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Risk of Human Papillomavirus (HPV) Infection and Cervical Neoplasia after Pregnancy

BMC Pregnancy and Childbirth volume 15, Article number: 244 (2015) Cite this article

Abstract

Background

Parity is well established as a risk factor for cervical cancer. It is not clear, however, how pregnancy influences the natural history of HPV infection and cervical neoplasia. Our objective was to study the risk of HPV infection and cervical squamous intraepithelial lesions (SIL) after pregnancy.

Methods

We used the Ludwig-McGill cohort study which includes 2462 women recruited in Sao Paulo, Brazil in 1993–97 and followed for up to 10 years. Cellular specimens were collected every 4–6 months for Pap cytology and HPV detection and genotyping by a polymerase chain reaction protocol. Study nurses recorded pregnancy occurrence during follow-up. HPV and Pap results from pregnant women were available before and after, but not during pregnancy. The associations between pregnancy and post-partum HPV infection/SIL were studied using generalized estimating equation models with logistic link. Adjusted odds ratios (OR) were estimated with empirical adjustment for confounding.

Results

We recorded 122 women with a history of pregnancy during follow-up. Of these, 29 reintegrated the cohort study after delivery. No association between HPV and pregnancy was found. A single SIL case (high grade SIL) occurred post-partum. Likewise, there was no association between pregnancy and risk of low grade SIL or any-grade SIL at the next visit (adjusted OR = 0.84, 95 % CI: 0.46-15.33) after controlling for confounders.

Conclusions

No associations were found between pregnancy and HPV or LSIL. The single observed case of HSIL post-partum was more than would be expected based on the rate of these abnormalities among non-pregnant women. As this association was found with only one case, caution is required in the interpretation of these results.

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Background

The central causal role of the so-called high oncogenic–risk (HR)-human papillomavirus (HPV) genotypes, such as HPV-16 in cervical carcinogenesis, has been established [1]. HPV is a necessary but not sufficient cause of virtually all cases of cervical cancer worldwide. HR-HPV infection also causes a substantial proportion of other anogenital neoplasms and oral squamous cell carcinomas [2]. HPV infections are one of the most common sexually transmitted conditions in the world although the vast majority are transient, with only a small proportion becoming persistent and leading the development of cervical cancer [3]. The fact that HPV infection does not always progress to neoplastic disease suggests that interpersonal variations in the immune system may play a role in the clearance of HPV infections and/or in their acquisition. Other viral or environmental factors may also play a role [4]. For example, parity is a well-established risk factor for cervical cancer [5]. It is not clear, however, exactly how pregnancy influences the natural history of human papillomavirus (HPV) infection and cervical neoplasia. To our knowledge, there is no prospective study of the risk conferred by pregnancy on both HPV infection and cervical intraepithelial neoplasia. The aim of this prospective study was to analyse the risk of HPV infection and cervical squamous intraepithelial lesion following pregnancy.

Method

Subject recruitment

The women included in this study were enrolled into the Ludwig-McGill cohort, a longitudinal investigation of the natural history of HPV infection and precursor lesions of cervical cancer. A detailed description of the design and methods of the study has been published previously [6]. Briefly, women attending a maternal and child health program catering to a low-income neighborhood in São Paulo (Brazil) were recruited between 1993 and 1997 and followed for up to 10 years. Women were eligible to participate if they: 1) were between 18 and 60 years of age, 2) were permanent residents of São Paulo, 3) were not currently pregnant and had no intention of becoming pregnant during the first year of follow-up, 4) had an intact uterus and no current referral for hysterectomy, 5) reported no use of vaginal medication in the previous 2 days and 6) had no reported treatment for cervical disease in the previous 6 months. Subjects gave a signed informed consent. The study protocol was approved by institutional ethical and research review boards of the participating institutions in Canada (McGill University Research and Ethics Board, Montreal) and in Brazil (Ludwig Institute for Cancer Research São Paulo Branch Institutional Review Board (IRB) and by the IRB of the Hospital e Maternidade Escola Vila Nova Cachoerinha Dr Mario Altenfender, São Paulo).

