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Cancer Epidemiology Biomarkers & Prevention 17, 680, March 1, 2008. doi: 10.1158/1055-9965.EPI-07-2739
© 2008 American Association for Cancer Research
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Nonsteroidal Anti-inflammatory Drug Use and Serum Total Estradiol in Postmenopausal Women

Alana G. Hudson1, Gretchen L. Gierach5, Francesmary Modugno1, Jennifer Simpson1, John W. Wilson2, Rhobert W. Evans1, Victor G. Vogel3,4 and Joel L. Weissfeld1,4

Departments of 1 Epidemiology and 2 Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh; 3 Department of Medicine, University of Pittsburgh School of Medicine; 4 University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania and 5 Cancer Prevention Fellowship Program, Office of Preventive Oncology, National Cancer Institute, NIH, Bethesda, Maryland

Requests for reprints: Alana G. Hudson, 516A Parran Hall, 130 DeSoto Street, Pittsburgh, PA 15261. Phone: 412-624-1913; Fax: 412-624-9326. E-mail: alg33{at}pitt.edu


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
Laboratory and epidemiologic evidence suggest that nonsteroidal anti-inflammatory drug (NSAID) use may be inversely related to the risk of breast cancer; however, the mechanism by which NSAIDs may protect against the development of this disease is uncertain. The objective of this observational study was to assess the relationship between current NSAID use and endogenous estradiol levels, an established breast cancer risk factor. To evaluate this aim, we conducted a cross-sectional investigation among 260 postmenopausal women who were not recently exposed to exogenous hormones. Information on current NSAID use (aspirin, cyclooxygenase-2 inhibitors, and other NSAIDs combined) was collected using a questionnaire at the time of blood draw. Estradiol was quantified in serum by radioimmunoassay. General linear models were used to evaluate the association between NSAID use and serum total estradiol. The age-adjusted and body mass index–adjusted geometric mean serum estradiol concentration among NSAID users (n = 124) was significantly lower than nonusers of NSAIDs (n = 136; 17.8 versus 21.3 pmol/L; P = 0.03). Further adjustment for additional potential confounding factors did not substantially alter estimates (17.7 versus 21.2 pmol/L; P = 0.03). To our knowledge, this report is the first to examine the relationship between NSAID use and serum estradiol in postmenopausal women. These cross-sectional findings suggest that NSAID use may be associated with lower circulating estradiol levels, potentially representing one mechanism through which NSAIDs exert protective effects on breast cancer. (Cancer Epidemiol Biomarkers Prev 2008;17(3):680–7)


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
Although breast cancer is a major public health problem, little is known about preventing this disease. Experimental studies have reported a protective effect of nonsteroidal anti-inflammatory drugs (NSAIDs), such as aspirin and ibuprofen, against mammary carcinogenesis (1-3), and accumulating evidence from both case-control and cohort studies suggests that use of NSAIDs may be associated with a modest decreased risk of breast cancer in women (4-10). However, findings are mixed (11-17). Clarifying the association between NSAID use and the development of breast cancer is potentially of great importance clinically. NSAIDs are widely used, readily available, and inexpensive agents. If they were shown to be chemopreventive, they could have a substantial effect on public health.

Although the mechanisms by which NSAIDs may protect against breast cancer are not fully understood, data suggest that the protective effect may be attributed in part to the ability of NSAIDs to decrease the formation of prostaglandin E2 (PGE2) by blocking cyclooxygenase (COX)-1 and/or COX-2 activity. One possible mechanism by which the COX/PGE2 cascade promotes breast cancer is via increasing estrogen production, as exposure to endogenous estrogens has been shown to play a causal role in the development of some breast cancers (18).

PGE2 up-regulates aromatase activity (19), the enzyme that converts androgens to estrogens, leading to increased estrogen synthesis. In postmenopausal women, aromatatic conversion of androgens is the primary source of circulating estrogens, and suppression of this enzyme has been shown to have a profound effect on both circulating estrogen levels (20) and breast cancer recurrence (21). Recently, dose-dependent decreases in aromatase activity were observed in breast cancer cells following treatment with NSAIDs, a COX-1 selective inhibitor, and COX-2 selective inhibitors (22). Therefore, NSAIDs may offer protection against breast cancer by reducing a woman's exposure to estrogen via the inhibition of aromatase activity. Indeed, laboratory results have shown that estradiol production is decreased in breast cells that are exposed to the selective COX-2 inhibitor celecoxib (23).

