- Research article
- Open Access
- Open Peer Review
Chronic inflammatory diseases, anti-inflammatory medications and risk of prostate cancer: a population-based case-control study
- Kerri Beckmann1, 2Email authorView ORCID ID profile,
- Beth Russell2,
- Debra Josephs2,
- Hans Garmo2, 3,
- Christel Haggstrom4, 5,
- Lars Holmberg2, 5,
- Pär Stattin5,
- Mieke Van Hemelrijck†2, 6 and
- Jan Adolfsson†7
© The Author(s). 2019
- Received: 18 December 2018
- Accepted: 17 June 2019
- Published: 21 June 2019
Whether chronic inflammation increases prostate cancer risk remains unclear. This study investigated whether chronic inflammatory diseases (CID) or anti-inflammatory medication use (AIM) were associated with prostate cancer risk.
Fifty-five thousand nine hundred thirty-seven cases (all prostate cancer, 2007–2012) and 279,618 age-matched controls were selected from the Prostate Cancer Database Sweden. CIDs and AIMs was determined from national patient and drug registers. Associations were investigated using conditional logistic regression, including for disease/drug subtypes and exposure length/dose.
Men with a history of any CID had slightly increased risk of any prostate cancer diagnosis (OR: 1.08; 95%CI: 1.04–1.12) but not ‘unfavourable’ (high-risk or advanced) prostate cancer. Generally, risk of prostate cancer was highest for shorter exposure times. However, a positive association was observed for asthma > 5 years before prostate cancer diagnosis (OR: 1.21; 95%CI: 1.05–1.40). Risk of prostate cancer was increased with prior use of any AIMs (OR: 1.26; 95%CI: 1.24–1.29). A positive trend with increasing cumulative dose was only observed for inhaled glucocorticoids (p < 0.011).
Detection bias most likely explains the elevated risk of prostate cancer with prior history of CIDs or use of AIMs, given the higher risk immediately after first CID event and lack of dose response. However, findings for length of time with asthma and dose of inhaled glucocorticoids suggest that asthma may increase risk of prostate cancer through other pathways.
- Prostate cancer
- Chronic inflammatory disease
- Autoimmune disease
- Anti-inflammatory medication
There is convincing evidence that some specific cancers are associated with chronic inflammatory diseases (CIDs). Examples include inflammatory bowel disease and colon cancer, Helicobacter Pylori infection and gastric cancer, hepatitis B and C infections and hepatocellular carcinoma . Evidence for chronic inflammation as a risk factor for prostate cancer is less clear. Several different lines of evidence suggest that inflammation plays a role in prostate cancer development. For example, a number of putative risk factors for prostate cancer induce prostate inflammation, including heterocyclic amines in highly cooked meat, prostatitis and sexually transmitted diseases (STDs) [2–5]. In addition to localised inflammation, there is evidence suggesting systemic inflammation may also increase prostate cancer risk. High levels of circulating C-reactive protein , a marker of inflammation, and increased Immunoglobulin (Ig) E levels , a marker of atopy, are associated with increased risk of prostate cancer. Increased risk of prostate cancer has been reported among men with asthma or other atopic conditions [7, 8] and among men with autoimmune diseases [9–12], though contradictory findings have also been reported [13–17]. On the other hand, reduced risk of prostate cancer has been reported with exposure to some anti-inflammatory medications (AIMs) used to manage CIDs, though again the evidence is mixed [18–21].
However, previous evidence of positive associations between CIDs/AIMs and prostate cancer may be affected by detection bias, resulting from frequent health service encounters or investigations leading to detection of prostate cancer, especially for men with localised inflammation arising from prostatitis or STDs .
The aim of this study was to investigate the link between chronic inflammation and risk of prostate cancer by examining the association between 1) history of CIDs, and 2) use of AIMs, and prostate cancer incidence, using population-wide registry-based data. Our a priori hypotheses were that risk of prostate cancer would be increased among men with CIDs due to persistent or recurring exposure to inflammatory mediators, while risk would be reduced among men who used AIMs, due to anti-inflammatory properties of these drugs.
