Developing therapies for heart failure with preserved ejection fraction: current state and future directions.
JACC Heart Fail. 2: 97-112Oghina S. Bougouin W. Bézard M. et al.The impact of patients with cardiac amyloidosis in HFpEF trials.
JACC Heart Fail. 9: 169-178Mohammed S.F. Mirzoyev S.A. Edwards W.D. et al.Left ventricular amyloid deposition in patients with heart failure and preserved ejection fraction.
JACC Heart Fail. 2: 113-122González-López E. Gagliardi C. Dominguez F. et al.Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths.
Eur Heart J. 38: 1895-1904Tanskanen M, Peuralinna T, Polvikoski T, et al. Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation inalpha2-macroglobulinandtau: a population-based autopsy study. Ann Med. 2008;40(3):232-239.
Gillmore J.D. Maurer M.S. Falk R.H. et al.Nonbiopsy diagnosis of cardiac transthyretin amyloidosis.
Circulation. 133: 2404-2412Sipe J.D. Benson M.D. Buxbaum J.N. et al.Nomenclature 2014: amyloid fibril proteins and clinical classification of the amyloidosis.
Amyloid. 21: 221-224Molecular mechanisms of amyloidosis.
N Engl J Med. 349: 583-596Rapezzi C. Merlini G. Quarta C.C. et al.Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types.
Circulation. 120: 1203-1212Amyloidosis: a convoluted story: historical review.
Br J Haematol. 114: 529-538Transthyretin amyloidosis: a little history of hereditary amyloidosis.
Amyloid. 24: 76-77History of amyloidosis.
J Intern Med. 232: 509-510Gorevic P.D. Prelli F.C. Wright J. et al.Systemic senile amyloidosis. Identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy.
J Clin Invest. 83: 836-843Connors L.H. Lim A. Prokaeva T. et al.Tabulation of human transthyretin (TTR) variants.
Amyloid. 10: 160-184Falk R.H. Gertz M.A. Benson M.D. et al.Rationale and Design of a Phase 3 study to evaluate the efficacy and safety of ION-682884 in patients with transthyretin-mediated amyloid cardiomyopathy (ATTR-CM).
Blood. 134: 5764Bandera F. Martone R. Chacko L. et al.Clinical importance of left atrial infiltration in cardiac transthyretin amyloidosis.
JACC Cardiovasc Imaging. 15: 17-29Connors L.H. Sam F. Skinner M. et al.Heart failure resulting from age-related cardiac amyloid disease associated with wild-type transthyretin: a prospective, observational cohort study.
Circulation. 133: 282-290Adams D. Koike H. Slama M. et al.Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease.
Nat Rev Neurol. 15: 387-404Maurer M.S. Hanna M. Grogan M. et al.Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (transthyretin amyloid outcome Survey).
J Am Coll Cardiol. 68: 161-172Suhr O.B. Svendsen I.H. Andersson R. et al.Hereditary transthyretin amyloidosis from a Scandinavian perspective.
J Intern Med. 254: 225-235Jacobson D.R. Pastore R.D. Yaghoubian R. et al.Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans.
N Engl J Med. 336: 466-473Booth D.R. Booth S.E. Persey M.R. et al.Three new amyloidogenic TTR mutations: PRO12, GLU18, and VAL33. Neuromuscular Disord. Three new amyloidogenic TTR mutations: PRO12, GLU18, and VAL33 Neuromuscular Disord.
. 6Reynolds M.M. Veverka K.K. Gertz M.A. et al.Ocular manifestations of familial transthyretin amyloidosis.
Am J Ophthalmol. 183: 156-162Kittleson M.M. Maurer M.S. Ambardekar A.V. et al.Cardiac amyloidosis: evolving diagnosis and management: a scientific statement from the American heart association.
Circulation. 142: e7-e22Quarta C.C. Buxbaum J.N. Shah A.M. et al.The amyloidogenic V122I transthyretin variant in elderly black Americans.
N Engl J Med. 372: 21-29Grogan M. Scott C.G. Kyle R.A. et al.Natural history of wild-type transthyretin cardiac amyloidosis and risk stratification using a novel staging system.
J Am Coll Cardiol. 68: 1014-1020Gillmore J.D. Damy T. Fontana M. et al.A new staging system for cardiac transthyretin amyloidosis.
Eur Heart J. 39: 2799-2806Cheng R.K. Levy W.C. Vasbinder A. et al.Diuretic dose and NYHA functional class are independent predictors of mortality in patients with transthyretin cardiac amyloidosis.
JACC Cardiooncol. 2: 414-424Sperry B.W. Reyes B.A. Ikram A. et al.Tenosynovial and cardiac amyloidosis inpatients undergoing carpal tunnel release.
J Am Coll Cardiol. 72: 2040-2050Geller H.I. Singh A. Alexander K.M. et al.Association between ruptured distal biceps tendon and wild-type transthyretin cardiac amyloidosis.
