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A systematic review and meta-analysis on tubal ligation and breast cancer risk



Based on previous studies, it has been hypothesized that tube sterilization may be associated with a lower risk of breast cancer. This study aims to investigate the relationship between tubal ligation and the risk of breast cancer through a systematic review and meta-analysis.


In this systematic review and meta-analysis, PubMed/Medline, Web of Science, Scopus, and Google Scholar were searched for relevant non randomized studies published up to November 2020. Then, we screened the papers to include the eligible papers in the meta-analysis. Finally, we pooled the extracted results of individual studies to estimate the summary effect size. All analyses were done using Stata software version 13 (Stata Corp, College Station, TX).


Four hundred sixty-four papers were retrieved from PubMed/Medline (160), Scopus (165), and Web of Science (139), and 21 papers from Google Scholar and manual search of references in selected full texts. After the removal of duplicates and screening of the papers, 11 articles (6 cohort and 5 case-control study) were included in the final analysis. The results of cohort (RR = 0.99, 95% CI = 0.97–1.0, I2 = 21.1%) and case control studies (OR = 0.87, 95% CI = 0.62–1.12, I2 = 88.9%) revealed that tubal ligation was not significantly associated with breast cancer risk.


According to our findings, tubal ligation cannot be considered as a risk factor associated with breast cancer risk.

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Permanent contraception, also known as female sterilization or tubal ligation, is a surgical procedure in which fallopian tubes are blocked or removed. This contraceptive method is one of the most popular methods of family planning around the world [1, 2], accounting for 21.8% of contraceptive users in 2014 after oral contraceptives by 25.3% [3]. The prevalence of tubal ligation use has increased to 24% in 2019, with 219 million women worldwide choosing this method as their favorite contraceptive [3, 4].

Based on previous studies, it has been hypothesized that tube sterilization may be associated with a lower risk of breast cancer [2], especially among women < 45 years of age [5]. Ovarian hormones are involved in the pathogenesis of breast cancer. Therefore, tubal ligation may alter the risk of breast cancer due to changes in hormone levels before menopause age [5]. However, tubal ligation can also damage surrounding tissues, disrupting blood flow to ovaries and their hormonal function, thereby reducing the risk of breast cancer [6].

Numerous case-control and cohort studies [5,6,7,8,9] have been conducted in different parts of the world with different methodologies to examine this relationship. The findings, however, have been inconsistent and there is still no consensus on the effect of tubal ligation on breast cancer risk. Although most studies have reported either no association or reduced risk of breast cancer following tubal ligation, there is also some evidence of an increased risk of breast cancer [9]. Besides, a study has reported that there is an inverse relationship between tubal ligation and breast cancer mortality [7].

In previous meta-analysis studies, the protective effect of tubal ligation on endometrial [10] and ovarian cancers [11, 12] was reported. Therefore, it is expected that tubal ligation, with a similar mechanism, can be associated with a reduction in breast cancer risk.

With the inconsistency of previous study findings and also the fact that the last meta-analysis on this topic was conducted a decade ago when due to lack of evidence only PubMed database was searched [2], this study aimed to investigate the relationship between tubal ligation and risk of breast cancer through a systematic review and meta-analysis on non-randomized studies.


Study design

The systematic review and meta-analysis were conducted following the standard guideline of “Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA)” [13] and “Cochrane Handbook for Systematic Reviews of Interventions” [14].

Search strategy

To extract the relevant articles, a specific search strategy was devised, using a variety of keywords, for the following three international databases: Medline via PubMed, Scopus, and Web of Science. Medical Subject Heading (MeSH) and our keywords (including “breast neoplasms,” “breast cancer,” “sterilization, tubal,” “tubal sterilization,” “tubal ligation,” “tubal occlusion,” “female sterilisation,” “sterilization, reproductive,” and “reproductive sterilization”) were searched in PubMed. The search was filtered to only subsume human and English language studies. The modified keywords were then used to search in Scopus and Web of Science databases. More detail on the search strategy is reported in Supplementary file 1. The searching activities were conducted by authors (AAH, SS, and SZR) on November 23. Finally, Google Scholar was searched for gray literature, and references of selected articles were also manually checked by authors to find the relevant articles.