Although the above-mentioned pathway through which NSAIDs may decrease the development of breast cancer has been highlighted previously (24, 25), the association between NSAID use and circulating estradiol in women is currently unknown. Therefore, in this cross-sectional investigation, we asked whether differences in serum estradiol levels could be observed between self-reported NSAID users and nonusers in a population of postmenopausal women not taking menopausal hormone therapy.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
Study Population
We used data from controls drawn from the Mammograms and Masses Study (MAMS), a case-control study of estrogen metabolites, mammographic breast density, and breast cancer risk. Details of the study methodologies have been presented elsewhere (26). In brief, 869 cancer-free women and 264 recently diagnosed breast cancer cases were recruited into the MAMS through the Magee-Womens Hospital Mammographic Screening and Diagnostic Imaging Program in the greater Pittsburgh area between September 2001 and May 2005. Women who were ages ≥18 years, who reported no previous personal history of cancer, with the exception of nonmelanoma skin cancer, and who could provide written informed consent were eligible for study enrollment. Participants in the MAMS include (a) breast cancer cases who were recruited from the Magee-Womens Surgical Clinic for an initial evaluation after newly diagnosed primary breast cancer (n = 264), (b) controls who were undergoing outpatient needle breast biopsy through the Breast Biopsy Service at Magee-Womens Hospital but who were not subsequently diagnosed with breast cancer (n = 313), (c) "healthy" controls who received screening mammography through Magee-Womens Hospital or through Pittsburgh Magee Womancare Centers (n = 538), and (d) an additional 18 participants whose blood was dedicated solely to an ancillary study of intraindividual cytokine and hormone level reproducibility. To increase recruitment of the "healthy" control group, study flyers were attached to screened negative mammogram reports mailed to patients between November 2003 and April 2005. The MAMS is approved by the University of Pittsburgh's Institutional Review Board and all participants provided written informed consent at the time of study entry.

Subsample Selection
Participants were selected for the present study if they met the following eligibility criteria: (a) healthy controls recruited only via study flyers through Magee-Womens Hospital or through Pittsburgh Magee Womancare Centers (n = 453), because these participants completed a self-administered questionnaire on the day of blood draw; (b) postmenopausal, defined as having no menstrual bleeding during the year before enrollment, having undergone a bilateral oophorectomy, or having a hysterectomy without bilateral oophorectomy and ages ≥50 years. We measured follicle-stimulating hormone for women ages <55 years at blood draw who had a hysterectomy without bilateral oophorectomy (n = 5); all five participants had follicle-stimulating hormone levels above 40 mIU/mL (range, 49.1-185.2), consistent with follicle-stimulating hormone elevation in the postmenopausal range (27); (c) did not use hormone therapy within 3 months of enrollment; and (d) did not report using vaginal estrogen creams, oral contraceptives, selective estrogen receptor modulators, or corticosteroids on the day of blood draw. Ninety-eight premenopausal women, 55 postmenopausal women using hormone therapy, 24 women using selective estrogen receptor modulators, 5 participants on corticosteroids, and 1 participant later found to have a personal history of breast cancer were excluded from the study. Two hundred and seventy participants met the above-mentioned criteria.

Covariate Information
A standardized, self-administered questionnaire was used to gather exposure information. Participants in the subsample completed the questionnaire at study enrollment on the day of blood draw. Information collected included demographic data, current use of medication and supplements, reproductive history, family medical history, past exogenous hormone use, and lifestyle factors, such as smoking status and alcohol intake. Alcohol use (g/d) in the past year was calculated as reported previously (28). Age at onset of menopause was defined according to the methods formerly described by the Women's Health Initiative (29), where age at menopause corresponded to the age of a woman's last natural menstrual bleeding, bilateral oophorectomy, or age a woman began using hormone therapy. For a hysterectomized woman without a bilateral oophorectomy, age at menopause was the earliest age at which she began using hormone therapy or first had menopausal symptoms. If neither occurred and her age at hysterectomy was ≥50 years, then age at menopause was her age at hysterectomy. Age at menopause was undeterminable in seven participants. Years since menopause were calculated by subtracting the age at menopause from the age at enrollment.

