Global Longitudinal Strain is Incremental to Left Ventricular Ejection Fraction for the Prediction of Outcome in Optimally Treated Dilated Cardiomyopathy Patients
Background Speckle tracking echocardiographic global longitudinal strain (GLS) predicts outcome in patients with new onset heart failure. Still, its incremental value on top of left ventricular ejection fraction (LVEF) in patients with nonischemic, nonvalvular dilated cardiomyopathy (DCM) after opti...
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Published in | Journal of the American Heart Association Vol. 11; no. 6; p. e024505 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley and Sons Inc
15.03.2022
Wiley |
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Abstract | Background Speckle tracking echocardiographic global longitudinal strain (GLS) predicts outcome in patients with new onset heart failure. Still, its incremental value on top of left ventricular ejection fraction (LVEF) in patients with nonischemic, nonvalvular dilated cardiomyopathy (DCM) after optimal heart failure treatment remains unknown. Methods and Results Patients with DCM were included at the outpatient clinics of 2 centers in the Netherlands and Italy. The prognostic value of 2-dimensional speckle tracking echocardiographic global longitudinal strain was evaluated when being on optimal heart failure medication for at least 6 months. Outcome was defined as the combination of sudden or cardiac death, life-threatening arrhythmias, and heart failure hospitalization. A total of 323 patients with DCM (66% men, age 55±14 years) were included. The mean LVEF was 42%±11% and mean GLS after optimal heart failure treatment was -15%±4%. Twenty percent (64/323) of all patients reached the primary outcome after optimal heart failure treatment (median follow-up of 6[4-9] years). New York Heart Association class ≥3, LVEF, and GLS remained associated with the outcome in the multivariable-adjusted model (New York Heart Association class: hazard ratio [HR], 3.43; 95% CI, 1.49-7.90,
=0.004; LVEF: HR, 2.13; 95% CI, 1.11-4.10,
=0.024; GLS: HR, 2.24; 95% CI, 1.18-4.29,
=0.015), whereas left ventricular end-diastolic diameter index, left atrial volume index, and delta GLS were not. The addition of GLS to New York Heart Association class and LVEF improved the goodness of fit (log likelihood ratio test
<0.001) and discrimination (Harrell's C 0.703). Conclusions Within this bicenter study, GLS emerged as an independent and incremental predictor of adverse outcome, which exceeded LVEF in patients with optimally treated DCM. This presses the need to routinely include GLS in the echocardiographic follow-up of DCM. |
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AbstractList | Background Speckle tracking echocardiographic global longitudinal strain (GLS) predicts outcome in patients with new onset heart failure. Still, its incremental value on top of left ventricular ejection fraction (LVEF) in patients with nonischemic, nonvalvular dilated cardiomyopathy (DCM) after optimal heart failure treatment remains unknown. Methods and Results Patients with DCM were included at the outpatient clinics of 2 centers in the Netherlands and Italy. The prognostic value of 2‐dimensional speckle tracking echocardiographic global longitudinal strain was evaluated when being on optimal heart failure medication for at least 6 months. Outcome was defined as the combination of sudden or cardiac death, life‐threatening arrhythmias, and heart failure hospitalization. A total of 323 patients with DCM (66% men, age 55±14 years) were included. The mean LVEF was 42%±11% and mean GLS after optimal heart failure treatment was −15%±4%. Twenty percent (64/323) of all patients reached the primary outcome after optimal heart failure treatment (median follow‐up of 6[4–9] years). New York Heart Association class ≥3, LVEF, and GLS remained associated with the outcome in the multivariable‐adjusted model (New York Heart Association class: hazard ratio [HR], 3.43; 95% CI, 1.49–7.90, P=0.004; LVEF: HR, 2.13; 95% CI, 1.11–4.10, P=0.024; GLS: HR, 2.24; 95% CI, 1.18–4.29, P=0.015), whereas left ventricular end‐diastolic diameter index, left atrial volume index, and delta GLS were not. The addition of GLS to New York Heart Association class and LVEF improved the goodness of fit (log likelihood ratio test P<0.001) and discrimination (Harrell’s C 0.703). Conclusions Within this bicenter study, GLS emerged as an independent and incremental predictor of adverse outcome, which exceeded LVEF in patients with optimally treated DCM. This presses the need to routinely include GLS in the echocardiographic follow‐up of DCM. Background Speckle tracking echocardiographic global longitudinal strain (GLS) predicts outcome in patients with new onset heart failure. Still, its incremental value on top of left ventricular ejection fraction (LVEF) in patients with nonischemic, nonvalvular dilated cardiomyopathy (DCM) after optimal heart failure treatment remains unknown. Methods and Results Patients with DCM were included at the outpatient clinics of 2 centers in the Netherlands and Italy. The prognostic value of 2-dimensional speckle tracking echocardiographic global longitudinal strain was evaluated when being on optimal heart failure medication for at least 6 months. Outcome was defined as the combination of sudden or cardiac death, life-threatening arrhythmias, and heart failure