Population-based type-specific prevalence of high-risk human papillomavirus infection in Estonia

Abstract

Background

Effective prophylactic vaccines are available against human papillomavirus (HPV) types 6, 11, 16, and 18 which are licensed for routine use among young women. Monitoring is needed to demonstrate protection against cervical cancer, to verify duration of protection, and assess replacement frequency of non-vaccine types among vaccinated cohorts.

Methods

Data from a population-based study were used to assess the type-specific prevalence of HPV in a non-vaccinated population in Estonia: 845 self-administered surveys and self-collected vaginal swabs were distributed, 346 were collected by mail and tested for HPV DNA from female participants 18-35 years of age.

Results

The overall HPV prevalence (weighted estimate to account for the sampling method) in the study population (unvaccinated women aged 18-35) was calculated to be 38% (95% CI 31-45%), with estimated prevalences of high- and low-risk HPV types 21% (95% CI 16-26%), and 10% (95% CI 7-14%), respectively. Of the high-risk HPV types, HPV 16 was detected most frequently (6.4%; 95% CI 4.0-9.8%) followed by HPV 53 (4.3%; 95% CI 2.3-7.2%) and HPV 66 (2.8%; 95% CI 1.3-5.2%).

Conclusions

We observed a high prevalence of total and high-risk type HPV in an Eastern European country. The most common high-risk HPV types detected were HPV 16, 53, and 66.

Background

Human papillomavirus (HPV) is thought to be the most common sexually transmitted infection in the world [1]. Genital HPV types are categorized according to their epidemiological association with cervical cancer. Infections with low-risk types, such as HPV types 6 and 11, can cause benign or low grade changes in cervical cells, genital warts, and recurrent respiratory papillomatosis. High-risk HPV types can cause cervical, anal, and other genital cancers. High-risk HPV types are detected in 99% of cervical cancers, and worldwide approximately 70% of cervical cancers are due to HPV types 16 and 18 [2]. Many developed countries have licensed vaccines that are highly effective against HPV types 6, 11, 16, and 18 for prophylactic use among young females [3]. With widespread use of the vaccine, decreases in the prevalence of HPV types covered by the vaccine would be expected [4]. Close monitoring is needed to demonstrate protection against cervical cancer, to verify duration of protection, and assess the replacement frequency of non-vaccine types among vaccinated cohorts, and potential barriers to vaccination coverage [5, 6]. However, before a vaccination program is undertaken, baseline HPV disease burden must be assessed to gauge the efficacy of the program and the vaccine itself. To date, there are limited data on the prevalence of HPV among women living in eastern European countries. We have therefore studied the pre-vaccine prevalence of different types of HPV in Estonia.

Methods

Sample

An age-stratified (18-20, 21-25, 26-30, 31-35) random sample of 845 women aged 18-35 years was derived from the Estonian Population Registry list for Tartu city (the second largest city in the country) and county residents (from a total of 22,904 women aged 18-35). The Estonian Population Registry is an electronic database containing personal data about people residing in Estonia.

Study procedures

Data collection was conducted from September 2005 to May 2006. Each participant was mailed a package containing a specimen collection kit (a cotton swab for vaginal swabbing on a plastic handle packed in an individual reclosable plastic sleeve; Eurotubo^® Collection swab, Deltalab, S.L.I., Barcelona, Spain), collection instructions and an informed consent form attached to a 35-item questionnaire requesting socio-demographic characteristics, sexual behaviour, and health care utilization data. For specimen collection, participants were instructed to wash their hands before opening the swab, to hold the swab by the end of the handle, to insert the foam swab into the vagina as if inserting a tampon, to gently turn the swab during a count of 10, and to replace the swab in the plastic sleeve, avoiding contact with the external genitalia.

Self-collected specimens (vaginal swabs) were mailed directly to the laboratory, in pre-stamped, pre-addressed envelopes. The swabs were transported in a dry state. Earlier studies have documented good performance of NAAT assays for the detection of HPV (and other genital pathogens) using self-obtained vaginal swabs shipped in a dry state to a laboratory [7–10]. Samples were tested in the ISO 15 189 accredited diagnostics laboratory of Quattromed HTI Laboratories Ltd. Study procedures complied with local regulations regarding mailing of biological materials. (Detailed description of the study design is provided elsewhere [11].)

