Volume 11, Issue 9 (12-2013)                   IJRM 2013, 11(9): 761-0 | Back to browse issues page

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Binesh F, Akhavan A, Davoodi M. Does oral contraceptive pill increase the risk of abnormal Pap smear?. IJRM 2013; 11 (9) :761-0
URL: http://ijrm.ir/article-1-464-en.html
1- Department of Pathology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran , Binesh44@yahoo.com
2- Department of Radiotherapy, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
3- Shahid Sadoughi University of Medical Sciences, Yazd, Iran
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Introduction
 
Invasive squamous cell carcinoma of the cervix is still the most common malignant tumor of the female genital tract in most countries (1). Due to the lack of a population-based universal national cancer registry center in Iran, there is no accurate data on the incidence of cancers. However, the prevalence of cervical cancer in Iran seems to be much lower than in other developing countries (2).
According to WHO declaration cervical cancer ranks as 12th most frequent cancer among women in Iran (3). Cervical dysplasia is a premalignant lesion that can progress to cervical cancer. Invasive cancer of the cervix has been considered a preventable cancer because it has a long pre invasive state, cervical cytology screening programs are available, and the treatment of pre invasive lesions is effective (4). Cytologic screening of cervical smears is the most effective screening test for cervical cancer ever developed (5).
Over the past several years, through improvements in screening and treatment, the incidence and mortality rates of cervical cancer have dramatically declined in developed countries (6). In spite of the preventable nature of this disease, 12,710 new cases of invasive cervical cancer resulting in 4290 deaths were anticipated in the United States in 2011 (7). Despite new modalities of treatment, up to 35% of patients diagnosed with cervical cancer will subsequently develop metastasis (8).
An association of cervical cancer with several risk factors including human papilloma virus infection, smoking, oral contraceptive consumption and male factor (multiple partners) have been shown in some studies (9-11). Additionally, it has been propounded that there are some host factors which are effective in progression of disease (12). Oral contraceptive pill (OCP) is the most universal modern method of contraception, followed by female sterilization, in the world (13).
In Iran, the use of OCP has been increased specially in the last two decades and is available to married couples, free of charge, at public clinics (14). Over the last 40 years, literature regarding OCPs has accentuated the “dark side” of the drug and pointed out how their numerous side effects adversely impact many users and even societies at large. A large body of epidemiological evidence suggests that cervical cancer risk might increase by using OCPs for a long period (15-17).
But results have been inconsistent across populations. For example in some studies (some of them are from Iran) no consistent association emerged between the risk of intraepithelial cervical neoplasm and oral contraceptive use (18-20). On the other hand there are some studies which suggest that OCP consuming for a long time, might raise cervical cancer risk (21-24). In this study, we investigated the effects of combined oral contraceptives on the prevalence of abnormal Pap smear among women who were referred to Shahid Sadoughi and Madar hospitals in Yazd.
 
Materials and methods
 
A cross-sectional descriptive study was conducted over a 2 years period from 2009 to 2011. The study was approved by the university ethics committee. As has been done previously by McFarlane-Anderson et al all cytological reports and slides at Cytopathology Department of Shahid Sadoughi and Madar hospitals in Yazd , within this period were reviewed (17). This covered 1286 women who have taken OCP and constituted the case group. The control group included women who had regular Pap test checkups as part of their routine screening during the same period of the study and they had not used OCP.
Both the case group and the control group were recruited from the same community and were demographically similar. Cervical samples from the subjects had been taken after oral consent. Women who were previously diagnosed with cervical cancer or who with known premalignant lesions and who have been received injectable contraceptive compound were excluded. The age of the cases and of the controls was matched. The age range for both groups was limited between 25 and 60 years. The duration of using the pills was at least 5 years. Abnormal Pap tests included atypical squamous cells of undetermined significance (ASCUS), dysplasia and carcinoma.
The 2001 Bethesda system was used to classify the epithelial abnormalities (25). Equipment indispensable for HPV DNA testing was not available in our laboratory and therefore, the procedure was not performed. Clinical data with regard to smoking, duration of OCP use and marital status, when available and accessible, were collected for the case and control. Since our local community is a rather conservative, we assumed that all our women do not smoke, do not drink alcohol and are not sexually promiscuous.
 
