Page 52 - Read Online
P. 52

Pica et al. Vessel Plus 2022;6:10  https://dx.doi.org/10.20517/2574-1209.2021.81  Page 11 of 11

               33.      Pan JA, Kerwin MJ, Salerno M. Native T1 mapping, extracellular volume mapping, and late gadolinium enhancement in cardiac
                   amyloidosis: a meta-analysis. JACC Cardiovasc Imaging 2020;13:1299-310.  DOI  PubMed  PMC
               34.      Bandula S, Banypersad SM, Sado D, et al. Measurement of Tissue interstitial volume in healthy patients and those with amyloidosis
                   with equilibrium contrast-enhanced MR imaging. Radiology 2013;268:858-64.  DOI  PubMed  PMC
               35.      Fontana M, Banypersad SM, Treibel TA, et al. AL and ATTR cardiac amyloid are different: native T1 mapping and ECV detect
                   different biology. J Cardiovasc Magn Reson 2014:16.  DOI
               36.      Fontana M, Banypersad SM, Treibel TA, et al. Differential myocyte responses in patients with cardiac transthyretin amyloidosis and
                   light-chain amyloidosis: a cardiac MR imaging study. Radiology 2015;277:388-97.  DOI  PubMed
               37.      Kotecha T, Martinez-Naharro A, Treibel TA, et al. Myocardial edema and prognosis in amyloidosis. J Am Coll Cardiol 2018;71:2919-
                   31.  DOI  PubMed
               38.      Sharpley FA, Fontana M, Martinez-Naharro A, et al. Cardiac biomarkers are prognostic in systemic light chain amyloidosis with no
                   cardiac involvement by standard criteria. Haematologica 2020;105:1405-13.  DOI  PubMed  PMC
               39.      Garcia-Pavia P, Rapezzi C, Adler Y, et al. Diagnosis and treatment of cardiac amyloidosis. A position statement of the European
                   Society of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur J Heart Fail 2021;23:512-26.  DOI  PubMed
               40.      Gertz MA, Comenzo R, Falk RH, et al. Definition of organ involvement and treatment response in immunoglobulin light chain
                   amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18-22
                   April 2004. Am J Hematol 2005;79:319-28.  DOI  PubMed
               41.      Grogan M, Scott CG, Kyle RA, et al. Natural history of wild-type transthyretin cardiac amyloidosis and risk stratification using a novel
                   staging system. J Am Coll Cardiol 2016;68:1014-20.  DOI  PubMed
               42.      Gillmore JD, Damy T, Fontana M, et al. A new staging system for cardiac transthyretin amyloidosis. Eur Heart J 2018;39:2799-806.
                   DOI  PubMed
               43.      Banypersad SM, Fontana M, Maestrini V, et al. T1 mapping and survival in systemic light-chain amyloidosis. Eur Heart J
                   2015;36:244-51.  DOI  PubMed  PMC
               44.      Messroghli DR, Moon JC, Ferreira VM, et al. Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2,
                   T2* and extracellular volume: a consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the
                   European Association for Cardiovascular Imaging (EACVI). J Cardiovasc Magn Reson 2017;19:75.  DOI  PubMed  PMC
               45.      Law S, Petrie A, Chacko L, et al. Disease progression in cardiac transthyretin amyloidosis is indicated by serial calculation of National
                   Amyloidosis Centre transthyretin amyloidosis stage. ESC Heart Fail 2020;7:3942-9.  DOI  PubMed  PMC
               46.      Raina S, Lensing SY, Nairooz RS, et al. Prognostic value of late gadolinium enhancement CMR in systemic amyloidosis. JACC
                   Cardiovasc Imaging 2016;9:1267-77.  DOI  PubMed
               47.      Boynton SJ, Geske JB, Dispenzieri A, et al. LGE provides incremental prognostic information over serum biomarkers in AL cardiac
                   amyloidosis. JACC Cardiovasc Imaging 2016;9:680-6.  DOI  PubMed
               48.      Lin L, Li X, Feng J, et al. The prognostic value of T1 mapping and late gadolinium enhancement cardiovascular magnetic resonance
                   imaging in patients with light chain amyloidosis. J Cardiovasc Magn Reson 2018;20:2.  DOI  PubMed  PMC
               49.      Dorbala S, Vangala D, Bruyere J Jr, et al. Coronary microvascular dysfunction is related to abnormalities in myocardial structure and
                   function in cardiac amyloidosis. JACC Heart Fail 2014;2:358-67.  DOI  PubMed  PMC
               50.      Chacko L, Kotecha T, Martinez-naharro A, et al. 1171Myocardial perfusion mapping in cardiac amyloidosis - exploring the spectrum
                   from infiltration to ischaemia. Eur Heart J 2019;40:ehz748.0013.  DOI
               51.      Palladini G, Milani P, Merlini G. Management of AL amyloidosis in 2020. Blood 2020;136:2620-7.  DOI  PubMed
               52.      Addison D, Slivnick JA, Campbell CM, Vallakati A, Jneid H, Schelbert E. Recent advances and current dilemmas in the diagnosis and
                   management of transthyretin cardiac amyloidosis. J Am Heart Assoc 2021;10:e019840.  DOI  PubMed  PMC
               53.      Martinez-Naharro A, Abdel-Gadir A, Treibel TA, et al. CMR-verified regression of cardiac AL amyloid after chemotherapy. JACC
                   Cardiovasc Imaging 2018;11:152-4.  DOI  PubMed
               54.      Maurer MS, Schwartz JH, Gundapaneni B, et al; ATTR-ACT Study Investigators. Tafamidis treatment for patients with transthyretin
                   amyloid cardiomyopathy. N Engl J Med 2018;379:1007-16.  DOI  PubMed
               55.      Solomon SD, Adams D, Kristen A, et al. Effects of patisiran, an RNA interference therapeutic, on cardiac parameters in patients with
                   hereditary transthyretin-mediated amyloidosis. Circulation 2019;139:431-43.  DOI  PubMed
               56.      Fontana M, Martinez-Naharro A, Chacko L, et al. Reduction in CMR derived extracellular volume with patisiran indicates cardiac
                   amyloid regression. JACC Cardiovasc Imaging 2021;14:189-99.  DOI  PubMed
   47   48   49   50   51   52   53   54   55   56   57