Abstract
Background
We investigated the efficacy of clinical and classic echocardiographic parameters in predicting the occurrence of nonsustained ventricular tachycardia (NsVT) in patients with hypertrophic cardiomyopathy (HCM).
Methods
The study comprised 59 patients with HCM (47 male, [80%]; mean age, 48.48 ± 14.16 years). Clinical, electrocardiographic, as well as classic two-dimensional and speckle-tracking echocardiography (STE) data were collected. All patients had Holter monitoring within 24–72 h of the echocardiographic examination. NsVT was defined as three or more consecutive premature wide QRS complexes with a heart rate of > 100 bpm. The patient population was categorized into groups based on the occurrence or absence of NsVT on the 24-h Holter recordings.
Results
NsVT was observed in 17 patients (29%). In these patients, higher twist (14.4 ± 3.8 vs.18 ± 7.9; p = 0.02), higher apical rotation (8.7 ± 4.2 vs. 12.2 ± 7; p = 0.02), higher sudden cardiac death risk score (4.4 ± 2.2 vs. 7 ± 3.3; p = 0.007), and decreased global longitudinal peak strain (GLPS; −12.8 ± 3.1 vs. −10.6 ± 2.8; p = 0.014) were observed. In the multivariate logistic regression analysis, including GLPS and twist, GLPS (Odds Ratio [OR]: 1.406; 95% CI: 1.087–1.818; p = 0.009) and twist (OR: 1.236; 95% CI: 1.056–1.446; p = 0.008) were found to be independent predictors of NsVT. In the receiver operating characteristic curve analysis, GLPS < −11.9% predicted NsVT with 82% sensitivity and 60% specificity (area under the curve [AUC]: 0.70; p = 0.014) and twist > 15.2° predicted NsVT with 70% sensitivity and 58% specificity (AUC: 0.69; p = 0.027).
Conclusion
Decreased GLPS and increased twist were predictive of NsVT in HCM patients. Parameters that can easily be measured with STE can help detect patients who may develop arrhythmia.
Zusammenfassung
Hintergrund
Die Autoren untersuchten die Bedeutung klinischer und klassischer Echokardiographieparameter für die Vorhersage des Auftretens einer nichtanhaltenden ventrikulären Tachykardie (NsVT) bei Patienten mit hypertropher Kardiomyopathie (HCM).
Methoden
Die Studie umfasste 59 Patienten mit HCM (47 m., d. h. 80 %; Durchschnittsalter: 48,48 ± 14,16 Jahre). Klinische, elektrokardiographische und klassische 2‑dimensionale sowie Speckle-Tracking-Echokardiographie(STE)-Daten wurden dokumentiert. Bei allen Patienten erfolgte ein Langzeit-EKG innerhalb von 24–72 h nach der echokardiographischen Untersuchung. NsVT war definiert als 3 oder mehr aufeinanderfolgende vorzeitige breite QRS-Komplexe mit einer Herzfrequenz von > 100/min. Die Patientenpopulation wurde in Gruppen eingeteilt, je nach Vorliegen von NsVT im 24-h-EKG.
Ergebnisse
NsVT wurde bei 17 Patienten festgestellt (29 %). Diese Patienten wiesen eine höhere Torsion auf (14,4 ± 3,8 vs.18 ± 7,9; p = 0,02), stärkere apikale Rotation (8,7 ± 4,2 vs. 12,2 ± 7; p = 0,02), einen höheren Risikowert für plötzlichen Herztod (4,4 ± 2,2 vs. 7 ± 3,3; p = 0,007) und eine verminderte globale longitudinale Spitzendeformation auf (GLPS; −12,8 ± 3,1 vs. −10,6 ± 2,8; p = 0,014). In der multivariaten logistischen Regressionsanalyse, einschließlich GLPS und Torsion, stellten sich GLPS (Odds Ratio, OR: 1,406; 95 %-KI: 1,087–1,818; p = 0,009) und Torsion (OR: 1,236; 95 %-KI: 1,056–1,446; p = 0,008) als unabhängige Prädiktoren einer NsVT heraus. In der Receiver-Operating-Characteristic(ROC)-Analyse ließ sich durch eine GLPS < −11,9 % eine NsVT mit 82 % Sensitivität und 60 % Spezifität (Fläche unter der Kurve, AUC: 0,70; p = 0,014) und durch eine Torsion > 15,2° eine NsVT mit 70 % Sensitivität und 58 % Spezifität (AUC: 0,69; p = 0,027) vorhersagen.
Schlussfolgerung
Eine verminderte GLPS und erhöhte Torsion waren Prädiktoren einer NsVT bei HCM-Patienten. Somit können einfach mit der STE zu bestimmende Parameter dazu beitragen, Patienten zu erkennen, bei denen sich möglicherweise eine Arrhythmie entwickelt.
Similar content being viewed by others
References
Decker JA, Rossano JW, Smith EO, Cannon B, Clunie SK, Gates C, Jefferies JL, Kim JJ, Price JF, Dreyer WJ, Towbin JA, Denfield SW (2009) Risk factors and mode of death in isolated hypertrophic cardiomyopathy in children. J Am Coll Cardiol 54(3):250–254
Kofflard MJ, Ten Cate FJ, van der Lee C, van Domburg RT (2003) Hypertrophic cardiomyopathy in a large community-based population: clinical outcome and identification of risk factors for sudden cardiac death and clinical deterioration. J Am Coll Cardiol 41(6):987–993
Cardim N, Galderisi M, Edvardsen T, Plein S, Popescu BA, D’Andrea A et al (2015) Role of multimodality cardiac imaging in the management of patients with hypertrophic cardiomyopathy: an expert consensus of the European Association of Cardiovascular Imaging endorsed by the Saudi Heart Association. Eur Heart J Cardiovasc Imaging 16:280
Saumarez RC, Camm AJ, Panagos A, Gill JS, Stewart JT, de Belder MA et al (1992) Ventricular fibrillation in hypertrophic cardiomyopathy is associated with increased fractionation of paced right ventricular electrograms. Circulation 86:467–474
Elliott PM, Anastasakis A, Borger MA, Borggrefe M, Cecchi F, Charron P, Hagege AA, Lafont A, Limongelli G, Mahrholdt H, McKenna WJ, Mogensen J, Nihoyannopoulos P, Nistri S, Pieper PG, Pieske B, Rapezzi C, Rutten FH, Tillmanns C, Watkins H (2014) 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). Eur Heart J 35(39):2733–2779
Buja G, Miorelli M, Turrini P, Melacini P, Nava A (1993) Comparison of QT dispersion in hypertrophic cardiomyopathy between patients with and without ventricular arrhythmias and sudden death. Am J Cardiol 72:973–976
D’Andrea A (2006) Prognostic value of intra-left ventricular electromechanical asynchrony in patients with hypertrophic cardiomyopathy. Eur Heart J 27:1311–1318
Adabag AS, Maron BJ, Appelbaum E, Harrigan CJ, Buros JL, Gibson CM et al (2008) Occurrence and frequency of arrhythmias in hypertrophic cardiomyopathy in relation to delayed enhancement on cardiovascular magnetic resonance. J Am Coll Cardiol 51:1369–1374
O’Mahony C, Jichi F, Pavlou M, Monserrat L, Anastasakis A, Rapezzi C et al (2014) A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk SCD). Eur Heart J 35:2010–2020
Moustafa SE, Kansal M, Alharthi M, Deng Y, Chandrasekaran K, Mookadam F (2011) Prediction of incipient left ventricular dysfunction in patients with chronic primary mitral regurgitation: a velocity vector imaging study. Eur J Echocardiogr 12(4):291–298
Tops LF, Delgado V, Marsan NA, Bax JJ (2017) Myocardial strain to detect subtle left ventricular systolic dysfunction. Eur J Heart Fail 19(3):307–313. https://doi.org/10.1002/ejhf.694
Haland TF, Almaas VM, Hasselberg NE, Saberniak J, Leren IS, Hopp E, Edvardsen T, Haugaa KH (2016) Strain echocardiography is related to fibrosis and ventricular arrhythmias in hypertrophic cardiomyopathy. Eur Heart J Cardiovasc Imaging 17(6):613–621