The study enrolled 2528 women, corresponding to a 70 % response rate and subsequently, 66 ineligible women were excluded. Follow-up for the remaining 2462 women consisted of 1 visit every 4 months for the first year and 2 visits per year thereafter. Cervical specimens were taken for Papanicolaou (Pap) cytology and HPV testing at every visit with a fixed-sampling area Accelon device. For the first 4 visits and for each annual visit thereafter, subjects answered a nurse-administered questionnaire designed to collect information on socio-demographic, lifestyle, sexual, reproductive and contraceptive characteristics. Pregnancy status was registered by study nurses along with date and procedures of visits, reasons of dropouts and reintegration, and other study-relevant incidents. Pregnant women were excluded from the study during pregnancy and offered to be reintegrated in the study after a minimum of 45 days following delivery, if there was no clinical impediment and if they consented. HPV and Pap results from pregnant women were available before and after, but not during pregnancy.

Cervical cells specimen

An Accelon biosampler (Medscand, Inc., Hollywood, Florida) was used to collect ecto- and endocervical samples for each visit and a Pap smear was prepared on a glass slide and fixed with 95 % ethanol. The sampler containing the residual exfoliated cells was immersed in a tube containing Tris-EDTA buffer (pH 7.4) and agitated to release the cells. The tubes containing cell suspensions were frozen until testing. Samples were then sent to the Ludwig Institute for storage and testing. Pap smears were sent to the study centre in Canada for cytology reading by one of the co-authors (AF). Cytopathology reports were based on the 1991 Bethesda system for cytological diagnoses [7]; the Pap smears were read ‘blinded’ to all other test results for the same sample and for the same woman and findings were classified as normal, atypical squamous cells of undetermined significance (ASCUS), atypical glandular cells of undetermined significance (AGUS), low grade squamous intraepithelial lesion (LSIL), or high grade squamous intraepithelial lesion (HSIL).

HPV DNA testing

The Accelon device containing ecto- and endocervical cells was placed in a tube containing Tris-EDTA buffer (pH 7.4). DNA was extracted, purified by spin column chromatography, and amplified by polymerase chain reaction (PCR), using the MY09/11 and PGMY protocols [8, 9] for detection of HPV DNA. Typing of amplified products was performed by dot-blot hybridization with individual oligonucleotide probes and by restriction fragment length polymorphism (RFLP) analysis. This method identified more than 40 HPV genital types. Amplified products that hybridized only with a generic probe and were unidentifiable in RFLP analysis were classified as positive for unknown types. The genotypes tested included high oncogenic risk (HR-) HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68, 73 and 82, and low oncogenic risk (LR-) HPV types 6, 11, 26, 32, 34, 40, 42, 44, 53, 54, 57, 61, 62, 67, 69, 70, 71, 72, 81, 83, 84 and 89 (unknown types considered LR-HPVs) [10, 11]. We included more than 30 type-specific positive controls in hybridization membranes to control for experimental variation between different membranes. DNA specimen quality was checked by amplification of a 268-bp human β–globin gene region [8]. Specimens were tested blindly and precautions were taken to prevent contamination. Samples that were negative for both HPV and β–globin were considered inadequate for analysis.

Statistical analysis

We explored the relationships between pregnancy and outcomes such as HPV infection and cervical squamous intraepithelial lesions (SIL) using generalized estimating equation (GEE) via a logistic regression link, which take into account the clustering within each individual caused by the repeated-measurements design. GEE models were based on an exchangeable correlation pattern. We studied the association between pregnancy and the presence of HPV, LSIL and HSIL. Post-partum visits were compared to other usual visits for the presence of HPV or SIL. We explored the relationship between HPV infection and pregnancy by considering grouped HPV genotypes per their oncogenic potential (high-risk and low-risk as described above), per their phylogenetic relationship within the genus Alpha-papillomavirus (species 3, 5, 6, 7, 9, 10) [12] and grouped HPV per their general tropism for the cervix or the vagina [13]. HPV group 1 (benign) included HPV types 6, 11, 32, 40, 42, 44 (cervical and vaginal species 1, 8, 10); HPV group 2 included HPV types 16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 67, 68, 69, 70, 82 (cervical species 5, 6, 7, 9, 11); and HPV group 3 included HPV types 57, 61, 71, 72, 62, 81, 83, 84, 89 (vaginal species 3, 4, 15).