JAMA. 318: 962Westermark P. Westermark G.T. Suhr O.B. et al.Transthyretin-derived amyloidosis: probably a common cause of lumbar spinal stenosis.
Ups J Med Sci. 119: 223-228Castaño A. Narotsky D.L. Hamid N. et al.Unveiling transthyretin cardiac amyloidosis and its predictors among elderly patients with severe aortic stenosis undergoing transcatheter aortic valve replacement.
Eur Heart J. 38: 2879-2887Scully P.R. Treibel T.A. Fontana M. et al.Prevalence of cardiac amyloidosis in patients referred for transcatheter aortic valve replacement.
J Am Coll Cardiol. 71: 463-464Ternacle J. Krapf L. Mohty D. et al.Aortic stenosis and cardiac amyloidosis: JACC review topic of the week.
J Am Coll Cardiol. 74: 2638-2651Galat A. Guellich A. Bodez D. et al.Aortic stenosis and transthyretin cardiac amyloidosis: the chicken or the egg?.
Eur Heart J. 37: 3525-3531Longhi S. Lorenzini M. Gagliardi C. et al.Coexistence of degenerative aortic stenosis and wild-type transthyretin-related cardiac amyloidosis.
JACC Cardiovasc Imaging. 9: 325-327Treibel T.A. Fontana M. Gilbertson J.A. et al.Occult transthyretin cardiac amyloid in severe Calcific aortic stenosis: prevalence and prognosis in patients undergoing Surgical aortic valve replacement.
Circ Cardiovasc Imaging. 9: e005066Nativi-Nicolau J. Maurer M.S.Amyloidosis cardiomyopathy: update in the diagnosis and treatment of the most common types.
Curr Opin Cardiol. 33: 571-579Kyriakou P. Mouselimis D. Tsarouchas A. et al.Diagnosis of cardiac amyloidosis: a systematic review on the role of imaging and biomarkers.
BMC Cardiovasc Disord. 18: 221Cyrille N.B. Goldsmith J. Alvarez J. et al.Prevalence and prognostic significance of low QRS voltage among the three main types of cardiac amyloidosis.
Am J Cardiol. 114: 1089-1093Amyloid cardiomyopathy.
Herz. 45: 267-271Di Nunzio D. Recupero A. de Gregorio C. et al.Echocardiographic findings in cardiac amyloidosis: inside two-dimensional, Doppler, and strain imaging.
Curr Cardiol Rep. 21https://doi.org/10.1007/s11886-019-1094-zMaurer M.S. Elliott P. Comenzo R. et al.Addressing common questions encountered in the diagnosis and management of cardiac amyloidosis.
Circulation. 135: 1357-1377Carvalho FP de Erthal F. Azevedo C.F.The role of cardiac MR imaging in the assessment of patients with cardiac amyloidosis.
Magn Reson Imaging Clin N Am. 27: 453-463Fontana M. Banypersad S.M. Treibel T.A. et al.Native T1 mapping in transthyretin amyloidosis.
JACC Cardiovasc Imaging. 7: 157-165Bokhari S. Castaño A. Pozniakoff T. et al.(99m)Tc-pyrophosphate scintigraphy for differentiating light-chain cardiac amyloidosis from the transthyretin-related familial and senile cardiac amyloidoses.
Circ Cardiovasc Imaging. 6: 195-201Glaudemans A.W.J.M. van Rheenen R.W.J. van den Berg M.P. et al.Bone scintigraphy with99mtechnetium-hydroxymethylene diphosphonate allows early diagnosis of cardiac involvement in patients with transthyretin-derived systemic amyloidosis.
Amyloid. 21: 35-44Quarta C.C. Gonzalez-Lopez E. Gilbertson J.A. et al.Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis.
Eur Heart J. 38: 1905-1908Ansari-Lari M.A. Ali S.Z.Fine-needle aspiration of abdominal fat pad for amyloid detection: a clinically useful test?.
Diagn Cytopathol. 30: 178-181Fine N.M. Arruda-Olson A.M. Dispenzieri A. et al.Yield of noncardiac biopsy for the diagnosis of transthyretin cardiac amyloidosis.
Am J Cardiol. 113: 1723-1727Bulawa C.E. Connelly S. Devit M. et al.Tafamidis, a potent and selective transthyretin kinetic stabilizer that inhibits the amyloid cascade.
Proc Natl Acad Sci U S A. 109: 9629-9634Maurer M.S. Bokhari S. Damy T. et al.Expert consensus recommendations for the suspicion and diagnosis of transthyretin cardiac amyloidosis.
Circ Heart Fail. 12: e006075Left ventricular systolic dysfunction precipitated by verapamil in cardiac amyloidosis.
Chest. 104: 618-620Gertz M.A. Skinner M. Connors L.H. et al.Selective binding of nifedipine to amyloid fibrils.
Am J Cardiol. 55: 1646Bozkurt B. Colvin M. Cook J. et al.Current diagnostic and treatment strategies for specific dilated cardiomyopathies: a scientific statement from the American heart association.
