Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Prevalence and risk factors of anal human papillomavirus infection among HIV-negative men who have sex with men in Urumqi city of Xinjiang Uyghur Autonomous Region, China

  • Tian Tian ,

    Contributed equally to this work with: Tian Tian, Peierdun Mijiti

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Resources, Validation, Writing – original draft

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

  • Peierdun Mijiti ,

    Contributed equally to this work with: Tian Tian, Peierdun Mijiti

    Roles Data curation, Formal analysis, Writing – original draft

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

  • Huang Bingxue,

    Roles Investigation, Resources, Software, Validation

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

  • Zhang Fadong,

    Roles Investigation, Resources

    Affiliation Surgery Department of Toutunhe District General Hospital, Urumqi, Xinjiang, China

  • Abidan Ainiwaer,

    Roles Investigation, Methodology, Resources

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

  • Sang Guoyao,

    Roles Investigation, Methodology, Resources

    Affiliation Clinical Laboratory of Xinjiang Medical University First Affiliated Hospital, Urumqi, Xinjiang, China

  • Zhang Zhanlin,

    Roles Investigation, Methodology, Resources

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

  • Yeledan Mahan,

    Roles Investigation, Resources

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

  • Tuo Xiaoqin,

    Roles Investigation, Resources, Software, Validation

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

  • Gong Zheng,

    Roles Investigation, Methodology, Resources

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

  • Dai Jianghong

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Project administration, Supervision, Writing – original draft

    438263678@qq.com

    Affiliation Department of Epidemiology and Biostatistics, School of Public Health, Xinjiang Medical University, Urumqi, Xinjiang, China

Abstract

Background

Infection with human papillomavirus (HPV) is the most common sexually transmitted infection among men who have sex with men (MSM). Study on prevalence and risk factors of anal HPV infection among HIV-negative MSM in Northwestern China was rare.

Methods

We performed a cross-sectional study of HPV prevalence using anal swab specimens among HIV-negative MSM in Urumqi city of Xinjiang Uyghur Autonomous Region, China between April 1st and October 30th in 2016. Prevalence of any anal HPV infection, high-risk and low-risk HPV infection was estimated. Risk factors associated with any anal HPV infection was analyzed using univariate and multivariate logistic regression models.

Results

Among 538 potential participants, 500(92.9%) were recruited in this study. The genotyping results of anal HPV infection were available for all. Of them, 259 (51.8%), 190 (38.0%) and 141(28.2%) were positive for at least one of the targeted 37 HPV genotypes, high-risk HPV genotypes, and any low-risk HPV genotypes. The most prevalent anal HPV genotype was HPV 6(11.8%), followed by HPV 16(11.2%), HPV 11(10.8%), HPV 51(7.0%) and HPV 18(5.4%).Among those infected with at least one of the targeted 37 anal HPV genotypes, 75(29.0%), 155(59.8%) and 191(73.7%) were infected with 2-valent, quadrivalent and 9-valent HPV vaccine-covered genotypes. Receptive anal intercourse in the past year was the only predictor of any anal HPV infection in multivariate logistic regression model.

Conclusion

Prevalence of any anal HPV infection and high-risk HPV infection among HIV-negative MSM in Urumqi city of Xinjiang is high. The majority of genotypes detected in our study were covered by quadrivalent and 9-valent HPV vaccines. Regular anal exams and early HPV vaccination among MSM may be considered in future HPV prevention programs in Xinjiang, China.

Introduction

Human papillomavirus (HPV) is the most common sexually transmissible infectious agent worldwide [1]. So far, more than 200 types of HPV have been identified, and around 40 of these infect the squamous epithelium of the genital tract including the anus, cervix, vulva and vagina [2]. Importantly, most of HPV infections are transient and asymptomatic, since they are rapidly cleared by an intact immune system. However, in some instances, HPV may cause clinical manifestations of variable severity, spanning from benign warts (condylomata), mainly caused by the low-risk HPV 6 and 11, to cancerous lesions, caused by high-risk (HR) types (e.g. HPV 16 and 18) [3]. HR-HPV infection was thought to be responsible for 7–8% of all human malignancies [4] and was associated with majority of cervical cancers, anal cancers, vaginal cancers, vulvar cancers, and oropharyngeal carcinomas [5].

