A Routine PET/CT Protocol with Streamlined Calculations for Assessing Cardiac Amyloidosis Using (18)F-Florbetapir
Dustin R Osborne, Shelley N Acuff, Alan Stuckey, Jonathan S Wall, Dustin R Osborne, Shelley N Acuff, Alan Stuckey, Jonathan S Wall
Abstract
Introduction: Cardiac amyloidosis is a rare condition characterized by the deposition of well-structured protein fibrils, proteoglycans, and serum proteins as amyloid. Recent work has shown that it may be possible to use (18)F-Florbetapir to image cardiac amyloidosis. Current methods for assessment include invasive biopsy techniques. This work enhances foundational work by Dorbala et al. by developing a routine imaging and analysis protocol using (18)F-Florbetapir for cardiac amyloid assessment.
Methods: Eleven patients, three healthy controls and eight myloid positive patients, were imaged using (18)F-Florbetapir to assess cardiac amyloid burden. Four of the patients were also imaged using (82)Rb-Chloride to evaluate possible (18)F-Florbetapir retention because of reduced myocardial blood flow. Quantitative methods using modeling, SUVs and SUV ratios were used to define a new streamlined clinical imaging protocol that could be used routinely and provide patient stratification.
Results: Quantitative analysis of (18)F-Florbetapir cardiac amyloid data were compiled from a 20-min listmode protocol with data histogrammed into two static images at 0-5, 10-15, or 15-20 min. Data analysis indicated the use of SUVs or ratios of SUVs calculated from regions draw in the septal wall were adequate in identification of all healthy controls from amyloid positive patients in this small cohort. Additionally, we found that it may be possible to use this method to differentiate patients suffering from AL vs. TTR amyloid.
Conclusion: This work builds on the seminal work by Dorbala et al. by describing a short (18)F-Florbetapir imaging protocol that is suitable for routine clinical use and uses a simple method for quantitative analysis of cardiac amyloid disease.
Keywords: Florbetapir; PET/CT; amyloid; amyloidosis; cardiac.
Figures
References
- Blancas-Mejía LM, Ramirez-Alvarado M. Systemic amyloidoses. Annu Rev Biochem (2013) 82(1):745–74.10.1146/annurev-biochem-072611-130030
- Banypersad SM, Moon JC, Whelan C, Hawkins PN, Wechalekar AD. Updates in cardiac amyloidosis: a review. J Am Heart Assoc (2012) 1(2):e000364.10.1161/JAHA.111.000364
- Ferris HW. Amyloidosis of lungs and heart. Am J Pathol (1936) 12(5):701–18.
- Esplin BL, Gertz MA. Current trends in diagnosis and management of cardiac amyloidosis. Curr Probl Cardiol (2013) 38(2):53–96.10.1016/j.cpcardiol.2012.11.002
- Dungu JN, Anderson LJ, Whelan CJ, Hawkins PN. Cardiac transthyretin amyloidosis. Heart (2012) 98(21):1546–54.10.1136/heartjnl-2012-301924
- Lie JT. Pathology of amyloidosis and amyloid heart disease. Appl Pathol (1984) 2(6):341–56.
- Dubrey SW, Cha K, Anderson J, Chamarthi B, Reisinger J, Skinner M, et al. The clinical features of immunoglobulin light-chain (al) amyloidosis with heart involvement. QJM (1998) 91(2):141–57.10.1093/qjmed/91.2.141
- Rapezzi C, Merlini G, Quarta CC, Riva L, Longhi S, Leone O, et al. Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. Circulation (2009) 120(13):1203–12.10.1161/CIRCULATIONAHA.108.843334
- Picken MM. Modern approaches to the treatment of amyloidosis: the critical importance of early detection in surgical pathology. Adv Anat Pathol (2013) 20(6):424–39.10.1097/PAP.0b013e3182a92dc3
- Palladini G, Campana C, Klersy C, Balduini A, Vadacca G, Perfetti V, et al. Serum n-terminal pro-brain natriuretic peptide is a sensitive marker of myocardial dysfunction in al amyloidosis. Circulation (2003) 107(19):2440–5.10.1161/01.CIR.0000068314.02595.B2
- Koyama J, Ray-Sequin PA, Falk RH. Prognostic significance of ultrasound myocardial tissue characterization in patients with cardiac amyloidosis. Circulation (2002) 106(5):556–61.10.1161/01.CIR.0000023530.86718.B0
- Bull S, Loudon M, Ntusi N, Joseph J, Francis J, Ferreira V, et al. Impaired myocardial perfusion in moderate asymptomatic aortic stenosis relates to longitudinal strain but not non-contrast t1 values. J Cardiovasc Magn Reson (2013) 15(Suppl 1):O24.10.1186/1532-429X-15-S1-O24
- Rapezzi C, Guidalotti P, Salvi F, Riva L, Perugini E. Usefulness of 99mtc-dpd scintigraphy in cardiac amyloidosis. J Am Coll Cardiol (2008) 51(15):1509–10.10.1016/j.jacc.2007.12.038
- Schaadt BK, Hendel HW, Gimsing P, Jonsson V, Pedersen H, Hesse B. 99mtc-aprotinin scintigraphy in amyloidosis. J Nucl Med (2003) 44(2):177–83.
