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  Vol. 162 No. 4, February 25, 2002 TABLE OF CONTENTS
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Aspirin, Postmenopausal Hormones, and C-Reactive Protein

Arch Intern Med. 2002;162:480-481.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Most oral preparations of postmenopausal hormones (PMHs) increase levels of C-reactive protein (C-RP), a sensitive marker of inflammation, within about 4 weeks of initiation of therapy.1-3 This increase is observed in patients who are given either estrogen alone or estrogen in combination with a progestin, which has now become the most common preparation of PMH used. These data derive from observational studies and randomized trials of apparently healthy women suggesting that the increase is not attributable to atherosclerotic burden or other risk factors for cardiovascular disease or to other inflammatory disorders.4

Elevated levels of C-RP predict increased risks of subsequent cardiovascular events in both men and women.5-6 The mechanisms by which this occurs are not clear. C-reactive protein may be a marker for predicting an increased risk of events or may have some direct proinflammatory and atherogenic properties. It is present in atherosclerotic plaques. Furthermore, recent data suggest that C-RP . . . [Full Text of this Article]



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Aspirin Use, Dose, and Clinical Outcomes in Postmenopausal Women With Stable Cardiovascular Disease: The Women's Health Initiative Observational Study
Berger et al.
Circ Cardiovasc Qual Outcomes 2009;2:78-87.
ABSTRACT | FULL TEXT  

Endogenous Salicylates, Aspirin, and Inflammation
Paterson and Lawrence
Arch Intern Med 2002;162:1531-1532.
FULL TEXT  





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