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Published on: November 7, 2017
Clinical and pathologic characteristics of dilated cardiomyopathy in hemodialysis patients
Jiro Aoki1, Yuji Ikari, Hiroyoshi Nakajima
1Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan. aokijiro@aol.com
Insights
Dialysis patients with dilated cardiomyopathy show severe heart muscle cell growth and fibrosis. Extensive heart fibrosis predicts cardiac death, necessitating close monitoring and treatment for these patients.
Area of Science:
- Cardiology
- Nephrology
- Pathology
Background:
- Dialysis patients often exhibit impaired left ventricular (LV) function without coronary artery disease, but their specific pathological changes and prognoses remain poorly understood.
- Dilated cardiomyopathy (DCM) in dialysis patients is characterized by reduced ejection fraction and enlarged LV end-diastolic volume index.
- The underlying cardiac pathology in this population requires further elucidation.
Purpose of the Study:
- To investigate the pathological characteristics of the left ventricle in hemodialysis patients with DCM.
- To determine the prognostic significance of these pathological findings, particularly left ventricular fibrosis, in relation to cardiac death.
Main Methods:
- Left ventricular endomyocardial biopsies were performed on 40 hemodialysis patients with DCM and 50 non-dialysis patients with idiopathic DCM (control group).
- Patients were followed for a mean of 3.1 years post-biopsy.
- Pathological features including myocyte hypertrophy, disarray, and fibrosis were assessed and correlated with clinical outcomes.
Main Results:
- Hemodialysis patients with DCM exhibited significantly severe myocyte hypertrophy and extensive interstitial fibrosis compared to controls, resembling the dilated phase of hypertrophic cardiomyopathy.
- A high percentage of left ventricular fibrosis was identified as the sole significant predictor of cardiac death in multivariate analysis (P=0.02).
- The 3-year event-free survival for cardiac death was markedly lower in dialysis patients with severe fibrosis (42%) versus those without (82%).
Conclusions:
- The primary cardiac pathologies in dialysis patients with DCM include interstitial fibrosis and severe myocyte hypertrophy.
- The extent of left ventricular fibrosis is a critical prognostic indicator for cardiac mortality in this patient group.
- Dialysis patients with significant left ventricular fibrosis require vigilant follow-up and tailored therapeutic strategies to mitigate cardiac event risk.
Background:
Some dialysis patients have impaired left ventricular (LV) function without coronary artery disease. The pathologic changes and prognoses of these patients have not been well described.
Methods:
We performed LV endomyocardial biopsies on 40 hemodialysis patients with dilated cardiomyopathy (DCM; an ejection fraction <50% and a left ventricular end-diastolic volume index >90 mL/m(2) without coronary artery disease), and on 50 nondialysis patients with idiopathic DCM as the control group. Following LV biopsies, the patients were followed-up for a mean of 3.1 +/- 2.3 years.
Results:
The pathologic characteristics of the dialysis group were severe myocyte hypertrophy (the mean myocyte diameter across the nucleus: 37.6 +/- 10.5 mum vs. 25.6 +/- 7.7 mum, P= 0.001), myocyte disarray (30%), and extensive fibrosis (the mean percent area of left ventricular fibrosis: 22.3 +/- 18.4% vs. 21.3 +/- 14.6%, P= NS). These pathologic characteristics resembled the dilated phase of hypertrophic cardiomyopathy. In the dialysis group, a high percent area of LV fibrosis was the only significant predictor of cardiac death by multivariate analysis (P= 0.02). The 3-year cumulative event-free survival rate for cardiac death in dialysis patients with severe fibrosis (more than 30%) was 42%, while that for patients without severe fibrosis was 82% (P= 0.03).
Conclusion:
The pathologic characteristics of the heart in dialysis patients with DCM are interstitial fibrosis and severe myocyte hypertrophy with occasional disarray. The extent of LV fibrosis is a strong predictor of cardiac death. Careful follow-up and treatment are necessary for dialysis patients with a high percent area of LV fibrosis.
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