Circulation. 134https://doi.org/10.1161/cir.0000000000000455Donnelly J.P. Sperry B.W. Gabrovsek A. et al.Digoxin use in cardiac amyloidosis.
Am J Cardiol. 133: 134-138Ritts A.J. Cornell R.F. Swiger K. et al.Current concepts of cardiac amyloidosis: diagnosis, clinical management, and the need for collaboration.
Heart Fail Clin. 13: 409-416Sperry B.W. Hanna M. Shah S.J. et al.Spironolactone in patients with an echocardiographic HFpEF phenotype suggestive of cardiac amyloidosis: results from TOPCAT.
JACC Heart Fail. 9: 795-802Mints Y.Y. Doros G. Berk J.L. et al.Features of atrial fibrillation in wild-type transthyretin cardiac amyloidosis: a systematic review and clinical experience: atrial fibrillation in wild-type transthyretin amyloidosis.
ESC Heart Fail. 5: 772-779El-Am E.A. Dispenzieri A. Melduni R.M. et al.Direct current cardioversion of atrial arrhythmias in adults with cardiac amyloidosis.
J Am Coll Cardiol. 73: 589-597Dli F. Syed I.S. Martinez M. et al.Intracardiac thrombosis and embolism in patients with cardiac amyloidosis.
Circulation. 119: 2490-2497Barbhaiya C.R. Kumar S. Baldinger S.H. et al.Electrophysiologic assessment of conduction abnormalities and atrial arrhythmias associated with amyloid cardiomyopathy.
Heart Rhythm. 13: 383-390Longhi S. Quarta C.C. Milandri A. et al.Atrial fibrillation in amyloidotic cardiomyopathy: prevalence, incidence, risk factors and prognostic role.
Amyloid. 22: 147-155Towbin J.A. McKenna W.J. Abrams D.J. et al.2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy.
Heart Rhythm. 16: e301-e372Donnellan E. Wazni O. Kanj M. et al.Atrial fibrillation ablation in patients with transthyretin cardiac amyloidosis.
Europace. 22: 259-264Kochav S.M. Dizon J. Maurer M.S.A peak into the pace of cardiac amyloidosis.
JACC Clin Electrophysiol. 6: 1155-1157Donnellan E. Wazni O.M. Saliba W.I. et al.Cardiac devices in patients with transthyretin amyloidosis: impact on functional class, left ventricular function, mitral regurgitation, and mortality.
J Cardiovasc Electrophysiol. 30: 2427-2432Giancaterino S. Urey M.A. Darden D.Hsu management of arrhythmias in cardiac amyloidosis.
J Am Coll Cardiol. 6: 351-361Lin G. Dispenzieri A. Kyle R. et al.Implantable cardioverter defibrillators in patients with cardiac amyloidosis: ICD in cardiac amyloidosis.
J Cardiovasc Electrophysiol. 24: 793-798Rehorn MR, Loungani RS, Black-Maier E, et al. Cardiac Implantable Electronic Devices: A Window Into the Evolution of Conduction Disease in Cardiac Amyloidosis. JACC Clin Electrophysiol 2020:6(9):1144-1154. doi:10.1016/j.jacep.2020.04.020. Epub 2020 Aug 26. PMID: 32972550.
Judge D.P. Heitner S.B. Falk R.H. et al.Transthyretin stabilization by AG10 in symptomatic transthyretin amyloid cardiomyopathy.
J Am Coll Cardiol. 74: 285-295Ibrahim M. Saint Croix G.R. Lacy S. et al.The use of diflunisal for transthyretin cardiac amyloidosis: a review.
Heart Fail Rev. https://doi.org/10.1007/s10741-021-10143-4Benson M.D. Waddington-Cruz M. Berk J.L. et al.Inotersen treatment for patients with hereditary transthyretin amyloidosis.
N Engl J Med. 379: 22-31Suhr O.B. Coelho T. Buades J. et al.Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose study.
Orphanet J Rare Dis. 10: 109Gillmore J.D. Gane E. Taubel J. et al.CRISPR-Cas9 in vivo gene editing for transthyretin amyloidosis.
N Engl J Med. 385: 493-502Griffin J.M. Rosenblum H. Maurer M.S.Pathophysiology and therapeutic approaches to cardiac amyloidosis.
Circ Res. 128: 1554-1575Berk J.L. Suhr O.B. Obici L. et al.Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial.
JAMA. 310: 2658Adams D. Gonzalez-Duarte A. O’Riordan W.D. et al.Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis.
N Engl J Med. 379: 11-21Maurer M.S. Schwartz J.H. Gundapaneni B. et al.Tafamidis treatment for patients with transthyretin amyloid cardiomyopathy.
N Engl J Med. 379: 1007-1016Elliott P. Drachman B.M. Gottlieb S.S. et al.Long-term survival with tafamidis in patients with transthyretin amyloid cardiomyopathy.
Circ Heart Fail. 15: e008193
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