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Associations of aspirin and other anti-inflammatory medications with breast cancer risk by the status of COX-2 expression.
Yaghjyan, Lusine; Eliassen, A Heather; Colditz, Graham; Rosner, Bernard; Schedin, Pepper; Wijayabahu, Akemi; Tamimi, Rulla M.
Afiliação
  • Yaghjyan L; Department of Epidemiology, College of Public Health and Health Professions and College of Medicine, University of Florida, 2004 Mowry Rd, Gainesville, FL, 32610, USA. lyaghjyan@ufl.edu.
  • Eliassen AH; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Colditz G; Department of Surgery, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
  • Rosner B; Institute for Public Health, Washington University in St. Louis, St. Louis, MO, USA.
  • Schedin P; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Wijayabahu A; Oregon Health and Science University, Portland, OR, USA.
  • Tamimi RM; Department of Epidemiology, College of Public Health and Health Professions and College of Medicine, University of Florida, 2004 Mowry Rd, Gainesville, FL, 32610, USA.
Breast Cancer Res ; 24(1): 89, 2022 12 09.
Article em En | MEDLINE | ID: mdl-36494710
ABSTRACT

BACKGROUND:

We investigated the associations of aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) with breast cancer risk by the status of COX-2 protein expression.

METHODS:

This study included 421 cases and 3,166 controls from a nested case-control study within the Nurses' Health Study (NHS) and Nurses' Health Study II (NHSII) cohorts. Information on medication use was first collected in 1980 (NHS) and 1989 (NHSII) and was updated biennially. Medication use was defined as none, past or current; average cumulative dose and frequency were calculated for all past or current users using data collected from all biannual questionnaires preceding the reference date. Immunochemistry for COX-2 expression was performed using commercial antibody (Cayman Chemical and Thermo Fisher Scientific). We used polychotomous logistic regression to quantify associations of aspirin and NSAIDs with the risk of COX2+ and COX2- breast cancer tumors, while adjusting for known breast cancer risk factors. All tests of statistical significance were two-sided.

RESULTS:

In multivariate analysis, we found no differences in associations of the aspirin exposures and NSAIDs with breast cancer risk by COX2 expression status. In stratified analyses by COX2 status, significant associations of these medications with breast cancer risk were observed for dosage of aspirin among current users in COX2- tumors (OR for > 5 tablets per week vs. none 1.71, 95% CI 1.01-2.88, p-trend 0.04). Regular aspirin use was marginally associated with the risk of COX2- tumors (p-trend = 0.06).

CONCLUSIONS:

Our findings suggested no differences in associations of aspirin and other NSAIDs with COX2+ and COX2- tumors.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Aspirina Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Aspirina Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article