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Lasofoxifene and Cardiovascular Events in Postmenopausal Women With Osteoporosis
Author(s) -
Kristine E. Ensrud,
Andrea Z. LaCroix,
John R. Thompson,
David D. Thompson,
Richard Eastell,
David M. Reid,
Slobodan Vukičević,
Jane A. Cauley,
Elizabeth BarrettConnor,
Róisín Armstrong,
Francine K. Welty,
Steven R. Cummings
Publication year - 2010
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/circulationaha.109.924571
Subject(s) - medicine , osteoporosis , postmenopausal osteoporosis , postmenopausal women , intensive care medicine , bone mineral
In the Postmenopausal Evaluation and Risk Reduction With Lasofoxifene (PEARL) trial, women assigned to lasofoxifene 0.5 mg/d had a lower risk of major coronary heart disease (CHD) events and stroke, whereas women assigned to lasofoxifene 0.25 mg/d had a lower risk of stroke. Both doses of lasofoxifene increased the risk of venous thromboembolic events. In this report, we provide comprehensive cardiovascular end-point data, including component events comprising the composite end point of major CHD events, and evaluate whether the effect of lasofoxifene 0.5 mg/d is consistent across different categories of CHD risk.

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