Laboratory methods

Specimen processing and DNA isolation

The vaginal swabs were held for up to three days at 4°C prior to DNA extraction. Material from swab specimens was suspended in PBS and collected by centrifugation at 16,060G for 20 minutes. The supernatant was discarded and the pellet was resolved in PBS. DNA was extracted using the High Pure PCR Template Preparation Kit (Roche Molecular Biochemicals, Mannheim, Germany) according to the manufacturer's instructions. Amplification of the human β-globin gene was performed to confirm the integrity of the DNA in the samples [12].

HPV genotyping

Human papillomaviruses were detected by single-round PCR using the degenerated oligo primers MY09/11 and HMB01 as described by Gravitt et al. [13] using an Eppendorf Mastercycler (Hamburg, Germany). The PCR products were detected by ethidium bromide-stained agarose gel electrophoresis. All positive results were genotyped by restriction fragment length polymorphism analysis as described in Mejer et al. [14] The HPV genotypes were classified using the systems proposed by Dunne EF et al. and Munos et al. [4, 15] The following HPV types were classified as high-risk: 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 73, 82 including probable high-risk types 26, 53, 66. Types 6, 11, 40, 42, 43, 44, 54, 61, 70, 72, 81 and 89 were classified as low-risk.

Statistical analysis

The HPV prevalence was calculated from the number of positive cases divided by the number of tested specimens. Weighted estimates of population prevalence were computed to adjust for the stratified sampling utilized in the study. Correlates of HPV prevalence were explored using the chi-square test for proportions, and multiple logistic regression analysis to assess confounding and interaction between variables. Factors with p < 0.05 in bivariate analysis were entered in a multivariate comparison. A conceptual framework approach was used for the multivariable analysis [16]. All analyses were performed with statistical software R (version 2.2.1 for Windows).

Ethical approval was obtained from the Ethics Review Board of the University of Tartu and the Institutional Review Board of the State University of New York at Albany. The study followed data protection legislation requirements from the Estonian Data Protection Inspectorate. Study participants received no financial incentive for participation.

Results

Study sample and socio-demographic characteristics

Study invitations reached 86% (723/845) of the targeted sample but 122 individuals could not be reached because the packet was undeliverable (e.g., moved, wrong address). These subjects were excluded from the analysis.

Women who returned the questionnaire or self-collected a vaginal sample (n = 346) were compared with those who did not (n = 377) using population registry data. There was no statistically significance difference in response proportion according to age, residency or ethnicity (data not shown) [11].

Respondents ranged in age from 18 to 35 years (mean 26.9, SD 5.5). Two out of three participants were either married (23%) or living with a sexual partner (41%).

HPV DNA Prevalence Overall and by Age

Of the 326 adequate specimens available for HPV DNA testing, 37% (95% CI 31-44%) were positive for any HPV DNA. After weighting for the source population distribution, the prevalence estimate was 38% (95% CI 31-45%) (Table 1). While the overall HPV prevalence was highest in the 21-25-year age group, greater high- risk HPV prevalence was documented for the youngest age group (aged 18-20 years).

Table 1 HPV prevalence among women in Estonia by age group (data from DNA analysis of self-collected vaginal swabs, 2006)

Prevalence of High-Risk, Low-Risk, and Specific Types

The overall prevalence of high- and low-risk HPV types was 21% (95% CI 16-26%) and 10% (95% CI 7-14%), respectively. The prevalence of unidentified HPV types was 7% (95% CI 4-10%). The most common HPV types detected were HPV 16, 53, 66 (high-risk types), and HPV 61, 81 (low-risk types) (Table 2).

Table 2 Type-specific HPV DNA prevalence amongst women in Estonia, 2006

Factors Associated With HPV DNA Detection

Detection of HPV DNA was significantly correlated in the bivariate analysis with age, and sexual behaviour (ever having sex, young age at debut, and higher number of sexual partners within the last 12 months). However, HPV DNA was detected in 6% of females who reported never having had sex. The final multivariate model demonstrated that age (> 26, OR = 0.4, 95% CI 0.2-0.9), age above 18 years at first sexual intercourse (OR = 0.4, 95% CI 0.2-0.8), and increasing numbers of sexual partners in the last 12 months (OR = 2.5, 95% CI 1.4-4.5) were independently associated with HPV DNA detection (Table 3).

