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Risk of uterine, ovarian and breast cancer following pelvic inflammatory disease: a nationwide population-based retrospective cohort study
- Cheng-Che Shen†1, 2, 3,
- Li-Yu Hu†1, 4,
- Albert C. Yang1, 5,
- Yung-Yen Chiang6,
- Jeng-Hsiu Hung7, 8 and
- Shih-Jen Tsai1, 5Email authorView ORCID ID profile
© The Author(s). 2016
Received: 15 December 2015
Accepted: 19 October 2016
Published: 3 November 2016
Pelvic inflammatory disease (PID) is characterized by infection and inflammation of the upper genital tract in women and is associated with health sequelae. We used a nationwide population-based retrospective cohort study to explore the relationship between PID and the subsequent development of gynecological cancers including ovarian, breast or uterine cancer.
We identified subjects diagnosed with PID between January 1st, 2000 and December 31st, 2002 in the Taiwan National Health Insurance Research Database. A comparison cohort constructed for patients without PID were matched according to age and sex. All PID patients and control groups were observed until diagnosed with ovarian, breast or uterine cancer, or until death, withdrawal from the NHI system, or until December 31st, 2009.
The PID cohort consisted of 32,268 patients, and an equal number of matched controls without PID. The adjusted hazard ratio (HR) of ovarian, breast or uterine cancer in subjects with PID were: HR 1.326 (95 % confidence interval: 0.775–2.269), HR: 1.039 (95 % confidence interval: 0.862–1.252), and HR: 1.439 (95 % confidence interval: 0.853–2.426) respectively in comparison with controls during follow-up.
This large nationwide population-based cohort study suggests that there is no increased risk for ovarian, breast or uterine cancer among women who have PID compared to a matching population.
KeywordsPelvic inflammatory disease Uterine cancer Ovarian cancer Breast cancer Retrospective cohort study
Pelvic inflammatory disease (PID) is a polymicrobial infection and inflammatory disorder of the upper female genital tract, including the uterus, fallopian tubes, and adjacent pelvic structures in women [1, 2]. It primarily affects young, sexually active women. Most women with PID can be treated successfully as outpatients with a course of antibiotics for at least two weeks .
Without adequate treatment, PID may lead to major sequelae, including ectopic pregnancy, pelvic pain, abscesses, and infertility. Since infertility and low parity are common complications of PID and are risk factors for ovarian cancer, a few studies have demonstrated that PID may increase the risk of ovarian cancer. A case-control study in Canada with 450 histologically verified primary epithelial ovarian cancer cases and 564 randomly selected population controls done by Risch and Howe, first reported that PID increased the risk of epithelial ovarian cancer . This association has been interpreted in terms of inflammatory changes of the ovarian surface epithelium . However, an Italian case–control study found no increased risk of ovarian cancer with a history of PID (OR 0.7, 95 % confidence interval, 0.4–1.3) . Genetic differences between racial or ethnic groups, culture, and climate may partly explain these controversial results. Recently, Lin and colleagues used a large, nationwide health insurance database in Taiwan, demonstrating that the adjusted hazard ratio (HR) for ovarian cancer in patients with PID was 1.92 (95 % CI 1 · 27–2 · 92) during the 3-year follow-up period . However, this study was limited by a short period between the PID and the diagnosis of ovarian cancer (1–3 years) . Furthermore, patients with International Classification of Diseases, ninth revision, clinical modification (ICD-9-CM) code 616 (inflammatory disease of cervix, vagina, and vulva) could have been wrongly classified in PID cases in that study . For these reasons, the first aim of this study is to explore whether PID increases the risk of developing ovarian cancer with the same database (Longitudinal Health Insurance Database 2005, LHID2005), but with a longer follow-up period excluding ICD-9-CM code 616 in PID cases. The second aim of this study to investigate whether women with PID raise the risk of developing uterine or breast cancer.
