Authors: Gitte Vrelits Sørensen, Deirdre P Cronin-Fenton, Henrik Toft Sørensen, Sinna Pilgaard Ulrichsen, Lars Pedersen, Timothy L Lash
Categories: Research Article
Source: Breast Cancer Research : BCR
Doi: 10.1186/bcr3106
Authors: Gitte Vrelits Sørensen, Deirdre P Cronin-Fenton, Henrik Toft Sørensen, Sinna Pilgaard Ulrichsen, Lars Pedersen, Timothy L Lash
Glucocorticoids are widely prescribed drugs. In the human body, glucocorticoid is the main stress hormone and controls a variety of physiological and cellular processes, including metabolism and immune response. It belongs to the same steroid superfamily as estrogens, which are known to play a role in breast cancer. However, the effect of glucocorticoid use on the risk of breast cancer is not clear.
We conducted a case-control study using population-based medical databases from Northern Denmark (1.8 million inhabitants) to investigate the association between glucocorticoid prescriptions and breast cancer risk. The study included 9,488 incident breast cancer cases diagnosed between 1994 and 2008 and 94,876 population controls. We estimated the odds ratios (ORs) and 95% confidence intervals (CIs) associating glucocorticoid use with breast cancer occurrence, controlling for prescriptions of postmenopausal hormone replacement therapy, anti-diabetics, immunosuppressive drugs, and hospital diagnosis of obesity, diabetes, chronic pulmonary diseases and autoimmune diseases.
We found no effect on breast cancer risk in ever users (> 2 prescriptions) of any glucocorticoids (adjusted odds ratio (aOR) = 1.0; 95% CI: 0.96, 1.1), systemic glucocorticoids (aOR = 1.0; 95% CI: 0.96, 1.1), or inhaled glucocorticoids (aOR = 1.0; 95% CI: 0.95, 1.1), each compared to never users of any glucocorticoids. Associations for recent use (preceding two years) and former use (more than two years earlier) were near null in all dose categories (low, medium and high number of prescriptions). Intensity of systemic glucocorticoid use (cumulative prednisolone equivalent doses), regardless of duration (< 1, 1 to 5, 5+ years), was also not associated with breast cancer risk.
Overall, our study provides no evidence that glucocorticoid use affects the risk of breast cancer.
Glucocorticoid is an adrenocortical hormone, belonging to the same steroid superfamily as estrogen, which is known to play a role in breast cancer risk [1]. Glucocorticoids mediate most of their effects through the intracellular glucocorticoid receptor (GR), which subsequently modulates downstream gene regulation [2]. The GR is expressed in breast tissue and has been shown to be involved in normal breast development during pregnancy [3]. In the human body, glucocorticoid is the main stress hormone and controls a variety of physiological and cellular processes including metabolism, cell growth, apoptosis, and immune response [2]. Thus, it could potentially play a role in the risk of breast cancer by several mechanisms.
Synthetic glucocorticoids affect immune function and are commonly used as anti-inflammatory and immunosuppressive therapy in diseases such as asthma, chronic obstructive pulmonary disease (COPD), inflammatory bowel disease (IBD), inflammatory arthritis, and other connective tissue disorders [4]. The immune system has a role in preventing cancer development and progression [5,6], so suppression of the immune system may promote tumor development. However, the role of the immune system in cancer is dual and complex, since it may also promote tumor growth [5]. In addition, decreased glucose tolerance, a well-known side effect of glucocorticoids [4], has been suggested to promote mammary carcinogenesis [7-9].
To our knowledge, only one study has previously been published on the relation between glucocorticoid use and breast cancer risk [10]. Our previous study included nearly 33,000 women, ascertained prescriptions for systemic glucocorticoids between 1989 and 1996, ascertained breast cancers until 1998, and recorded a total of 367 breast cancer cases. We reported no association between glucocorticoid prescriptions and breast cancer risk. Due to a relatively short average follow-up time (mean 5.8 years), we were not able to investigate the effect of long-term use. Also, we were only able to control for age as a potential confounder.
A recent review called for further research investigating the potential association between glucocorticoid use and breast cancer risk, criticizing our previous study for lack of clinical details and the possibility of confounding [11]. We, therefore, conducted a large population-based case-control study with prospectively collected prescription data to examine the association between glucocorticoid use and breast cancer risk. In addition to following a larger population over a longer period, we have extended our previous study [10] by incorporating more information on potential confounders, such as parity, age at first birth, use of postmenopausal hormone replacement therapy (HRT), anti-diabetic medicine, immunosuppressive drugs, any history of hospital diagnosed obesity, diabetes, COPD, asthma, rheumatoid arthritis (RA), IBD and other autoimmune diseases (see Additional file 1).
