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International Journal of Reproductive Biomedicine logoLink to International Journal of Reproductive Biomedicine
. 2017 May;15(5):305–310.

Relative frequency of human papillomavirus genotypes and related sociodemographic characteristics in women referred to a general hospital in Tehran, 2014-2015: A cross-sectional study

Mahin Jamshidi Makiani 1, Sara Minaeian 2, Soheila Amini Moghaddam 3, Seyed Akbar Moosavi 4, Zahra Moeini 5, Vajihe Zamani 6, Mahnaz Karbalaei Sabbagh 7, Hosein Forghani 8
PMCID: PMC5510584  PMID: 28744526

Abstract

Background:

Human papilloma virus (HPV) is one of the major public health problems and the main causes of cervical cancer. The prevalence HPV infection in developing countries with low financial resources is high.

Objective:

This study aimed to determine the relative frequency of HPV genotypes and its sociodemographic characteristics in women referred to a general hospital in Tehran, Iran from 2014-2015.

Materials and Methods:

This cross-sectional study was performed in 400 women with Pap smear samples, referring to to a general hospital in Tehran, Iran from 2014-2015. The detection of 28 HPV genotypes was performed by using the Multiplex PCR technique. The sociodemographic survey was conducted for each HPV positive woman.

Results:

HPV-positive infection was detected in 155 (38.75%) women aged 17-85 years. HPV 16 (19.1%) was the most prevalent type, followed by HPV 39 (12.5%) and HPV 18 (8.9%). The highest rate of HPV infection was observed at the age of 36 years (7.7%). The level of education and economic situation of each woman were showed most of HPV-positive women had a high school diploma (34.6%) and average economic situation (67,9%). 60.9% of these women were a housewife, and 67.3% lived in the capital .

Conclusion:

Determination of HPV genotype and risk factor related to HPV infection in each geographical region can lead to the production of effective vaccines against the HPV virus. It can also be useful for disease management and high sensitivity diagnosis of cervical intraepithelial neoplasia.

Key Words: Human papilloma virus, Frequency, Multiplex PCR, Socioeconomic factors

Introduction

Human papilloma virus (HPV) is one of the major public health problems and the main causes of cervical cancer (1). It is the considerable challenge in developing countries with low financial resources (2). HPV is a member of the Papillomaviridae family (3) which is divided into high-risk, possibly high-risk, and Low-risk HPV groups. Up to now, the sequences of 150 HPV types have been determined (4). According to studies performed persistent HPV infections can lead to cervical cancer (5, 6). Some types of high risks HPV, such as HPV 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 and 70 can lead to cervical carcinoma (7, 8).

The worldwide prevalence of HPV has been varied from 2-44% (9). In a meta-analysis, which was accomplished by Bruni et al the global prevalence of HPV was 11.7%. The HPV prevalence was 24% in Sub-Saharan Africa, 21.4% in Eastern Europe, 16.1% in Latin America (10). According to the research that has been accomplished in Iran in 2012; the prevalence of HPV infection among women was 7% (11). Among the different types of HPV that have been observed in Iran, the prevalence of HPV 16 and HPV 18 was 7.3% and 2.8%, respectively (12). The socioeconomic situation, the level of education, living in deprived areas and regional customs and habits have a significant effect on HPV infection rate (13, 14).Smoking, alcohol consumption, and women’s sex history are some of the important risk factors of acquisition of HPV infection (15).

It has been proven HPV detection and organized screening program can be essential strategies against cervical cancer. Thus providing accurate and rapid methods for detection and identification of HPV would be very useful and helpful (16). Multiplex PCR, which is easy to use with high sensitivity and specificity, plays an important role in the detection of many viruses such as HPV (4, 17).

By identifying risk factors contributing to HPV infection according to the customs and habits of each specific area, effective prevention methods and rapid detection of HPV infection can be achieved. It could help us to reduce the prevalence of HPV in the society significantly. Most studies within the field of HPV prevalence which has been performed in Iran have only focused on determination of the HPV types. However, in this study, we decided to survey socioeconomic and demographic characteristic’s data in addition to the relative frequency of HPV.

The main aim of this investigation was to detect the frequency of HPVs genotypes and study of risk factors associated with HPV infection in the part of the Tehran city.

