back to reference Ferreira N, Saraiva MJ, Almeida MR (2011) Natural polyphenols inhibit different steps of the process of transthyretin (TTR) amyloid fibril formation. FEBS Lett 585:2424–2430PubMedCrossRef Ferreira N, Saraiva MJ, Almeida MR (2011) Natural polyphenols inhibit different steps of the process of transthyretin (TTR) amyloid fibril formation. FEBS Lett 585:2424–2430PubMedCrossRef
42.
go back to reference Benson MD, Teague SD, Kovacs R, Feigenbaum H, Jung J, Kincaid JC (2011) Rate of progression of transthyretin amyloidosis. Am J Cardiol 108:285–289PubMedCrossRef Benson MD, Teague SD, Kovacs R, Feigenbaum H, Jung J, Kincaid JC (2011) Rate of progression of transthyretin amyloidosis. Am J Cardiol 108:285–289PubMedCrossRef
43.
go back to reference Morner S, Hellman U, Suhr OB, Kazzam E, Waldenstrom A (2005) Amyloid heart disease mimicking hypertrophic cardiomyopathy. J Intern Med 258:225–230PubMedCrossRef Morner S, Hellman U, Suhr OB, Kazzam E, Waldenstrom A (2005) Amyloid heart disease mimicking hypertrophic cardiomyopathy. J Intern Med 258:225–230PubMedCrossRef
44.
go back to reference Ng B, Connors LH, Davidoff R, Skinner M, Falk RH (2005) Senile systemic amyloidosis presenting with heart failure: a comparison with light chain-associated amyloidosis. Arch Intern Med 165:1425–1429PubMedCrossRef Ng B, Connors LH, Davidoff R, Skinner M, Falk RH (2005) Senile systemic amyloidosis presenting with heart failure: a comparison with light chain-associated amyloidosis. Arch Intern Med 165:1425–1429PubMedCrossRef
45.
go back to reference Rapezzi C, Merlini G, Quarta CC, Riva L, Longhi S, Leone O, Salvi F, Ciliberti P, Pastorelli F, Biagini E, Coccolo F, Cooke RM, Bacchi-Reggiani L, Sangiorgi D, Ferlini A, Cavo M, Zamagni E, Fonte ML, Palladini G, Salinaro F, Musca F, Obici L, Branzi A, Perlini S (2009) Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. Circulation 120:1203–1212PubMedCrossRef Rapezzi C, Merlini G, Quarta CC, Riva L, Longhi S, Leone O, Salvi F, Ciliberti P, Pastorelli F, Biagini E, Coccolo F, Cooke RM, Bacchi-Reggiani L, Sangiorgi D, Ferlini A, Cavo M, Zamagni E, Fonte ML, Palladini G, Salinaro F, Musca F, Obici L, Branzi A, Perlini S (2009) Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. Circulation 120:1203–1212PubMedCrossRef
46.
go back to reference Connors LH, Doros G, Sam F, Badiee A, Seldin DC, Skinner M (2011) Clinical features and survival in senile systemic amyloidosis: comparison to familial transthyretin cardiomyopathy. Amyloid 18(Suppl 1):152–154PubMed Connors LH, Doros G, Sam F, Badiee A, Seldin DC, Skinner M (2011) Clinical features and survival in senile systemic amyloidosis: comparison to familial transthyretin cardiomyopathy. Amyloid 18(Suppl 1):152–154PubMed
47.
go back to reference Kristen AV, Haufe S, Schonland SO, Hegenbart U, Schnabel PA, Rocken C, Hardt S, Lohse P, Ho AD, Haberkorn U, Dengler TJ, Altland K, Katus HA (2011) Skeletal scintigraphy indicates disease severity of cardiac involvement in patients with senile systemic amyloidosis. Int J Cardiol Jul 15 [epub ahead of print] Kristen AV, Haufe S, Schonland SO, Hegenbart U, Schnabel PA, Rocken C, Hardt S, Lohse P, Ho AD, Haberkorn U, Dengler TJ, Altland K, Katus HA (2011) Skeletal scintigraphy indicates disease severity of cardiac involvement in patients with senile systemic amyloidosis. Int J Cardiol Jul 15 [epub ahead of print]
48.