We estimated crude and adjusted odd ratios (ORs) with respective 95 % confidence intervals (CI). For adjusted estimates, we controlled for empirical confounders using a 5 % change-in-estimate method (variables that changed the estimates by +/− 5 % were included in the model) considering the following variables: age at enrolment (linear), race (white, non-white), marital status (single, married, widowed, separated, unmarried but living with partner), income (quartiles of income), smoking (never, current, former), age at first sexual intercourse (≤15, 16–17, 18–19, 20+), number of previous pregnancies (0–1, 2–3, 4–6, 7+), Pap testing before enrollment in the cohort (yes, no) and lifetime number of sexual partners (0–1, 2–3, 4+). For the analysis concerning the association between SIL and pregnancy, we also considered HPV status (negative, LR-HPV only, any HR-HPV) as a potential confounder or mediator.

Results

A total of 2475 women were included and provided altogether 24,558 visits. The mean and median follow-up time were 5.1 (SD = 3.2 years) and 6.4 (inter-quartile range = 1.0-7.5) years, respectively. The mean age at enrolment was 32.7 years (SD = 8.8; median = 32, range: 18–59) and most women were white (64 %). We recorded 122 women with a history of pregnancy during follow-up. After giving birth, 29 (23.8 %) women reentered the study. The mean time between visits for reintegration into the cohort was 3.9 years (SD = 1.6).

Table 1 describes the characteristics at baseline (enrolment) according to the pregnancy status in the course of follow-up. Women who became pregnant over the course of follow-up were younger than those in the remainder of the cohort. The distribution of other age-dependent variables also differed according to pregnancy outcomes, e.g., women who did not become pregnant were more likely to have a normal cytology result and to be HPV negative at baseline. Table 1 also provides baseline data for women who had a pregnancy but who did not reintegrated the cohort after pregnancy. Overall, women lost to follow-up after pregnancies were largely comparable to those who reintegrated into the cohort after giving birth.

Table 1 Characteristics at baseline (at enrolment in the cohort) according to pregnancy status in the course of follow-up
Full size table

Table 2 presents the crude and adjusted ORs for the association between pregnancy and post-partum HPV infection and SILs. Six of the post-pregnancy visits were HPV positive (20.7 %), whereas 3787 out of 23,735 (16.0 %) visits without an intervening pregnancy yielded the same finding. We found no evidence that pregnancy increased the risk of detecting HPV at the next visit post-partum irrespective of the categories used to group HPV genotypes (range of adjusted ORs: 0.80-1.86; none statistically significant). Table 2 also shows the association between pregnancy and cytological abnormalities. A single SIL case (an HSIL) occurred post-partum. Likewise, there was no association between pregnancy and LSIL or any-grade SIL at the next visit (adjusted OR = 0.84, 95 % CI: 0.46-15.33) after controlling for confounders. The single observed case of HSIL post-partum was more than would be expected based on the rate of these abnormalities among non-pregnant women even after accounting for multiple confounders (OR = 8.75, 95 % CI: 1.00-77.03).

Table 2 Crude and adjusted odds ratios (ORs) for the association between HPV detection or squamous intraepithelial lesion (SIL) and pregnancy
Full size table

Discussion

In this longitudinal study, we analysed the risk of HPV infection and cytological abnormality following pregnancy. No association was detected between pregnancy and LSIL, nor for post-partum HPV infection. Although, the single observed case of HSIL post-partum was more than would be expected based on the rate of these abnormalities among non-pregnant women, this association was found with only one case, which calls for caution in interpreting these findings.

There are plausible mechanisms whereby pregnancy may influence the natural history of HPV infection and progression to clinical lesions. Increased levels of estrogen or growth hormone associated with pregnancy such as human chorionic gonadotropin (hCG) may increase HPV molecular activity [14, 15]. Studies on condyloma acuminata and laryngeal recurrent respiratory papillomatosis have shown that these lesions increase in number and size during pregnancy [16]. Others suggested that a reduced humoral response to HPV may occur in pregnant women [17].