We conducted this population-based case-control study among female residents of the Central and North Denmark Regions between 1 February 1994 and 31 December 2008. Together, these regions represent about one-third of the Danish population (approximately 1.8 million inhabitants). The Danish National Health Service provides tax-supported health-care to all residents of the country and refunds part of the patients' expenditures on most physician-prescribed drugs, including glucocorticoids [12].
All health-related services are registered to individual patients by use of their civil personal registration (CPR) number, assigned to all Danish citizens since 1968 by the Danish Civil Registration System (CRS). This number encodes gender and date of birth [13] and facilitates accurate individual-level linkage between population-based registries.
The Danish regions are served by pharmacies equipped with computerized accounting systems through which data are sent to a regional prescription database hosted by Aarhus University [12], with key information about prescriptions for refundable drugs. Thus, the prescription database includes information on each patient's CPR number; the type and quantity of drug prescribed according to the Anatomical Therapeutic Chemical classification system (ATC), and the date the prescription was filled [12,14]. The Danish regions were until 1 January 2007 divided into counties. Because the different counties started contributing data to the prescription database at different times, they differ with respect to the earliest availability of prescription data, with the earliest being 1989 [12]. To ensure that we had at least minimal prescription data history for each case and their corresponding controls, we only included women who had more than 5 years of prescription history before their index date (as defined below). Women who were resident in the study area for less than five years before index date were excluded from the source population, as were women with any malignant cancer diagnosis before their index dates (except non-melanoma skin cancers).
The sample size was determined by using the Danish Cancer Registry (DCR) to identify all women with an incident diagnosis of breast cancer in the region during the study period (see Additional file 1 for International Classification of Diseases (ICD) codes). The DCR has recorded all incident cancers through 31 December 2008 [15] and has near 100% completeness for breast cancer diagnosis [16]. With this sample size, our study had 90% power to detect an odds ratio of 1.1 or greater.
Controls were identified using the CRS [13,17]. A pool of eligible individuals with the same birth year and county/region of residence as each breast cancer patient was sampled from the general-population among all women alive and free of breast cancer on the date of the matched case's breast cancer diagnosis. This date of diagnosis, therefore, served as the index date for the case and all of the controls matched to the case. Ten individuals from this pool were randomly selected for each case. All eligible controls were included when the risk-set of matched controls included fewer than ten individuals.
The prescription database [12] was used to identify all prescriptions before index date for systemic (oral and injected), inhaled and local-acting glucocorticoids with intestinal anti-inflammatory effect ('local glucocorticoids' hereafter). The following preparations were available and prescribed during the study period (see Additional file 1 for ATC codes): betamethasone, dexamethasone, methylprednisolone, prednisolone, prednisone, triamcinolone, cortisone, hydrocortisone, beclomethason, budesonide, flunisolide, fluticasone, and mometasone.
The prescription database also provided information on use of the following potential confounding drugs before the index date (see Additional file 1 for ATC codes): postmenopausal HRT [18], anti-diabetics [19], and use of immunosuppressive drugs as a marker of immune-related disease.
The Danish National Patient Registry (DNPR) contains information about all non-psychiatric hospital admissions since 1977, and since 1995 also outpatient visits [20]. From the DNPR we retrieved data on hospital diagnoses of the following diseases before the index obesity, diabetes, COPD, asthma, RA, IBD (ulcerative colitis or Crohn's disease), and a list of 'other autoimmune diseases' (see Additional file 1 for the list of diseases and associated ICD codes).
To obtain information about parity and age at first birth we used the CRS [13]. In the CRS, the CPR numbers of parents are linked to their child, as long as the child lived with the parents in 1968 or later. We limited the analysis adjusted for parity and age at first birth to women born later than 1949, for whom the CRS allows reconstruction of childbearing history with better than 95% completeness [21].
We categorized glucocorticoid use as never versus ever use. Ever users were further subdivided into two dose one or two prescriptions or more than two prescriptions. We examined the association of overall glucocorticoid use with breast cancer and then examined the association of systemic and inhaled glucocorticoid use separately. To examine the temporality of glucocorticoid use and the risk of breast cancer, we divided ever use into recent use (only prescriptions within two years of the index date) and former use (prescriptions earlier than two years of the index date). In the group of any glucocorticoid users we further divided the number of prescriptions into low (one or two prescriptions), medium (three to nine) and high (more than nine). We based these cut-offs on the distribution of prescription counts among the controls with more than two prescriptions.