Instituted in 1995, the National Health Insurance (NHI) program is a mandatory health insurance program that offers comprehensive medical care coverage, including outpatient, inpatient, emergency, and traditional Chinese medicine, to all residents of Taiwan, with a coverage rate of up to 98 % . The NHI research database (NHIRD) contains comprehensive information regarding clinical visits, prescription details and diagnostic codes based on ICD-9-CM. NHIRD is managed by the National Health Research Institutes, and confidentiality is maintained according to the directives of the Bureau of NHI. We used LHID2005 as our study data source. LHID2005 contains all the original claim data of 1,000,000 beneficiaries, randomly sampled from the year 2005 Registry for Beneficiaries (ID) of the NHIRD; everyone who was a beneficiary of the National Health Insurance Program within 2005 is in the population for random sampling. There are approximately 25.68 million individuals in this registry. All registration and claim data of the 1,000,000 individuals collected by the National Health Insurance Program constitute the LHID2005. There were no significant differences in gender distribution, age distribution, or average insured payroll-related amount between the patients in the LHID2005 and those in the original NHIRD (http://nhird.nhri.org.tw/en/index.htm). Recently, using LHID2005, we have demonstrated an increased risk of uterine but not ovarian and breast cancer in women with polycystic ovary syndrome .
Using data extracted from the LHID2005, we conducted a retrospective cohort study of patients who were newly diagnosed with PID by an obstetrician-gynecologist between January 1st, 2000 and December 31st, 2002. To ensure diagnostic validity and patient homogeneity, we selected only patients who had at least two consensus PID diagnoses for the study group. We excluded patients who were diagnosed with PID between January 1st, 1996, and December 31st, 1999. We also excluded patients who were diagnosed with malignancies (ICD-9-CM codes: 140-208) before they were diagnosed with PID. For every PID patient included in the final cohort, one age- and sex-matched control without PID, and any malignancy was randomly selected from LHID 2005 in the same time period as PID patient. Random assignment procedures were performed by SAS statistical software and were based on random numbers generated from the uniform distribution. All PID patients and controls were observed until diagnosed with breast cancer (ICD-9-CM code: 174-175), ovarian cancer (ICD-9-CM codes: 183), uterine cancer (ICD-9-CM codes: 179, 181 and 182), or until death, withdrawal from the NHI system, or until December 31st, 2009. Our main dependent variable was the occurrence of breast cancer, ovarian cancer, or uterine cancer, as reported in the Registry for Catastrophic Illness. For a diagnosis of cancer to be reported in the Registry, histological confirmation is required. Common co-morbidities including hypertension, diabetes mellitus, dyslipidemia, congestive heart failure, chronic pulmonary diseases, coronary artery diseases, and cerebrovascular diseases were also compared between PID and controls. The study design and the criteria had been used in similar studies [10–12].
The incidences of newly diagnosed breast cancer, ovarian cancer, or uterine cancer in PID patients and controls were calculated, and independent t tests and chi-squared tests were used to examine differences in demographic characteristics between the PID patients and controls. A Cox proportional-hazards regression model was constructed to calculate the hazard ratio (HR) of breast cancer, ovarian cancer, or uterine cancer of the PID and control cohorts, respectively. Control variables, such as age, urbanization, monthly income, common co-morbidities including hypertension, diabetes mellitus, dyslipidemia, congestive heart failure, chronic pulmonary diseases, coronary artery diseases, and cerebrovascular diseases were included as covariates in the multivariate model to calculate adjusted HR. SAS statistical software for Windows, version 9.3 (SAS Institute, Cary, NC, USA), was used for data extraction, computation, data linkage, processing, and sampling. All other statistical analyses were performed using SPSS statistical software for Windows, version 20 (IBM, Armonk, NY, USA). Results for comparisons with a P value of less than .05 were considered as a statistically significant relationship.
Case control study design
For further confirmation of our study results, we also designed a case control study. All subjects who were aged 20 and older and were newly diagnosed with uterine, ovarian or breast cancer, respectively in 2009 were included as case group. The controls were matched to cases by age, sex, and index date with a ratio of 1:4. Diagnosis of PID before index events was recorded during period of 2000-2009. The percentage of PID diagnosis in patients with uterine, ovarian, breast cancer and three control cohorts were calculated respectively. Odds ratios and 95 % confidence intervals were also estimated by using multiple logistic regression.