Statistical analysis
Statistical analysis included Chi-Squared test and Fischer’s exact test. The odds ratio (OR) and 95% confidence interval (95% CI) were applied to estimate the relative risk of negative and positive Pap tests of the cases and the controls. Test results with a probability p<0.05 were considered to be statistically significant. Statistical Package for Social Sciences (SPSS, Chicago, IL) version 15.0 software was used to perform the statistical analysis.
 
Results
 
There were 1286 cases and 1218 controls involved in this study. Ages ranged from 25-60 years with a mean age of 35 years. Demographic characteristics are depicted (Table I). The mean ages of the cases and the controls were 34.14±6.48 and 35.93±7.56, respectively.
Five (0.4%) women who had used OCP showed abnormal Pap tests. All of these abnormal Pap tests indicated ASCUS. The 
control group had three (0.2%) women with abnormal Pap tests in which two of the cytology reports were compatible with ASCUS and one result disclosed low- grade squamous intraepithelial lesion (LSIL). According to the calculated p-value (p=0.727), no association between OCP consumption and abnormal Pap smear was observed.
The estimated Odds ratio for the cases (OR=1.579, 95% CI=0.378-6.591) was not significantly superior to the estimated Odds ratio for the controls (OR=0.999, 95% CI=0.996-1.003). The mean duration of OCP consumption in women with normal Pap smear was 7.66±2.6 years and in women with abnormal Pap smear was 10.8±3.6 years. According to p=0.019 there is a significant difference between women with normal and abnormal Pap smear regarding duration of OCP consumption.