Materials and methods

Sample collection and DNA extraction

In this cross-sectional study, a total of 400 women referred to the Women’s Clinic of a general hospital in Tehran, Iran during the period of one year from September 2014 to September 2015 were recruited. Our inclusion criteria were all women who referred to Women’s Clinic, needed gynecological examination and agreed to have examination. Women who were in menstrual period, pregnancy, had a history of HPV vaccination, or had a contraindication of gynecological examination were excluded.

All participants were interviewed for their level of education, sociodemographic characteristics, age, the age of menarche, marriage or menopause, pregnancy contraception methods, underlying disease, history of sexually transmitted diseases, history of smoking, and sexual or reproductive history. Then they were undergoing a gynecologic examination and a Pap smear test by vaginal cytology brush through the liquid-based thin perb pap method. HPV DNA was extracted using the EZ DNA Methylation™ Extraction Kit (TBG, USA) according to the manufacturer’s instruction and then multiplex polymerase-chain-reaction (PCR) tests for HPV DNA were performed.

Multiplex PCR test

HPV genotyping was performed using the HPV-HCR Genotype-Eph kit (AmpliSens(R), Russia).The kit is based on simultaneous amplifying in one tube (multiplex-PCR) of four types of HPV DNA and allows the user to detect infections and co-infections of high-risk HPV genotypes. DNA from each HPV genotype was used as a positive control and distilled water in place of template DNA run at the same conditions as a negative control.

Each PCR was performed in a DNA thermal cycler (Sensquest, Germany) with the following condition: The amplification was carried out with initial enzyme activation at 95oC for 15 min, followed by 42 cycles, including 1 sec denaturation at 95oC, 3 sec annealing at 63oC and 40 sec chain elongation at 72oC and a final elongation at 72oC for 1 min and cooling at 4oC. PCR products were visualized on 1.5% agarose gel by ethidium bromide staining (18, 19).

A participant was considered HPV-positive if the test results by PCR or genotyping were positive. Samples that were negative for HPV DNA were amplified with primers for the cKi-ras gene to ensure the integrity of the samples. Samples in which neither HPV DNA nor the cKi-ras gene was amplified were considered inadequate for analysis and were excluded.

Ethical consideration

Informed consent was obtained from all women enrolled, and the study was approved by the Ethics Committee of the Iran University of Medical Sciences (Ref. number: IR.IUMS.REC.1391-17028).

Statistical analysis

Data analysis, which was obtained from Multiplex PCR test and the questionnaires were entered into an Excel spreadsheet and then data were performed using Statistical Package for the Social Sciences, version 18.0, SPSS Inc, Chicago, Illinois, USA (SPSS) software. All quantitative variables were evaluated by the mean±SEM and type-specific prevalence of HPV were summarized using frequency distributions.

Results

Demographic and Sociodemographic Characteristics

The mean±SD age of participants in this study was 42.58±12.21 yr old (ranging from 17-89 yr old). Among 400 women included in this analysis, overall HPV prevalence was 38.75% [positive HPV (n=155) and negative HPV (n=245)]. The mean age of HPV-positive women was 40.47 yr old (ranging from 20-80 yr old). Also, the mean age of menarche and marriage among the HPV-infected women were 13.28±1.57 and 19.38±4.96 yr, respectively and 70.4% of them had not experienced menopause until this study was underway. The mean age of menopause among HPV-positive women was 47.29±6.93 yr.

22.4% of HPV-positive women had never been used any contraception method (Table I). 87.2% of them did not have a history of sexually transmitted diseases (STDs), 93.6% did not have any malignancy history, and only 31.4% of them had the underlying disease. Study of the questionnaires was indicated that 0.6% were not married and were not a virgin, 87.2% married once, 7.1% had a second marriage, and 5.8% did not answer this question. Among them, 80.8% were a mother and the mean age of the first pregnancy was 20.94±4.801.

Table I.

