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Title: Mode of action of triethylenetetramine dihydrochloride on copper metabolism in Wilson's disease. Author: Siegemund R, Lössner J, Günther K, Kühn HJ, Bachmann H. Journal: Acta Neurol Scand; 1991 Jun; 83(6):364-6. PubMed ID: 1887758. Abstract: The drug of choice for the initial treatment of "decoppering" in Wilson's disease, an inherited disorder of copper metabolism, is the chelating agent D-penicillamine. In the case of harmful side-effects an alternative drug is triethylenetetramine dihydrocholoride (trien or trientine). Using the 24-h-urine excretion of copper and the oral copper loading test with copper-64, a double function for trien was found: trien increases the urine copper excretion and decreases the intestinal copper absorption respectively.[Abstract] [Full Text] [Related] [New Search]