Assessment of NSAID Use
The primary exposure variable "current NSAID use" was collected on the day of blood draw. On the self-administered questionnaire, participants were asked to report all prescribed and over-the-counter medications that were currently being used. The question asked, "Are you CURRENTLY taking any medications (prescription or over-the-counter, including aspirin and ibuprofen)?" If a participant responded affirmatively, she was prompted to "please list them in this table." Dosage data were collected but not analyzed as many participants knew only the number of tablets taken rather than the actual dose. The questionnaire was reviewed for completeness by a trained research nurse (study coordinator), who queried participants if further clarification was needed. Each medication reported in the table was subsequently assigned a code using a therapeutic classification system as indexed in the Nurse Practitioners' Prescribing Reference, which is updated quarterly (30). Participants who listed aspirin, COX-2 inhibitor, or other non-aspirin NSAID use on the questionnaire were considered "current NSAID users." Participants who did not list using a NSAID were considered "current NSAID nonusers." Because acetaminophen is generally reported to be a poor inhibitor of the COX-1/COX-2 enzymes (31) and its mechanism of action has yet to be resolved, we classified acetaminophen users as nonusers of NSAIDs (n = 12) unless they also reported taking a NSAID (n = 6).

Two additional NSAID exposure variables were considered in relation to estradiol levels, a secondary exposure variable and a NSAID variable constructed from the primary and secondary variables. The secondary NSAID exposure variable was from the participant's yes-or-no response to the study phlebotomist's question at blood draw, "Have you taken any aspirin or anti-inflammatory agents in the last 48 h?" No effort was undertaken to determine the specific agent the participant had used. Therefore, this variable is more subjective in that responses were based solely on each individual's perception of what constitutes an anti-inflammatory agent and aspirin. The secondary exposure variable was used in conjunction with the primary NSAID exposure variable to construct a third variable labeled "consistent NSAID use." "Consistent NSAID users" listed on the questionnaire that they were currently taking a medication that was an aspirin, COX-2 inhibitor, or non-aspirin NSAID and also verbally reported that they took an aspirin or other anti-inflammatory agent in the past 48 h. "Consistent NSAID nonusers" did not list using any NSAID nor did they state having taken an aspirin or anti-inflammatory agent in the past 48 h. This latter variable was created as an attempt to reduce potential NSAID use/nonuse misclassification. None of the participants in this analysis were missing any of the NSAID exposure variable data. Exposure data were collected and coded without knowledge of estradiol levels.

Clinical Measures
The study coordinator obtained physical measurements (height and weight) and recorded information on a standardized form. After the participant removed her shoes and heavy clothing, weight was measured at a standing position to the nearest 0.1 kg using a standard balance beam; standing height was measured at full inspiration to the nearest 0.1 cm. All anthropometric measurements were taken twice and were repeated if the first two measurements differed by more than 0.5 cm or 0.5 kg. The mean of the measurements was used in the analysis. Body mass index (BMI) was calculated as weight (kg) divided by the square of height (m2).

Forty milliliters of peripheral nonfasting blood were collected from the participants at study enrollment. All samples were processed on site at the Magee-Womens Hospital Satellite General Clinical Research Center according to standard protocols. After processing, the samples were aliquoted into 1 mL cryovials in which RBC, serum, plasma, and buffy coat were separated. Samples were stored at or below -70°C before laboratory analyses.

Laboratory Analyses
Serum samples were used for the quantification of total estradiol (sex hormone binding globulin and albumin-bound plus unbound estradiol) and were assayed at the Royal Marsden Hospital in England. Estradiol concentrations were measured by RIA after ether extraction, using a highly specific rabbit antiserum raised against an estradiol-6-carboxymethyloxime-bovine serum albumin conjugate (EIR) and Third-Generation Estradiol [I125] reagent DSL 39120 (Diagnostic Systems Laboratories; ref. 32). The assay detection limit was 3 pmol/L by calculation from the 95% confidence limits of the zero standard. A random subset of 27 replicate quality-control samples was included to assess reproducibility; the calculated coefficient of variation between duplicates for estradiol was 14.5%. Laboratory personnel were masked to both subject identification and quality-control status.

Statistical Analyses
Wilcoxon's rank-sum test was used to compare selected continuous characteristics between current users and nonusers of NSAIDs and the {chi}2 test or the Fisher's exact test was used to assess differences in categorical variables. The Kruskal-Wallis test was used to test for significant differences in continuous characteristics across estradiol tertile categories. A log transformation was applied to serum estradiol concentrations to obtain homoscedacity and an approximately normal distribution for linear model residuals. One participant was excluded from analyses because total estradiol levels were deemed unreliable by the laboratory. An additional nine participants with outlying estradiol values, defined as >2 SD from the mean of estradiol concentration (>150 pmol/L; range, 150-847 pmol/L), were removed from analyses because such high levels likely indicated that the women were not postmenopausal or did not correctly report current hormone use. Thus, the final analytic subsample included 260 women.

