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The clinical course of idiopathic dilated cardiomyopathy. A population-based study
D D Sugrue1, R J Rodeheffer, M B Codd
1Mayo Clinic, Rochester, Minnesota.
Insights
Idiopathic dilated cardiomyopathy has a more favorable prognosis in the general population than previously thought, based on referral center studies. This population-based study shows improved survival rates for this heart condition.
Area of Science:
- Cardiology
- Epidemiology
- Public Health
Background:
- Idiopathic dilated cardiomyopathy (IDCM) is a significant cause of heart failure.
- Previous prognostic data for IDCM primarily derived from referral center case series, potentially overestimating disease severity.
- Population-based studies are crucial for understanding the true clinical course of chronic diseases.
Purpose of the Study:
- To determine the prognosis of individuals diagnosed with IDCM within a defined population.
- To compare the survival outcomes of this population-based cohort with a historical referral center case series of IDCM.
Main Methods:
- A cohort study design was employed.
- Utilized a population-based sample from Olmsted County, Minnesota, identifying 40 residents diagnosed with IDCM between 1975 and 1984.
- Follow-up extended through July 1, 1989, with survival data compared to 104 patients from a 1960-1973 Mayo Clinic referral series.
Main Results:
- One-year survival was significantly higher in the population-based cohort (95%) compared to the referral series (69%).
- Five-year survival also showed a marked difference: 80% for the population cohort versus 36% for the referral series (P < 0.001).
- Despite better outcomes than referral cases, the population cohort had impaired long-term survival compared to age- and sex-matched controls, with older age and lower ejection fraction predicting poorer outcomes.
Conclusions:
- Population-based data suggest that the clinical course of IDCM may be more favorable than commonly perceived from referral center studies.
- These findings challenge existing clinical perceptions of IDCM prognosis.
- Further research into community-based IDCM management and outcomes is warranted.
Objective:
To describe the prognosis of individuals with idiopathic dilated cardiomyopathy in a population-based sample and to compare this with the prognosis of patients in a previous referral center case series of idiopathic dilated cardiomyopathy.
Design:
Cohort study.
Setting:
Population-based in Olmsted County, Minnesota.
Patients:
Forty residents of Olmsted County, Minnesota with idiopathic dilated cardiomyopathy initially diagnosed between 1975 and 1984 who were followed through 1 July 1989 and 104 patients from a Mayo Clinic referral case series from 1960 to 1973.
Measurements:
Survival for the population-based cohort at 1 year and 5 years.
Results:
Survival at 1 year differed dramatically between the population-based cohort and the referral case series at 1 year (95% compared with 69%, respectively) and at 5 years (80% compared with 36%, respectively) (P less than 0.001). Long-term survival for the population-based cohort was nonetheless impaired when compared with an age- and sex-matched cohort, that is, the 1980 Minnesota white population (8-year survival: observed, 58% compared with expected, 83%; P less than 0.001). Among community patients, older age (adjusted Cox model hazard ratio for 10-year increase in age, 1.59; 95% CI, 1.08 to 2.35) and lower left ventricular ejection fraction (adjusted hazard ratio for 10% decrease, 1.90; CI, 1.04 to 3.50) were independently associated with impaired survival.
Conclusions:
These population-based data challenge the clinical perception of the clinical course of idiopathic dilated cardiomyopathy based on referral practice prognostic studies and suggest that the clinical course of this condition may be more favorable than previously recognized.
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