Debonnaire P, Thijssen J, Leong DP, Joyce E, Katsanos S, Hoogslag GE, Schalij MJ, Atsma DE, Bax JJ, Delgado V, Marsan NA (2014) Global longitudinal strain and left atrial volume index improve prediction of appropriate implantable cardioverter defibrillator therapy in hypertrophic cardiomyopathy patients. Int J Cardiovasc Imaging 30(3):549–558
Funabashi N, Takaoka H, Horie S, Ozawa K, Daimon M, Takahashi M, Yajima R, Saito M, Fujiwara K, Tani A, Kamata T, Uehara M, Kataoka A, Kobayashi Y (2013) Regional peak longitudinal-strain by 2D speckle-tracking TTE provides useful information to distinguish fibrotic from non-fibrotic lesions in LV myocardium on cardiac MR in hypertrophic cardiomyopathy. Int J Cardiol 168(4):4520–4523
Notomi Y, Lysyansky P, Setser RM et al (2005) Measurement of ventricular twist by two-dimensional ultrasound speckle tracking imaging. J Am Coll Cardiol 45:2034–2041
Zhang HJ, Wang H, Sun T, Lu MJ, Xu N, Wu WC, Sun X, Wang WG, Lin QW (2014) Assessment of left ventricular twist mechanics by speckle tracking echocardiography reveals association between LV twist and myocardial fibrosis in patients with hypertrophic cardiomyopathy. Int J Cardiovasc Imaging 30(8):1539–1548. https://doi.org/10.1007/s10554-014-0509-6
Pedersen CT, Kay GN, Kalman J, Borggrefe M, Della-Bella P, Dickfeld T, Dorian P, Huikuri H, Kim YH, Knight B, Marchlinski F, Ross D, Sacher F, Sapp J, Shivkumar K, Soejima K, Tada H, Alexander ME, Triedman JK, Yamada T, Kirchhof P, Lip GY, Kuck KH, Mont L, Haines D, Indik J, Dimarco J, Exner D, Iesaka Y, Savelieva I (2014) EHRA/HRS/APHRS expert consensus on ventricular arrhythmias. Europace 16(9):1257–1283. https://doi.org/10.1093/europace/euu194
Lang RM, Badano LP, Mor-Avi V, Afilalo J, Armstrong A, Ernande L (2015) Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. Eur Heart J Cardiovasc Imaging 16(3):233–270
Schabelman S, Schiller NB, Silverman NH, Ports TA (1981) Left atrial volume estimation by twodimensional echocardiography. Cathet Cardiovasc Diagn 7(2):165–178
Jalanko M, Tarkiainen M, Sipola P, Jääskeläinen P, Lauerma K, Laine M, Nieminen MS, Laakso M, Heliö T, Kuusisto J (2016) Left ventricular mechanical dispersion is associated with nonsustained ventricular tachycardia in hypertrophic cardiomyopathy. Ann Med 48(6):417–427
Correia E, Rodrigues B, Santos LF, Moreira D, Gama P, Cabral C, Santos O (2011) Longitudinal left ventricular strain in hypertrophic cardiomyopathy: correlation with nonsustained ventricular tachycardia. Echocardiography 28(7):709–714. https://doi.org/10.1111/j.1540-8175.2011.01427.x
Di Salvo G, Pacileo G, Limongelli G, Baldini L, Rea A, Verrengia M (2010) Nonsustained ventricular tachycardia in hypertrophic cardiomyopathy and new ultrasonic derived parameters. J Am Soc Echocardiogr 23:581–590
Monserrat L, Elliott PM, Gimeno JR, Sharma S, Penas-Lado M, McKenna WJ (2003) Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: an independent marker of sudden death risk in young patients. J Am Coll Cardiol 42(5):873–879
McKenna WJ, Sadoul N, Slade AK, Saumarez RC (1994) The prognostic significance of nonsustained ventricular tachycardia in hypertrophic cardiomyopathy. Circulation 90(6):3115–3117