Cohen's {kappa} statistic was calculated as a measure of agreement between the primary and secondary NSAID exposure variables. Differences in mean log estradiol levels between users and nonusers of NSAIDs were tested by the Student's t test. The general linear model approach was performed to calculate multivariable-adjusted estradiol levels and to assess differences in levels between NSAID users and nonusers. Adjusted means and confidence intervals for each NSAID category were quantified using the least-squares mean option of PROC GLM. Two adjusted models are presented. The first model was adjusted for age and BMI, which were deemed necessary covariates given their previously reported associations with both NSAID use (33) and estradiol levels (34, 35). The second model was further adjusted for variables found to be associated with NSAID use or estradiol levels within the study population (univariate association P < 0.15). The final multivariable model was adjusted for age (continuous), BMI (continuous), years since menopause (continuous), race (White versus non-White), and regular alcohol intake in the past year (none, <12 g/d, ≥12 g/d, entered as an indicator variable). Additional adjustment for family history of breast cancer, past hormone therapy use, smoking status, sex hormone binding globulin, and various reproductive factors yielded similar results and are not presented. The geometric mean estradiol concentrations were calculated by taking the anti-log of the least-squares means after adjustment. For each model, a plot of the studentized residuals versus the predicted values was examined to check whether the equality of variance assumption was met. A normal probability plot of the residuals was examined to assess normality. Assumptions of normality and homogeneity of variance were met for all models presented. Tests of statistical significance were two tailed, and given the exploratory nature of this work, we reported our results at the P < 0.05 significance level rather than correct for multiple comparisons. All analyses were done using SAS software version 9.1 (SAS Institute).


   Results
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
Characteristics of the study population are shown in Table 1 . The majority of participants (66.9%) were overweight or obese (BMI ≥ 25 kg/m2) and White (93.1%). Overall, 124 (47.7%) participants reported current NSAID use at the time of blood draw (Table 2 ). In this study, 25.0%, 12.3%, and 2.3% participants reported using only aspirin, non-aspirin NSAIDs, and COX-2 selective inhibitors, respectively, whereas 8.1% reported using at least two different types of NSAIDs (data not shown). One hundred forty (53.8%) women reported that they took aspirin or another anti-inflammatory agent within 48 h of blood draw. One hundred (38.5%) participants listed current use of a NSAID on the baseline questionnaire and verbally reported aspirin or anti-inflammatory use within 48 h of blood draw, and 96 (36.9%) reported no use of NSAIDs in both settings. The agreement between the primary and secondary exposure variables was moderate with a {kappa} value of 0.51.


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  		Table 1. Distribution of selected characteristics by NSAID use among 260 postmenopausal women in the MAMS

 

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  		Table 2. Self-reported NSAID use in the MAMS

 
With the exception of race, current NSAID users and nonusers were statistically similar with regard to all other demographic characteristics (Table 1). Current users of NSAIDs were more likely to be White than nonusers (96.8% versus 89.7%; P = 0.03). Demographic differences between users and nonusers for all NSAID exposure variables (primary, secondary, and constructed) were similar, with the exception of BMI. Participants who reported aspirin or anti-inflammatory drug use within the past 48 h and those who were consistent users not greater BMIs than participants who reported no use (data not shown).

The geometric mean serum estradiol concentration for the study population was 19.5 pmol/L, with levels ranging from 3.3 to 140.0 pmol/L. As illustrated in Table 3 , higher serum estradiol levels were associated with increasing BMI (P < 0.0001) and negatively associated with alcohol intake (P = 0.003). Although not statistically significant, it was observed that women with higher circulating estradiol levels were on average fewer years from menopause (P = 0.11). With the exception of alcohol intake, all associations persisted after controlling for BMI (data not shown). The association between alcohol intake and estradiol diminished after controlling for BMI.


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  		Table 3. Distribution of selected characteristics by tertile of serum estradiol concentration among 260 postmenopausal women in the MAMS

 
After adjustment for age and BMI, current NSAID use was significantly inversely associated with serum estradiol concentrations (17.8 versus 21.3 pmol/L; P = 0.03; Table 4 ), with ~16.4% lower levels in users than nonusers of NSAIDs. The age- and BMI-adjusted association between use of the secondary NSAID exposure variable (aspirin or anti-inflammatory agent in the past 48 h) and estradiol was suggestive of an inverse effect, but this finding was not statistically significant (18.5 versus 20.9 pmol/L; P = 0.14). A slightly stronger association between NSAID use and estradiol levels was observed when comparing consistent users with consistent nonusers (17.5 versus 21.5 pmol/L; P = 0.03). Further adjustment for race, alcohol intake, and years menopausal only slightly increased the strength of association observed in the age- and BMI-adjusted analyses.