Table I. Patients characteristics and Pap smear results in both groups




Discussion
 
In this study we found no association between OCP consumption and abnormal Pap smear. The possible association between the use of OCP and the development of cervical neoplasia has been the subject of many epidemiological investigations, but the nature of the association remains unclear (26). A remarkable amount of epidemiologic evidence suggests that OCP consuming for a long time, might raise cervical cancer risk, but results have been inconsistent across populations (21).
In addition, it is difficult to separate the effect of oral contraceptive pill use on the risk of contracting HPV infection. Animal studies has shown that Rhesus monkeys that were given high doses of medroxy progesterone developed cervical cancer (27). Furthermore, in 1993 a massive worldwide study conducted by the World Health Organization was published which examined the risk established between OCP use and invasive squamous cervical carcinoma among 2,300 women who had cervical carcinoma and found a strong correlation (22).
In a large study group, Herrero et al showed that women who had received injectable progestins for at least 5 years and who had used them at least 5 years ago suffered a 430% increased risk of developing cervical cancer (23). Also, Briton revealed that usage of OCP for more than 10 years could increase the risk of cervical cancer (24). One study has shown that current use of combined OCPs, a positive HIV test and multiparity are significant predictors of high-grade cervical lesions (11).
On the other hand, in some studies this association has fallen in to suspicion. Molina and coworkers did not find any risk for neoplasia in women who ever used OCP after controlling for the possible confounders and two other studies even showed a protective effect of OCP on severe cervical dysplasia (18-20). The inconsistent reports of an association between hormonal contraception and cervical dysplasia and cancer may be related, in part, to confounding risk factors that include sexual and lifestyle behaviors (28). These factors are difficult to control.
It should be noted that the causal link between HPV and cervical dysplasia and cancer is now generally accepted (29). The literature is overwhelmed with evidential data supporting that human papilloma virus (HPV) is a necessary etiological factor in the pathogenesis of cervical dysplasia and carcinoma (30). However, it is believed that a high proportion of HPV-infected women do not develop serious cervical neoplasia and that other co-factors may be necessary to ultimately culminate severe disease (31). OCP use has been suggested as one possible factor (32).
Other cofactors that may play a role in the carcinogenesis process include smoking, other sexually transmitted diseases and prolonged immunosuppression (33). Given that HPV infection is now considered the major factor in development of cervical cancer, it would seem that OCP may be acting as an enhancer of neoplastic growth. In addition to any direct effect of OCP on the development of cervical dysplasia, either as an initiator or promoter of carcinogenesis, the use of hormonal contraceptives could result in women indulging in more unprotected sexual activity, putting them at more risk of HPV infection and other sexually transmitted infections and their sequel (34). In this study we found no association between OCP consumption and abnormal Pap smear.
To explain these results, it should be taken into account that pathogenesis of cervical cancer and precancerous lesions in Muslim countries might be different compared with western societies due to the difference in the risk factors. The incidence of abnormal Pap smear in Iran is relatively low compared with other studies performed in industrialized countries (35). We are in agreement with others, that we do have a relatively lower prevalence of cervical carcinoma and cervical premalignant lesions. In one study the rate of abnormal Pap smear in Iran has been reported to be 0.2-1% (36). This is most likely related to the sexual behaviors conducted under Islamic rules. In Iran, sexual activity typically starts only after marriage and the cultural and religious traditions of our conservative society restrict the likelihood of multiple sexual partners.
This fact by itself decreases the possibility of HPV and other sexually transmitted infections. However other practices such as male circumcision, which is customary in our country and very low rate of smoking among Iranian women due to cultural context, may play an important role as well. From above-mentioned findings, it is clear that our society has a lower prevalence of HPV infection and cervical neoplasia and as a result, the association between OCP and abnormal Pap smear is weak. On the contrary, in this study there was a significant difference between women with normal and abnormal Pap smear regarding duration of OCP consumption. Thus, long term exposure to OCP conferred more risk for induction of cervical premalignant and malignant changes.
Moreover, other studies have shown that prolonged use of OCP (more than 8-10 years) had a significant influence on the increased risk of cervical cancer (37). Therefore, women using OCP for a prolonged period of time should be encouraged to do regular Pap smear screening. It should be noted that our study had some limitations: 1) The most important limitation was the lack of information about HPV infection, 2) We used conventional pap smear test which had high rate of false-negative results. 3) There were some difficulties in interview because questions related to sexual and reproductive behaviour are considered taboo in Muslim countries such as Iran.
 
Conclusion
 
Results from current study did not show an association between OCP consumption and abnormal Pap smear results. More prospective studies are required.
 
Acknowledgements
 
The authors would like to thank the staff of Pathology Laboratories, Shahid Sadoughi Hospital and Madar Hospital, especially Mrs. Khadijeh Arab for their support and help. This work was supported by Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
 
Conflict of interest
 
Not declared.
 