Maron BJ, Bonow RO, Cannon RO 3rd, Leon MB, Epstein SE (1987) Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1). N Engl J Med 316(13):780–789. https://doi.org/10.1056/NEJM198703263161305
Petersen SE, Jerosch-Herold M, Hudsmith LE, Robson MD, Francis JM, Doll HA, Selvanayagam JB, Neubauer S, Watkins H (2007) Evidence for microvascular dysfunction in hypertrophic cardiomyopathy: new insights from multiparametric magnetic resonance imaging. Circulation 8;115(18):2418–2425
Funabashi N, Kataoka A, Horie S, Ozawa K, Takaoka H, Takahashi M, Yajima R, Saito M, Umazume T, Fujiwara K, Kamata T, Uehara M, Kobayashi Y (2013) Distinguishing 320 slice CT-detected focal fibrotic lesions and non-fibrotic lesions in hypertrophic cardiomyopathy by assessment of regional myocardial strain using two dimensional speckle tracking echocardiography. Int J Cardiol 30;169(6):e109–13
Paraskevaidis IA, Farmakis D, Papadopoulos C, Ikonomidis I, Parissis J, Rigopoulos A, Iliodromitis EK, Kremastinos DT (2009) Two-dimensional strain analysis in patients with hypertrophic cardiomyopathy and normal systolic function: a 12-month follow-up study. Am Heart J 158(3):444–450
Hartlage GR, Kim JH, Strickland PT, Cheng AC, Ghasemzadeh N, Pernetz MA, Clements SD, Williams BR 3rd (2015) The prognostic value of standardized reference values for speckle-tracking global longitudinal strain in hypertrophic cardiomyopathy. Int J Cardiovasc Imaging 31(3):557–565
Ternacle J, Bremont C, d’Humieres T, Faivre L, Doan HL, Gallet R, Oliver L, Dubois-Randé JL, Lim P (2017) Left ventricular dyssynchrony and 2D and 3D global longitudinal strain for differentiating physiological and pathological left ventricular hypertrophy. Arch Cardiovasc Dis 2136(16):30213–30213
Reant P, Mirabel M, Lloyd G, Peyrou J, Lopez Ayala JM, Dickie S, Bulluck H, Captur G, Rosmini S, Guttmann O, Demetrescu C, Pantazis A, Tome-Esteban M, Moon JC, Lafitte S, McKenna WJ (2016) Global longitudinal strain is associated with heart failure outcomes in hypertrophic cardiomyopathy. Heart 15;102(10):741–747
De S, Borowski AG, Wang H, Nye L, Xin B, Thomas JD, Tang WH (2011) Subclinical echocardiographic abnormalities in phenotype-negative carriers of myosin-binding protein C3 gene mutation for hypertrophic cardiomyopathy. Am Heart J 162(2):262–267.e3
Ozawa K, Funabashi N, Takaoka H, Kobayashi Y (2017) Successful MACE risk stratification in hypertrophic cardiomyopathy patients using different 2D speckle-tracking TTE approaches. Int J Cardiol 1;228:1015–1021
Almaas VM, Haugaa KH, Strøm EH, Scott H, Dahl CP, Leren TP, Geiran OR, Endresen K, Edvardsen T, Aakhus S, Amlie JP (2013) Increased amount of interstitial fibrosis predicts ventricular arrhythmias, and is associated with reduced myocardial septal function in patients with obstructive hypertrophic cardiomyopathy. Europace 15(9):1319–1327. https://doi.org/10.1093/europace/eut028
Maron BJ (2010) Contemporary insights and strategies for risk stratification and prevention of sudden death in hypertrophic cardiomyopathy. Circulation 121(3):445–456