Recently, the interest on the burden of anal HPV infection has been growing because of increasing incidence of anal cancers among some at-risk population such as men who have sex with men (MSM) and HIV-infected individuals. Due to their sexual habits, MSM show a particularly high prevalence of HPV in the anal canal and develop lesions at this body site more frequently than any other population [6]. The prevalence of anal HPV infection among MSM was inconsistently reported in previous studies [7]. Prevalence of anal HPV infection among HIV-positive MSM in China was well documented [811]; however, data on prevalence of anal HPV among HIV-negative MSM, particularly in Northwestern China where reported number of MSM was increasing, was scarce. A better understanding of anal HPV infection among MSM may help inform strategies for the prevention of anal cancer in this population. In this study, we aimed to find out the prevalence and predictors of anal HPV infection among HIV-negative MSM in Urumqi city, China.

Materials and methods

Ethical statement

Xinjiang Medical University First Affiliated Hospital Ethics Committee reviewed and approved this study. Written informed consent obtained from each study participant before the interview and testing. All private information from questionnaire were kept confidential and used for population analysis only.

Study population

We performed a cross-sectional study of HPV prevalence using anal swab specimens among HIV-negative MSM in Urumqi city of Xinjiang, China between April 1st and October 30th in 2016. Participants were recruited, through local non-government organization (Tianshan Volunteers Workstation), using the methods of website advertisement, WeChat group (Chinese social media mobile application software), MSM bars, sexually transmitted disease clinics, and voluntary HIV counseling and testing clinics. Additionally, those recruited were also encouraged to refer their peers to attend the study. Potential participants were invited to Tianshan Volunteers Workstation for questionnaire interview, HPV swabs, and HIV testing during the study period. Participants were eligible if they were male and at least 18 years old, self-reported having sex with men in the past year, were willing to provide anal swab specimens for HPV testing and blood for HIV testing, and were able to provide written informed consent. All participants were compensated 30 Chinese yuan (approximately four and half US dollar).

Data collection

Data were collected using a questionnaire administered by trained interviewers who were also MSM in a private room. The questionnaire included information on socio-demographic characteristics (e.g. age group, ethnicity, education level, marital status, etc.), self-reported sexual orientation, heterosexual behavior in the past year, experience of anal intercourse in the past year, sexual role, commercial sex experience, circumcision status, STD infection in the past year, smoking status, and alcohol consumption.

Specimen collection and laboratory testing

Human immunodeficiency virus infection status was determined by an enzyme immunoassay (Wantai Biological Pharmacy, Beijing, China) and was confirmed by HIV-1/2 Western blot assay (HIV Blot 2.2 WB; Genelabs Diagnostics, Singapore, Singapore).

Trained physician collected anal samples by inserting a saline water moistened nylon flocked swab 3–5cms in the anal canal and gently rotating it for about 2 minutes. The swab was then kept in 3 mL of sample transport medium for Hybribio 37 HPV GenoArray Diagnostic Kit (Hybribio Biotech Limited Corporation, Chaozhou, China). Hybribio 37 HPV GenoArray Diagnostic Kit Test is based on a flow-through hybridization and gene-chip method. The low-density gene chip was pre-fixed with 37 type-specific oligonucleotides and the genotype was analyzed using HybriMax (Hybribio Biotech Limited Corporation, Chaozhou, China).The final results were detected by colorimetric change on the membrane under direct visualization. Positive and negative controls were included in the GenoArray test kit in every PCR analysis as well as during the hybridization process for quality control. Mixtures of different specific probes can be used in the same well of a 42-well plate format allowing for multiplex analysis. Blue-purple spots were recognized as HPV positive. This testing kit can detect 37 common types of HPV, including 23 oncogenic or HR-HPV (16, 18, 26, 31, 33, 35,39, 45, 51, 52, 56, 58, 59, 66, 68, 82,83,53, 55, 34, 57, 69, and 71) and 14 non-oncogenic or LR-HPV (06, 11, 40, 42, 44, 54,61, 67, 70, 72, 73, 81, and 84). Study participants with genotyping positive for any HPV type were determined to be currently infected with HPV. The operating protocol has been described in detail elsewhere [12, 13].