Data source and variables
We used data from Prostate Cancer Database Sweden (PCBaSe), a population-wide database linkage between the National Prostate Cancer Registry (NPCR), the National Patient Register (NPR), the National Prescribed Drug Register (from Jan 1, 2006) and the Swedish longitudinal integration database for health insurance and labour market studies (LISA), through Swedish personal identification numbers . In addition to men diagnosed with prostate cancer, PCBaSe also includes disease-free population controls, selected using an incident density sampling approach . The NPCR has near complete coverage (98%) of prostate cancer diagnoses across Sweden since 1988. Information collected in NPCR includes date of diagnosis, age, tumour stage and grade, levels of prostate specific antigen (PSA) at diagnosis, and primary treatment.
We used a case-control design to study the association between CIDs/AIMs and risk of prostate cancer diagnosis. The main outcome of this study was a diagnosis of prostate cancer, recorded in NPCR. All men diagnosed with prostate cancer between Jan 1, 2007 and Dec 31, 2012 were selected as cases. Five population controls, free of prostate cancer at the time of diagnosis of the corresponding index case, matched on year of birth and area of residence, were selected for each case.
The two broad exposures of interest were 1) prior history of CIDs and 2) exposure to AIMs. For the CIDs component, the analytic study population was restricted to men diagnosed from 2007 to 2009 plus controls, due to incomplete data on rare conditions from 2010 onwards. Prior history of CIDs was derived from International classification of diseases, 10th edition (ICD-10) codes recorded in the NPR for any single hospital inpatient or outpatient episode from 1998 onwards. CIDs were classified into the following subcategories: chronic inflammatory and infectious diseases; allergies; and autoimmune diseases (further sub-grouped as auto-antibody negative; auto-antibody positive – systemic; and auto-antibody positive - organ specific diseases). Type 1 diabetes mellitus (T1DM) was excluded from the organ specific autoimmune category given likely misclassification of type 2 diabetes mellitus. Likewise, prostatitis was excluded from the chronic inflammatory diseases category due to likely detection bias from more intensive investigation of the prostate. Both were analysed separately. The full list of included diseases and respective ICD-10 codes is provided in the Additional file 2.
For analysis of AIMs, the whole study population was included. Exposure to selected AIMs was determined through linkage to Sweden’s National Prescribed Drug register, based on Anatomical Therapeutic Chemical (ATC) codes for drugs commonly prescribed for the management of CIDs: Non-aspirin non-steroidal anti-inflammatory drugs (NSAID) (M01A), systemic glucocorticoids (H02AB), inhaled glucocorticoids (R03BA), non-steroidal asthma medications (R03AC, R03CC, R03AK, R03BB, R03DC), immuno-suppressants (L04A), and anti-gout medications (M04A). One previous prescription was considered to be sufficient to be classified as exposed. Data were extracted on class of drug, date of first prescription and cumulative dose before diagnosis. These data were only available from July 1, 2005, onwards. For both CIDs and AIMs, length of exposure and cumulative dose were determined for similar periods for cases and controls, with date of diagnosis of the case being used as the reference date for selected controls.
Charlson comorbidity index  (CCI) was derived from data hospital admission records prior to diagnosis of prostate cancer. Marital status and education level were extracted from LISA, while data on prostate cancer risk categories (grade, clinical stage, and prostate serum antigen (PSA) level at diagnosis) were extracted from NPCR. To determine whether CIDs or AIMs were associated with disease severity at diagnosis we classified men with Prostate cancer according to risk categories. The ‘favourable risk prostate cancer’ group included low and intermediate risk categories (Gleason Score < =7, clinical stage T1–2, PSA ≤ 20, N0/X and M0/X]), while the ‘unfavourable risk’ prostate cancer group included high-risk, regionally-advanced and metastatic disease (Gleason score = 8–10, PSA > 20, N1 or M1). These terms are used below to refer to different risk groupings.
Associations between CIDs/AIMs and prostate cancer risk were examined using multivariable conditional logistic regression. Separate analyses were undertaken for any prior CIDs and any AIMs exposure, as well as each CID and AIM subtype. In all cases the reference group were all men not previously exposed to the specific condition or medication of interest. To assess the potential for detection bias, we examined length of time since first recorded diagnosis of CID (< 12, 12- < 36, 36- < 60, 60+ months) and total cumulative dose for subtypes of AIMs (< 50, 50- < 200, 200- < 500, 500+ daily dose equivalents) prior to prostate cancer diagnosis. Models were adjusted for education level (low< 10 years, middle 10–12 years, high>12 years); marital status (married, not married), and comorbidity (CCI =0, 1, 2, 3+). Wald tests were used to test trends according to categories of exposure for CIDs and cumulative daily dose for AIMs. Separate subgroup analyses were also undertaken restricted to ‘favourable’ and ‘unfavourable’ risk groups and their respective controls.