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  		Table 4. Unadjusted and adjusted geometric mean (95% CI) estradiol concentrations according to categories of NSAID use

 
Figure 1 presents the adjusted geometric mean serum estradiol concentration by subcategory of NSAID use as defined by the cross-tabulation of the primary and secondary NSAID exposure variables. Three categories were defined, the two concordant groups (that is, "No NSAIDs on medication list/No NSAIDs verbally" and "Yes NSAIDs on medication list/Yes NSAIDs verbally") remained as separate exposure categories, whereas the two discordant groups (that is, "No NSAIDs on medication list/Yes NSAIDs verbally" and "Yes NSAIDs on medication list/No NSAIDs verbally") were collapsed into a single category. The three groups had significantly different adjusted mean estradiol levels (Ptrend = 0.02). Mean estradiol was lowest for participants who reported NSAID use for both measures and highest for participants who did not report use for either measure.


Figure 1
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  		Figure 1. Adjusted geometric mean (95% CI) of estradiol according to self-reported NSAID use. Serum total estradiol was adjusted for age at blood draw, BMI, race, years menopausal, and current alcohol intake in a general linear model (n = 7 missing data). No/No = Participant's current medication list did not indicate use of a NSAID and the participant verbally responded that she did not consume an aspirin or anti-inflammatory agent within 48 h of blood draw. No/Yes = Participant's current medication list did not indicate use of a NSAID but participant verbally responded that she consumed an aspirin or anti-inflammatory agent within 48 h of blood draw. Yes/No = Participant's current medication list indicated use of a NSAID but the participant verbally responded that she did not consume an aspirin or anti-inflammatory agent within 48 h of blood draw. Yes/Yes = Participant's current medication list indicated use of a NSAID and the participant verbally responded that she consumed an aspirin or anti-inflammatory agent within 48 h of blood draw.

 
To assess the possible effects of acetaminophen use on the findings, all analyses were repeated, excluding acetaminophen users from the NSAID nonuser groups. Results did not differ substantially (data not shown). We also assessed unadjusted and adjusted relationships between all NSAID exposure variables and log-transformed sex hormone binding globulin, but no statistically significant relationships were observed (data not shown).


   Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
In this cross-sectional investigation, we observed lower circulating estradiol levels among postmenopausal women reporting NSAID use. Specifically, we observed ~16% lower estradiol levels among current users than nonusers. Decreased estradiol levels were consistent regardless of how NSAID use was assessed (that is, self-reported current NSAID use on questionnaire, verbal reporting of use in past 48 h, and the agreement between these two variables). Further, the strength of association was slightly stronger when comparing participants who reported NSAID use at both the time of blood draw and within 48 h of blood draw to those who reported no use of NSAIDs for both measures. Associations were independent of age, BMI, and other potential confounding variables. As elevated serum estradiol levels have been linked to breast cancer risk, these results provide support to the growing body of evidence linking NSAID use to decreased breast cancer incidence.

Although findings in the literature are not completely consistent, results of several epidemiologic studies suggest that use of NSAIDs may reduce the risk of breast cancer (reviewed in ref. 36). The inconsistent findings across studies may be explained in part by differences in the definition of NSAID use, dosage and frequency data, and NSAID assessment periods. Notably, some studies suggest the decreased risk is stronger among estrogen receptor–positive breast cancers (37, 38) and, if true, would strengthen the hypothesis of an estrogen modulatory effect by NSAIDs. However, this relationship is not consistently observed (10, 39).

The reduced risk of breast cancer observed among NSAID users in epidemiologic studies may in part be mediated through the favorable effects of NSAIDs on PGE2 production. Decreased PGE2 synthesis may result in suppressed estradiol production in postmenopausal women and subsequently reduced breast cancer risk. In accordance with this biological paradigm, we observed that postmenopausal participants reporting NSAID use had lower estradiol levels. Therefore, this study adds credence to the epidemiologic data illustrating a protective effect between NSAID use and breast cancer incidence. As NSAID use is modifiable, a chemoprotective action attributed to its use could have a considerable public health effect. However, the risk-to-benefit ratio would need to be considered because NSAIDs have potentially serious side effects (40, 41).

The present study has limitations that deserve attention and that should be considered when evaluating the study findings. First, as this is a cross-sectional investigation, we cannot ascertain the temporal relationship between NSAID use and serum estradiol and causal conclusions cannot be made. Multiple measurements of NSAID use and serum estradiol may have resulted in more precise estimates. Additional limitations of this study include our inability to assess duration of NSAID use or dosage information, as duration of NSAID use was not collected and dosage data were deemed unreliable. Women exposed to a longer duration of NSAID use or larger doses may have more pronounced effects on circulating estradiol levels than occasional NSAID users (that is, as-needed) or those consuming smaller doses (that is, low-dose aspirin).