Statistical analysis

Questionnaires and laboratory results were entered using EpiData version 3.1(The Epi Data Association Odense, Denmark). Data were analyzed using SPSS version 17.0 (SPSS Inc., Chicago, IL, USA). Unconditional univariate logistic regression models were used to evaluate the association between each variable and any anal HPV infection. Multivariate logistic regression was applied to determine predictors of any anal HPV infection. All variables with p-values< 0.2 in univariate analyses were entered into the multivariate logistic model. Crude odds ratios (COR) and adjusted odds ratios (adjusted OR) were calculated, as appropriate along with 95% confidence intervals (CI).

Results

Characteristics of study participants

538 potential participants were invited for interview, HPV swabs and HIV testing. 16 did not give written consent, 12 did not provide blood for HIV testing, and eight did not show up at study site. Therefore, 502 individuals were recruited and two were positive for HIV. Finally, only data of 500 eligible HIV-negative participants were analyzed. Of them, 250 (50.0%) were aged≤ 29 years old, 277 (55.4%) were local residents, 457(91.4%) were of Han ethnicity, and 258(51.6%) had received education at the high school level or lower. In addition, 108 (21.6%) reported having sex with women in the past year, 439(87.8%) reported experience of anal intercourse in the past six months, 185 (37.0%) reported having been circumcised, only 44 (8.8%) reported having had STDs in the past year, and only 17 (3.4%) reported experience of commercial sex in the past year.

Prevalence of HPV infection

The genotyping results of anal HPV were available for all participants (Table 1). Of them, 259 (51.8%) were positive for at least one of the targeted 37 HPV genotypes. All were negative for HPV 26, HPV 35, HPV 71, HPV 40 and HPV 67. Among those positive for any 37 HPV genotypes, 118(45.6%) were exclusively infected with HR-HPV, 69(26.6%) were exclusively infected with LR-HPV, and 72 (27.8%) were infected with both LR-HPV and HR-HPV. Among those exclusively infected with HR-HPV, 29.7% were multiple infections, while it was 13.0% among those with exclusively infected with LR-HPV.HPV 16 (11.2%) and HPV51 (7.0%) were found to be the most prevalent HR-HPV genotypes; HPV6 (11.8%) and HPV11 (10.8%) were the most prevalent LR-HPV genotypes. The prevalence of 2-valent, quadrivalent and 9-valent HPV vaccine genotypes among participants all tested for HPV were 15.0%, 31.0% and 38.2%, respectively. However, among those infected with at least one of the targeted 37 anal HPV genotypes, 75(29.0%), 155(59.8%) and 191(73.7%) were infected with 2-valent, quadrivalent and 9-valent HPV vaccine-covered genotypes.

thumbnail
Table 1. HPV detection and genotyping among 500 HIV-negative MSM.

https://doi.org/10.1371/journal.pone.0187928.t001

Risk factors associated with HPV infections

Univariate and multivariate logistic regression analyses were performed to assess the associations between variables and any HPV infection among HIV-negative MSM. Multivariate logistic regression analysis indicated that receptive anal intercourse in the past year was the only predictor of any anal HPV infection (Table 2 and Table 3).

thumbnail
Table 2. Characteristics of 500 study participants and univariate analysis of association between variables and any anal HPV infection [n (%)].

https://doi.org/10.1371/journal.pone.0187928.t002

thumbnail
Table 3. Multivariate analysis of risk factors for any HPV infection.