Study selection

To select the relevant articles, the retrieved articles were entered into Endnote version X8. Duplicate articles were removed in this stage. Then, the titles and abstracts of the remaining articles were screened and the irrelevant articles were excluded. After that, the full texts of the remaining articles were evaluated and unrelated articles were discarded. The required information was finally extracted from the remaining related articles. In cases where an article was relevant but the necessary data was not reported, the corresponding author was contacted. All stages of the study selection were performed by two people (AAH and SM). In the case of controversies, decisions were made in consultation with other authors.

Inclusion and exclusion criteria

Non-randomized articles that were published in the English language, up to November 2020, and examining the association between tubal ligation and breast cancer were included in the study. Moreover, only case-control and cohort studies were included, and other types of articles namely randomized interventional studies, letters to the editors, case reports, case series, editorials, review articles, and commentaries were excluded.

Data extraction

Data were extracted from the full-text of retrieved articles by the authors (AAH, MS2, SM, and SZR), and in the cases of disagreements, decisions were made in consultation with other authors. Data extracted from each article included first author’s name, year of publication, study design, type of effect size (e.g., odds ratio (OR) and risk ratio (RR)), effect size (and its 95% confidence interval (95% CI)), place of study, the quality score of the article, and studied population. In cohort studies, RR was extracted, and in case-control studies, OR was extracted.

Risk of bias

Qualitative evaluation of the included studies was performed by two authors based on the Newcastle-Ottawa Quality Assessment Scale (NOS), adapted for case-control and cohort studies. This scale is introduced to assess the quality of observational studies. The NOS evaluates each study based on six items in three overarching headings of selection, comparability, and exposure. Each item is given a star and its score ranges from 0 to 9. The articles were finally categorized into three groups with a score of more than 6 as high, 3 to 6 as moderate, and less than 3 as low quality.

Statistical analysis

To check the heterogeneity across the studies, the I2 statistic with a chi-square test was used. Also, in cases where there was significant heterogeneity, the random-effect model was used, and in other cases, the fixed-effect model was conducted to pool the effect sizes with “metan” command [15]. To explore the publication bias, Egger’s linear regression, Begg’s test (with “metabias” command [16]), and funnel plot (with “metafunnel” command [17]) were used. Moreover, a sensitivity analysis was performed to identify the effect of each study on the summary effect size with “metainf” command [18]. All analyses were done using Stata software version 13 (Stata Corp, College Station, TX, USA).


Study selection and study characteristics

The PRISMA flow diagram regarding the selection of the articles is displayed in Fig. 1. Searching the three international databases, we retrieved 464 papers (PubMed/Medline: 160, Scopus: 165, and Web of Science: 139). Twenty-one papers were retrieved from Google Scholar and a manual search of the references of all selected full texts. After the removal of duplicate papers, 369 papers remained from which 345 papers were excluded following their titles and abstracts screening. Then, the full texts of the remaining 24 articles were evaluated, and 13 articles were excluded due to irrelevance, lack of meeting inclusion criteria, or lack of sufficient data reporting. Finally, 11 articles [2, 5, 6, 8, 9, 19,20,21,22,23,24] were included in the meta-analysis.

Fig. 1
figure 1

Flow diagram of the literature search for studies included in the meta-analysis

The eleven studies that met the inclusion criteria are summarized in Table 1. Five were case-control [5, 9, 19,20,21] and six were cohort study designs [2, 6, 8, 22,23,24]. The oldest study was published in 1988 [9] and the latest in 2016 [24]. There were 6 articles from the USA [2, 5, 6, 8, 9, 21], 3 articles from Europe [19, 22, 24], and 2 articles from Asia [20, 23]. The adjusted effect size was reported in all the articles except for a study from Korea. More details about the selected studies are reported in Table 1.