Type of Study: Original Article |

References
1. Rosai J. Ackerman's surgical pathology, female reproductive system, uterus-cervix. 10th Ed. Elsevier Mosbey; 2011: 1447-1448.
2. Farjadian S, Asadi E, Doroudchi M, Dehaghani AS, Tabei SZ, Kumar VP, et al. High risk HPV types in southern Iranian patients with cervical cancer. Pathol Oncol Res 2003; 9:121-125. [DOI:10.1007/BF03033756]
3. World Health Organization. ICO Information Center on HPV and Cervical Cancer (HPV Information Center): Human papillomavirus and related cancers. Sum Rep Update 2010.
4. Jafari Shobeiri M, Halimi M, Dastranj A, Shahamphar J. Screening for cervical cancer and precancerous lesions in Tabriz. MJIRI 2007; 21: 1-10.
5. Thomison J, Thomas LK, Shroyer KR. Human papillomavirus: molecular and cytologic/ histologic aspects related to cervical intraepithelial neoplasia and carcinoma. Hum Pathol 2008; 39: 154-166. [DOI:10.1016/j.humpath.2007.11.002]
6. Gichangi P, Estambale B, Bwayo J, Rogo K, Ojwang S, Opiyo A, et al. Knowledge and practice about cervical cancer and Pap smear testing among patients at Kenyatta National Hospital, Nairobi, Kenya. Intl J Gynecol Cancer 2003; 13: 827-833. [DOI:10.1111/j.1525-1438.2003.13612.x]
7. Jonathan S. Berek, cervical cancer, Deborah L. Berek MA, Berek and Novak's Gynecology. 15th Ed united-state of America, Lippincott Williams and Wilkins 2012; 1305.
8. Santin AD, Zhan F, Bignotti E, Siegel ER, Cané S, Bellone S, et al. Gene expression profiles of primary HPV16-and HPV18-infected early stage cervical cancers and normal cervical epithelium: identification of novel candidate molecular markers for cervical cancer diagnosis and therapy. Virology 2005; 331: 269-291. [DOI:10.1016/j.virol.2004.09.045]
9. Sohail R, Nazir R, Latif Y, Zaman F. Evaluation of cervical smear in women attending gynecological OPD. J Surg Pak (Int) 2008; 13: 3.
10. Sohail R, Nazir R, Latif Y, Zaman F. Evaluation of cervical smear in women attending gynecological OPD. J Surg Pakn (Int) 2008; 13: 121-123.
11. Kiatiyosnusorn R, Suprasert P, Srisomboon J, Siriaree S, Khunamornpong S, Kietpeerakool, C. High-grade histologic lesions in women with low-grade squamous intraepithelial lesion cytology from a region of Thailand with a high incidence of cervical cancer. Int J Gynaecol Obstet 2010; 110: 133-136. [DOI:10.1016/j.ijgo.2010.03.022]
12. Marshall K. Cervical dysplasia: early intervention. Altern Med Rev 2003; 8: 156-170.
13. Edlow AG, Bartz D. Hormonal contraceptive options for women with headache: A review of the evidence. Rev Obstet Gynecol 2010; 3: 55-65.
14. Saadatnia M, Naghavi N, Fatehi F, Zare M, Tajmirriahi M. Oral contraceptive misuse as a risk factor for cerebral venous and sinus thrombosis. J Res Med Sci 2012; 17: 344-347.
15. Ye Z, Thomas DB, Ray RM. Combined oral contraceptives and risk of cervical carcinoma in situ. Int J Epidemiol 1995; 24: 19-26. [DOI:10.1093/ije/24.1.19]
16. Mafuva C, Djarova T, Matarira HT. Influence of combined oral contraceptives on the onset of cervical intraepithelial neoplasia. Afr J Health Sci 2002; 9: 129-137.
17. McFarlane-Anderson N, Patience E, Bazuaye M, Jackson D, Monica S, Horace M Fletcher, Cervical dysplasia and cancer and the use of hormonal contraceptives in Jamaican women. BMC Womens Health 2008; 8: 9. [DOI:10.1186/1472-6874-8-9]
18. Molina R, Thomas DB, Dabancens A, Lopez J, Ray RM, Martinez L, et al. Oral contraceptives and cervical carcinoma in situ in Chile. Cancer Res 1988; 48: 1011-1015.
19. Sayednozadi S, Hassany M, Ramezani MA. Association of oral contraceptives and abnormal Pap smear. Am J Appl Sci 2005; 2: 1150-1152. [DOI:10.3844/ajassp.2005.1150.1152]
