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Published on: June 14, 2016
Increased circulating soluble form of Fas in patients with dilated cardiomyopathy
H Kawakami1, Y Shigematsu, T Ohtsuka
1The Second Department of Internal Medicine, Ehime University School of Medicine, Japan.
Insights
Circulating soluble Fas (sFas) levels are elevated in dilated cardiomyopathy (DCM) patients and correlate with heart failure severity. Higher sFas may indicate a better prognosis, independent of heart geometry.
Area of Science:
- Cardiology
- Immunology
- Biomarkers
Background:
- Dilated cardiomyopathy (DCM) is a significant cause of heart failure.
- The prognostic role of circulating soluble Fas (sFas) in DCM remains unclear.
- Fas pathway dysregulation is implicated in various cardiovascular diseases.
Purpose of the Study:
- To investigate the prognostic value of circulating soluble Fas (sFas) in patients with DCM.
- To assess the relationship between sFas levels and heart failure severity.
- To determine if sFas provides prognostic information independent of left ventricular geometry.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) was used to measure circulating sFas levels.
- 33 DCM patients and 12 age-matched normal controls (NC) were included.
- DCM patients were stratified into two groups based on sFas levels relative to NC mean + 2SD.
Main Results:
- Circulating sFas levels were significantly higher in DCM patients compared to NC (2.42±1.02 vs 1.66±0.20 ng/ml, p=0.015).
- Elevated sFas levels correlated positively with heart failure severity and left ventricular end-diastolic pressure in DCM.
- Group II (lower sFas) experienced 5 deaths from heart failure, while Group I (higher sFas) had no deaths during follow-up.
Conclusions:
- Circulating sFas levels are elevated in DCM patients.
- sFas levels increase proportionally with heart failure severity.
- Circulating sFas may serve as an independent prognostic marker in DCM, irrespective of left ventricular dimensions.
Abstract:
To examine the prognostic role of the circulating soluble form of Fas (sFas), circulating sFas levels were measured in 33 patients with dilated cardiomyopathy (DCM) and 12 age-matched normal control subjects (NC) using an enzyme-linked immunosorbent assay (ELISA). Circulating sFas levels in DCM were significantly higher than those in NC (2.42+/-1.02 vs 1.66+/-0.20 ng/ml, p=0.015). Patients with DCM were stratified into 2 groups [group I (n=15): sFas > or =2.06 ng/ml; group II (n=18): sFas <2.06 ng/ml] on the basis of the mean value plus 2SD of circulating sFas level in NC. The circulating sFas level was significantly increased in relation to the severity of heart failure and correlated positively to left ventricular end-diastolic pressure in DCM. However, there were no significant differences in left ventricular dimension between the 2 groups. There were 5 deaths from worsening heart failure in group II, but there were no deaths in group I during the follow-up period. In conclusion, circulating sFas levels were increased in patients with DCM. Circulating sFas levels are increased in proportion to the severity of heart failure and may provide prognostic information independent of left ventricular geometry.
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