Improved detection of myocardial involvement in acute inflammatory cardiomyopathies using T2 mapping

Paaladinesh Thavendiranathan, Michael Walls, Shivraman Giri, David Verhaert, Sanjay Rajagopalan, Sean Moore, Orlando P Simonetti, Subha V Raman, Paaladinesh Thavendiranathan, Michael Walls, Shivraman Giri, David Verhaert, Sanjay Rajagopalan, Sean Moore, Orlando P Simonetti, Subha V Raman

Abstract

Background: T2-weighted cardiac magnetic resonance imaging is useful in diagnosing acute inflammatory myocardial diseases, such as myocarditis and tako-tsubo cardiomyopathy (TTCM). We hypothesized that quantitative T2 mapping could better delineate myocardial involvement in these disorders versus T2-weighted imaging.

Methods and results: Thirty patients with suspected myocarditis or TTCM, referred for cardiac magnetic resonance imaging, who met established diagnostic criteria underwent myocardial T2 mapping. T2 values were averaged in involved and remote myocardial segments, both defined by a reviewer blinded to T2 data. In myocarditis, T2 was 65.2±3.2 ms in the involved myocardium versus 53.5±2.1 ms in the remote myocardium (P<0.001). In TTCM, T2 was 65.6±4.0 ms in the involved myocardium versus 53.6±2.7 ms in the remote segments (P<0.001). T2 values were similar across remote myocardial segments in patients and all myocardial segments in controls (P>0.05 for all). T2 maps provided diagnostic data even in patients with difficulty breath holding. A T2 cutoff of 59 ms identified areas of myocardial involvement, with sensitivity and specificity of 94% and 97%, respectively. T2 mapping revealed regions of abnormal T2 beyond those identified by wall motion abnormalities or late gadolinium-enhancement positivity. Conventional T2-weighted short tau inversion recovery images were uninterpretable in 7 patients because of artifact and unremarkable in 2 patients who had elevated T2 values. T2-prepared steady-state-free precession images showed areas of signal hyperintensity in only 17 of 30 patients.

Conclusions: Quantitative T2 mapping reliably identifies myocardial involvement in patients with myocarditis and TTCM. T2 mapping delineated a greater extent of myocardial disease in both conditions compared with that identified by wall motion abnormalities, T2-weighted short tau inversion recovery imaging, T2-prepared steady-state-free precession, or late gadolinium enhancement. Quantitative T2 mapping warrants consideration as a robust technique to identify myocardial injury in patients with acute myocarditis or TTCM.

Figures

Figure 1
Figure 1
Averaged T2 values in the involved and remote segments in patients with myocarditis (N=20) and TTCM (N=10) and controls (N=30) are shown. The centerline in each box represents the median, while the lower and upper limits of each box represent 25th and 75th percentiles, respectively. *p<0.001 for comparison to controls (ANOVA with Bonferroni post hoc analysis), †p<0.001 for comparison to remote segments.
Figure 2
Figure 2
T2 maps, T2W-STIR, and LGE images in 3 representative patients with myocarditis. (A) A 25 year-old male presented with gastrointestinal symptoms with ST elevations and a troponin of 31.1mg/dL. Three involved and 3 remote segments are shown. (B) A 29 year-old male presented with chest pain worse with inspiration and lying flat. He had diffuse ST elevations with a peak troponin of 17.3mg/dL. Two involved and two remote segments are shown (C) A 24 year old male who presented with syncope. Peak troponin was 4.5mg/dL. All illustrated segments show elevated T2 values.
Figure 3
Figure 3
SSFP diastolic and systolic images, T2 maps, and LGE images in 2 patients with TTCM. (A)72 year old female presented with shortness of breath, found to have normal coronaries. (B) 49 year old female presented with chest pain, found to have normal coronaries. CMR images show apical ballooning of both left and right ventricle. In both cases, the T2 maps show elevated T2 values in the mid and/or apical segments with normal values involving the basal segments
Figure 4
Figure 4
ROC curves. (A) Comparison of involved myocardial segments in either myocarditis or TTCM in comparison to healthy controls. (B) Comparison of involved myocardial segments with remote segments in the same patients.
Figure 5
Figure 5
T2 values measured in an area of myocardium with epicardial delayed enhancement versus subendocardial myocardium in the same regions. (A) Short axis delayed enhancement image, (B) short axis T2 image from the same slice position.
Figure 6
Figure 6
T2 maps, T2W-STIR, and LGE images in 3 representative patients with myocarditis with no obvious edema on T2 STIR imaging. (A) 44 year old male with chest pain and a peak troponin of 33.3mg/dL. T2 values in the involved and remote segments were 65 and 54ms respectively. (B) 20 year old female with shortness of breath and chest pain with a peak troponin of 4.0mg/dL. T2 values in the involved and remote segments were 66 and 56ms respectively. (C) 39 year old male with gastrointestinal symptoms and fever with a peak troponin of 12.4mg/dL. Involved and remote segments T2 values were 67 and 45ms respectively.
Figure 7
Figure 7
Comparison between T2 maps and T2p-SSFP images is shown. The upper left panel shows the T2 map from a patient with tako-tsubo cardiomyopathy and negative LGE imaging; the affected region (arrow) had an abnormally elevated T2 of 65.9 ms compared to 53.0 ms in the remote myocardium. The same patient’s T2p-SSFP image (upper right panel) was visually rated as normal by two expert reviewers. The bottom left panel shows the T2 map from a patient with myocarditis whose LGE showed epicardial hyperenhancement in the inferolateral and apical segments; these segments were also abnormal by T2 mapping (T2 = 67.0 in the affected region vs. 53.0 ms in the remote myocardium). The apical region was identified as abnormal by visual assessment of the T2p-SSFP image (bottom right panel, arrow).
Figure 8
Figure 8
Bland-Altman plots for interobserver agreement in the measurement of T2 values for patients with myocarditis or TTCM. (A) Involved myocardial segments, (B) remote myocardial segments, and for (C) controls. LOA, level of agreement 1 standard deviation.

