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Pentoxifylline in ischemic, hypertensive and idiopathic-dilated cardiomyopathy: effects on left-ventricular function,
Philipp Bahrmann1, Uta M Hengst, Babara M Richartz
1Clinic of Internal Medicine I, Friedrich-Schiller-University, Erlanger Allee 101, 07740 Jena, Germany. philipp.bahrmann@med.uni-jena.de
Insights
Pentoxifylline did not improve left-ventricular ejection fraction or other heart failure markers in patients with ischemic, hypertensive, or idiopathic-dilated cardiomyopathy over six months.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Elevated tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) are observed in congestive heart failure (CHF).
- Pentoxifylline, a xanthine derivative, inhibits TNF-alpha and IL-6 production.
- Previous studies suggested pentoxifylline improved cardiac function in idiopathic-dilated cardiomyopathy.
Purpose of the Study:
- To investigate the efficacy of pentoxifylline as an add-on therapy in patients with CHF.
- To evaluate its effects on left-ventricular function and inflammatory markers across different etiologies of cardiomyopathy.
Main Methods:
- A randomized controlled trial involving 47 patients with compensated CHF (LVEF ≤ 40%) and various cardiomyopathy types.
- Patients received pentoxifylline (600 mg BID) or placebo for 6 months, alongside standard CHF treatment.
- Primary endpoint: change in left-ventricular ejection fraction (LVEF) via echocardiography; secondary endpoints included inflammatory markers and functional capacity.
Main Results:
- After 6 months, no significant difference in LVEF was observed between the pentoxifylline and placebo groups (e.g., 29±7% to 33±10% vs. 27±9% to 34±9%, P=NS).
- Secondary endpoints, including inflammatory cytokine levels and functional capacity, also showed no significant changes.
- The study included patients with ischemic, hypertensive, and idiopathic-dilated cardiomyopathy.
Conclusions:
- Pentoxifylline as an additional treatment demonstrated a neutral effect on left-ventricular function.
- It did not significantly alter inflammatory cytokine levels or clinical symptoms in patients with CHF.
- The findings suggest pentoxifylline offers no additional benefit for cardiac function or inflammatory status in these CHF patient groups.
Introduction:
Tumor necrosis factor (TNF)-alpha and interleukin-6 (IL-6) are significantly elevated in patients with congestive heart failure (CHF). Pentoxifylline, a xanthin-derived agent, is known to inhibit the production of TNF-alpha and IL-6. Recent studies have shown that pentoxifylline produces an increase in ejection fraction, a decrease in left-ventricular chamber size and an improvement in clinical status in patients with idiopathic-dilated cardiomyopathy. Therefore, we studied the effects of pentoxifylline in ischemic, hypertensive and idiopathic-dilated cardiomyopathy.
Methods:
Primary endpoint was left-ventricular ejection fraction (LVEF) assessed by contrast 2D echocardiography. Secondary endpoints were concentrations of TNF-alpha, IL-6, brain natriuretic peptide, maximal oxygen uptake (VO(2 max)) assessed by cardiopulmonary exercise testing and Minnesota Living with Heart Failure Questionnaire score or New York Heart Association scale.
Results:
Forty-seven patients (31.9% ischemic, 21.3% hypertensive, 10.6% ischemic and hypertensive, 36.2% idiopathic-dilated cardiomyopathy) were randomly assigned to pentoxifylline 600 mg BID (n=23) or placebo (n=24) if they had a compensated CHF with a LVEF less than or equal to 40% and had taken their standard treatment consisting of angiotensin-converting enzyme inhibitors, diuretics and beta-blockers for at least 3 months. Baseline demographic and clinical characteristics of each group were similar. Forty-one patients completed the study protocol and were analysed for primary and secondary endpoints. After 6 months of treatment, LVEF was unchanged in the pentoxifylline group compared with placebo (29+/-7 to 33+/-10% vs. 27+/-9 to 34+/-9%, respectively, P=NS). Also the secondary endpoints did not significantly change during follow-up.
Conclusion:
Additional treatment with pentoxifylline is neutral with regard to left-ventricular function, inflammatory cytokines and symptoms in patients with ischemic, hypertensive and idiopathic-dilated cardiomyopathy.
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