Table 3 Bivariable and multivariable factors associated with HPV DNA positivity amongst women in Estonia, 2006

Discussion

Cervical cancer is the second most common cancer in women worldwide. It is the sixth most frequent cancer among Estonian women of all ages, and the second most frequent cancer among young Estonian women (aged between 15 and 44 years) [17]. The availability of effective HPV vaccines has prompted a discussion about their use within public health vaccine programs. Geographical data on the HPV type distribution for women with cervical cancers as well as among women in the general population are essential for estimating the impact of cervical screening and vaccination programs [18]. Several recent studies have documented pre-vaccination HPV prevalence [4, 19–23] varying according to the study design (sampling), study cohorts (clinic based, population based) and time period. These studies have typically used cervical samples obtained during a gynecological examination in the context of routine screening. In countries where cervical cancer screening is not widely implemented, such studies may not represent the general population and a non-invasive method acceptable to a representative sample of women is needed. One such option is the self-obtained vaginal sample. Several studies have documented that self-sampling has similar sensitivity to physician-obtained sampling to detect HPV DNA, suggesting that it is a viable screening option and may be a suitable alternative method for studies on HPV transmission and vaccine trials [24, 25]. Studies utilizing HPV DNA testing of asymptomatic women in the general population estimate the prevalence of HPV infection to be in the range of 2-44% [26]. Self-collected vaginal samples likely pick up a mixture of cervical and vaginal cells. Previous analyses have established that genotypes within phylogenetic species tend to be similar with respect to the anatomic site of infection [27, 28]. Studies comparing HPV detection in paired cervical and vaginal specimens have shown that the carcinogenic HPV types (alpha9 phylogenetic species, i.e. HPV 16) have a similar affinity for vaginal and cervical epithelium (resulting in similar recorded prevalences for any carcinogenic HPV type in vaginal and cervical specimens) [28], but non-carcinogenic HPV types of the alpha3/alpha15 (i.e. HPV 61) phylogenetic species may have a stronger affinity for vaginal epithelium [28].

Consistent with published data, we found that HPV 16 was the most prevalent HPV type (6.4%). We found a relatively low HPV 18 prevalence. In the light of studies documenting similar prevalence of any high-risk HPV in paired cervical and vaginal specimens this finding is of importance [28, 29], and we would expect to see a low prevalence of HPV 18 in cervical samples from the same population. A low prevalence of HPV 18 among women from post-Soviet countries has been documented in other studies [30]. HPV 6 and 11 (alpha10 phylogenetic species) are relatively rarely isolated from vaginal/cervical specimens (HPV 6 < 1.5% and HPV 11 < 0.5% from cervical and vaginal specimens in Castle et al 2007 [29]; HPV 6 < 2% and HPV 11 < 0.5% from cervical specimens in Butsch Kovacic et al 2006 [31]; and HPV 6 from vaginal specimens either physician or patient-collected < 3.5% in Moscicki et al [32]), findings that are similar to those in our study.

Based on the most recent studies (Table 4) we surmise that Estonia represents a typical eastern European country with higher HPV and high-risk HPV prevalences than those reported from neighboring countries with well-developed population-based cervical cancer screening programs (i.e. Finland, Sweden, Denmark).

Table 4 Studies describing HPV and high-risk type-specific prevalence from different countries

The overall HPV prevalence in our study population was high with the highest overall HPV prevalence among those aged 21-25 years (and the highest prevalence of high-risk HPV occurring in the 18-20 year age group) and declining with age. It is well known that sexually active young adults are most at risk for acquiring HPV. Beside young age, predictors of HPV infection included younger age at first sexual intercourse and higher number of sexual partners in the 12 months before the study. Our results are also in line with existing information on HPV epidemiology [26, 33, 34].

Our study has several limitations. This study was not originally designed to assess HPV prevalence, thus we do not have data on cervical cytology from participating women. The degree to which the study is representative of the general population may be affected by the low response rate and selection factors associated with response. It is very probable that non-responders and women who were not reachable are at higher risk of exposure to HPV. However, in our study, the probability of not responding was not related to ethnicity, residency or age, despite the correlation between young age and infection. Also, we were unable to include preadolescent women as this would have been ethically unjustifiable and impractical from a logistical standpoint. While it is reasonable to assume that the prevalence estimates from this study are somewhat inflated due to selective participation, the estimate is probably better than that based on traditional clinic-based findings which are not representative in Estonia.

Conclusion

Several factors affecting cervical cancer control are changing, including a better understanding of the natural history of HPV, reliable assays for detecting high-risk HPV infections, and the availability of effective preventive vaccines. However, there are important differences in the relevant policy questions for different settings. Local data including information on HPV (type specific) prevalence is needed for modeling in a decision analytic framework to identify those factors most likely to influence outcomes, provide insight into the cost-effectiveness of different strategies, and assist in early decision-making when weighed against equity, public preferences, and political and cultural constraints. Our study provides valuable baseline data about prevalence and type distribution of HPV prior to the introduction of HPV vaccination.