20. Becker TM, Wheeler CM, McGOUGH NS, Stidley CA, Parmenter CA, Dorin MH, et al. Contraceptive and reproductive risks for cervical dysplasia in southwestern Hispanic and non-Hispanic white women. Int J Epidemiol 1994; 23: 913-922. [DOI:10.1093/ije/23.5.913]
21. Nygård J, Skare G, Thoresen SØ. The cervical cancer screening programme in Norway, 1992-2000: changes in Pap smear coverage and incidence of cervical cancer. J Med Screen 2002; 9: 86-91. [DOI:10.1136/jms.9.2.86]
22. Berry G, Maclennan R, Shearman R, Jelihovsky T, Booth JC, Molina R, et al. Invasive squamous‐cell cervical carcinoma and combined oral contraceptives: Results from a multinational study. Int J Cancer 1993; 55: 228-236. [DOI:10.1002/ijc.2910550211]
23. Herrero R, Brinton LA, Reeves WC, Brenes MM, De Britton RC, Tenorio F, et al. Injectable contraceptives and risk of invasive cervical cancer: evidence of an association. Int J Cancer 2006; 46: 5-7. [DOI:10.1002/ijc.2910460103]
24. Brinton LA. Oral contraceptives and cervical neoplasia. Contraception 1991; 43: 581-595. [DOI:10.1016/0010-7824(91)90005-Z]
25. Solomon D, Nayar R. The Bethesda System for reporting cervical cytology: definitions, criteria, and explanatory notes: Springer; 2004. [DOI:10.1007/978-1-4612-2042-8]
26. Celentano DD, Klassen A, Weisman CS, Rosenshein NB. The role of contraceptive use in cervical cancer: the Maryland cervical cancer case-control study. Am J Epidemiol 1987; 126: 592-604. [DOI:10.1093/oxfordjournals.aje.a114699]
27. Dallenbach-Hellweg G. On the origin and histological structure of adenocarcinoma of the endocervix in women under 50 years of age. Pathol Res Prac 1984; 179: 38-50. [DOI:10.1016/S0344-0338(84)80059-X]
28. Marc A, Fritz, Leon S peroff, Oral contraception, Marc A. Fritz, Leon Speroff, Clinical gynecologic endocrinology and infertility. 8th Ed. United State of America, Lippincott Williams and Wilkins; 2011: 996-997.
29. Green J, De Gonzalez AB, Smith J, Franceschi S, Appleby P, Plummer M, et al. Human papillomavirus infection and use of oral contraceptives. Br J Cancer 2003; 88: 1713-1720. [DOI:10.1038/sj.bjc.6600971]
30. Walboomers JMM, Jacobs MV, Manos MM, Bosch FX, Kummer JA, Shah KV, et al. Human papillomavirus is a necessary cause of invasive cervical cancer worldwide. J Pathol 1999; 189: 12-19. https://doi.org/10.1002/(SICI)1096-9896(199909)189:1<12::AID-PATH431>3.0.CO;2-F [DOI:10.1002/(SICI)1096-9896(199909)189:13.0.CO;2-F]
31. Hausen HZ. Human genital cancer: Synergism between two virus infections or synergism between a virus infection and initiating events? Lancet 1982; 320: 1370-1372. [DOI:10.1016/S0140-6736(82)91273-9]
32. Negrini BP, Schiffman MH, Kurman RJ, Barnes W, Lannom L, Malley K, et al. Oral contraceptive use, human papillomavirus infection, and risk of early cytological abnormalities of the cervix. Cancer Res 1990; 50: 4670-4675.
33. Gayed M, Bernatsky S, Ramsey-Goldman R, Clarke A, Gordon C. Lupus and cancer. Lupus 2009; 18: 479-485. [DOI:10.1177/0961203309102556]
34. Smith JS, Green J, de Gonzalez AB, Appleby P, Peto J, Plummer M, et al. Cervical cancer and use of hormonal contraceptives: a systematic review. Lancet 2003; 361: 1159-1167. [DOI:10.1016/S0140-6736(03)12949-2]
35. Greenlee RT, Murray T, Bolden S, Wingo PA. Cancer statistics, 2000. CA Cancer J Clin 2008; 50: 7-33. [DOI:10.3322/canjclin.50.1.7]
36. Mosavi-Jarrahi A, Mohagheghi M, Zeraatti H, Mortazavi H. Cancer registration in Iran. Asian Pac J Cancer Prev 2001; 2: 25-29.
37. Schlesselman JJ. Net effect of oral contraceptive use on the risk of cancer in women in the United States. Obstet Gynecol 1995; 85: 793-801. [DOI:10.1016/0029-7844(95)00022-J]

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