https://doi.org/10.1371/journal.pone.0187928.t003

Discussion

In this study, we investigated the prevalence of anal HPV infection among HIV-negative MSM in Urumqi city of Xinjiang province. The prevalence of any anal HPV infection among HIV-negative MSM in our study was 51.8%, which was within the range of results reported by various studies in China (33.8%-62.8%) [10, 11, 1314]. However, it was lower than studies conducted in other countries (70%-85.3%) [1518]. The discrepancy between these studies might be due to different characteristics of target population (e.g. source of recruitment, whether community-based or clinics, demographic characteristics, behavioral factors) or the HPV testing methods. Hybrid Capture and polymerase chain reaction (PCR)-based assays (e.g. Linear Array, MY09/11, GP5+/6+, etc.) were widely used for HPV detection and genotyping in epidemiological studies [18]. FDA-approved Hybrid Capture 2 system can detect five LR-genotypes and 13 HR-genotypes, but it only distinguishes between the high-risk and low-risk groups and does not permit identification of specific HPV genotypes [19]. Additionally, the detection limit of approximately 5000 genome equivalents makes it less sensitive than PCR[20].The sensitivity and specificity of PCR-based assays may be varied due to choice of primers, size of PCR products, and methods of sequence-analysis of PCR products. In addition, the number of HPV genotypes detected by PCR-based assays is varied as well [21]. PCR followed by flow-through hybridization and gene chip technology was used in our study, and its sensitivity, specificity, and number of HPV genotypes detected (37 genotypes) were quite similar to the popular PCR-based Linear Array assay [22,23]. Therefore, comparison of anal HPV prevalence among MSM groups should be careful and cautious.

Approximately 90% of invasive anal cancers are attributed to single infections with a HR-HPV type [24]. Of HPV-positive anal cancers, the great majority are associated with HPV 16 type (85%), followed by HPV 18 (7%), with a combined HPV 16 and HPV 18 prevalence of 90% irrespective of geographic location [25].Therefore, screening for anal HR-HPV infection and HPV-related anal lesions may help to reduce the burden of anal cancer in this high risk population [26]. In our study, the prevalence of any HR-HPV type among HIV-negative MSM was 38.0%; this was higher than the results reported among HIV-negative MSM in Netherlands (33.6%), Thailand (36.6%) and China (27.1%) [14, 27, 28], but it was lower than the results of a study conducted in three cities of China (48.2%) [10]. Furthermore, the most prevalent HPV genotype in anal canal in our study was HPV 6(11.8%), followed by HPV 16(11.2%), HPV 11(10.8%), HPV 51(7.0%) and HPV 18(5.0%). The distribution of HPV genotype in anal canal was similar to that reported in other studies in China [10,14] and South Africa[15], but different from that reported in Thailand[29], in which the most common HPV types were HPV 16 (27%), HPV 58 (23%), HPV 51(18%), and HPV 39 (14%). These results implied HPV genotype distribution might be varied among different MSM groups, and thus understanding the distribution of HPV genotypes among local MSM may help to guide the introduction of proper HPV vaccine in the local MSM community.

It is noticeable that the great majority of HPV genotypes detected in our study were covered by both quadrivalent and 9-valent HPV vaccines. This implies a great number of HPV cases in MSM in Urumqi might be prevented by these two vaccines. However, until very recently 2-valent HPV vaccine became available in Chinese markets and it is the only available HPV vaccine in China. In addition, results from a previous study suggested very low awareness and acceptability of HPV vaccine among MSM in China, in which only 18.4% of MSM had heard of HPV, 10.2% had heard of HPV vaccine, and 20.2% were willing to take HPV vaccine before sexual debut [30]. Joint efforts should be made by MSM media and MSM community organizations and clinicians to enhance health education about HPV vaccination among MSM at proper age.