Our finding of no increased risk of HPV detection with pregnancy concurs with other reports [18–27]. Only a few showed a higher risk of HPV infection in pregnant women [28–30]. The higher risk of HPV infection in these studies could be explained by confounding variables related to sexual activity, as pregnancy and HPV infection are both acquired through sex. Some studies have shown a higher risk of HSIL with pregnancy. Morimura et al. (2002) [31] have shown that the proportion of women with of abnormal Pap test results was significantly higher during pregnancy. Jensen and colleagues (2013) [32] found that childbirth increased the risk of HSIL, over and above the risk of persistent HPV infection. Taken together, those studies suggest, that careful monitoring of HPV positive women in the post-partum period may be warranted.

It is not clear however, whether or not the risk of progression of HPV infection to cervical neoplasia (preinvasive and invasive cancer) is higher when detected during pregnancy. Studies on the progression of biopsy proven cervical neoplasia during pregnancy are rare, since biopsies tend to be avoided during pregnancy. When Pap results are used to estimate risk, reports provide a wide range of estimates: 10–70 % of cytological abnormalities found during pregnancy regress, 25–89 % persist without progression and 3–30 % progress [33–46]. Studies on evolution of HSIL during pregnancy and the post-partum period show a range of progression to micro-invasive carcinoma from 0 to 14.2 % and a very low risk of progression to frankly invasive cancer (0.1 %) (reviewed in Serati et al., [44]).

This study has limitations. It is possible that residual confounding may explain our findings. For example, lack of control for women’s partners’ sexual behaviour could create confounding if pregnancy is associated with a higher likelihood of partners’ extra-conjugal sexual relationships. However, this potential confounding bias is unlikely to have occurred, as no association was found for HPV infection or LSIL. We also used cytology and not histology results in this analysis. However, Morimura et al. (2002) [31] has shown that the accuracy of cytology Pap testing is similar between pregnant and non-pregnant women. As this potential information bias is non differential, it would have only underestimated the relative risk we found. Finally, most of the women in our cohort already had their children at the time of recruitment and only a small number of women experienced a pregnancy within the cohort. Moreover, a criterion for recruitment in our cohort was not being currently pregnant and no intention of becoming pregnant during the first year of follow-up, which reduced the number of pregnancies in the cohort and the number of women who reentered the cohort after birth.

One of the strengths of our study was the use of a longitudinal design approach including prospective collection of data before and after pregnancy. This limits the potential for bias that would have occurred if pregnant women were more likely to be screened compared to non-pregnant women because all pregnant women in our study were similarly followed-up in the cohort prior to becoming pregnant. We also applied a conservative control for confounding including sexual behaviour and variables that were different between pregnant and non pregnant women such as age.

Conclusions

In conclusion, we found no association between pregnancy and HPV infection and cervical lesions but admittedly, our cohort included a limited number of pregnant women. A single SIL case (an HSIL) occurred post-partum which calls for caution in interpretation.

References

  1. de Sanjosé S, Quint WGV, Alemany L, Geraets DT, Klaustermeier JE, Lloveras B, et al. Human papillomavirus genotype attribution in invasive cervical cancer: a retrospective cross-sectional survey. Lancet Oncol. 2010;11:1048–56.

    Article  PubMed  Google Scholar 

  2. Trottier H, Burchell AN. Epidemiology of mucosal human papillomavirus (HPV) infection and HPV -associated diseases. Public Health Genomics. 2009;12(5–6):291–307.

    Article  PubMed  Google Scholar 

  3. Trottier H, Franco EL. Human papillomavirus (HPV) and cervical cancer: burden and epidemiology. Am J Manag Care. 2006;12(17 Suppl):S462–72.

    PubMed  Google Scholar 

  4. Trottier H, Franco EL. The epidemiology of genital human papillomavirus infection. Vaccine. 2006;24 Suppl 1:S1–15.

    PubMed  Google Scholar 

  5. Muñoz N, Franceschi S, Bosetti C, Moreno V, Herrero R, Smith JS, et al. Bosch FX; International Agency for Research on Cancer. Role of parity and human papillomavirus in cervical cancer: the IARC multicentric case–control study. Lancet. 2002;359(9312):1093–101.

