Phosphodiesterase Type 5 Inhibition Is a Novel Therapeutic Option in Raynaud Disease
Author(s) -
Evren Caglayan,
Michael Huntgeburth,
Thomas Karasch,
Julia Weihrauch,
Nicolas Hunzelmann,
Thomas Krieg,
Erland Erdmann,
Stephan Rosenkranz
Publication year - 2006
Publication title -
archives of internal medicine
Language(s) - English
Resource type - Journals
eISSN - 1538-3679
pISSN - 0003-9926
DOI - 10.1001/archinte.166.2.231
Subject(s) - vardenafil , medicine , cgmp specific phosphodiesterase type 5 , connective tissue disease , connective tissue , sildenafil , population , laser doppler velocimetry , blood flow , gastroenterology , surgery , disease , tadalafil , pathology , autoimmune disease , environmental health
Raynaud disease (RD) is a common disorder affecting 3% to 5% of the healthy population, and occurs in more than 90% of patients with connective tissue diseases. The therapeutic options remain limited, particularly in patients with secondary RD due to connective tissue disease. Theoretical considerations lead to the expectation that phosphodiesterase type 5 inhibitors may improve clinical symptoms and digital blood flow in patients with RD.
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