hospitalization. A total of 323 patients with DCM (66% men, age 55±14 years) were included. The mean LVEF was 42%±11% and mean GLS after optimal heart failure treatment was -15%±4%. Twenty percent (64/323) of all patients reached the primary outcome after optimal heart failure treatment (median follow-up of 6[4-9] years). New York Heart Association class ≥3, LVEF, and GLS remained associated with the outcome in the multivariable-adjusted model (New York Heart Association class: hazard ratio [HR], 3.43; 95% CI, 1.49-7.90, =0.004; LVEF: HR, 2.13; 95% CI, 1.11-4.10, =0.024; GLS: HR, 2.24; 95% CI, 1.18-4.29, =0.015), whereas left ventricular end-diastolic diameter index, left atrial volume index, and delta GLS were not. The addition of GLS to New York Heart Association class and LVEF improved the goodness of fit (log likelihood ratio test <0.001) and discrimination (Harrell's C 0.703). Conclusions Within this bicenter study, GLS emerged as an independent and incremental predictor of adverse outcome, which exceeded LVEF in patients with optimally treated DCM. This presses the need to routinely include GLS in the echocardiographic follow-up of DCM. Background Speckle tracking echocardiographic global longitudinal strain (GLS) predicts outcome in patients with new onset heart failure. Still, its incremental value on top of left ventricular ejection fraction (LVEF) in patients with nonischemic, nonvalvular dilated cardiomyopathy (DCM) after optimal heart failure treatment remains unknown. Methods and Results Patients with DCM were included at the outpatient clinics of 2 centers in the Netherlands and Italy. The prognostic value of 2-dimensional speckle tracking echocardiographic global longitudinal strain was evaluated when being on optimal heart failure medication for at least 6 months. Outcome was defined as the combination of sudden or cardiac death, life-threatening arrhythmias, and heart failure hospitalization. A total of 323 patients with DCM (66% men, age 55±14 years) were included. The mean LVEF was 42%±11% and mean GLS after optimal heart failure treatment was -15%±4%. Twenty percent (64/323) of all patients reached the primary outcome after optimal heart failure treatment (median follow-up of 6[4-9] years). New York Heart Association class ≥3, LVEF, and GLS remained associated with the outcome in the multivariable-adjusted model (New York Heart Association class: hazard ratio [HR], 3.43; 95% CI, 1.49-7.90, P=0.004; LVEF: HR, 2.13; 95% CI, 1.11-4.10, P=0.024; GLS: HR, 2.24; 95% CI, 1.18-4.29, P=0.015), whereas left ventricular end-diastolic diameter index, left atrial volume index, and delta GLS were not. The addition of GLS to New York Heart Association class and LVEF improved the goodness of fit (log likelihood ratio test P<0.001) and discrimination (Harrell's C 0.703). Conclusions Within this bicenter study, GLS emerged as an independent and incremental predictor of adverse outcome, which exceeded LVEF in patients with optimally treated DCM. This presses the need to routinely include GLS in the echocardiographic follow-up of DCM.Background Speckle tracking echocardiographic global longitudinal strain (GLS) predicts outcome in patients with new onset heart failure. Still, its incremental value on top of left ventricular ejection fraction (LVEF) in patients with nonischemic, nonvalvular dilated cardiomyopathy (DCM) after optimal heart failure treatment remains unknown. Methods and Results Patients with DCM were included at the outpatient clinics of 2 centers in the Netherlands and Italy. The prognostic value of 2-dimensional speckle tracking echocardiographic global longitudinal strain was evaluated when being on optimal heart failure medication for at least 6 months. Outcome was defined as the combination of sudden or cardiac death, life-threatening arrhythmias, and heart failure hospitalization. A total of 323 patients with DCM (66% men, age 55±14 years) were included. The mean LVEF was 42%±11% and mean GLS after optimal heart failure treatment was -15%±4%. Twenty percent (64/323) of all patients reached the primary outcome after optimal heart failure treatment (median follow-up of 6[4-9] years). New York Heart Association class ≥3, LVEF, and GLS remained associated with the outcome in the multivariable-adjusted model (New York Heart Association class: hazard ratio [HR], 3.43; 95% CI, 1.49-7.90, P=0.004; LVEF: HR, 2.13; 95% CI, 1.11-4.10, P=0.024; GLS: HR, 2.24; 95% CI, 1.18-4.29, P=0.015), whereas left ventricular end-diastolic diameter index, left atrial volume index, and delta GLS were not. The addition of GLS to New York Heart Association class and LVEF improved the goodness of fit (log likelihood ratio test P<0.001) and discrimination (Harrell's C 0.703). Conclusions Within this bicenter study, GLS emerged as an independent and incremental predictor of adverse outcome, which exceeded LVEF in patients with optimally treated DCM. This presses the need to routinely include GLS in the echocardiographic follow-up of DCM. |
Author | Henkens, Michiel T. H. M. Weerts, Jerremy Sinagra, Gianfranco Boscutti, Andrea Manca, Paolo Knackstedt, Christian Heymans, Stephane R. B. Stolfo, Davide Hazebroek, Mark R. Nuzzi, Vincenzo Merlo, Marco Verdonschot, Job A. J. van den Broek, Wout W. A. Raafs, Anne G. |