Characteristics of patients with pelvic inflammatory disease and comparison subjects
Age (years) a
34.48 (27.46 – 42.06)
34.48 (27.47 – 42.06)
Distribution of age
20 – 39
40 – 59
Coronary artery disease
Congestive heart failure
Chronic pulmonary disease
Degree of urbanization
Follow-up, years a
8.84 (8.04 – 9.51)
8.84 (8.04 – 9.51)
Newly diagnosed cancers, N (%)
Age of diagnosis of cancer (years) a
45.50 (40.75 – 59.00)
46.50 (41.25 – 51.75)
46.00 (40.00 – 52.00)
45.00 (41.00 – 50.00)
47.00 (40.00 – 56.00)
52.00 (45.00 – 55.00)
PID on risks of ovarian cancer, breast cancer, and uterine cancer
Hazard ratios of developing cancer between patients with pelvic inflammatory disease and comparison subjects
Crude HR (95 % CI)
Adjusted HR (95 % CI)a
1.42 (0.84 – 2.39)
1.33 (0.78 – 2.27)
1.03 (0.85 – 1.24)
1.04 (0.86 – 1.25)
1.35 (0.81 – 2.24)
1.44 (0.853 – 2.43)
Results of case control study design
Odds ratio of history of pelvic inflammatory disease on ovarian cancer
Ovarian cancer group
(N = 55)
(N = 220)
OR = 1.40
(95 % CI 0.72–2.70)
P = 0.32
Odds ratio of history of pelvic inflammatory disease on breast cancer
Breast cancer group
(N = 356)
(N = 1424)
OR = 1.12
(95% CI 0.84–1.51)
P = 0.44
Odds ratio of history of pelvic inflammatory disease on uterine cancer
Uterine cancer group
(N = 70)
(N = 280)
OR = 1.64
(95 % CI 0.90–2.97)
P = 0.11
In a nationwide population-based study of ovarian cancer among PID patients in Taiwan, it was found that patients with PID had an increased risk of ovarian cancer than patients without PID . However, in our nationwide population-based study in Taiwan with the same database, no significantly increased risk of subsequent ovarian cancer was observed after a diagnosis of PID. The discrepancy between such study and our study may have come from differences in study periods (3 years versus 10 years), physician specialties for PID diagnosis (obstetrician-gynecologist and other specialties versus obstetrician–gynecologist), differences in diagnosis restrictions for ovarian cancer (only patients with catastrophic illness certificate in our study) and PID ICD-9-CM coding (ICD-9-CM codes 614-616 versus ICD-9-CM codes: 614-615). In the cohort studied by Lin and colleagues, at least two episodes of PID in relation to diagnosis of ovarian cancer had to occur within 1–3 years . In such a short period, a causal relation between PID and ovarian cancer seems less likely, and the inverse relationship between ovarian cancer risk factor and PID cannot be excluded . Furthermore, both ICD-9-CM codes 614 and 615 refer to inflammatory disease of the ovary, fallopian tube, pelvic cellular tissue, peritoneum, and uterus, except cervix, respectively, which fit the diagnosis of PID. However, PID cases in Lin and colleagues’ study also included ICD- 9-CM code 616, which refers to the inflammatory disease of cervix, vagina, and vulva. These infections affect only the lower genital tract which is unrelated to or has not yet progressed to PID. Thus, it would be inappropriate to include diseases pertinent to code 616 in this survey . In addition, our main dependent variables, the occurrence of breast cancer, ovarian cancer, or uterine cancer, are collected from the Registry for Catastrophic Illness and histological confirmation is required for a diagnosis of cancer to be reported in the Registry, Therefore, the diagnosis of cancer in our study is more precise.
Furthermore, our analysis showed that hypertension, dyslipidemia and diabetes were more prevalent in women with PID than in women without PID (Table 1). Medical conditions associated with metabolic syndrome such as hypertension, dyslipidemia and diabetes may alter immune response and increase the risk of PID in women [13, 14].
Ovarian, uterine and breast cancers are associated with several risk factors, such as low parity and infertility , which are common complications of PID [16, 17]. In addition, inflammatory response triggered by bacterial or viral infection is a major factor for human carcinogenesis [18, 19]. In addition of ovarian cancer, earlier reports have suggested PID diagnosis is a risk factor for cervical intra-epithelial neoplasia , cervical cancer  and colorectal cancer . In this study, we investigated the hypothesis that PID may increase the risk of uterine and breast cancers using a national health insurance database. Our study suggests that there are no increased risks for both cancers among people who have PID compared to a matching population.
Based on the relatively small number of patients diagnosed with cancer in our study, we collected annual number and incidence of ovarian, breast and uterine cancer of Taiwan from Health Promotion Administration, Ministry of Health and Welfare of Taiwan (https://cris.hpa.gov.tw/) and compared above figures with our study. The results showed that incidence rate of ovarian, breast or uterine cancer was similar between general population of Taiwan and subjects of our study (Additional file 1: Table S1). Hence, we think the results of our study were representative and valid.