    Article  PubMed  Google Scholar 

  6. Franco E, Villa L, Rohan T, Ferenczy A, Petzl-Erler M, Matlashewski G. Design and methods of the Ludwig-McGill longitudinal study of the natural history of human papillomavirus infection and cervical neoplasia in Brazil. Ludwig-McGill Study Group. Rev Panam Salud Publica. 1999;6:223–33.

    Article  CAS  PubMed  Google Scholar 

  7. Broder S. The Bethesda System for Reporting Cervical/Vaginal Cytologic Diagnoses—Report of the 1991 Bethesda Workshop. JAMA. 1992;267:1892.

    Article  CAS  PubMed  Google Scholar 

  8. Bauer HM, Ting Y, Greer CE, Chambers JC, Tashiro CJ, Chimera J et al. Genital human papillomavirus infection in female university students as determined by a PCR-based method. JAMA. 1991;265:472–7.

    Article  CAS  PubMed  Google Scholar 

  9. Gravitt PE, Peyton CL, Alessi TQ, Wheeler CM, Coutlée F, Hildesheim A, et al. Improved amplification of genital human papillomaviruses. J Clin Microbiol. 2000;38:357–61.

    CAS  PubMed  PubMed Central  Google Scholar 

  10. International Agency for Research on Cancer (IARC). Monographs on the evaluation of carcinogenic risks to humans. Human Papillomaviruses, vol. 90. Lyon, France: International Agency for Research on Cancer (IARC); 2007.

    Google Scholar 

  11. Muñoz N, Bosch FX, de Sanjose S, Herrero R, Castellsagué X, Shah KV, et al. Epidemiologic classification of human papillomavirus types associated with cervical cancer. N Engl J Med. 2003;348:518–27.

    Article  PubMed  Google Scholar 

  12. de Villiers EM, Fauquet C, Bernard HU, Broker TR, zur Hausen H. Classification of papillomaviruses. Virology. 2004;324:17–27.

    Article  PubMed  Google Scholar 

  13. Schiffman M, Herrero R, Desalle R, Hildesheim A, Wacholder S, Rodriguez AC, et al. The carcinogenicity of human papillomavirus types reflects viral evolution. Virology. 2005;337(1):76–84.

    Article  CAS  PubMed  Google Scholar 

  14. Nair HB, Luthra R, Kirma N, Liu YG, Flowers L, Evans D, et al. Induction of aromatase expression in cervical carcinomas: effects of endogenous estrogen on cervical cancer cell proliferation. Cancer Res. 2005;65:11164–73.

    Article  CAS  PubMed  Google Scholar 

  15. Delvenne P, Herman L, Kholod N, Caberg JH, Herfs M, Boniver J, et al. Role of hormone cofactors in the human papillomavirus-induced carcinogenesis of the uterine cervix. Mol Cell Endocrinol. 2007;264:1–5.

    Article  CAS  PubMed  Google Scholar 

  16. Scurry Jr WC, McGinn JD. Recurrent respiratory papillomatosis in pregnancy: a case of emergent airway management. Ear Nose Throat J. 2008;87(6):E8–11.

    PubMed  Google Scholar 

  17. Sethi S, Muller M, Schneider A, Blettner M, Smith E, Turek L, et al. Serologic response to the E4, E6, and E7 proteins of human papillomavirus type 16 in pregnant women. Am J Obstet Gynecol. 1998;178:360–4.

    Article  CAS  PubMed  Google Scholar 

  18. Smith EM, Johnson SR, Jiang D, Zaleski S, Lynch CF, Brundage S, et al. The association between pregnancy and human papilloma virus prevalence. Cancer Detect <?show [?A3B2 show $6#?]?>Prev. 1991;15:397–402.

  19. Soares VR, Nieminen P, Aho M, Vesterinen E, Vaheri A, Paavonen J. Human papillomavirus DNA in unselected pregnant and non-pregnant women. Int J STD AIDS. 1990;1:276–8.