References

    1. Eitel I, Behrendt F, Schindler K, Kivelitz D, Gutberlet M, Schuler G, Thiele H. Differential diagnosis of suspected apical ballooning syndrome using contrast-enhanced magnetic resonance imaging. Eur Heart J. 2008;29:2651–2659.
    1. Abdel-Aty H, Cocker M, Friedrich MG. Myocardial edema is a feature of Tako-Tsubo cardiomyopathy and is related to the severity of systolic dysfunction: insights from T2-weighted cardiovascular magnetic resonance. Int J Cardiol. 2009;132:291–293.
    1. Abdel-Aty H, Boye P, Zagrosek A, Wassmuth R, Kumar A, Messroghli D, Bock P, Dietz R, Friedrich MG, Schulz-Menger J. Diagnostic performance of cardiovascular magnetic resonance in patients with suspected acute myocarditis: comparison of different approaches. J Am Coll Cardiol. 2005;45:1815–1822.
    1. Friedrich MG, Sechtem U, Schulz-Menger J, Holmvang G, Alakija P, Cooper LT, White JA, Abdel-Aty H, Gutberlet M, Prasad S, Aletras A, Laissy JP, Paterson I, Filipchuk NG, Kumar A, Pauschinger M, Liu P. Cardiovascular magnetic resonance in myocarditis: A JACC White Paper. J Am Coll Cardiol. 2009;53:1475–1487.
    1. Pennell D. Myocardial salvage: retrospection, resolution, and radio waves. Circulation. 2006;113:1821–1823.
    1. Giri S, Chung YC, Merchant A, Mihai G, Rajagopalan S, Raman SV, Simonetti OP. T2 quantification for improved detection of myocardial edema. J Cardiovasc Magn Reson. 2009;11:56.
    1. Eitel I, Lucke C, Grothoff M, Sareban M, Schuler G, Thiele H, Gutberlet M. Inflammation in takotsubo cardiomyopathy: insights from cardiovascular magnetic resonance imaging. Eur Radiol. 2010;20:422–431.
    1. Prasad A, Lerman A, Rihal CS. Apical ballooning syndrome (Tako-Tsubo or stress cardiomyopathy): a mimic of acute myocardial infarction. Am Heart J. 2008;155:408–417.
    1. Giri S, Xue H, Shah S, Dharmakumar R, Verhaert D, Guehring J, Zuehlsdorff S, Raman S, Simonetti O. Inline non-rigid motion-corrected t2 mapping of myocardium. Journal of Cardiovascular Magnetic Resonance. 2010;12:P229.
    1. Simonetti OP, Finn JP, White RD, Laub G, Henry DA. “Black blood” T2-weighted inversion-recovery MR imaging of the heart. Radiology. 1996;199:49–57.
    1. Sievers B, Elliott MD, Hurwitz LM, Albert TS, Klem I, Rehwald WG, Parker MA, Judd RM, Kim RJ. Rapid detection of myocardial infarction by subsecond, free-breathing delayed contrast-enhancement cardiovascular magnetic resonance. Circulation. 2007;115:236–244.
    1. Cerqueira MD, Weissman NJ, Dilsizian V, Jacobs AK, Kaul S, Laskey WK, Pennell DJ, Rumberger JA, Ryan T, Verani MS. Standardized myocardial segmentation and nomenclature for tomographic imaging of the heart: a statement for healthcare professionals from the Cardiac Imaging Committee of the Council on Clinical Cardiology of the American Heart Association. Circulation. 2002;105:539–542.
    1. Hor KN, Gottliebson WM, Carson C, Wash E, Cnota J, Fleck R, Wansapura J, Klimeczek P, Al-Khalidi HR, Chung ES, Benson DW, Mazur W. Comparison of magnetic resonance feature tracking for strain calculation with harmonic phase imaging analysis. JACC Cardiovasc Imaging. 2010;3:144–151.