Study of contraception methods in HPV-positive women

Contraception methods Frequency n (%)
Oral contraceptive 10 (6.41)
Tubal ligation 15 (9.6)
Vasectomy 6 (3.8)
Condoms 26 (16.66)
Oral contraceptives and natural family planning 1 (0.6)
Oral contraceptives and vasectomy 1 (0.6)
Condom and natural family planning 3 (1.9)
No method 35 (22.43)
withdrawal method during intercourse 59 (37.82)
Total 156 (100)

Socioeconomic analysis of HPV-positive women was performed. This means that level of education and economic situation of each were evaluated. Most of HPV-positive women had a high school diploma (34.6%) and average economic situation (67.9%). 60.9% of these women were a housewife, and 67.3% lived in the capital. A survey of the HPV-positive women showed that 96.8% of them were not smokers and 93.6% were not the hookah smokers (Table II). Twenty-eight different types of HPV were detected. The highest prevalence of HPV type was HPV16 (19.1%) and as follows HPV39 (12.5%) and HPV18 (8.9%). The lower types of HPV were HPVs 15, 17, 40, 53, 67, 69, 70, and 75 had the lowest prevalence (Figure 1).

Table II.

Survey of smoking and Hookah smoker in HPV-positive women

Frequency n(%)
Smoking 5/156 (3.2)
Hookah smoker 10/156 (6.4)

Figure 1.

Figure 1

The prevalence of different HPV types among HPV DNA- positive samples

Discussion

It has been proven persistent HPV infection can lead to cervical cancer and intraepithelial neoplasia (16, 20). Serological methods and culture are not the reliable and sensitive methods for detection of HPV, thus uses the accurate and rapid test are taken under consideration (21, 22).

According to our results, 155/400 (38.75%) studied women were positive and infected by one or more types of HPV. Also, the most prevalent types of HPV were HPV16 (20.2%). 22 types of HPV were observed, including HPV 15, 16, 17, 18, 31, 33, 35, 39, 40, 45, 51, 52, 53, 56, 58, 59, 66, 67, 68, 70, 73 and 75.The prevalence of HPV types was changeable in different geographic regions, but HPV 16 were reported as the most prevalent and cancerous type among the other types of Human papillomavirus (23). According to studies performed in Iran, the prevalence of HPV 16 was higher than other types of HPV (24-26). In the study which was performed in Iran, the total prevalence of HPV in Iran among 7655 women was 9.4% and the prevalence of HPV 16 and 18 were respectively 2.03% and 1.7% (27).

The prevalence of HPV 16 was 76% in 2 hospitals in Tehran, 7.3% in the other hospital in Tehran, and 15.21% in Isfahan (25, 26, 28). Clifford et al reported that HPV 18, 45, 31, and 33 were respectively the most common types of HPV after HPV 16 (29). In Asia, HPV 52 and 58 respectively, were more prevalent after HPV 16 and 18 (30). Our survey showed that after HPV 16, HPV 39 (16.2%) and HPV 18 (12.6%) were respectively the most prevalent type of HPV. However, Salehi-Vaziri and colleagues reported HPV 35 (9.1%) was the most common types of HPV after HPV 16 (32.8%) in Iran (24). As mentioned before, differences among the types of HPV can be due to various geographical distributions of this virus(9).

In our study, the highest rate of HPV prevalence was observed at the age 36 yr (7.7%) followed by age 46 yr (5.8%). In the study was performed by Dunne et al the prevalence of HPV infection was increased from aged 14-24 yr and in the older ages, the rate of HPV infection was decreased gradually. The highest rate of HPV infection prevalence was observed at the age under 20 yr. The prevalence of HPV was 19.6% in women who were in the fifties, 25.2% in forties, and 27.5% in the thirties (31). It could be due to differences in the number and type of study population. Studies in different countries indicated that the rate of HPV infection in the young women was high. It may be due to high sexual activity of them during this period of life. But the rate of HPV infection in the fourth or fifth decades of life was reduced gradually (7, 32, 33).

However, the risk of HPV infection in women who were sexually active existed in all ages (34). Kim et al have reported that age was one of the significant risk factors for acquisition high-risk HPV infection and high-risk HPV infection was decreased with advancing women age (35). The results from this study indicated that in all age categories, the most infectious type was HPV 16 (19.1%), and the highest rate of infection was observed at the age of 38 years. Generally, in Iran, the mean age of menarche is reported 12.81 yr (36).