- Administration, U. F, Drug. Aprotinin Injection (Marketed as Trasylol) Information, Food and Drug Administration in Rockville, MD: (2008).
- Fergusson DA, Hebert PC, Mazer CD, Fremes S, MacAdams C, Murkin JM, et al. A comparison of aprotinin and lysine analogues in high-risk cardiac surgery. N Engl J Med (2008) 358(22):2319–31.10.1056/NEJMoa0802395
- Cueto-Garcia L, Reeder GS, Kyle RA, Wood DL, Seward JB, Naessens J, et al. Echocardiographic findings in systemic amyloidosis: spectrum of cardiac involvement and relation to survival. J Am Coll Cardiol (1985) 6(4):737–43.10.1016/S0735-1097(85)80475-7
- Penugonda N. Cardiac MRI in infiltrative disorders: a concise review. Curr Cardiol Rev (2010) 6(2):134–6.10.2174/157340310791162668
- Antoni G, Lubberink M, Estrada S, Axelsson J, Carlson K, Lindsjo L, et al. In vivo visualization of amyloid deposits in the heart with 11c-pib and pet. J Nucl Med (2013) 54(2):213–20.10.2967/jnumed.111.102053
- Okamura N, Yanai K. Florbetapir (18f), a pet imaging agent that binds to amyloid plaques for the potential detection of Alzheimer’s disease. IDrugs (2010) 13(12):890–9.
- Dorbala S, Vangala D, Semer J, Strader C, Bruyere JR, Jr, Di Carli MF, et al. Imaging cardiac amyloidosis: a pilot study using f-florbetapir positron emission tomography. Eur J Nucl Med Mol Imaging (2014) 41(9):1652–62.10.1007/s00259-014-2787-6
- Osborne D, Wells K, Stuckey A, Wilson S, Wall J, Solomon A. Determination of cardiac amyloid involvement using 18f florbetapir and dynamic pet. J Nucl Med (2013) 54(2):2071.
- Wells K, Osborne D, Stuckey A, Wilson S, Wall J, Solomon A. 18f florbetapir pet/ct cardiac amyloid imaging in patients with systemic amyloidosis. J Nucl Med (2013) 54(2):294.
- Gertz MA, Comenzo R, Falk RH, Fermand JP, Hazenberg BP, Hawkins PN, 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(4):319–28.10.1002/ajh.20381
- Lortie M, Beanlands RS, Yoshinaga K, Klein R, Dasilva JN, DeKemp RA. Quantification of myocardial blood flow with 82rb dynamic pet imaging. Eur J Nucl Med Mol Imaging (2007) 34(11):1765–74.10.1007/s00259-007-0478-2
- Tahari A, Lee A, Rajaram M, Fukushima K, Lodge MA, Lee BC, et al. Absolute myocardial flow quantification with 82rb pet/ct: comparison of different software packages and methods. Eur J Nucl Med Mol Imaging (2014) 41(1):126–35.10.1007/s00259-013-2537-1
- deKemp RA, Declerck J, Klein R, Pan X-B, Nakazato R, Tonge C, et al. Multisoftware reproducibility study of stress and rest myocardial blood flow assessed with 3d dynamic pet/ct and a 1-tissue-compartment model of 82rb kinetics. J Nucl Med (2013) 54(4):571–7.10.2967/jnumed.112.112219
- Devereux RB, Alonso DR, Lutas EM, Gottlieb GJ, Campo E, Sachs I, et al. Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol (1986) 57(6):450–8.10.1016/0002-9149(86)90771-X
- Lin KJ, Hsu WC, Hsiao IT, Wey SP, Jin LW, Skovronsky D, et al. Whole-body biodistribution and brain pet imaging with [18f]av-45, a novel amyloid imaging agent–a pilot study. Nucl Med Biol (2010) 37(4):497–508.10.1016/j.nucmedbio.2010.02.003
- Choi SR, Golding G, Zhuang Z, Zhang W, Lim N, Hefti F, et al. Preclinical properties of 18f-av-45: a pet agent for abeta plaques in the brain. J Nucl Med (2009) 50(11):1887–94.10.2967/jnumed.109.065284
Source: PubMed