Table 1 Characteristics of the primary studies included in the meta-analysis

Risk of bias within studies

The quality of each study was checked according to the NOS and all studies were of high quality. However, we could not check the quality of a study from Korea [20] due to a lack of access to the full-text.

Quantitative data synthesis

In this study, the results of cohort and case-control studies was not combined together and the results pooled separately. Because of significant heterogeneity between primarily included case-control studies, a random-effects model with a Mantel-Hansel approach was used to summarize the findings, while cohort studies were combined using the fixed-effects model. The results of cohort (RR = 0.99, 95% CI = 0.97–1.0, I2 = 21.1%) and case control studies (OR = 0.87, 95% CI = 0.62–1.12, I2 = 88.9%) revealed that tubal ligation was not significantly associated with breast cancer risk (Figs. 2 and 3).

Fig. 2
figure 2

Forest plot describing the association between tubal ligation and breast cancer risk among cohort studies

Fig. 3
figure 3

Forest plot describing the association between tubal ligation and breast cancer risk among case-control studies

Heterogeneity and meta-regression

The results suggested a significant heterogeneity between primary case control studies (heterogeneity chi-squared = 36.1, (d.f. = 4), p = 0.001, I2 (variation in ES attributable to heterogeneity) = 88.9%, estimate of between-study variance tau-squared = 0.066), and the results revealed that there is no significant heterogeneity among cohort studies (heterogeneity chi-squared = 6.3, (d.f. = 5), p = 0.275, I2 (variation in ES attributable to heterogeneity) = 21.1%, estimate of between-study variance tau-squared = 0.001). Therefore, a random-effects model was used to summarize the effect sizes in case control studies and fixed-effects model was used in cohort studies.

Additional analysis

Based on previous evidence [25,26,27], the OR is a good estimate of the RR if the incidence of the disease is rare. Assuming that breast cancer is rare in people with and without a history of tubal ligation, we combined the effect sizes of all studies (11 studies). Overall, the pooled effect size in the meta-analysis revealed that tubal ligation was not significantly associated with breast cancer risk (summary effect size (SES) = 0.97, 95% CI = 0.89–1.04, I2 = 76.8%, random-effects model).

Risk of bias across studies

Begg’s and Egger’s tests were used to check the possibility of publication bias. The findings, however, suggested that there was no evidence of publication bias among case-control (Begg’s test p value = 0.462, Egger’s test p value = 0.36) and cohort studies (Begg’s test p value = 0.133, Egger’s test p value = 0.34).

Sensitivity analysis

Based on sensitivity analysis, the results showed that in both cohort and case-control studies, there was no association between tubal ligation and breast cancer risk by removing each individual studies. Also, overall sensitivity analysis showed that the highest estimate of summary effect size was related to the time when Shin et al. study [20] was excluded from the meta-analysis (SES = 1.01, 95% CI = 0.95–1.07). The lowest estimate on the other hand was related to the time when Irwin et al. study [9] was excluded from the meta-analysis (SES = 0.96, 95% CI = 0.89–1.02).


In this study, we collected and analyzed non-randomized articles examining the relationship between tubal ligation and breast cancer risk in a systematic review and meta-analysis. The results of the study strongly support the lack of an association between tubal ligation and breast cancer risk. Regardless of the statistically significant level, the estimated summary effect size was close to its null value of one, suggesting that the observed association was not clinically important (i.e., not in favor of a protective effect of tubal ligation on breast cancer risk). In addition, the small confidence intervals obtained from the models implicate accurate results.