There is much controversy over the menarche age as an independent risk factor in HPV infection (37, 38).In our research, the menarche age of most HPV-positive women was 13 years old and HPV 16 was the most prevalent type among them. The highest frequency of age in menopausal women was observed in the age 50 yr. Most of them were infected with HPV 16. The finding of the current study was consistent with Smith et al study who showed HPV 16 was the most prevalent type among menopausal women (39). It had shown that long duration use of oral contraception could amplify the risk of HPV infection while using a condom could reduce it (40). In the current study, HPV16 was the most common type in women who used IUD and natural withdrawal method during intercourse. In the women who had the history of the sexually transmitted disease and the history of malignancy HPV16 was the most prevalent type. HPV35 and HPV38 were detected as dominant types in women who had the underlying disease, but HPV16 was further observed in those who didn’t have.

In Iran, the rate of cigarette smokers among women varied from 0.04-10.5%, and in comparison to the rates reported by WHO, it was the lowest rate (41). The results of this study indicated that among women who smoked and used Hookah, HPV 16 was further observed compared to other types of HPV. In study was performed in the northeast region of India HPV16 was the more prevalent type among head and neck cancer patients who had tobacco chewing habit (42). Studies have shown HPV 16 infection and use of cigarette were two significant factor, which can enhance the development of cervical cancer (43, 44). It should be noted that in Iran, smoking is not common among women.

According to the finding of Giorgi Rossi et al lower socioeconomic women had a little knowledge about HPV infection and cervical cancer (45). Similarly, in another study it was mentioned that lower levels of education and economic status were inversely associated with the incidence of cancers are caused by HPV infection (46). In current study women with an average socioeconomic status, had the highest rate of HPV infection and HPV 16 was observed more frequently in this group. It can be due to less referring to women who were in the lower socioeconomic status group to the physician. This evidence can also be observed in the lower literacy level of HPV-positive women. An investigation by Catarino et al revealed that being a housewife could be a risk factor to acquire HPV infection (47). Also, we found that 60.9% of HPV-positive women were housewives, with a high prevalence of HPV16. After that, HPV 18 and HPV 39 had the highest prevalence of HPV infection among the other type of HPV.

Conclusion

Our study provides that HPV16 was the most prevalent type (19.1%) in HPV positive women. In all risk factors investigated in this study HPV16 was the most prevalent type. HPV genotyping and detection of risk factors associated with HPV acquisition in each region can lead to develop an effective screening program and increase the level of awareness of community members. It can also be useful for disease management and high sensitivity diagnosis of cervical intraepithelial neoplasia. Further studies should be done to investigate the HPV genotyping of the other region of Iran or the other part of the world.

Acknowledgments

The study was supported by Iran University of Medical Sciences, Tehran, Iran.

Conflict of interest

Vaccination against HPV is not mandatory in Iran. Study of prevalence of Human Papillomavirus genotypes and related sociodemographic characteristics will allow us to have sufficient information about this infection and will be led to perform routine immunization against HPV in Iran.