We also investigated interaction between history of CIDs and major classes of anti-inflammatory medications. For these analyses, interaction terms for CIDs and AIMs subtype were included in regression models for overall risk of prostate cancer, along with other covariates. Differences in log likelihood between models with and without interaction terms were used to determine any statistically significant effect modification in men with CID history.
Finally we undertook a series of sensitivity analyse to examine the robustness of our findings with respect to AIMs and prostate cancer risk. These included 1) altering our definition of AIMs exposure to 2 or more prior prescriptions, 2) restricting the cohort to men diagnosed with prostate cancer from 2010 to 2012 to allow for longer time for AIMs exposure given prescription data were only available from 2006, and 3) excluding cases whose prostate cancer diagnosis was within 12 months of their first prescription.
All statistical analyses were undertaken using Stata v 14.0 (Stata Corporation, College Station, Texas USA). This study was approved by the Research Ethics Board, Umeå University, Sweden.
Characteristics of the study population
n = 55,937
n = 279,618
Age at diagnosis (years)
Charlson Comorbidity Index
Period of diagnosis/inclusion
Chronic inflammatory conditions and prostate cancer risk
Prior history of chronic inflammatory disease (CID) and odds of prostate cancer, overall and by disease categorya
Prior record of chronic inflammatory diseaseb
Controls n = 139,311
Cases n = 27,874
Favourable risk PCa
Unfavourable risk PCa
OR c (95% CI)
OR c (95% CI)
OR c (95% CI)
Any chronic inflammatory /autoimmune disease (excl. Prostatitis and T1DM)
Chronic inflammatory / infectious diseases (excl. Prostatitis)
Allergies (including Asthma)
Autoimmune diseases (any excluding T1DM):
Autoantibody positive - systemic
1.06 (0.89 = 1.27)
Autoantibody positive - organ specific
Autoantibody positive - organ specific (excl. T1DM)
Associations between CIDs and prostate cancer risk groups are also shown in Table 2. For all CIDs combined, and for the inflammatory/infectious diseases and allergies subcategories, risk was only increased for favourable risk prostate cancer. Only history of chronic prostatitis was associated with both favourable (OR: 2.03; 95%CI: 1.63–2.52) and unfavourable risk prostate cancer (OR: 1.56; 95%CI: 1.18–2.07), with the former having the stronger association. The negative association observed for T1DM was evident for both favourable (OR: 0.64; 95%CI: 0.56–0.80) and unfavourable risk prostate cancer (OR: 0.80; 95%CI: 0.71–0.91), with a stronger association for favourable risk prostate cancer.
Time interval from first recorded episode for specific inflammatory disease groups and odds of prostate cancer diagnosis
Time from first hospital episode to diagnosis/inclusion date
12- < 36 months
≥ 36 months
> 60 months
ORa (95% CI)
OR (95% CI)
OR (95% CI)
OR (95% CI)
DISEASE GROUPS (reference: no recorded episode)
Any chronic inflammatory /autoimmune disease (excl. Prostatitis and T1DM)
Chronic inflammatory/infectious diseases (excl. prostatitis)
Allergies (including asthma)
Auto-immune diseases (excluding T1DM)
Antibody positive - systemic
Antibody positive - organ confined (excl. T1DM)
Anti-inflammatory medications and prostate cancer risk
Prior exposure to anti-inflammatory medications and the odds of prostate cancer, overall and by disease categorya
Exposure anti-inflammatory medicationsb
Controls n = 279,618
Cases n = 55,937
ORc (95% CI)
ORc (95% CI)
ORc (95% CI)
Any Anti-inflammatory medication
Acetic acid derivatives
Propionic acid derivatives
Other non-Aspirin NSAIDs
Any non-topical glucocorticoid
Any (nonsteroidal) asthma medications
Short term b-agonists
Long term b-agonists
With respect to disease severity, exposure to any AIMs was positively associated with both favourable (OR: 1.34; 95%CI: 1.31–1.38) and unfavourable risk prostate cancer (OR: 1.17; 95%CI: 1.13–1.20) but associations were stronger for the favourable risk group. Similar patterns was observed for most AIMs subtypes.