go back to reference Bellenger NG, Burgess MI, Ray SG, Lahiri A, Coats AJ, Cleland JG, Pennell DJ (2000) Comparison of left ventricular ejection fraction and volumes in heart failure by echocardiography, radionuclide ventriculography and cardiovascular magnetic resonance; are they interchangeable? Eur Heart J 21:1387–1396PubMedCrossRef Bellenger NG, Burgess MI, Ray SG, Lahiri A, Coats AJ, Cleland JG, Pennell DJ (2000) Comparison of left ventricular ejection fraction and volumes in heart failure by echocardiography, radionuclide ventriculography and cardiovascular magnetic resonance; are they interchangeable? Eur Heart J 21:1387–1396PubMedCrossRef
49.
go back to reference Reichek N, Devereux RB, Rocha RA, Hilkert R, Hall D, Purkayastha D, Pitt B (2009) Magnetic resonance imaging left ventricular mass reduction with fixed-dose angiotensin-converting enzyme inhibitor-based regimens in patients with high-risk hypertension. Hypertension 54:731–737PubMedCrossRef Reichek N, Devereux RB, Rocha RA, Hilkert R, Hall D, Purkayastha D, Pitt B (2009) Magnetic resonance imaging left ventricular mass reduction with fixed-dose angiotensin-converting enzyme inhibitor-based regimens in patients with high-risk hypertension. Hypertension 54:731–737PubMedCrossRef
50.
go back to reference Hughes DA, Elliott PM, Shah J, Zuckerman J, Coghlan G, Brookes J, Mehta AB (2008) Effects of enzyme replacement therapy on the cardiomyopathy of Anderson-Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa. Heart 94:153–158PubMedCrossRef Hughes DA, Elliott PM, Shah J, Zuckerman J, Coghlan G, Brookes J, Mehta AB (2008) Effects of enzyme replacement therapy on the cardiomyopathy of Anderson-Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa. Heart 94:153–158PubMedCrossRef
51.
go back to reference Sohns C, Sossalla S, Schmitto JD, Jacobshagen C, Raab BW, Obenauer S, Maier LS (2010) Visualization of transcoronary ablation of septal hypertrophy in patients with hypertrophic obstructive cardiomyopathy: a comparison between cardiac MRI, invasive measurements and echocardiography. Clin Res Cardiol 99:359–368PubMedCrossRef Sohns C, Sossalla S, Schmitto JD, Jacobshagen C, Raab BW, Obenauer S, Maier LS (2010) Visualization of transcoronary ablation of septal hypertrophy in patients with hypertrophic obstructive cardiomyopathy: a comparison between cardiac MRI, invasive measurements and echocardiography. Clin Res Cardiol 99:359–368PubMedCrossRef
52.
go back to reference Yuan J, Qiao S, Zhang Y, You S, Duan F, Hu F, Yang W (2010) Follow-up by cardiac magnetic resonance imaging in patients with hypertrophic cardiomyopathy who underwent percutaneous ventricular septal ablation. Am J Cardiol 106:1487–1491PubMedCrossRef Yuan J, Qiao S, Zhang Y, You S, Duan F, Hu F, Yang W (2010) Follow-up by cardiac magnetic resonance imaging in patients with hypertrophic cardiomyopathy who underwent percutaneous ventricular septal ablation. Am J Cardiol 106:1487–1491PubMedCrossRef
53.
go back to reference Prinz C, Farr M, Hering D, Horstkotte D, Faber L (2010) Reduction in ECG abnormalities and improvement of regional left ventricular function in a patient with Fabry’s disease during enzyme-replacement therapy. Clin Res Cardiol 99:53–55PubMedCrossRef Prinz C, Farr M, Hering D, Horstkotte D, Faber L (2010) Reduction in ECG abnormalities and improvement of regional left ventricular function in a patient with Fabry’s disease during enzyme-replacement therapy. Clin Res Cardiol 99:53–55PubMedCrossRef
54.