Kauer F, van Dalen BM, Michels M, Schinkel AF, Vletter WB, van Slegtenhorst M, Soliman OI, Geleijnse ML (2017) Delayed and decreased LV untwist and unstrain rate in mutation carriers for hypertrophic cardiomyopathy. Eur Heart J Cardiovasc Imaging 18(4):383–389. https://doi.org/10.1093/ehjci/jew213
Sade LE, Demir Ö, Atar I, Müderrisoglu H, Özin B (2008) Effect of mechanical dyssynchrony and cardiac resynchronization therapy on left ventricular rotational mechanics. Am J Cardiol 101:1163–1169
Bertini M, Nucifora G, Marsan NA, Delgado V, van Bommel RJ, Boriani G et al (2009) Left ventricular rotational mechanics in acute myocardial infarction and in chronic (ischemic and nonischemic) heart failure patients. Am J Cardiol 103:1506–1512
Han W, Xie M, Wang X, Lu Q (2008) Assessment of left ventricular global twist in essential hypertensive heart by speckle tracking imaging. J Huazhong Univ Sci Technol Med Sci 28:114–117
Candan O, Hatipoglu Akpinar S, Dogan C, Demirkıran A, Dindar B, Bayram Z, Yılmaz F, Kaymaz C, Ozdemir N (2017) Twist deformation for predicting postoperative left ventricular function in patients with mitral regurgitation: A speckle tracking echocardiography study. Echocardiography 34(3):422–428. https://doi.org/10.1111/echo.13462
van Dalen BM, Kauer F, Michels M, Soliman OI, Vletter WB, van der Zwaan HB, ten Cate FJ, Geleijnse ML (2009) Delayed left ventricular untwisting in hypertrophic cardiomyopathy. J Am Soc Echocardiogr 22(12):1320–1326. https://doi.org/10.1016/j.echo.2009.07.021
Chang SA, Kim HK, Kim DH, Kim JC, Kim YJ, Kim HC, Sohn DW, Oh BH, Park YB (2010) Left ventricular twist mechanics in patients with apical hypertrophic cardiomyopathy: assessment with 2D speckle tracking echocardiography. Heart 96(1):49–55. https://doi.org/10.1136/hrt.2009.166629
Vriesendorp PA, Schinkel AF, Liebregts M, Theuns DA, van Cleemput J, Ten Cate FJ, Willems R, Michels M (2015) Validation of the 2014 European Society of Cardiology guidelines risk prediction model for the primary prevention of sudden cardiac death in hypertrophic cardiomyopathy. Circ Arrhythm Electrophysiol 8(4):829–835 (Aug)
Fernández A, Quiroga A, Ochoa JP, Mysuta M, Casabé JH, Biagetti M, Guevara E, Favaloro LE, Fava AM, Galizio N (2016) Validation of the 2014 European Society of Cardiology sudden cardiac death risk prediction model in hypertrophic cardiomyopathy in a reference center in South America. Am J Cardiol 118(1):121–126
Maron BJ, Casey SA, Chan RH, Garberich RF, Rowin EJ, Maron MS (2015) Independent assessment of the European Society of Cardiology sudden death risk model for hypertrophic cardiomyopathy. Am J Cardiol 116(5):757–764 (Sep)
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
O. Candan, C. Gecmen, A. Kalaycı, E. Bayam, A. Guner, S. Gunduz, S. Cersit, and M. Ozkan declare that they have no competing interests.
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Rights and permissions
About this article
Cite this article
Candan, O., Gecmen, C., Kalaycı, A. et al. Left ventricular twist in hypertrophic cardiomyopathy. Herz 44, 238–246 (2019). https://doi.org/10.1007/s00059-017-4633-7
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00059-017-4633-7
Keywords
- Cardiac arrhythmia
- Cardiomyopathy, hypertrophic obstructive
- Sudden cardiac death
- Echocardiography
- Heart rate