Cumulative dose for selected classes of anti-inflammatory medications and risk of prostate cancer
Cumulative dose of anti-inflammatory medication a
> 500 dd
ORb (95% CI)
ORb (95% CI)
ORb (95% CI)
ORb (95% CI)
Any na-NSAID (reference: no prescriptions)
Acetic acid derivatives
Propionic acid derivatives
Non-steroidal asthma medications
With respect to interaction between CIDs and AIMs, we observed a slight decrease in the strength of association between prior non-aspirin-NSAID use and overall prostate cancer risk among men with a history of CIDs (P < 0.04). Similar interactions were observed for acetic acid derivative (p = 0.007) and for systemic glucocorticoid exposure (p = 0.001) but again the effects was only slightly weaker in men with history of CIDs (Additional file 1: Table S2).
This comprehensive, population-wide observational study found no convincing evidence of increased risk of prostate cancer among men with a history of any CIDs. While the odds ratio for any prior CID was slightly elevated (OR = 1.08), this only applied to favourable risk disease, with no elevated risk for less favourable risk prostate cancer. For specific CIDs, our results suggest increased risk of prostate cancer for chronic prostatitis and for allergies, but decreased risk among those hospitalised with T1DM. Our analyses of AIMs revealed moderately increased risk of prostate cancer with any use of AIMs, and specifically for non-aspirin-NSAID, glucocorticoids and other non-steroidal asthma medications.
Detection bias most likely explains the association between prostate cancer and history of any CID or use of AIMs, given more frequent contact with the healthcare system would increase the opportunity for prostate cancer detection through blood tests which include PSA measurement. As in most other countries, routine PSA screening is not recommended in Sweden . Nevertheless, opportunistic screening occurs frequently in Sweden, with a 5-year prevalence estimated at 60% in 2010 [26, 27]. Physicians attitudes and recommendations influence uptake of PSA testing [28, 29] and PSA testing frequency appears to be increased among those in regular contact with the healthcare system .
While several previous studies have reported associations between prostatitis and prostate cancer, debate is ongoing regarding whether the association is causal –i.e. via inflammatory pathways – or due to detection bias given more prostate-specific examinations . Our results support the role of detection bias, since risk was highest for chronic prostatitis admissions within 12 months of diagnosis. However, given the elevated odds for chronic prostatitis > 60 months prior to prostate cancer diagnosis, it is possible that other pathways may be involved, though this is difficult to disentangle from ongoing prostatic investigations.
Previous studies have consistently reported lower risk of prostate cancer in men with diabetes [31–34]. Proposed explanations include decreased hormone levels which may slow prostate carcinogenesis, potential effects of diabetes or anti-diabetic medications on serum PSA levels or prostate tissue pathology which lead to delays in diagnosis, and reduced screening/health seeking behaviour among diabetic men which may reduce opportunities for diagnosis . Though most of this evidence relates to type-2 diabetes mellitus, a multinational study using diabetes registry data has reported lower risk of prostate cancer among men with T1DM . While our findings also suggest decreased risk in men with T1DM, concerns remain about the accuracy of hospital records for type of diabetes, given the higher than expected prevalence of T1DM in our cohort.
With respect to allergies/asthma, we also observed higher risk for first hospitalisation within 12 months, which indicates detection bias may play a role. However, risk was also significantly elevated for first hospitalisation > 5 years earlier suggesting the association may also involve pathways other than detection bias. Increased risk of prostate cancer has been reported previously among men with atopic diseases, specifically asthma , those using anti-asthma medications  and those positive for serum allergen-specific IgE, a marker of atopy . However, the effect size in our study was more modest than other studies.
Counter to expectations, we observed a positive association between use of AIMs and risk of prostate cancer, with the strongest effects for non-aspirin-NSAIDs. Given the association was only observed for favourable risk prostate cancer and there was no clear dose response, we again suspect this finding reflects detection bias. While our findings are consistent with those of other large population-based studies (e.g. Skriver et al. 2016 , Denmark; Murad et al. 2011, UK ), they are inconsistent with meta-analyses which conclude that there is no association [18, 37] or a negative association  between prostate cancer and use of non-aspirin-NSAIDs. The meta-analysis by Lui et al. however, did indicate a positive association between non-aspirin-NSAIDs and prostate cancer risk in studies undertaken in Europe. Authors of the Danish population-based study also concluded that the positive association they observed was not likely to be causal . However, findings from studies on the use of non-aspirin-NSAIDs and prostate cancer risk within the context of PSA screening trials do not support effects due to detection bias alone [19, 38].