go back to reference Weidemann F, Niemann M, Breunig F, Herrmann S, Beer M, Stork S, Voelker W, Ertl G, Wanner C, Strotmann J (2009) Long-term effects of enzyme replacement therapy on fabry cardiomyopathy: evidence for a better outcome with early treatment. Circulation 119:524–529PubMedCrossRef Weidemann F, Niemann M, Breunig F, Herrmann S, Beer M, Stork S, Voelker W, Ertl G, Wanner C, Strotmann J (2009) Long-term effects of enzyme replacement therapy on fabry cardiomyopathy: evidence for a better outcome with early treatment. Circulation 119:524–529PubMedCrossRef
55.
go back to reference Al Zahrani GB, Bellavia D, Pellikka PA, Dispenzieri A, Hayman SR, Oh JK, Miyazaki C, Miller FA Jr (2009) Doppler myocardial imaging compared to standard two-dimensional and Doppler echocardiography for assessment of diastolic function in patients with systemic amyloidosis. J Am Soc Echocardiogr 22:290–298PubMedCrossRef Al Zahrani GB, Bellavia D, Pellikka PA, Dispenzieri A, Hayman SR, Oh JK, Miyazaki C, Miller FA Jr (2009) Doppler myocardial imaging compared to standard two-dimensional and Doppler echocardiography for assessment of diastolic function in patients with systemic amyloidosis. J Am Soc Echocardiogr 22:290–298PubMedCrossRef
56.
go back to reference Butz T, Piper C, Langer C, Wiemer M, Kottmann T, Meissner A, Plehn G, Trappe HJ, Horstkotte D, Faber L (2010) Diagnostic superiority of a combined assessment of the systolic and early diastolic mitral annular velocities by tissue Doppler imaging for the differentiation of restrictive cardiomyopathy from constrictive pericarditis. Clin Res Cardiol 99:207–215PubMedCrossRef Butz T, Piper C, Langer C, Wiemer M, Kottmann T, Meissner A, Plehn G, Trappe HJ, Horstkotte D, Faber L (2010) Diagnostic superiority of a combined assessment of the systolic and early diastolic mitral annular velocities by tissue Doppler imaging for the differentiation of restrictive cardiomyopathy from constrictive pericarditis. Clin Res Cardiol 99:207–215PubMedCrossRef
57.
go back to reference Perdrix L, Mansencal N, Cocheteux B, Chatellier G, Bissery A, Diebold B, Mousseaux E, Abergel E (2011) How to calculate left ventricular mass in routine practice? An echocardiographic versus cardiac magnetic resonance study. Arch Cardiovasc Dis 104:343–351PubMedCrossRef Perdrix L, Mansencal N, Cocheteux B, Chatellier G, Bissery A, Diebold B, Mousseaux E, Abergel E (2011) How to calculate left ventricular mass in routine practice? An echocardiographic versus cardiac magnetic resonance study. Arch Cardiovasc Dis 104:343–351PubMedCrossRef
58.
60.
go back to reference Suhr O, Danielsson A, Holmgren G, Steen L (1994) Malnutrition and gastrointestinal dysfunction as prognostic factors for survival in familial amyloidotic polyneuropathy. J Intern Med 235:479–485PubMedCrossRef Suhr O, Danielsson A, Holmgren G, Steen L (1994) Malnutrition and gastrointestinal dysfunction as prognostic factors for survival in familial amyloidotic polyneuropathy. J Intern Med 235:479–485PubMedCrossRef
Metadata
Title
Green tea halts progression of cardiac transthyretin amyloidosis: an observational report
Authors
Arnt V. Kristen
Stephanie Lehrke
Sebastian Buss
Derliz Mereles
Henning Steen
Philipp Ehlermann
Stefan Hardt
Evangelos Giannitsis
Rupert Schreiner
Uwe Haberkorn
Philipp A. Schnabel
Reinhold P. Linke
Christoph Röcken
Erich E. Wanker
Thomas J. Dengler
Klaus Altland
Hugo A. Katus
Publication date
01-10-2012
Publisher
Springer-Verlag
Published in
Clinical Research in Cardiology / Issue 10/2012
Print ISSN: 1861-0684
Electronic ISSN: 1861-0692
DOI
https://doi.org/10.1007/s00392-012-0463-z

Other articles of this Issue 10/2012

Clinical Research in Cardiology 10/2012 Go to the issue