Risk factors associated with any anal HPV infection among MSM were various in previous studies. The most consistently reported risk factors for anal HPV infection were a past history of receptive anal intercourse, recent receptive anal intercourse and a higher number of male sexual partners in the past months [3134]. Similarly, receptive anal intercourse in the past year was associated with anal HPV infection in our study. However, frequency of condom use during homosexual behaviors in the past six month and number of male sexual partners in the past six month were not associated with any anal HPV infection among MSM in our study. Results for these associations were not consistent in previous studies either [3, 34, 3536]. Importantly, HPV transmission can occur through other non-intercourse anal sexual practices such as fingering, fisting and oral sex [37], this may partially explain why the association of frequency of condom use during homosexual behaviors with anal HPV infection was not observed in our study. Racial difference in anal HPV infection among MSM was observed in several studies [9, 31]. In our study, we found other ethnic minority groups were more likely to have anal HPV infection compared to Han ethnic group after adjustment of potential confounders, although this association was marginal (p = 0.072). This marginal racial disparity may be real or due to recruitment of a small number of ethnic minorities in our study. 25% of the total population of Urumqi city are ethnic minorities (2016 Statistical Yearbook of Xinjiang Uyghur Autonomous Region, China), and majority of them are Muslim. Recruitment of Muslim MSM participant in scientific studies is quite difficult because MSM of Muslim background often conceal their homosexual identity to avoid harsh stigma and discrimination by Islamic society [38, 39]. MSM with different religious belief and those irreligious may differ in homosexual behaviors, and religiosity may play an important role in transmission of infectious disease among MSM in China [40]. Future study should be done among Muslim MSM in Xinjiang region to investigate the real prevalence and risk factors of HPV infection among them.

The results in our study should be interpreted with caution. First, due to the nature of convenience sampling and source of recruitment, participants in our study may not represent all MSM in Urumqi city. This may lead to selection bias in our study. Second, cross-sectional detection of HPV may be transient deposition only, thus it is difficult to predict how many of the cases would persist. Third, we used interviewer-based questionnaire rather than self-administered questionnaire, this may introduce some information bias given the sensitivity of the topic (e.g. selective reporting of sexual behavior/habits due to prejudice/stigma, etc.). Fourth, HIV-positive MSM were not included in our study due to very low prevalence of HIV infection in our sample. Future HPV prevalence study should be focused on HIV-positive MSM in Xinjiang province.

Conclusions

In conclusion, high prevalence of any anal HPV infection (51.8%) and any HR-HPV infection (38.0%) was observed among HIV-negative MSM in Urumqi city. The most prevalent HPV genotype was HPV 6, followed by HPV 16, HPV 11, HPV 51 and HPV 18, most of which were covered by quadrivalent and 9-valent HPV vaccine. Receptive anal intercourse in the past year was the only risk factor associated with any anal HPV infection in our study population. Regular anal exams and early HPV vaccination among MSM may be considered in future HPV prevention programs in Xinjiang, China.

Acknowledgments

We thank volunteers from Tianshan Volunteers Workstation for their great efforts on enrollment of study participants.

