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PMID: 17389287 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Long-term aspirin use and mortality in women.

Archives of internal medicine ·Vol. 167 ·No. 6 ·2007-03-26 ·Pages 562-72

Chan AT, Manson JE, Feskanich D, Stampfer MJ, Colditz GA, Fuchs CS

Abstract

The influence of long-term use of aspirin on total mortality in women remains uncertain. We conducted a prospective, nested, case-control study of 79 439 women enrolled in the Nurses' Health Study who had no history of cardiovascular disease or cancer. Women provided data on medication use biennially since 1980. We assessed relative risk (RR) of death according to aspirin use before diagnosis of incident cardiovascular disease or cancer and during the corresponding period for each control subject. During 24 years, we documented 9477 deaths from all causes. In women who reported current aspirin use, the multivariate RR of death from all causes was 0.75 (95% confidence interval, 0.71-0.81) compared with women who never used aspirin regularly. The risk reduction was more apparent for death from cardiovascular disease (RR, 0.62; 95% confidence interval, 0.55-0.71) than for death from cancer (RR, 0.88; 95% confidence interval, 0.81-0.96). Use of aspirin for 1 to 5 years was associated with significant reductions in cardiovascular mortality (RR, 0.75; 95% confidence interval, 0.61-0.92). In contrast, a significant reduction in risk of cancer deaths was not observed until after 10 years of aspirin use (P(linear trend) = .005). The benefit associated with aspirin was confined to low and moderate doses and was significantly greater in older participants (P(interaction)< .001) and those with more cardiac risk factors (P(interaction) = .02). In women, low to moderate doses of aspirin are associated with significantly lower risk of all-cause mortality, particularly in older women and those with cardiac risk factors. A significant benefit is evident within 5 years for cardiovascular disease, whereas a modest benefit for cancer is not apparent until after 10 years of use.

MeSH Terms
Adult Age Factors Aspirin/therapeutic use Cardiovascular Diseases/mortality Case-Control Studies Cause of Death Female Follow-Up Studies Humans Middle Aged Multivariate Analysis Neoplasms/mortality Platelet Aggregation Inhibitors/therapeutic use Prospective Studies Risk Risk Factors United States/epidemiology
Chemicals
Platelet Aggregation Inhibitors Aspirin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Chan Andrew T
Gastrointestinal Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA 0214, USA.
Manson JoAnn E
Feskanich Diane
Stampfer Meir J
Colditz Graham A
Fuchs Charles S
Article Info
Journal
Archives of internal medicine
Abbr.
Arch Intern Med
ISSN
0003-9926
Published
2007-03-26
Pages
562-72
Language
English
Region
United States
NLM ID
0372440
Subset
IM
Grants
NCI NIH HHS · CA 107412 · United States
NCI NIH HHS · CA 87969 · United States
NHLBI NIH HHS · HL 34594 · United States
Corrections
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