    1. Bansal M, Cho GY, Chan J, Leano R, Haluska BA, Marwick TH. Feasibility and accuracy of different techniques of two-dimensional speckle based strain and validation with harmonic phase magnetic resonance imaging. J Am Soc Echocardiogr. 2008;21:1318–1325.
    1. Pirat B, Khoury DS, Hartley CJ, Tiller L, Rao L, Schulz DG, Nagueh SF, Zoghbi WA. A novel feature-tracking echocardiographic method for the quantitation of regional myocardial function: validation in an animal model of ischemia-reperfusion. J Am Coll Cardiol. 2008;51:651–659.
    1. Verhaert D, Thavendiranathan P, Giri S, Mihai G, Rajagopalan S, Simonetti OP, Raman SV. Direct t2 quantification of myocardial edema in acute ischemic injury. JACC Cardiovasc Imaging. 2011;4:269–278.
    1. Sole MJ, Liu P. Viral myocarditis: a paradigm for understanding the pathogenesis and treatment of dilated cardiomyopathy. J Am Coll Cardiol. 1993;22:99A–105A.
    1. Rolf A, Nef HM, Mollmann H, Troidl C, Voss S, Conradi G, Rixe J, Steiger H, Beiring K, Hamm CW, Dill T. Immunohistological basis of the late gadolinium enhancement phenomenon in tako-tsubo cardiomyopathy. Eur Heart J. 2009;30:1635–1642.
    1. Arai AE. Using magnetic resonance imaging to characterize recent myocardial injury: utility in acute coronary syndrome and other clinical scenarios. Circulation. 2008;118:795–796.
    1. Eitel I, Friedrich MG. T2-weighted cardiovascular magnetic resonance in acute cardiac disease. J Cardiovasc Magn Reson. 2011;13:13.
    1. Aletras AH, Kellman P, Derbyshire JA, Arai AE. ACUT2E TSE-SSFP: a hybrid method for T2-weighted imaging of edema in the heart. Magn Reson Med. 2008;59:229–235.
    1. Kellman P, Aletras AH, Mancini C, McVeigh ER, Arai AE. T2-prepared SSFP improves diagnostic confidence in edema imaging in acute myocardial infarction compared to turbo spin echo. Magn Reson Med. 2007;57:891–897.
    1. Friedrich MG, Strohm O, Schulz-Menger J, Marciniak H, Luft FC, Dietz R. Contrast media-enhanced magnetic resonance imaging visualizes myocardial changes in the course of viral myocarditis. Circulation. 1998;97:1802–1809.
    1. Nef HM, Mollmann H, Kostin S, Troidl C, Voss S, Weber M, Dill T, Rolf A, Brandt R, Hamm CW, Elsasser A. Tako-Tsubo cardiomyopathy: intraindividual structural analysis in the acute phase and after functional recovery. Eur Heart J. 2007;28:2456–2464.
    1. Cooper LT, Virmani R, Chapman NM, Frustaci A, Rodeheffer RJ, Cunningham MW, McNamara DM. National Institutes of Health-sponsored workshop on inflammation and immunity in dilated cardiomyopathy. Mayo Clin Proc. 2006;81:199–204.
    1. Stensaeth KH, Fossum E, Hoffmann P, Mangschau A, Klow NE. Clinical characteristics and role of early cardiac magnetic resonance imaging in patients with suspected ST-elevation myocardial infarction and normal coronary arteries. Int J Cardiovasc Imaging. 2010;27:355–365.

Source: PubMed

3
Se inscrever