The sample size was not large enough to assess the effects of the different NSAIDs (e.g., aspirin and selective COX-2 inhibitors) on estradiol levels. Further, we cannot rule out exposure misclassification. The result of nondifferential misclassification of our exposure variable (NSAID use versus NSAID nonuse) would most likely bias the findings toward the null hypothesis and possibly underestimate the true association between NSAID use and serum estradiol. We attempted to reduce misclassification by repeating analyses limiting the sample to women who consistently reported NSAID use or nonuse. Further, although we attempted to control for potential confounders in the statistical analyses, we cannot rule out the possibility that women who are users of NSAIDs had a factor in common that we did not measure that is related to lower serum estradiol levels. Contrary to our findings, previous studies have observed positive associations between alcohol intake and postmenopausal endogenous estradiol levels; however, our results are consistent with others observing no association between alcohol and estradiol levels after adjustment for BMI (42). Finally, the lack of ethnic diversity and exclusion of premenopausal women in our sample limits the generalizability of the results.

Strengths of our study include the use of standardized instruments, reproducible measures of total estradiol, and the assessment of NSAID use on the same day as blood draw. The last strength is important, because the effect of NSAIDs on the inhibition of COX enzymes and PGE2 synthesis occurs rapidly (43). Finally, the observed distribution of postmenopausal total estradiol levels and the self-reported prevalence of NSAID use in this population were similar to previous reports (35, 44).

In summary, we believe this to be one of the first reports on the association between NSAID use and postmenopausal estradiol levels. We found NSAID users to have significantly lower serum estradiol than nonusers which may account for the protective effect NSAID use has been observed to exhibit on breast cancer development. However, continued research efforts are needed to verify our findings.


   Acknowledgments
 
We thank Glenn Allen, Katherine Reeves, Betty Kotowski, and Elizabeth Wentzel for contributions to MAMS and Dr. Mitch Dowsett and Dr. Elizabeth Folkerd and Ms. Debbie Doody for conducting the serum estradiol assays.


   Footnotes
 
Grant support: NIH grants R25-CA57703, K07-CA80668, R21-CA95113, and P20 CA103730-02; Department of Defense grants DAMD17-02-1-0553 and W81XWH-06-1-0532; and Pennsylvania Department of Health grant P2777693. Additional support was provided by funds received from the NIH/National Center for Research Resources/General Clinical Research Center grant MO1-RR000056.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Received 10/27/07; revised 12/13/07; accepted 12/21/07.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