References

  • 1.Minaeian S, Rahbarizadeh F, Zarkesh-Esfahani SH, Ahmadvand D, Broom OJ. Neutralization of human papillomavirus by specific nanobodies against major capsid protein L1. J Microbiol Biotechnol. 2012;22:721–728. doi: 10.4014/jmb.1112.12001. [DOI] [PubMed] [Google Scholar]
  • 2.Parkin DM, Bray F. The burden of HPV-related cancers. Vaccine. 2006;24:S11–S25. doi: 10.1016/j.vaccine.2006.05.111. [DOI] [PubMed] [Google Scholar]
  • 3.De Villiers E-M, Fauquet C, Broker TR, Bernard H-U, zur Hausen H. Classification of papillomaviruses. Virology. 2004;324:17–27. doi: 10.1016/j.virol.2004.03.033. [DOI] [PubMed] [Google Scholar]
  • 4.Tsakogiannis D, Diamantidou V, Toska E, Kyriakopoulou Z, Dimitriou T, Ruether I, et al. Multiplex PCR assay for the rapid identification of human papillomavirus genotypes 16, 18, 45, 35, 66, 33, 51, 58, and 31 in clinical samples. Arch Virol. 2015;160:207–214. doi: 10.1007/s00705-014-2261-6. [DOI] [PubMed] [Google Scholar]
  • 5.Moscicki A-B, Schiffman M, Kjaer S, Villa LL. Updating the natural history of HPV and anogenital cancer. Vaccine. 2006;24:S42–S51. doi: 10.1016/j.vaccine.2006.06.018. [DOI] [PubMed] [Google Scholar]
  • 6.Koshiol J, Lindsay L, Pimenta JM, Poole C, Jenkins D, Smith JS. Persistent human papillomavirus infection and cervical neoplasia: a systematic review and meta-analysis. Oxford Univ Press; 2008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Burd EM. Human papillomavirus and cervical cancer. Clin Microbiol Rev. 2003;16:1–17. doi: 10.1128/CMR.16.1.1-17.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Sasagawa T, Basha W, Yamazaki H, Inoue M. High-risk and multiple human papillomavirus infections associated with cervical abnormalities in Japanese women. Cancer Epidemiol Prevent Biomark. 2001;10:45–52. [PubMed] [Google Scholar]
  • 9.Orozco-Colín A, Carrillo-García A, Méndez-Tenorio A, Ponce-de-León S, Mohar A, Maldonado-Rodríguez R, et al. Geographical variation in human papillomavirus prevalence in Mexican women with normal cytology. Int J Infect Dis. 2010;14:1082–1087. doi: 10.1016/j.ijid.2010.07.007. [DOI] [PubMed] [Google Scholar]
  • 10.Bruni L, Diaz M, Castellsagué M, Ferrer E, Bosch FX, de Sanjosé S. Cervical human papillomavirus prevalence in 5 continents: meta-analysis of 1 million women with normal cytological findings. J Infect Dis. 2010;202:1789–1799. doi: 10.1086/657321. [DOI] [PubMed] [Google Scholar]
  • 11.Khorasanizadeh F, Hassanloo J, Khaksar N, Taheri SM, Marzaban M, Rashidi BH, et al. Epidemiology of cervical cancer and human papilloma virus infection among Iranian women-Analyses of national data and systematic review of the literature. Gynecol Oncol. 2013;128:277–281. doi: 10.1016/j.ygyno.2012.11.032. [DOI] [PubMed] [Google Scholar]
  • 12.Yousefzadeh A, Mostafavizadeh SM, Jarollahi A, Raeisi M, Garshasbi M, Siavashvahabi Z, et al. Human papillomavirus (HPV) prevalence and types among women attending regular gynecological visit in Tehran, Iran. Clin Lab. 2013;60:267–273. doi: 10.7754/clin.lab.2013.130221. [DOI] [PubMed] [Google Scholar]
  • 13.Graham JE, Mishra A. Global challenges of implementing human papillomavirus vaccines. Int JEquit Health. 2011;10:27. doi: 10.1186/1475-9276-10-27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Giorgi Rossi P, Baldacchini F, Ronco G. The possible effects on socio-economic inequalities of introducing HPV testing as primary test in cervical cancer screening programs. Front Oncol. 2014;4:20. doi: 10.3389/fonc.2014.00020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Dempsey AF. Human papillomavirus: the usefulness of risk factors in determining who should get vaccinated. Rev Obstet Gynecol. 2008;1:122. [PMC free article] [PubMed] [Google Scholar]
  • 16.Minaeian S, Rahbarizadeh F, Zarkesh Esfahani SH, Ahmadvand D. Characterization and enzyme-conjugation of a specific anti-l1 nanobody. J Immunoassay Immunochem. 2012;33:422–434. doi: 10.1080/15321819.2012.665407. [DOI] [PubMed] [Google Scholar]
