Related Experiment Video
Updated: May 18, 2026

Studying Left Ventricular Reverse Remodeling by Aortic Debanding in Rodents
Published on: July 14, 2021
Left ventricular reverse remodeling in long-term (>12 years) survivors with idiopathic dilated cardiomyopathy
Yoshihisa Matsumura1, Eri Hoshikawa-Nagai, Toru Kubo
1Department of Medicine and Geriatrics, Kochi Medical School, Kochi University, Kochi, Japan. matsumur@kochi-u.ac.jp
Insights
Left ventricular reverse remodeling (LVRR) is uncommon in long-term survivors of idiopathic dilated cardiomyopathy. However, even mild LVRR in these patients is linked to a better prognosis.
Area of Science:
- Cardiology
- Heart Failure Research
- Echocardiography
Background:
- Idiopathic dilated cardiomyopathy (IDC) prognosis is often poor.
- Long-term outcomes and reverse remodeling in IDC survivors are not well understood.
Purpose of the Study:
- To investigate left ventricular reverse remodeling (LVRR) in long-term survivors (>12 years) of IDC.
- To correlate LVRR with survival and echocardiographic parameters.
Main Methods:
- Retrospective analysis of 59 IDC patients with >12 years follow-up.
- Echocardiography used to assess LV dimensions and function.
- LVRR defined as LV end-diastolic dimension ≤ 55 mm and fractional shortening ≥ 25%.
Main Results:
- 37% of long-term survivors showed LVRR; 63% had persistent LV dysfunction but reduced LV end-systolic dimension.
- Patients who died or underwent transplantation had significantly increased LV size and no LVRR.
- LVRR was associated with a favorable prognosis in long-term IDC survivors.
Conclusions:
- Left ventricular reverse remodeling, even if mild, is linked to improved survival in idiopathic dilated cardiomyopathy.
- Persistent LV dysfunction with reduced LV end-systolic dimension is common in survivors.
- Significant LV enlargement predicts a poorer outcome in IDC patients.
Abstract:
Little is known about left ventricular (LV) reverse remodeling (LVRR) in long-term survivors with idiopathic dilated cardiomyopathy. We studied 59 patients with idiopathic dilated cardiomyopathy who had a potential clinical and echocardiographic follow-up period of >12 years. LVRR was defined as LV end-diastolic dimension ≤ 55 mm and fractional shortening ≥ 25% on the last echocardiogram. Of the 59 patients, 38 died (heart failure in 20, sudden death in 11, and other causes in 7), 2 underwent transplantation, and 19 survived. In the survivors, the LV size had significantly decreased and LV fractional shortening had significantly increased on the last echocardiogram. LVRR occurred in 37% of the survivors. The remaining 63% of the survivors still had LV dysfunction, but the LV end-systolic dimension had decreased significantly. In patients who died or underwent transplantation, the LV size significantly increased. No patient who died or underwent transplantation had LVRR. In conclusion, >60% of the long-term (>12 years) survivors with idiopathic dilated cardiomyopathy still had LV systolic dysfunction, but the LV end-systolic dimension had decreased significantly. In contrast, patients who died or underwent transplantation had significant LV enlargement. These results suggest that LVRR, even if it is not marked, is associated with a favorable prognosis.
More Related Videos
09:37Permanent Ligation of the Left Anterior Descending Coronary Artery in Mice: A Model of Post-myocardial Infarction Remodelling and Heart Failure
Published on: December 2, 2014
07:41A Model of Reverse Vascular Remodeling in Pulmonary Hypertension Due to Left Heart Disease by Aortic Debanding in Rats
Published on: March 1, 2022
Related Concept Videos
Heart Failure II: Pathophysiology
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Mitral Regurgitation I: Introduction
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy