Guest guest Posted January 19, 2007 Report Share Posted January 19, 2007 Bosentan improves myocardial function in systemic sclerosis patients 1/18/2007 By: Reuters Health NEW YORK (Reuters Health), Jan 18 - Short-term treatment with the endothelin antagonist bosentan improves myocardial perfusion and function in patients with systemic sclerosis (SSc), according to a report in the December 2006 issue of the Journal of Rheumatology. Endothelin antagonists are not only useful in SSc when pulmonary arterial hypertension has occurred, but they also have the potential to be a general treatment for the disease, Dr. Yannick Allanore from Hopital Cochin in Paris, France, told Reuters Health. " The concept is that systemic sclerosis, which is a severe disease characterized by systemic fibrosis, is at the beginning mainly a vascular disease, and we hypothesize that using major vascular drugs (calcium channel blockers, endothelin antagonists, prostacyclins, phosphodiesterase inhibitors, etc.) from the beginning and at appropriate dosage may interfere with the fibrotic process which seems secondary, " Dr. Allanore explained. Based on bosentan's demonstrated efficacy in pulmonary hypertension related to collagen vascular diseases such as SSc, Dr. Allanore and colleagues investigated the myocardial effects of bosentan in 18 patients with SSc using cardiac MRI and tissue-Doppler echocardiography (TDE). Four weeks of treatment with bosentan increased median myocardial perfusion index from 0.17 to 0.22, the authors report, a level similar to that seen in healthy controls. Peak systolic and diastolic strain rates also increased significantly after bosentan treatment, the results indicate, although systolic and diastolic blood pressures were not affected. There were no serious adverse events during the study, the researchers note, and none of the lab values were significantly altered by treatment. " Ideally, a randomized controlled long-term (24-36 months) study would be needed to compare the cardiovascular changes in the bosentan compared to placebo group for cardiovascular complications (myocardial function, pulmonary arterial hypertension, digital ulceration) and to demonstrate the 'protective' effects of the drug regarding the vascular progression of the disease, " Dr. Allanore commented. By Will Boggs, M.D. Last Updated: 2007-01-17 14:11:16 -0400 (Reuters Health) J Rheumatol 2006;33:2464-2469 http://www.auntminnie.com/index.asp?Sec=sup & Sub=car & Pag=dis & ItemId=74303 & wf=1591 Not an MD Quote Link to comment Share on other sites More sharing options...
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