A new drug called avosentan may slow the progression of diabetic kidney disease and help prevent end stage disease. This new agent inhibits the actions of endothelin, a hormone that induces strong vasocontriction and stimulates the growth of vascular, cardiac, and kidney cells. Seen here René R. Wenzel. Photo Credit: Paracelsus UniversityFebruary 14, 2009, (Sawf News) - A new drug called avosentan may slow the progression of diabetic kidney disease and help prevent end stage disease. This new agent inhibits the actions of endothelin, a hormone that induces strong vasocontriction and stimulates the growth of vascular, cardiac, and kidney cells.
The drug significantly lowers urinary protein excretion—an important marker of kidney disease progression—in patients with diabetic kidney disease, according to an international clinical trial appearing in the March 2009 issue of the Journal of the American Society Nephrology (JASN).
A high level of protein excreted in the urine, called proteinuria, is a hallmark of kidney disease that often develops due to uncontrolled diabetes. Because a reduction in proteinuria correlates with a marked improvement in kidney prognosis, researchers have been searching for ways to lower urinary protein excretion rates in patients with diabetic kidney disease.
René R. Wenzel, MD, of the Paracelsus University in Salzburg, Austria, and his colleagues recently investigated the potential avosentan for reducing proteinuria.
In their trial conducted in 58 European centers, Dr. Wenzel and his team randomized 286 patients with diabetic kidney disease to receive a placebo or four different doses of avosentan (5mg, 10mg, 25mg, 50mg) for 12 weeks in addition to standard therapy. The results showed that there was a marked and significant reduction of albuminuria (one of the major proteins excreted in the urine in diabetic kidney disease) even with lower doses of avosentan. Compared with values measured at the start of the study, all avosentan doses decreased patients’ mean relative urinary albumin excretion rates (–16.3% to –29.9%) while the placebo did not (+35.5%). Because there seemed to be no additional beneficial effect with doses of avosentan above 25 mg, the optimal dose in terms of risk-benefit-ratio is likely to be 10 mg and below.
According to the authors, this study indicates that avostentan given in addition to standard treatments could have a protective effect on the kidneys. They noted that a larger clinical trial is needed to confirm the study’s findings and to determine whether avosentan’s effects result in long-term benefits.
News Copyright © Sawf News. May not be reproduced without explicit written permission