References

  1. 1. Crosbie EJ, Einstein MH, Franceschi S, Kitchener HC.Human papillomavirus and cervical cancer.Lancet.2013; 382(9895):889–99. pmid:23618600
  2. 2. Doorbar J, Egawa N, Griffin H, Kranjec C, Murakami I.Human papillomavirus molecular biology and disease association.Rev Med Virol.2015; 25 Suppl 1:2–23.
  3. 3. Benevolo M, Donà MG, Ravenda PS, Chiocca S.Anal human papillomavirus infection: prevalence, diagnosis and treatment of related lesions.Expert Rev Anti Infect Ther.2016; 14(5):465–77. pmid:27050294
  4. 4. Cobos C, Figueroa JA, Mirandola L, Colombo M, Summers G, Figueroa A, et al. The role of human papilloma virus (HPV) infection in non-anogenital cancer and the promise of immunotherapy: a review.Int Rev Immunol.2014; 33(5):383–401. pmid:24811210
  5. 5. IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. A Review of Human Carcinogens. Part B: Biological Agents. Lyon, France: IARC; 2009. Chapter 6, Human papillomaviruses, pp. 255–313.
  6. 6. Machalek DA, Grulich AE, Jin F, Templeton DJ, Poynten IM.The epidemiology and natural history of anal human papillomavirus infection in men who have sex with men. Sex Health. 2012; 9(6):527–37. pmid:23380235
  7. 7. Giuliano AR, Anic G, Nyitray AG. Epidemiology and pathology of HPV disease in males.Gynecol Oncol. 2010; 117(2 Suppl):S15–9.
  8. 8. Li Z, Zhang H, Li X, Yang Y, Xin H, Li M, et al. Anal Human Papillomavirus Genotyping among HIV-Positive Men Who Have Sex with Men in Xi'an, China. PLoS One. 2015; 10(4):e0125120. pmid:25923768
  9. 9. Gao L, Zhou F, Li X, Yang Y, Ruan Y, Jin Q.Anal HPV infection in HIV-positive men who have sex with men from China. PLoS One. 2010; 5(12):e15256. pmid:21151900
  10. 10. Li X, Li M, Yang Y, Zhong X, Feng B, Xin H, et al. Anal HPV/HIV co-infection among Men Who Have Sex with Men: a cross-sectional survey from three cities in China. Sci Rep. 2016;6:21368. pmid:26892938
  11. 11. Hu Y, Qian HZ, Sun J, Gao L, Yin L, Li X, et al. Anal human papillomavirus infection among HIV-infected and uninfected men who have sex with men in Beijing, China. J Acquir Immune Defic Syndr. 2013; 64(1):103–14. pmid:23732908
  12. 12. Liu SS, Leung RC, Chan KK, Cheung AN, Ngan HY.Evaluation of a newly developed GenoArray human papillomavirus (HPV) genotyping assay and comparison with the Roche Linear Array HPV genotyping assay. J Clin Microbiol. 2010;48(3):758–64. pmid:20042614
  13. 13. Zhang DY, Yin YP, Feng TJ, Hong FC, Jiang N, Wang BX, et al. HPV infections among MSM in Shenzhen, China. PLoS One. 2014;9(5):e96364. pmid:24801331
  14. 14. Ren X, Ke W, Zheng H, Yang L, Huang S, Qin X, et al. Human Papillomavirus Positivity in the Anal Canal in HIV-Infected and HIV-Uninfected Men Who Have Anal Sex with Men in Guangzhou, China: Implication for Anal Exams and Early Vaccination. BIOMED RES INT. 2017;2017:1–9.
  15. 15. Müller EE, Rebe K, Chirwa TF, Struthers H, McIntyre J, Lewis DA. The prevalence of human papillomavirus infections and associated risk factors in men-who-have-sex-with-men in Cape Town, South Africa. BMC Infect Dis. 2016;16(1):440. pmid:27549219
  16. 16. Blas MM, Brown B, Menacho L, Alva IE, Silva-Santisteban A, Carcamo C. HPV Prevalence in Multiple Anatomical Sites among Men Who Have Sex with Men in Peru. PLoS One. 2015; 10(10):e0139524. pmid:26437318
  17. 17. Supindham T, Chariyalertsak S, Utaipat U1, Miura T, Ruanpeng D, Chotirosniramit N, et al. High Prevalence and Genotype Diversity of Anal HPV Infection among MSM in Northern Thailand. PLoS One. 2015, 10(5):e0124499. pmid:25932915