  1. Carter CA, Ip MM, Ip C. A comparison of the effects of the prostaglandin synthesis inhibitors indomethacin and carprofen on 7,12-dimethylbenz[a]anthracene-induced mammary tumorigenesis in rats fed different amounts of essential fatty acid. Carcinogenesis 1989;10:1369–74.[Abstract/Free Full Text]
  2. Lala PK, Al-Mutter N, Orucevic A. Effects of chronic indomethacin therapy on the development and progression of spontaneous mammary tumors in C3H/HEJ mice. Int J Cancer 1997;73:371–80.[CrossRef][Medline]
  3. Robertson FM, Parrett ML, Joarder FS, et al. Ibuprofen-induced inhibition of cyclooxygenase isoform gene expression and regression of rat mammary carcinomas. Cancer Lett 1998;122:165–75.[CrossRef][Medline]
  4. Schreinemachers DM, Everson RB. Aspirin use and lung, colon, and breast cancer incidence in a prospective study. Epidemiology 1994;5:138–46.[Medline]
  5. Harris RE, Kasbari S, Farrar WB. Prospective study of nonsteroidal anti-inflammatory drugs and breast cancer. Oncol Rep 1999;6:71–2.[Medline]
  6. Sharpe CR, Collet JP, McNutt M, Belzile E, Boivin JF, Hanley JA. Nested case-control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage. Br J Cancer 2000;83:112–20.[CrossRef][Medline]
  7. Johnson TW, Anderson KE, Lazovich D, Folsom AR. Association of aspirin and nonsteroidal anti-inflammatory drug use with breast cancer. Cancer Epidemiol Biomarkers Prev 2002;11:1586–91.[Abstract/Free Full Text]
  8. Harris RE, Chlebowski RT, Jackson RD, et al. Breast cancer and nonsteroidal anti-inflammatory drugs: prospective results from the Women's Health Initiative. Cancer Res 2003;63:6096–101.[Abstract/Free Full Text]
  9. Harris RE, Beebe-Donk J, Alshafie GA. Cancer chemoprevention by cyclooxygenase 2 (COX-2) blockade: results of case control studies. Subcell Biochem 2007;42:193–212.[Medline]
  10. Kirsh VA, Kreiger N, Cotterchio M, Sloan M, Theis B. Nonsteroidal antiinflammatory drug use and breast cancer risk: subgroup findings. Am J Epidemiol 2007;166:709–16.[Abstract/Free Full Text]
  11. Langman MJ, Chen KK, Gilman EA, Lancashire RJ. Effect of anti-inflammatory drugs on the overall risk of common cancer: case control study in general practice research database. Br Med J 2000;320:1642–6.[Abstract/Free Full Text]
  12. Neuget AI, Rosenbert DJ, Ahsan H, et al. Association between coronary heart disease and cancers of the breast, prostate, and colon. Cancer Epidemiol Biomarkers Prev 1998;7:869–73.[Abstract]
  13. Egan KM, Stampfer MJ, Giovannucci E, Rosner BA, Colditz GA. Prospective study of regular aspirin use and the risk of breast cancer. J Natl Cancer Inst 1996;88:988–93.[Abstract/Free Full Text]
  14. Friis S, Sorensen HT, McLaughlin JK, Johnsen SP, Blot WJ, Olsen JH. A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin. Br J Cancer 2003;88:684–8.[CrossRef][Medline]
  15. Sorensen HT, Friis S, Norgard B, et al. Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study. Br J Cancer 2003;88:1687–92.[CrossRef][Medline]
  16. Jacobs EJ, Thun MJ, Connell CJ, et al. Aspirin and other nonsteroidal anti-inflammatory drugs and breast cancer incidence in a large U.S. cohort. Cancer Epidemiol Biomarkers Prev 2005;14:261–4.[Abstract/Free Full Text]
  17. Cook NR, Lee IM, Gaziano JM, et al. Low-dose aspirin in the primary prevention of cancer: the Women's Health Study: a randomized controlled trial. JAMA 2005;294:47–55.[Abstract/Free Full Text]
  18. The Endogenous Hormones Breast Cancer Collaborative Group. Endogenous sex hormones and breast cancer in postmenopausal women: reanalysis of nine prospective studies. J Natl Cancer Inst 2002;94:606–16.[Abstract/Free Full Text]
  19. Zhao Y, Agarwal VR, Mendelson CR, Simpson ER. Estrogen biosynthesis proximal to a breast tumor is stimulated by PGE2 via cyclic AMP, leading to activation of promoter II of the CYP19 (aromatase) gene. Endocrinology 1996;137:5739–42.[Abstract]
  20. Bajetta E, Martinetti A, Zilembo N, et al. Biological activity of anastrozole in postmenopausal patients with advanced breast cancer: effects on estrogens and bone metabolism. Ann Oncol 2002;13:1059–66.[Abstract/Free Full Text]
  21. Baum M, Budza AU, Cuzick J, et al. Anastrozole alone or in combination with tamoxifen versus tamoxifen alone for adjuvant treatment of postmenopausal women with early breast cancer: first results of the ATAC randomized trial. Lancet 2002;359:2131–9.[CrossRef][Medline]
  22. Brueggemeier RW, Su B, Sugimoto Y, Diaz-Cruz ES, Davis DD. Aromatase and COX in breast cancer: enzyme inhibitors and beyond. J Steroid Biochem Mol Biol 2007;106:16–23.[Medline]