With respect to inhaled glucocorticoids and prostate cancer risk we did find evidence of a dose-response effect, suggesting there may be a causal relationship. However, it is difficult to disentangle the effects of inhaled glucocorticoids from the effects of asthma, since most prescriptions would be for asthma. There are a number of plausible explanations for increased risk with frequent use of glucocorticoids. Firstly, immunosuppressive effects of glucocorticoids may weaken the body’s defence against nascent or developing tumours . Secondly, metabolic changes induced through sustained use of glucocorticoids (i.e. metabolic syndrome, obesity, hyperglycaemia) have been linked to increased cancer risk . Thirdly, glucocorticoids may directly impact prostate cancer development through ‘cross-talk’ signalling of androgen receptors, leading to upregulation of androgen pathways which stimulate prostate cell growth . However, the lack of dose response with systemic glucocorticoids, and only a weak association with unfavourable risk prostate cancer lessen the argument for a causal relationship. Even if the association between inhaled glucocorticoids and prostate cancer was causal, the effect of prolonged use of these drugs is very modest and would not outweigh the benefits in terms of controlling asthma.
We have used high-quality, registry-based databases to investigate the association between CIDs/AIMs and prostate cancer risk. In the context of autoimmune diseases, which are quite rare, having such a large study population and population-wide coverage is a major strength. Furthermore, we were able to investigate dose-response relationships with respect to duration of CIDs and cumulative dose of AIMs. However, basing our exposure measure on hospital admission data will underestimate the true extent of CIDs since less severe inflammatory diseases (e.g. mild asthma, allergies) are often managed in community or outpatient settings. Likewise, prescription data may also be inaccurate since patients may not complete the course of medication prescribed. In addition we do not have information on prescription-free NSAID use. Furthermore, many AIMs have broad application beyond the management of inflammatory conditions (though this does not nullify their effect on prostate cancer). In terms of timing of initial diagnosis of CIDs, hospital admission data from 1998 may provide too short a time window to completely capture CID history, since conditions may have been diagnosed decades earlier. Even though we examined prostate cancer risk categories and trends according to exposure duration/dose, disentangling the effect of detection bias remains difficult without further information about primary health care visits and frequency of PSA testing.
This study found no consistent evidence linking prostate cancer risk to history of CIDs or use of AIMs. In general, the increased risk of prostate cancer is likely to be due to detection bias. However, findings suggesting possible associations with asthma/allergies and inhaled glucocorticoids warrant further investigation. More detailed clinical and translational research is required to better understand the relationship between chronic inflammation and prostate cancer risk, given limitations inherent in observational studies.
This project was made possible by the continuous work of the National Prostate Cancer Register of Sweden steering group: Pär Stattin (Chairman), Camilla Thellenberg Karlsson, Ove Andrén, Ann-Sofin Fransson, Magnus Törnblom, Stefan Carlsson, Marie Hjälm-Eriksson, David Robinson, Mats Andén, Jonas Hugosson, Ingela Franck Lissbrant, Johan Stranne, Maria Nyberg, Göran Ahlgren, René Blom, Lars Egevad, Fredrik Sandin, and Karin Hellström. The authors also wish to acknowledge the expert advice provided by Sophia Karagiannis and Deborah Enting in relation to this study.
Data collection and management within the National Prostate Cancer Register/PCBaSe is supported by the Swedish Cancer Society (grant 2013/472). Dr. Beckmann is funded through a NHMRC Early Career Research Fellowship. The funding bodies had no input into the design, analysis and interpretation of this study, nor writing or approving this manuscript.
Study design and conception: MV, JA; acquisition of data: HG, PS; Statistical analysis of data: KB, BR, HG; interpretation of results: KB, BR, DJ, CH, LH, PS MV, JA; drafting manuscript KB: revision of manuscript: KB, BR, DJ, CH, LH, PS MV, JA. All authors approved the final manuscript.
Ethics approval and consent to participate
This study was approved by Research Ethics Board, Umeå University, Sweden. Waiver of informed consent has been granted for Register-based data.
Consent for publication
The authors declare that they have no competing interests.
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