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La salud de la mujer / Woman's Health

29 Mayo 2007

La aspirina reduce a largo plazo la mortalidad femenina

La aspirina en pequeñas dosis reduce todas las causas de mortalidad en la mujer, especialmente entre las mayores y las que tienen riesgo cardiovascular.

PhotoEl beneficio de la aspirina, reduciendo la mortalidad, se debe sobre todo a la reducción de las muerte de origen cardiovascular. Sin embargo, sobre la base de estudios anteriores, las mujeres que no tienen riesgo cardiovascular no deben iniciar tratamiento con aspirina para prevenir la muerte. Los estudios previos habían demostrado la reducción de muertes del corazón y por cáncer. Por eso, se pone en duda que pueda reducir todas las causas de muerte.

El estudio que demuestra la reducción de mortalidad femenina por aspirina se refiere al Nurses' Health Study que incluye 79.439 mujeres. Todas las mujeres estaban libres de enfermedades de corazón y de cáncer. En 24 años murieron 9.477 mujeres; el uso de aspirina produjo reducción del 25% en la mortalidad. Este beneficio se relacionó 30% con menos riesgo cardiovascular y 12% por menos tasa de cáncer. Para prevenir el riesgo cardiovascular hay que tomar aspirina por lo menos un año, y para reducir cáncer al menos 10 años.


Arch Intern Med. 2007 Mar 26;167(6):562-72.Click here to read

Comment in: Arch Intern Med. 2007 Mar 26;167(6):535-6.

Long-term aspirin use and mortality in women.
Chan AT, Manson JE, Feskanich D, Stampfer MJ, Colditz GA, Fuchs CS. Gastrointestinal Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA 0214, USA.

BACKGROUND: The influence of long-term use of aspirin on total mortality in women remains uncertain. METHODS: 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. RESULTS: 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). CONCLUSIONS: 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.

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