Given that tubal ligation has a significant effect on reducing the risk of ovarian [11, 12] and endometrial cancers [10], our hypothesis in this study was that this association, with a similar mechanism, might be established for breast cancer too. On the contrary, we showed that there was no sufficient evidence to support this hypothesis, and it was concluded that tubal ligation is not associated with breast cancer risk. The lack of association between tubal ligation and breast cancer risk reinforces a hypothesis that the association between tubal ligation and ovarian cancer might be due to a mechanical barrier against ascending carcinogenic agents or due to screening effect (i.e., selective removal of suspicious ovaries during tubal ligation) [2].

From a total of 11 articles included in the meta-analysis, one study showed a significant increase [9] and one a significant decrease [20] in breast cancer following tubal ligation. The rest of the studies reported that there was no such association according to their findings. In fact, in line with our study, several studies have reported that tubal ligation cannot reduce the risk of breast cancer. In one study conducted by Calle et al. [7], however, the relationship between tubal ligation and the mortality rate of breast cancer was examined, and the authors concluded that there was an inverse relationship between tubal ligation and breast cancer mortality rate. To be precise, they reported that breast cancer mortality rate in those with a history of tubal ligation was 0.82 times higher than that of the control group, especially among women who were sterilized before age 35.

Previous studies have also suggested that women who have a history of tubal ligation are more prone to uterine surgery and hysterectomy [28], and bilateral oophorectomy [29], and these issues can act as a factor to reduce the risk of breast cancer. Given this, it can be hypothesized that tubal ligation alone may not play a role in reducing the risk of breast cancer but rather the surgery that occurs after tubal ligation might be a factor.

One of the important issues in meta-analysis studies is that the unadjusted data of individual studies are usually extracted and summarized. Fortunately, in this study, the adjusted effect size was reported in most of the primary papers where the effect of various confounding variables was controlled. Besides, the possibility of publication bias is another concern in these kinds of meta-analysis studies. Our analyses, however, showed that there is no evidence in favor of publication biases in individual studies. In this study, there was considerable heterogeneity between the included studies. Heterogeneity refers to any variation across primary included articles which mainly include clinical or methodological heterogeneity. No two studies can be identical, so systematic reviews require methods to evaluate the variability of studies to make reasonable decisions about data summarizing and comparisons [30]. Due to significant heterogeneity across the studies, we performed a sub-group analysis (based on study design) and also a random and fixed-effects model to pool the data.

One of the strengths of this study is that unlike a previous meta-analysis that only searched PubMed database a decade ago, three international databases including Scopus, Medline/PubMed, and Web of Science were searched and a general conclusion was made about the association between tubal ligation and breast cancer risk. One of the limitations of this study, however, is that only articles in the English language were reviewed. Moreover, due to the review nature of the study, it was not possible to assess the effect of time (number of years elapsed) since tubal ligation on the risk of breast cancer.

It should be highlighted that combining different study designs and different effect sizes leads to increased heterogeneity between studies, and in some cases, it is not recommended to combine them. In this study, the results of case control and cohort studies were reviewed, and we analyzed the case control (odds ratio) and cohort studies (risk ratio) separately, and because the results of these two types of studies did not differ, the results of these studies were merged as an additional analysis with random-effects model.

In this study, the statistical heterogeneity quantified by the I2 statistic, and because of a significant heterogeneity, random-effects model preferred to the fixed-effects model. Accordingly, because the number of studies is usually small, there is also the possibility of small study bias that the results should be used with caution.

In this study, some of reported effect size were adjusted for potential confounders and some of them were not adjusted. According to the Cochrane Handbook, the use of adjusted model is preferable if both unadjusted and adjusted intervention effects are reported.

In summary, in this study, we pooled the results of eleven individual studies and our findings did not suggest tubal ligation as a risk factor associated with breast cancer.

Availability of data and materials

All data generated or analyzed during this study are included in this published article (and its supplementary information files).