AuthorAffiliation | 3 Netherlands Heart Institute (Nl‐HI) Utrecht The Netherlands 1 Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands 4 Department of Clinical Genetics Maastricht University Medical Center Maastricht The Netherlands 2 Cardiothoracovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI) University of Trieste Trieste Italy 5 Department of Cardiovascular Research University of Leuven Leuven Belgium |
AuthorAffiliation_xml | – name: 2 Cardiothoracovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI) University of Trieste Trieste Italy – name: 5 Department of Cardiovascular Research University of Leuven Leuven Belgium – name: 1 Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands – name: 3 Netherlands Heart Institute (Nl‐HI) Utrecht The Netherlands – name: 4 Department of Clinical Genetics Maastricht University Medical Center Maastricht The Netherlands |
Author_xml | – sequence: 1 givenname: Anne G. orcidid: 0000-0001-9228-8045 surname: Raafs fullname: Raafs, Anne G. organization: Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands – sequence: 2 givenname: Andrea surname: Boscutti fullname: Boscutti, Andrea organization: Cardiothoracovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI)University of Trieste Trieste Italy – sequence: 3 givenname: Michiel T. H. M. orcidid: 0000-0001-6222-071X surname: Henkens fullname: Henkens, Michiel T. H. M. organization: Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands, Netherlands Heart Institute (Nl‐HI) Utrecht The Netherlands – sequence: 4 givenname: Wout W. A. orcidid: 0000-0002-4083-9957 surname: van den Broek fullname: van den Broek, Wout W. A. organization: Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands – sequence: 5 givenname: Job A. J. orcidid: 0000-0001-5549-1298 surname: Verdonschot fullname: Verdonschot, Job A. J. organization: Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands, Department of Clinical Genetics Maastricht University Medical Center Maastricht The Netherlands – sequence: 6 givenname: Jerremy orcidid: 0000-0002-9369-3453 surname: Weerts fullname: Weerts, Jerremy organization: Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands – sequence: 7 givenname: Davide orcidid: 0000-0002-4538-6811 surname: Stolfo fullname: Stolfo, Davide organization: Cardiothoracovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI)University of Trieste Trieste Italy – sequence: 8 givenname: Vincenzo orcidid: 0000-0002-9643-2697 surname: Nuzzi fullname: Nuzzi, Vincenzo organization: Cardiothoracovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI)University of Trieste Trieste Italy – sequence: 9 givenname: Paolo surname: Manca fullname: Manca, Paolo organization: Cardiothoracovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI)University of Trieste Trieste Italy – sequence: 10 givenname: Mark R. orcidid: 0000-0002-2151-7178 surname: Hazebroek fullname: Hazebroek, Mark R. organization: Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands – sequence: 11 givenname: Christian orcidid: 0000-0002-5457-3010 surname: Knackstedt fullname: Knackstedt, Christian organization: Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands – sequence: 12 givenname: Marco surname: Merlo fullname: Merlo, Marco organization: Cardiothoracovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI)University of Trieste Trieste Italy – sequence: 13 givenname: Stephane R. B. orcidid: 0000-0001-9477-7803 surname: Heymans fullname: Heymans, Stephane R. B. organization: Department of Cardiology and Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center+ Maastricht The Netherlands, Netherlands Heart Institute (Nl‐HI) Utrecht The Netherlands, Department of Cardiovascular Research University of Leuven Leuven Belgium – sequence: 14 givenname: Gianfranco surname: Sinagra fullname: Sinagra, Gianfranco organization: Cardiothoracovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI)University of Trieste Trieste Italy |
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ContentType | Journal Article |
Copyright | 2022 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. |
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Keywords | global longitudinal strain deformation imaging optimal medical treatment prognosis dilated cardiomyopathy |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 For Sources of Funding and Disclosures, see page 8. Supplemental Material for this article is available at https://www.ahajournals.org/doi/suppl/10.1161/JAHA.121.024505 A. G. Raafs and A. Boscutti are co‐first authors. C. Knackstedt, M. Merlo, S. R. B. Heymans, and G. Sinagra are joint senior authors. |
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Snippet | Background Speckle tracking echocardiographic global longitudinal strain (GLS) predicts outcome in patients with new onset heart failure. Still, its... |
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SubjectTerms | Adult Aged Cardiomyopathy, Dilated - complications Cardiomyopathy, Dilated - diagnostic imaging Cardiomyopathy, Dilated - drug therapy deformation imaging dilated cardiomyopathy Female global longitudinal strain Heart Failure Humans Male Middle Aged optimal medical treatment Original Research Prognosis Risk Factors Stroke Volume Ventricular Dysfunction, Left Ventricular Function, Left |
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Title | Global Longitudinal Strain is Incremental to Left Ventricular Ejection Fraction for the Prediction of Outcome in Optimally Treated Dilated Cardiomyopathy Patients |
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