    CAS  PubMed  Google Scholar 

  20. De Roda Husman AM, Walboomers JM, Hopman E, Bleker OP, Helmerhorst TM, Rozendaal L, et al. HPV prevalence in cytomorphologically normal cervical scrapes of pregnant women as determined by PCR: The age-related pattern. J Med Virol. 1995;46:97–102.

    Article  PubMed  Google Scholar 

  21. Chang-Claude J, Schneider A, Smith E, Blettner M, Wahrendorf J, Turek L. Longitudinal study of the effects of pregnancy and other factors on detection of HPV. Gynecol Oncol. 1996;60:355–62.

    Article  CAS  PubMed  Google Scholar 

  22. Tenti P, Zappatore R, Migliora P, Spinillo A, Maccarini U, De Benedittis M, et al. Latent human papillomavirus infection in pregnant women at term: A case– control study. J Infect Dis. 1997;176:277–80.

    Article  CAS  PubMed  Google Scholar 

  23. Chan PK, Chang AR, Tam WH, Cheung JL, Cheng AF. Prevalence and genotype distribution of cervical human papillomavirus infection: Comparison between pregnant women and non-pregnant controls. J Med Virol. 2002;67:583–8.

    Article  PubMed  Google Scholar 

  24. Nobbenhuis MA, Helmerhorst TJ, van den Brule AJ, Rozendaal L, Bezemer PD, Voorhorst FJ, et al. High-risk human papillomavirus clearance in pregnant women: trends for lower clearance during pregnancy with a catch-up postpartum. Br J Cancer. 2002;87:75–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Minkoff H, Shen X, Watts DH, Leighty R, Hershow R, Palefsky J, et al. Relationship of pregnancy to human papillomavirus among human immunodeficiency virus-infected women. Obstet Gynecol. 2006;108:953–60.

    Article  PubMed  Google Scholar 

  26. Banura C, Franceschi S, van Doorn LJ, Arslan A, Kleter B, Wabwire-Mangen F, et al. Prevalence, incidence and clearance of human papillomavirus infection among young primiparous pregnant women in Kampala. Uganda Int J Cancer. 2008;123(9):2180–7.

    Article  CAS  PubMed  Google Scholar 

  27. Schmeink CE, Melchers WJ, Hendriks JC, Quint WG, Massuger LF, Bekkers RL. Human papillomavirus detection in pregnant women: a prospective matched cohort study. J Womens Health (Larchmt). 2012;21(12):1295–301.

    Article  Google Scholar 

  28. Fife KH, Katz BP, Roush J, Handy VD, Brown DR, Hansell R. Cancer-associated human papillomavirus types are selectively increased in the cervix of women in the first trimester of pregnancy. Am J Obstet Gynecol. 1996;174:1487–93.

    Article  CAS  PubMed  Google Scholar 

  29. Gopalkrishna V, Murthy NS, Sharma JK, Roy M, Das DK, Luthra UK, et al. Increased human papillomavirus infection with the increasing number of pregnancies in Indian women. J Infect Dis. 1995;171:254–5.

    Article  CAS  PubMed  Google Scholar 

  30. Hernandez-Giron C, Smith JS, Lorincz A, Lazcano E, Hernandez-Avila M, Salmeron J. High-risk human papillomavirus detection and related risk factors among pregnant and nonpregnant women in Mexico. Sex Transm Dis. 2005;32:613–18.

    Article  PubMed  Google Scholar 

  31. Morimura Y, Fujimori K, Soeda S, Hashimoto T, Takano Y, Yamada H, et al. Cervical cytology during pregnancy--comparison with non-pregnant women and management of pregnant women with abnormal cytology. Fukushima J Med Sci. 2002;48(1):27–37.

    Article  PubMed  Google Scholar 

  32. Jensen KE, Schmiedel S, Norrild B, Frederiksen K, Iftner T, Kjaer SK. Parity as a cofactor for high-grade cervical disease among women with persistent human papillomavirus infection: a 13-year follow-up. Br J Cancer. 2013;108(1):234–9.

    Article  CAS  PubMed  Google Scholar 

  33. Ahdoot D, Van Nostrand KM, Nguyen NJ, Tewari DS, Kurasaki T, DiSaia PJ, et al. The effect of route of delivery on regression of abnormal cervical cytologic findings in the postpartum period. Am J Obstet Gynecol. 1998;178:1116–20.