Summary odds ratio


Odds ratio


Confidence interval


Summary adjusted odds ratio


Intrauterine device


Medical Subject Headings


Preferred Reporting Items for Systematic Review and Meta-Analysis


  1. Chan LM, Westhoff CL. Tubal sterilization trends in the United States. Fertility and Sterility. 2010;94(1):1–6.

    Article  Google Scholar 

  2. Gaudet MM, Patel AV, Sun J, Teras LR, Gapstur SM. Tubal sterilization and breast cancer incidence: results from the cancer prevention study II nutrition cohort and meta-analysis. Am J Epidemiol. 2013;177(6):492–9.

    Article  Google Scholar 

  3. Braaten KP, Dutton C. Overview of female permanent contraception 2020 [updated Nov 24, 2020]. Available from:

  4. United Nations, Department of Economic and Social Affairs, Population Division. Contraceptive Use by Method 2019: Data Booklet 2020. Available from:

  5. Press DJ, Sullivan-Halley J, Ursin G, Deapen D, McDonald JA, Strom BL, et al. Breast cancer risk and ovariectomy, hysterectomy, and tubal sterilization in the women's contraceptive and reproductive experiences study. Am J Epidemiol. 2011;173(1):38–47.

    Article  Google Scholar 

  6. Eliassen AH, Colditz GA, Rosner B, Hankinson SE. Tubal sterilization in relation to breast cancer risk. Int J Cancer. 2006;118(8):2026–30.

    Article  CAS  Google Scholar 

  7. Calle EE, Rodriguez C, Walker KA, Wingo PA, Petrelli JM, Thun MJ. Tubal sterilization and risk of breast cancer mortality in US women. Cancer Causes Control. 2001;12(2):127–35.

    Article  CAS  Google Scholar 

  8. Nichols H, Baird D, DeRoo L, Kissling G, Sandler D. Tubal ligation in relation to menopausal symptoms and breast cancer risk. Br J Cancer. 2013;109(5):1291–5.

    Article  CAS  Google Scholar 

  9. Irwin KL, Lee NC, Peterson HB, Rubin GL, Wingo PA, Mandel MG, et al. Hysterectomy, tubal sterilization, and the risk of breast cancer. Am J Epidemiol. 1988;127(6):1192–201.

    Article  CAS  Google Scholar 

  10. Loghmani L, Saedi N, Omani-Samani R, Safiri S, Sepidarkish M, Maroufizadeh S, et al. Tubal ligation and endometrial cancer risk: a global systematic review and meta-analysis. BMC Cancer. 2019;19(1):942.

    Article  Google Scholar 

  11. Cibula D, Widschwendter M, Májek O, Dusek L. Tubal ligation and the risk of ovarian cancer: review and meta-analysis. Hum Reprod Update. 2010;17(1):55–67.

    Article  Google Scholar 

  12. Rice MS, Murphy MA, Tworoger SS. Tubal ligation, hysterectomy and ovarian cancer: a meta-analysis. J Ovarian Res. 2012;5(1):13.

    Article  Google Scholar 

  13. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151(4):264–9.w264.

    Article  Google Scholar 

  14. Higgins JP, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, et al. Cochrane handbook for systematic reviews of interventions. Wiley; 2019.

  15. Harris RJ, Deeks JJ, Altman DG, Bradburn MJ, Harbord RM, Sterne JA. Metan: fixed-and random-effects meta-analysis. Stata J. 2008;8(1):3–28.

    Article  Google Scholar 

  16. Harbord R, Harris RJ, Sterne JA, Steichen T. METABIAS: Stata module to test for small-study effects in meta-analysis; 2009, Boston College Department of Economics, Statistical Software Components S.404901.

    Google Scholar 

  17. Sterne J. METAFUNNEL: Stata module to produce funnel plots for meta-analysis; 2003, Boston College Department of Economics, Statistical Software Components, S434101.

    Google Scholar 

  18. Steichen T. METANINF: Stata module to evaluate influence of a single study in meta-analysis estimation; 2001, Statistical Software Components, Boston College Department of Economics, S419201.