To examine whether breast cancer risk was associated with the intensity and duration of glucocorticoid use, we restricted the analyses to systemic glucocorticoid users and calculated prednisolone equivalent cumulative doses based on the equivalency table in Kelly's *Textbook of Rheumatology *[22] and grouped into the four < 200 mg, 200 to 399 mg, 400 to 999 mg and ≥ 1,000 mg (for calculations see Additional file 2). The duration was defined as the number of days from the date of the first prescription to the date of the last prescription, plus the duration of the last prescription (estimated to be on average 30 days). We divided the duration of glucocorticoid use into short-term (less than one year), medium-term (one to five years), and long-term (more than five years).
The covariates ever use of immunosuppressive drugs, ever use of postmenopausal HRT, COPD, asthma, IBD, obesity, and RA were coded individually as dichotomous variables. Other autoimmune diseases (see Additional file 1) were merged into a dichotomous variable. Since diabetes and metformin use may have counteracting effects on breast cancer risk [19], we coded diabetes and anti-diabetic medicine use as a categorical variable with three possible no diabetes or use of anti-diabetic medicine, diabetes or use of anti-diabetic medicine with ever use of metformin, and diabetes or use of anti-diabetic medicine without ever use of metformin.
We computed the frequency and proportion of cases and controls within categories of demographic variables and covariates.
In all analyses, we used never use of any glucocorticoids as the reference group. For the use of any glucocorticoids, systemic glucocorticoids, and inhaled glucocorticoids, we stratified by all covariates and calculated crude and stratum-specific odds ratios (ORs) to evaluate potential confounding and effect measure modification. We used conditional logistic regression analysis to compute crude and adjusted ORs (aORs) and their associated confidence intervals (95% CI), with simultaneous adjustment for the use of postmenopausal HRT, immunosuppressive drugs, hospital diagnosed obesity, diabetes (plus/minus a history of metformin use), COPD, asthma, IBD, RA and 'other autoimmune disease.' Since we used risk set sampling of controls, the ORs are unbiased estimates of the corresponding incidence rate ratio in the underlying population [23]. We report estimates of association stratified by age categories (< 45, 45 to 55 and > 55, as estimated ranges for pre-, peri- and post-menopausal status). In the group of women < 45, we were able to make additional adjustment for parity and age at first birth, using the combined variable (see Table 1).
We used Stata 11.0 (StataCorp LP, College Station, TX, USA) and SAS 9.2 (SAS Institute Inc., Cary, NC, USA) for the data analyses. This study was approved by the Danish Data Protection Agency (reference #2004-41-4693). According to Danish law, registry-based studies such as this one do not require further approval by an ethical review board or informed consent by the members of the study population.
We identified 9,488 breast cancer cases and 94,876 population controls. Median age at the index date was 62.1 years. Characteristics of cases and controls are shown in Table 1. As expected, a higher proportion of cases than controls had ever used postmenopausal HRT by their index date (24% versus 19%). In the subgroup of women born later than 1949 (*n *= 31,130), a lower proportion of cases than controls had a first birth before age 25 (45% versus 49%) and had three or more children (25% versus 27%). In all other characteristics, there were no important differences between cases and controls.
We found no effect on breast cancer risk in ever users (> 2 prescriptions) of any glucocorticoids compared to never users (aOR = 1.0; 95% CI: 0.96, 1.1). The association among former users with a high number of prescriptions (> 9) was null (aOR = 1.0; 95% CI: 0.93, 1.1). In addition, among recent users who only had prescriptions within the two years before their index date, we found null associations. Restricting the analysis to systemic or inhaled glucocorticoid use also showed no associations. Ever use (> 2 prescriptions) of systemic (aOR = 1.0; 95% CI: 0.96, 1.1) or inhaled glucocorticoids (aOR = 1.0; 95% CI: 0.95, 1.1), each compared to never use of any glucocorticoids, were both null (Table 2). Intensity of systemic glucocorticoid use (cumulative prednisolone equivalent doses), regardless of duration (< 1, 1 to 5, 5+ years), showed no pattern of association (Table 3). Stratifying into estimates of pre-, peri-, and post-menopausal status by age group also did not show any pattern of association. In the subgroups of women < 45 years old (Table 4) and all women born later than 1949 (*n *= 31,130), additional adjustment for parity and age at first birth did not change our overall estimates of null association. In the latter group, the aOR for > 2 glucocorticoid prescriptions ever, compared to never, was 1.0 (95% CI 0.88, 1.2).