  • 17.Elnifro EM, Ashshi AM, Cooper RJ, Klapper PE. Multiplex PCR: optimization and application in diagnostic virology. Clin Microbiol Rev. 2000;13:559–570. doi: 10.1128/cmr.13.4.559-570.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Haghshenas M, Golini-Moghaddam T, Rafiei A, Emadeian O, Shykhpour A, Ashrafi GH. Prevalence and type distribution of high-risk human papillomavirus in patients with cervical cancer: a population-based study. Infect Agents Cancer. 2013;8:20. doi: 10.1186/1750-9378-8-20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Romero-Pastrana F. Detection and typing of human papilloma virus by multiplex PCR with type-specific primers. ISRN Microbiol. 2012;2012 doi: 10.5402/2012/186915. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Braaten KP, Laufer MR. Human papillomavirus (HPV), HPV-related disease, and the HPV vaccine. Rev Obstet Gynecol. 2008;1:2. [PMC free article] [PubMed] [Google Scholar]
  • 21.Möbius G. Cytological early detection of cervical carcinoma: possibilities and limitations Analysis of failures. J Cancer Res Clin Oncol. 1993;119:513–521. doi: 10.1007/BF01686460. [DOI] [PubMed] [Google Scholar]
  • 22.Bashizadeh-Fakhar H, Ghane M, Faraji R, Ashoorizadeh B. Identifying Human Papilloma Virus (HPV) in Women with Genital Warts by Multiplex–PCR Method. Zahedan J Res Med Sci. 2013;15:45–48. [Google Scholar]
  • 23.Clifford G, Gallus S, Herrero R, Munoz N, Snijders P, Vaccarella S, et al. Worldwide distribution of human papillomavirus types in cytologically normal women in the International Agency for Research on Cancer HPV prevalence surveys: a pooled analysis. Lancet. 2005;366:991–998. doi: 10.1016/S0140-6736(05)67069-9. [DOI] [PubMed] [Google Scholar]
  • 24.Salehi-Vaziri M, Sadeghi F, Hashemi FS, Haeri H, Bokharaei-Salim F, Monavari SH, et al. Distribution of Human Papillomavirus genotypes in Iranian women according to the severity of the cervical lesion. Iran Red Crescent Med J. 2016;18:e24458. doi: 10.5812/ircmj.24458. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Shafaghi B, Jarollahi A, Yousefzadeh B, Ameri A, Moghadam S, Mostafavi M. Human Papilloma Virus Prevalence and Types among Iranian Women Attending Regular Gynecological visits. Reports of Radiotherapy and Oncology. 2013;1:73–79. [Google Scholar]
  • 26.Ghaffari SR, Sabokbar T, Mollahajian H, Dastan J, Ramezanzadeh F, Ensani F, et al. Prevalence of human papillomavirus genotypes in women with normal and abnormal cervical cytology in Iran. Asian Pacific J Cancer Prevent. 2006;7:529. [PubMed] [Google Scholar]
  • 27.Malary M, Moosazadeh M, Hamzehgardeshi Z, Afshari M, Moghaddasifar I, Afsharimoghaddam A. The prevalence of cervical human papillomavirus infection and the most at-risk genotypes among Iranian healthy women: A systematic review and meta-analysis. Int J Prevent Med. 2016;7:70. doi: 10.4103/2008-7802.181756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Allameh T, Moghim S, Farahbod F. Reviewing the Prevalence of Human Papillomavirus (HPV) in married women aged 18-60 years with normal Pap smear referring to gynecology clinics in hospitals affiliated to Isfahan University of Medical Sciences, Iran. J Isfahan Medl School. 2012;29 [Google Scholar]
  • 29.Clifford G, Smith JS, Plummer M, Munoz N, Franceschi S. Human papillomavirus types in invasive cervical cancer worldwide: a meta-analysis. Br JCancer. 2003;88:63–73. doi: 10.1038/sj.bjc.6600688. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Meijer CJ, Snijders PJ, Castle PE. Clinical utility of HPV genotyping. Gynecol Oncol. 2006;103:12–17. doi: 10.1016/j.ygyno.2006.07.031. [DOI] [PubMed] [Google Scholar]
  • 31.Dunne EF, Unger ER, Sternberg M, McQuillan G, Swan DC, Patel SS, et al. Prevalence of HPV infection among females in the United States. JAMA. 2007;297:813–819. doi: 10.1001/jama.297.8.813. [DOI] [PubMed] [Google Scholar]
  • 32.Trottier H, Franco EL. Human papillomavirus and cervical cancer: burden of illness and basis for prevention. Am J Manag Care. 2006;12:462–472. [PubMed] [Google Scholar]