    Article  CAS  PubMed  Google Scholar 

  34. Palle C, Bangsboll S, Andreasson B. Cervical intraepithelial neoplasia in pregnancy. Acta Obstet Gynecol Scand. 2000;79:306–10.

    Article  CAS  PubMed  Google Scholar 

  35. Vlahos G, Rodolakis A, Diakomanolis E, Stefanidis K, Haidopoulos D, Abela K, et al. Conservative management of cervical intraepithelial neoplasia (CIN(2–3)) in pregnant women. Gynecol Obstet Invest. 2002;54:78–81.

    Article  CAS  PubMed  Google Scholar 

  36. Coppola A, Sorosky J, Casper R, Anderson B, Buller RE. The clinical course of cervical carcinoma in situ diagnosed during pregnancy. Gynecol Oncol. 1997;67:162–5.

    Article  CAS  PubMed  Google Scholar 

  37. Baldauf JJ, Dreyfus M, Ritter J, Philippe E. Colposcopy and directed biopsy reliability during pregnancy: a cohort study. Eur J Obstet Gynecol Reprod Biol. 1995;62(1):31–6.

    Article  CAS  PubMed  Google Scholar 

  38. Yost N, Santoso JT, McIntire D, Iliya FA. Postpartum regression rates of antepartum cervical intraepithelial neoplasia II and III lesions. Obstet Gynecol. 1999;93:359–62.

    CAS  PubMed  Google Scholar 

  39. Paraskevaidis E, Koliopoulos G, Kalantaridou S, Pappa L, Navrozoglou I, Zikopoulos K, et al. Management and evolution of cervical intraepithelial neoplasia during pregnancy and postpartum. Eur J Obstet Gynecol Reprod Biol. 2002;104:67–9.

    Article  PubMed  Google Scholar 

  40. Douvier S, Filipuzzi L, Sagot P. Management of cervical intra-epithelial neoplasm during pregnancy. Gynecol Obstet Fertil. 2003;31(10):851–5.

    Article  CAS  PubMed  Google Scholar 

  41. Siddiqui G, Kurzel RB, Lampley EC, Kang HS, Blankstein J. Cervical dysplasia in pregnancy: progression versus regression post-partum. Int J Fertil Womens Med. 2001;46(5):278–80.

    CAS  PubMed  Google Scholar 

  42. Kaplan KJ, Dainty LA, Dolinsky B, Rose GS, Carlson J, McHale M, et al. Prognosis and recurrence risk for patients with cervical squamous intraepithelial lesions diagnosed during pregnancy. Cancer. 2004;102:228–32.

    Article  PubMed  Google Scholar 

  43. Frega A, Scirpa P, Corosu R, Verrico M, Scarciglia ML, Primieri MR, et al. Clinical management and follow-up of squamous intraepithelial cervical lesions during pregnancy and postpartum. Anticancer Res. 2007;27(4C):2743–6.

    PubMed  Google Scholar 

  44. Serati M, Uccella S, Laterza RM, Salvatore S, Beretta P, Riva C, et al. Natural history of cervical intraepithelial neoplasia during pregnancy. Acta Obstet Gynecol Scand. 2008;87:1296–300.

    Article  PubMed  Google Scholar 

  45. Cubo-Abert M, Centeno-Mediavilla C, Franco-Zabala P, Merced-Vázquez C, Castellví J, García A, et al. Risk factors for progression or persistence of squamous intraepithelial lesions diagnosed during pregnancy. J Low Genit Tract Dis. 2012;16(1):34–8.

    Article  PubMed  Google Scholar 

  46. Coppolillo EF, DE Ruda Vega HM, Brizuela J, Eliseth MC, Barata A, Perazzi BE. High-grade cervical neoplasia during pregnancy: diagnosis, management and postpartum findings. Acta Obstet Gynecol Scand. 2013;92(3):293–7.