The strength of our study is the use of a population-based data set with an enrollment of a large number of subjects, enabling us to trace the subsequent risk of gynecologic cancers in PID subjects and controls. Furthermore, diagnosis of cancer in our study must be confirmed by histological confirmation. In addition, our study design included an unbiased participant selection process. Because participation in NHI is mandatory and all residents of Taiwan can access health care with low copayments, referral biases were low with high follow-up compliance.
Certain limitations to our findings should, however, be considered: First, LHID2005 did not contain some important information regarding the studied subjects. Some of the patient information which may influence the risk of gynecologic cancers, such as smoking, alcohol consumption, parity, infertility, age at menarche, and family history of gynecologic cancers, were not available for analysis . Thus, we were unable to control these potentially confounding factors. Second, diagnosis of PID can only be confirmed with a positive bacteriological test for lower genital tract infection such as chlamydia or gonorrhea . PID diagnosis was entirely determined using the ICD codes from the National Health Insurance claim database, and there may be concerns regarding the diagnostic accuracy of the database. Third, the follow-up duration in this study (median follow-up time 8.84 years) may have been insufficient for detecting the carcinogenesis of certain types of cancer. Most ovarian, uterine, and breast cancer occur after age 50 and the short follow-up time in this study may underestimate any possible association. Thus, future studies with longer follow-up periods are required to determine the long-term risk of cancer among PID patients. Forth, our study is based on Taiwan National Health Insurance research database and it’s difficult to apply the results of our study to other regions with complete different population composition, culture, or climate due to limited geographical coverage. Finally, prevalence of PID diagnoses were identified using the ICD-9 codes from the database may be underestimated as only subjects seeking medical evaluation can be identified, leading to a likely underestimation of the association between PID and gynecologic cancers.
In summary, our study did not support the idea that the risk of ovarian cancer is higher in PID patients as shown in an earlier report with same nationally representative cohort database. We also demonstrated that PID diagnosis is not a risk factor for breast or uterine cancers.
The study was based on data from the National Health Insurance Research Database (provided by the Bureau of National Health Insurance of the Department of Health, Taiwan, and managed by the National Health Research Institute, Taiwan). The interpretation and conclusions contained in this article do not represent those of the Bureau of National Health Insurance, the Department of Health, or the National Health Research Institute. The authors alone are responsible for the content and writing of the paper.
This work was supported by grant MOST 104-2314-B-075 -072 -MY3 from Taiwan Ministry of Science and Technology and grant V104C-018 from the Taipei Veterans General Hospital. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
The datasets during and/or analysed during the current study available from the corresponding author on reasonable request.
Conceived and designed the experiments: SJT, CCS. Performed the experiments and analyzed the data: CCS, LYH, YYC. Contributed reagents/materials/analysis tools: SJT, ACY, JHH. Wrote the paper: CCS, SJT. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The Institutional Review Board of the Taipei Veterans General Hospital approved this study. Written consent from study patients was not obtained because the NHI dataset consists of de-identified secondary data for research purposes, and the Institutional Review Board of Taipei Veterans General Hospital issued a formal written waiver for the need for consent.
