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Increased Mortality With Long-Term Platelet Glycoprotein IIb/IIIa Antagonists: An Explanation?
Author(s) -
Jos Vermylen,
Marc Hoylaerts,
Jef Arnout
Publication year - 2001
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circ.104.20.e109
Subject(s) - medicine , platelet , term (time) , platelet membrane glycoprotein , glycoprotein , pharmacology , biochemistry , physics , chemistry , quantum mechanics
To the Editor:The increased mortality during long-term administration of oral glycoprotein IIb/IIIa antagonists as secondary prevention reported by Chew et al1 is indeed unexpected and perplexing. A possible hint may be given by the recent in vitro observations of Li et al.2 When platelets are activated with collagen in hirudinized whole blood in the presence of a glycoprotein IIb/IIIa antagonist, more platelet-leukocyte conjugates are formed. Conjugate formation is a consequence of P-selectin expression on the activated platelets and interaction of P-selectin with P-selectin glycoprotein ligand-1 and CD15 on leukocytes. Presumably because of the inhibition of platelet-platelet aggregation by glycoprotein IIb/IIIa antagonists, more activated platelets are …

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