  23. Prosperi JR, Robertson FM. Cyclooxygenase-2 directly regulates gene expression of P450 Cyp19 aromatase promoter regions pII, pI.3 and pI.7 and estradiol production in human breast tumor cells. Prostaglandins Other Lipid Mediat 2006;81:55–70.[CrossRef][Medline]
  24. Diaz-Cruz ES, Brueggemeier RW. Interrelationships between cyclooxygenases and aromatase: unraveling the relevance of cyclooxygenase inhibitors in breast cancer. Anticancer Agents Med Chem 2006;6:221–32.[Medline]
  25. DuBois RN. Aspirin and breast cancer prevention: the estrogen connection. JAMA 2004;291:2488–9.[Free Full Text]
  26. Reeves KW, Gierach GL, Modugno F. Recreational physical activity and mammographic breast density characteristics. Cancer Epidemiol Biomarkers Prev 2007;16:934–42.[Abstract/Free Full Text]
  27. Randolph JF, Jr., Crawford S, Dennerstein L, et al. The value of follicle-stimulating hormone concentration and clinical findings as markers of the late menopausal transition. J Clin Endocrinol Metab 2006;91:3034–40.[Abstract/Free Full Text]
  28. Modugno F, Ness RB, Allen GO. Alcohol consumption and the risk of mucinous and nonmucinous epithelial ovarian cancer. Obstet Gynecol 2003;102:1336–43.[CrossRef][Medline]
  29. Chen Z, Maricic M, Bassford TL, et al. Fracture risk among breast cancer survivors: results from the Women's Health Initiative Observational Study. Arch Intern Med 2005;165:552–8.[Abstract/Free Full Text]
  30. Nurse Practitioners' Prescribing Reference. New York (NY): Prescribing Reference, Inc.; 2004.
  31. Chandrasekharan NV, Dai H, Roos KL, et al. COX-3, a cyclooxygenase-1 variant inhibited by acetaminophen and other analgesic/antipyretic drugs: cloning, structure, and expression. Proc Natl Acad Sci U S A 2002;99:13926–31.[Abstract/Free Full Text]
  32. Dowsett M, Goss PE, Powles TJ, et al. Use of the aromatase inhibitor 4-hydroxyandrostenedione in postmenopausal breast cancer: optimization of therapeutic dose and route. Cancer Res 1987;47:1957–61.[Abstract/Free Full Text]
  33. Curhan GC, Bullock AJ, Hankinson SE, Willett WC, Speizer FE, Stampfer MJ. Frequency of use of acetaminophen, nonsteroidal anti-inflammatory drugs, and aspirin in US women. Pharmacoepidemiol Drug Saf 2002;11:687–93.[Medline]
  34. Erman A, Chen-Gal B, van Dijk DJ, et al. Ovarian angiotensin-converting enzyme activity in humans: relationship to estradiol, age, and uterine pathology. J Clin Endocrinol Metab 1996;81:1104–7.[Abstract]
  35. McTiernan A, Wu L, Chen C, et al. Relation of BMI and physical activity to sex hormones in postmenopausal women. Obesity (Silver Spring) 2006;14:1662–77.[CrossRef][Medline]
  36. Harris RE, Beebe-Donk J, Doss H, Burr Doss D. Aspirin, ibuprofen, and other non-steroidal anti-inflammatory drugs in cancer prevention: a critical review of non-selective COX-2 blockade [review]. Oncol Rep 2005;13:559–83.[Medline]
  37. Terry MB, Gammon MD, Zhang FF, et al. Association of frequency and duration of aspirin use and hormone receptor status with breast cancer risk. JAMA 2004;291:2433–40.[Abstract/Free Full Text]
  38. Marshall SF, Bernstein L, Anton-Culver H, et al. Nonsteroidal anti-inflammatory drug use and breast cancer risk by stage and hormone receptor status. J Natl Cancer Inst 2005;97:805–12.[Abstract/Free Full Text]
  39. Zhang Y, Coogan PF, Palmer JR, Strom BL, Rosenberg L. Use of nonsteroidal antiinflammatory drugs and risk of breast cancer: the Case-Control Surveillance Study revisited. Am J Epidemiol 2005;162:165–70.[Abstract/Free Full Text]
  40. Wolfe MM, Lichtenstein DR, Singh G. Gastrointestinal toxicity of nonsteroidal antiinflammatory drugs. N Engl J Med 1999;340:1888–99.[Free Full Text]
  41. Lanas A, Perez-Aisa MA, Feu F, et al. A nationwide study of mortality associated with hospital admission due to severe gastrointestinal events and those associated with nonsteroidal antiinflammatory drug use. Am J Gastroenterol 2005;100:1685–93.[CrossRef][Medline]
  42. Purohit V. Moderate alcohol consumption and estrogen levels in postmenopausal women: a review. Alcohol Clin Exp Res 1998;22:994–7.[CrossRef][Medline]
  43. Giagoudakis G, Markantonis SL. Relationships between the concentrations of prostaglandins and the nonsteroidal antiinflammatory drugs indomethacin, diclofenac, and ibuprofen. Pharmacotherapy 2005;25:18–25.[CrossRef][Medline]
  44. Paulose-Ram R, Hirsch R, Dillon C, Losonczy K, Cooper M, Ostchega Y. Prescription and non-prescription analgesic use among the US adult population: results from the third National Health and Nutrition Examination Survey (NHANES III). Pharmacoepidemiol Drug Saf 2003;12:315–26.[CrossRef][Medline]



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