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- Crossman SH. The challenge of pelvic inflammatory disease. Am Fam Physician. 2006;73(5):859–64.PubMedGoogle Scholar
- Mitchell C, Prabhu M. Pelvic inflammatory disease: current concepts in pathogenesis, diagnosis and treatment. Infect Dis Clin North Am. 2013;27(4):793–809.View ArticlePubMedGoogle Scholar
- Gradison M. Pelvic inflammatory disease. Am Fam Physician. 2012;85(8):791–6.PubMedGoogle Scholar
- Risch HA, Howe GR. Pelvic inflammatory disease and the risk of epithelial ovarian cancer. Cancer Epidemiol Biomark Prev. 1995;4(5):447–51.Google Scholar
- Parazzini F, La Vecchia C, Negri E, Moroni S, dal Pino D, Fedele L. Pelvic inflammatory disease and risk of ovarian cancer. Cancer Epidemiol Biomarkers Prev. 1996;5(8):667–9.PubMedGoogle Scholar
- Lin HW, Tu YY, Lin SY, Su WJ, Lin WL, Lin WZ, Wu SC, Lai YL. Risk of ovarian cancer in women with pelvic inflammatory disease: a population-based study. Lancet Oncol. 2011;12(9):900–4.View ArticlePubMedGoogle Scholar
- van de Laar R, Massuger LF. Pelvic inflammatory disease and ovarian cancer. Lancet Oncol. 2011;12(13):1184. author reply 1184-1185.View ArticlePubMedGoogle Scholar
- Cheong KM. Pelvic inflammatory disease and ovarian cancer. Lancet Oncol. 2011;12(13):1183–4. author reply 1184-1185.View ArticlePubMedGoogle Scholar
- Wu CY, Chen YJ, Ho HJ, Hsu YC, Kuo KN, Wu MS, Lin JT. Association between nucleoside analogues and risk of hepatitis B virus-related hepatocellular carcinoma recurrence following liver resection. JAMA. 2012;308(18):1906–14.View ArticlePubMedGoogle Scholar
- Shen CC, Yang AC, Hung JH, Hu LY, Tsai SJ. A nationwide population-based retrospective cohort study of the risk of uterine, ovarian and breast cancer in women with polycystic ovary syndrome. Oncologist. 2015;20(1):45–9.View ArticlePubMedGoogle Scholar
- Hung JH, Hu LY, Tsai SJ, Yang AC, Huang MW, Chen PM, Wang SL, Lu T, Shen CC. Risk of psychiatric disorders following polycystic ovary syndrome: a nationwide population-based cohort study. PLoS ONE. 2014;9(5):e97041.View ArticlePubMedPubMed CentralGoogle Scholar
- Lee YT, Hu LY, Shen CC, Huang MW, Tsai SJ, Yang AC, Hu CK, Perng CL, Huang YS, Hung JH. Risk of psychiatric disorders following irritable bowel syndrome: a nationwide population-based cohort study. PLoS ONE. 2015;10(7):e0133283.View ArticlePubMedPubMed CentralGoogle Scholar
- Paragh G, Seres I, Harangi M, Fulop P. Dynamic interplay between metabolic syndrome and immunity. Adv Exp Med Biol. 2014;824:171–90.View ArticlePubMedGoogle Scholar
- Roep BO, Tree TI. Immune modulation in humans: implications for type 1 diabetes mellitus. Nat Rev Endocrinol. 2014;10(4):229–42.View ArticlePubMedGoogle Scholar
- Cetin I, Cozzi V, Antonazzo P. Infertility as a cancer risk factor - a review. Placenta. 2008;29 Suppl B:169–77.View ArticlePubMedGoogle Scholar
- Haggerty CL, Totten PA, Tang G, Astete SG, Ferris MJ, Norori J, Bass DC, Martin DH, Taylor BD, Ness RB. Identification of novel microbes associated with pelvic inflammatory disease and infertility. Sex Transm Infect. 2016;92(6):441–6.Google Scholar
- Westrom L. Incidence, prevalence, and trends of acute pelvic inflammatory disease and its consequences in industrialized countries. Am J Obstet Gynecol. 1980;138(7 Pt 2):880–92.View ArticlePubMedGoogle Scholar
- Coussens LM, Werb Z. Inflammation and cancer. Nature. 2002;420(6917):860–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Rosin MP, Anwar WA, Ward AJ. Inflammation, chromosomal instability, and cancer: the schistosomiasis model. Cancer Res. 1994;54(7 Suppl):1929s–33.PubMedGoogle Scholar
- Giraud J, Coiffic J, Poulain P, Kerisit J. High prevalence of cervical intra-epithelial neoplasia in women treated for pelvic inflammatory disease. Eur J Obstet Gynecol Reprod Biol. 1998;81(1):51–4.View ArticlePubMedGoogle Scholar
- Skapinyecz J, Smid I, Horvath A, Jeney C, Kardos L, Kovacs P. Pelvic inflammatory disease is a risk factor for cervical cancer. Eur J Gynaecol Oncol. 2003;24(5):401–4.PubMedGoogle Scholar
- Hsu MI, Lin HW. Risk of colorectal cancer in women with pelvic inflammatory disease: a matched cohort study. BJOG. 2014;121(3):337–42.View ArticlePubMedGoogle Scholar
- Bevan CD, Johal BJ, Mumtaz G, Ridgway GL, Siddle NC. Clinical, laparoscopic and microbiological findings in acute salpingitis: report on a United Kingdom cohort. Br J Obstet Gynaecol. 1995;102(5):407–14.View ArticlePubMedGoogle Scholar