    Article  PubMed  Google Scholar 

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Acknowledgments

Ludwig–McGill cohort study team members: affiliated with the Ludwig Institute for Cancer Research in Sao Paulo, Brazil: Maria Luiza Baggio, Lenice Galan, João Simão Sobrinho, José Carlos Mann Prado, Silvaneide Ferreira, Lara Termini, Maria Cecília Costa, Romulo Miyamura, Andrea Trevisan, Patricia Thomann, João Candeias, Laura Sichero, Paula Rahal, Antonio Ruiz, Jane Kaiano, Monica Santos, Patricia Savio, Paulo Maciag, Tatiana Rabachini, Luisa Villa (Co-Principal Investigator). Affiliated with McGill University in Montreal, Canada: Marie-Claude Rousseau, Salaheddin Mahmud, Nicolas Schlecht, Helen Trottier, Alex Ferenczy, Thomas Rohan, Myriam Chevarie-Davis, Joseph Tota, Agnihotram Ramanakumar, Eliane Duarte, Sophie Kulaga, Juliette Robitaille, Robert Platt, Eduardo Franco (Principal Investigator).

We are grateful to Silvaneide Ferreira and Rache Hessel for study coordination and to Romulo Myamura, João Simão Sobrinho, José Carlos Mann Prado and Maria Cecilia Costa for HPV DNA testing and typing.

This study was supported by an intramural grant from the Ludwig Institute for Cancer Research to LLV and ELF and by grants from the U.S. National Cancer Institute (CA70269) and the Canadian Institutes of Health Research (MA13647) to ELF. MHM holds a salary award (chercheur-boursier) from the Fonds de la recherche du Québec en santé (FRQ-S). HT holds a salary award (chercheur-boursier) from the FRQ-S and from Canadian Institutes of Health Research (CIHR).

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Authors and Affiliations

  1. Division of Cancer Epidemiology, Department of Oncology, McGill University, Montreal, Canada

    Helen Trottier & Eduardo L. Franco

  2. Department of Social and Preventive Medicine, Université de Montréal, Montreal, Canada

    Helen Trottier & Marie-Hélène Mayrand

  3. Sainte-Justine Hospital Research Center, Department of Social and Preventive Medicine, Université de Montréal, 3175 Côte Sainte-Catherine, Room A-830, Montreal, QC, H3T 1C5, Canada

    Helen Trottier

  4. Department of Obstetrics and Gynecology, Université de Montréal and CRCHUM, Montreal, Canada

    Marie-Hélène Mayrand

  5. Ludwig Institute for Cancer Research, São Paulo, Brazil

    Maria Luiza Baggio, Lenice Galan & Luisa L. Villa

  6. Department of Pathology, McGill University and Jewish General Hospital, Montreal, Canada

    Alex Ferenczy

  7. Department of Radiology and Oncology, School of Medicine, University of São Paulo, São Paulo, Brazil

    Luisa L. Villa

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for the Ludwig-McGill Cohort Study Group

Corresponding author

Correspondence to Helen Trottier.

Additional information

Competing interests

HT has served as a paid consultant for and has received travel assistance from GlaxoSmithKline Biologicals, Merck, and Gilead Science. MHM has received consulting and lecture fees from Merck, Pfizer, Roche and GlaxoSmithKline. EF has received occasional lecture or consultation fees from Merck, GlaxoSmithKline, Roche and Gen-Probe. AF is a paid consultant for Merck, BD, Roche Diagnostic Systems, Hologic (GenProbe), Cepheid and Inovio. LV has received occasional lecture or consultation fees from Merck, Sharp and Dohme.

Authors’ contribution

All authors of this research paper have directly contributed to the conception and design (ELF, LLV), or acquisition of data (MLB, LG, AF), or analysis and interpretation (HT, MHM, AF, LLV, ELF) of the study. HT, MHM and ELF wrote the first draft of the manuscript. All authors have subsequently read, revised, and approved the version that is now being submitted.

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Trottier, H., Mayrand, MH., Baggio, M.L. et al. Risk of Human Papillomavirus (HPV) Infection and Cervical Neoplasia after Pregnancy. BMC Pregnancy Childbirth 15, 244 (2015). https://doi.org/10.1186/s12884-015-0675-0

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Keywords

BMC Pregnancy and Childbirth

ISSN: 1471-2393

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