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Association between indoxyl sulfate and cardiac dysfunction and prognosis in patients with dilated cardiomyopathy
Shuzo Shimazu1, Akihiro Hirashiki, Takahiro Okumura
1Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Insights
Serum indoxyl sulfate (IS) is linked to worse cardiac function and higher cardiac event risk in dilated cardiomyopathy (DCM) patients. IS may serve as a novel prognostic marker for DCM progression.
Area of Science:
- Cardiology
- Nephrology
- Biochemistry
Background:
- Serum indoxyl sulfate (IS) is a known uremic toxin that exacerbates chronic kidney disease (CKD) progression.
- The association between serum IS and hemodynamic parameters or cardiac events in nonischemic dilated cardiomyopathy (DCM) remains unclear.
Purpose of the Study:
- To investigate the relationship between serum IS levels and hemodynamic parameters.
- To determine if serum IS is associated with cardiac events in DCM patients.
Main Methods:
- Serum IS and plasma brain natriuretic peptide (BNP) levels were measured in 76 DCM patients.
- Echocardiography was performed, and patients were stratified into low IS (<0.9 µg/ml) and high IS (≥ 0.9 µg/ml) groups.
- Statistical analyses were conducted to assess associations and predictive values.
Main Results:
- Patients with high IS levels exhibited significantly greater E/e' values compared to those with low IS levels.
- E/e' was identified as an independent determinant of serum IS levels.
- The high IS group showed a significantly higher risk of cardiac events, and IS predicted events independently of BNP.
Conclusions:
- Cardiac dysfunction in DCM patients is associated with elevated serum IS levels.
- Serum IS may function as a novel prognostic biomarker for DCM patients, including those with normal renal function or mild-to-moderate CKD.
Background:
Serum indoxyl sulfate (IS) is a uremic toxin that accelerates the progression of chronic kidney disease (CKD). The aim of this study was to determine whether serum IS is associated with hemodynamic parameters or cardiac events in patients with nonischemic dilated cardiomyopathy (DCM).
Methods And Results:
The 76 patients with DCM had their serum IS and plasma brain natriuretic peptide (BNP) levels measured, and underwent echocardiographic examination. Mean (± standard deviation) left ventricular ejection fraction (LVEF) and BNP levels in the patients were 32.5 ± 10.7% and 204 ± 219 pg/ml, respectively. Patients were divided into 2 groups, low IS (<0.9 µg/ml) and high IS (≥ 0.9 µg/ml), based on the median value of serum IS. Although there were no significant differences in LVEF and BNP between the groups, E/e' was significantly greater in the high IS group than in the low IS group. Furthermore, E/e' was an independent determinant of serum IS level. The risk of a cardiac event was significantly higher in the high IS group than in the low IS group (P=0.014). Moreover, serum IS was a significant predictor of cardiac events even after adjustment for BNP.
Conclusions:
Cardiac dysfunction is associated with the serum IS level, which might serve as a new prognostic marker in DCM patients with normal renal function or mild to moderate CKD.
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