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Ursodeoxycholic acid may counter heart failure


The European Society of Cardiology (ESC) has welcomed an “intriguing” study published in the Journal of the American College of Cardiology (JACC), featuring a completely novel approach for improving endothelial function in heart failure.

In the “hypothesis generating” study, ursodeoxycholic acid (UDCA) delivered significant improvements in peak post ischemic blood flow in the arm, a trend for improvement in peak post ischemic blood flow in the leg, but failed to show benefits in exercise capacity and several inflammatory markers.

Despite such conflicting data, the ESC believes that further exploration of UCDA is now justified in larger populations of heart failure patients.


“Although the study failed on two out of three counts, the observed improvements in post ischemic arm and leg blood flow make it highly unlikely such findings would have occurred purely by chance,” said Professor Kenneth Dickstein, an ESC spokesperson.

“The results are enough to pique real interest and suggest the approach has the potential to offer another string to our bow for improving heart failure symptoms.”

It is also noteworthy, adds Dickstein from the University of Bergen (Stavanger University Hospital, Norway), that JACC felt the study to be of sufficient merit to commission an editorial.

The theory underlying the use of UDCA centres on the finding that abdominal congestion leads to increased gut permeability, allowing endotoxins produced by gram negative bacteria to enter the circulation.

The increased levels of proinflammatory cytokines can then further exacerbate symptoms of heart failure.

UDCA is able to form a complex around a component of the cell-wall of the gram-negative bacteria, thereby decreasing levels of proinflammatory cytokines and offering the potential to improve peripheral blood flow and ultimately increase exercise tolerance.

In the last 10 to 15 years studies have explored modifying inflammation in heart failure patients (through anti-inflammatory agents, antibiotics and statins), but all have proved neutral or in some cases even resulted in worse outcomes for patients.

In the current prospective double-blind, cross-over study, Stephan von Haehling, from the Charité Medical School (Berlin, Germany), and colleagues from Poland, UK, Austria and Italy, assessed the effects of UDCA on endothelial function and inflammatory markers in 17 chronic heart failure patients who received 500 mg UDCA twice daily for four weeks, followed by placebo for another four weeks.

Results showed that in comparison with placebo, UDCA significantly improved peak post-ischemic blood flow in the arm (p=0.038), and showed a trend for improved peak blood flow in the leg (p=0.079).

No change, however, occurred in the six-minute walk test and for New York Heart Association functional class, and furthermore, levels of tumour necrosis factor a and interleukin-6 remained unchanged

Recent registries showing a 5 to 8% annual mortality for chronic heart failure patients underline the urgent need for new heart failure treatments in addition to the standard ACE inhibitors, ARBs, beta blockers, aldosterone blockers and devices.

Journal of the American College of Cardiology

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