Overall, this population-based case-control study of more than 100,000 women provided no evidence of an association between glucocorticoid use and breast cancer risk. The null association was consistent when dividing the use of glucocorticoids into recent and former use, intensity and duration of use, and also consistent with our previous study [10]. Our results answer the need for research on the role of glucocorticoids in breast cancer risk, which has not been well studied [11].
Our study has several strengths. The uniformly organized Danish healthcare system with complete hospital history and access to appropriate population controls allows a population-based case-control design. The use of population-based prescription registries, with a completeness approaching 100% [12,14] ensured unbiased assessment of exposure data preceding breast cancer diagnosis and the registry source eliminated recall bias. In all our analyses, we included only persons with at least 5 years of prescription history, thus potential bias due to left censoring of exposure information was reduced compared with the earlier study [10].
Our study also had limitations. We had no data regarding adherence with prescriptions, potentially leading to non-differential misclassification of some non-users as users. However, our drug exposure assessment was based on redeemed prescriptions, and because patients had to pay a proportion of the drug cost, our estimates are likely to reflect actual use, especially in women with more than two prescriptions. In support of this expectation, a validation study on postmenopausal HRT by Danish women showed good agreement between self-reported use and prescription data in the registry [24]. We also had no information on body mass index, alcohol consumption or family history of breast cancer, and other factors that may impact the risk of breast cancer [25]. To confound our results substantially they would also have to be related to glucocorticoid use conditional on adjustment for the measured covariates, which we have no reason to expect.
A more important limitation might be our inability to examine the impact of glucocorticoid use on breast cancer risk by specific breast cancer characteristics such as hormone receptor status. Studies have addressed the possibility of cross-talk between estrogen receptors and glucocorticoid receptors in mammary epithelial cells [26] and recently *in vivo *studies have suggested that glucocorticoids may stimulate the expression of the sulfotransferase SULT1E1, which plays a role in deactivating estrogen [27]. Thus, estrogen levels and estrogen receptor expression might well impact the action of glucocorticoids. Glucocorticoid response may also vary due to glucocorticoid receptor gene polymorphisms. The increased risk of squamous cell carcinoma in glucocorticoid users is more pronounced in the presence of the allele with the common genetic variant in the glucocorticoid receptor gene, compared with the homozygote wild types [28] but we were unable to evaluate this gene-drug interaction. Finally, glucocorticoids increase the expression of insulin-like growth factor-1 (IGF-1) receptors [29] and the levels of circulating IGF-1 [30]. IGF-1 receptor expression patterns in epithelial cells of normal breast tissue biopsies were associated with an increased risk of subsequent breast cancer [31] and a meta-analysis from 2010 concluded that circulating IGF-1 levels are positively related to estrogen-receptor-positive breast tumors, regardless of menopausal status [32]. Our study did not, however, have measurements of IGF-1 receptor or circulating IGF-1 available for analyses.
There are several mechanisms by which glucocorticoid prescriptions might affect breast cancer risk in subpopulations defined by molecular subcharacteristics. Evaluations of these associations would require a study with detailed biological data. Overall, however, our results provide no evidence of an increased risk of breast cancer in glucocorticoid users compared with never users.
aOR: adjusted odds ratio; ATC: Anatomical Therapeutic Chemical; CI: confidence interval; COPD: chronic obstructive pulmonary disease; CPR civil personal registration number; CRS: Civil Registration System; DCR: Danish Cancer Registry; DNPR: Danish National Patient Registry; GR: glucocorticoid receptor; IBD: inflammatory bowel disease; ICD: International Classification of Diseases; IGF-1: insulin-like growth factor-1; HRT: hormone replacement therapy; OR: odds ratio; RA: rheumatoid arthritis.
None of the authors received any fees, honoraria, grants or consultancies that would constitute a conflict of interest with the current study. The Department of Clinical Epidemiology, Aarhus University Hospital, receives funding for other studies from pharmaceutical companies in the form of research grants to (and administered by) Aarhus University. None of these studies have any relation to the present study.
GVS designed the study, performed statistical analysis, interpreted the data, and drafted the manuscript. TLL conceived of the study and its design, provided epidemiological expertise, contributed to the interpretation of the data and critically revised the manuscript and contributed to major revisions. HTS and DCF conceived the study, and participated in its design, interpretation of data, and critically revised the manuscript. LP and SPU provided statistical expertise, analyzed the data, contributed to the interpretation of the data and critically reviewed the manuscript. All authors have read and approved the manuscript for publication.