  • 33.Castle PE, Schiffman M, Herrero R, Hildesheim A, Rodriguez AC, Bratti MC, et al. A prospective study of age trends in cervical human papillomavirus acquisition and persistence in Guanacaste, Costa Rica. J Infect Dis. 2005;191:1808–1816. doi: 10.1086/428779. [DOI] [PubMed] [Google Scholar]
  • 34.Castellsagué X, Schneider A, Kaufmann AM, Bosch FX. HPV vaccination against cervical cancer in women above 25 years of age: key considerations and current perspectives. Gynecol Oncol. 2009;115:S15–S23. doi: 10.1016/j.ygyno.2009.09.021. [DOI] [PubMed] [Google Scholar]
  • 35.Kim KD, Kim JJ, Kim SM, No JH, Kim YB. Prevalence and determinants of high-risk human papillomavirus infection in women with high socioeconomic status in Seoul, Republic of Korea. Asian Pacific J Cancer Prevent. 2012;13:269–273. doi: 10.7314/apjcp.2012.13.1.269. [DOI] [PubMed] [Google Scholar]
  • 36.Bahrami N, Soleimani MA, Chan YH, Ghojazadeh M, Mirmiran P. Menarche age in Iran: A meta-analysis. Iran JNurs Midwif Res. 2014;19:444–450. [PMC free article] [PubMed] [Google Scholar]
  • 37.Syrjänen K, Shabalova I, Petrovichev N, Kozachenko V, Zakharova T, Pajanidi J, et al. Age at menarche is not an independent risk factor for high-risk human papillomavirus infections and cervical intraepithelial neoplasia. Int J STD AIDS. 2008;19:16–25. doi: 10.1258/ijsa.2007.007042. [DOI] [PubMed] [Google Scholar]
  • 38.Winer RL, Feng Q, Hughes JP, O'reilly S, Kiviat NB, Koutsky LA. Risk of female human papillomavirus acquisition associated with first male sex partner. J Infect Dis. 2008;197:279–282. doi: 10.1086/524875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Smith E, Johnson S, Ritchie J, Feddersen D, Wang D, Turek L, et al. Persistent HPV infection in postmenopausal age women. Int J Gynecol Obstet. 2004;87:131–137. doi: 10.1016/j.ijgo.2004.07.013. [DOI] [PubMed] [Google Scholar]
  • 40.Winer RL, Hughes JP, Feng Q, O'reilly S, Kiviat NB, Holmes KK, et al. Condom use and the risk of genital human papillomavirus infection in young women. New Eng J Med. 2006;354:2645–2654. doi: 10.1056/NEJMoa053284. [DOI] [PubMed] [Google Scholar]
  • 41.Halimi L, Haghdoost AA, Alizadeh SM. Prevalence of cigarette smoking among Iranian women: a systematic review and meta-analysis. Med J. 2013;27:132. [PMC free article] [PubMed] [Google Scholar]
  • 42.Kumar R, Rai AK, Das D, Das R, Kumar RS, Sarma A, et al. Alcohol and tobacco increases risk of high risk HPV infection in head and neck cancer patients: Study from North-East Region of India. PloS One. 2015;10:e0140700. doi: 10.1371/journal.pone.0140700. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Dimitrov G, Džikova E, Dimitrov G, Babushku G, Antovska V. The influence of HPV16, smoking and coitarche in the development of cervical dysplasia in the stage where conization is the treatment of choice. Acta Facult Med Naissens. 2012;29:181–186. [Google Scholar]
  • 44.Gunnell AS, Tran TN, Torrång A, Dickman PW, Sparén P, Palmgren J, et al. Synergy between cigarette smoking and human papillomavirus type 16 in cervical cancer in situ development. Cancer Epidemiol Biomark Preven. 2006;15:2141–2147. doi: 10.1158/1055-9965.EPI-06-0399. [DOI] [PubMed] [Google Scholar]
  • 45.Rossi PG, Baldacchini F, Ronco G. The possible effects on socio-economic inequalities of introducing HPV testing as primary test in cervical cancer screening programs. Frontiers Oncol. 2014:4. doi: 10.3389/fonc.2014.00020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Benard VB, Johnson CJ, Thompson TD, Roland KB, Lai SM, Cokkinides V, et al. Examining the association between socioeconomic status and potential human papillomavirus‐associated cancers. Cancer. 2008;113:2910–2918. doi: 10.1002/cncr.23742. [DOI] [PubMed] [Google Scholar]
  • 47.Catarino R, Vassilakos P, Tebeu P-M, Schäfer S, Bongoe A, Petignat P. Risk factors associated with human papillomavirus prevalence and cervical neoplasia among Cameroonian women. Cancer Epidemiol. 2016;40:60–66. doi: 10.1016/j.canep.2015.11.008. [DOI] [PubMed] [Google Scholar]

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