    Google Scholar 

  19. Braga C, Negri E, La Vecchia C, Parazzini F, Dal Maso L, Franceschi S. Fertility treatment and risk of breast cancer. Hum Reprod (Oxford, England). 1996;11(2):300–3.

    Article  CAS  Google Scholar 

  20. Shin MH, Kim DH, Lee HK, Yang JH, Choi KJ, Ahn YO. The effect of tubal ligation on the protection from breast cancer: a case-control study in Korea. Am J Epidemiol. 1996;143(11):232.

    Google Scholar 

  21. Brinton L, Gammon M, Coates R, Hoover R. Tubal ligation and risk of breast cancer. Br J Cancer. 2000;82(9):1600–4.

    Article  CAS  Google Scholar 

  22. Iversen L, Hannaford PC, Elliott AM. Tubal sterilization, all-cause death, and cancer among women in the United Kingdom: evidence from the Royal College of General Practitioners’ Oral Contraception Study. Am J Obstet Gynecol. 2007;196(5):447.e441–8.

    Article  Google Scholar 

  23. Dorjgochoo T, Shu XO, Li HL, Qian HZ, Yang G, Cai H, et al. Use of oral contraceptives, intrauterine devices and tubal sterilization and cancer risk in a large prospective study, from 1996 to 2006. Int J Cancer. 2009;124(10):2442–9.

    Article  CAS  Google Scholar 

  24. Gaitskell K, Coffey K, Green J, Pirie K, Reeves GK, Ahmed AA, et al. Tubal ligation and incidence of 26 site-specific cancers in the Million Women Study. Br J Cancer. 2016;114(9):1033–7.

    Article  Google Scholar 

  25. Cummings P. The relative merits of risk ratios and odds ratios. Arch Pediatr Adolesc Med. 2009;163(5):438–45.

    Article  Google Scholar 

  26. King G, Zeng L. Estimating risk and rate levels, ratios and differences in case-control studies. Stat Med. 2002;21(10):1409–27.

    Article  Google Scholar 

  27. Diaz-Quijano FA. A simple method for estimating relative risk using logistic regression. BMC Med Res Methodol. 2012;12(1):14.

    Article  Google Scholar 

  28. Hillis SD, Marchbanks PA, Tylor LR, Peterson HB. Higher hysterectomy risk for sterilized than nonsterilized women: findings from the US Collaborative Review of Sterilization. Obstet Gynecol Surv. 1998;53(5):281–2.

    Article  Google Scholar 

  29. Lowder JL, Oliphant SS, Ghetti C, Burrows LJ, Meyn LA, Balk J. Prophylactic bilateral oophorectomy or removal of remaining ovary at the time of hysterectomy in the United States, 1979-2004. Am J Obstet Gynecol. 2010;202(6):538.e531–9.

    Article  Google Scholar 

  30. Ryan R, Communication Review Group. Heterogeneity and subgroup analyses in Cochrane Consumers and Communication Group reviews: planning the analysis at protocol stage. London, United Kingdom: Cochrane Consumers and Communication; 2016.

    Google Scholar 

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We would like to thank the vice chancellor for the research of Arak University of Medical Sciences for their financial and scientific supports.


This study was funded by Arak University of Medical Sciences. The funder had no role in the study design data collection, analyses, interpretation of the results, or decision to submit results.

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NN, AE, MS1, SN, and AAH conceived the study. All authors contributed to the title and full-text screening. AAH, SZR, MS2, and SM extracted the data. All authors contributed equally to the initial draft of the manuscript. AAH, SS, MS2, and SM analyzed the data, and all authors have read and revised and approved the final version of the manuscript.

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Correspondence to Amir Almasi-Hashiani.

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Supplementary Information

Additional file 1.

Search strategy.

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Najdi, N., Esmailzadeh, A., Shokrpour, M. et al. A systematic review and meta-analysis on tubal ligation and breast cancer risk. Syst Rev 11, 126 (2022).

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