  18. 18. Machalek DA, Poynten M, Jin F, Fairley CK, Farnsworth A, Garland SM, et al. Anal human papillomavirus infection and associated neoplastic lesions in men who have sex with men: a systematic review and meta-analysis.Lancet Oncol.2012; 13(5):487–500. pmid:22445259
  19. 19. Hubbard RA. Human papillomavirus testing methods. Arch Pathol Lab Med. 2003; 127(8):940–5. pmid:12873165
  20. 20. Molijn A, Kleter B, Quint W, van Doorn LJ. Molecular diagnosis of human papillomavirus (HPV) infections.J ClinVirol. 2005;32 Suppl 1:S43–51.
  21. 21. Molecular detection and genotyping of human papillomavirus. vanDoorn LJ, Kleter B, Quint WG. Expert Rev MolDiagn. 2001;1(4):394–402.
  22. 22. Wong OG, Lo CK, Chow JN, Tsun OK, Szeto E, Liu SS,et al. Comparison of the GenoFlow human papillomavirus (HPV) test and the Linear Array assay for HPV screening in an Asian population. J ClinMicrobiol. 2012; 50(5):1691–7.
  23. 23. Tao P, Zheng W, Wang Y, Bian ML.Sensitive HPV genotyping based on the flow-through hybridization and gene chip. J Biomed Biotechnol. 2012;2012:938780. pmid:23193367
  24. 24. Parkin DM, Bray F. Chapter 2: The burden of HPV-related cancers. Vaccine 2006; 24 Suppl 3:S3/11–25.
  25. 25. Hoots BE, Palefsky JM, Pimenta JM, Smith JS. Human papillomavirus type distribution in anal cancer and anal intraepithelial lesions. Int J Cancer. 2009;124(10):2375–83. pmid:19189402
  26. 26. Fox P. Anal cancer screening in men who have sex with men. CurrOpin HIV AIDS. 2009; 4(1):64–7. pmid:19343830
  27. 27. van Rijn VM, Mooij SH, Mollers M, Snijders PJ, Speksnijder AG, King AJ, et al. Anal, penile, and oral high-risk HPV infections and HPV seropositivity in HIV-positive and HIV-negative men who have sex with men. PLOS ONE. 2014; 9(3):e92208. pmid:24651691
  28. 28. Phanuphak N, Teeratakulpisarn N, Pankam T, Kerr SJ, Barisri J, Deesua A, et al. Anal human papillomavirus infection among Thai men who have sex with men with and without HIV infection: prevalence, incidence, and persistence. J Acquir Immune Defic Syndr. 2013; 63(4):472–9. pmid:23514956
  29. 29. Taweewat Supindham, Suwat Chariyalertsak, Utaiwan Utaipat, Toshiyuki Miura, Darin Ruanpeng, Nuntisa Chotirosniramit, et al. High Prevalence and Genotype Diversity of Anal HPV Infection among MSM in Northern Thailand. PLoS One. 2015; 10(5): e0124499. pmid:25932915
  30. 30. Zou H, Meng X, Jia T, Zhu C, Chen X, Li X, et al. Awareness and acceptance of human papillomavirus (HPV) vaccination among males attending a major sexual health clinic in Wuxi, China: A cross-sectional study. Hum Vaccin Immunother. 2016;12(6):1551–9. pmid:26467510
  31. 31. Goldstone S, Palefsky JM, Giuliano AR, Moreira ED Jr, Aranda C, Jessen H, et al. Prevalence of and risk factors for human papillomavirus (HPV) infection among HIV-seronegative men who have sex with men. J Infect Dis. 2011; 203(1):66–74. pmid:21148498
  32. 32. Chin-Hong PV, Vittinghoff E, Cranston RD, Buchbinder S, Cohen D, Colfax G, et al. Age-Specific prevalence of anal human papillomavirus infection in HIV-negative sexually active men who have sex with men: the EXPLORE study. J Infect Dis. 2004;190(12):2070–6. pmid:15551204
  33. 33. Guimarães MD, Grinsztejn B, Melo VH, Rocha GM, Campos LN, Pilotto JH, et al. Anal HPV prevalence and associated factors among HIV-seropositive men under antiretroviral treatment in Brazil. J Acquir Immune Defic Syndr. 2011; 57 Suppl 3:S217–24.
  34. 34. Nyitray AG, Carvalho da Silva RJ, Baggio ML, Lu B, Smith D, Abrahamsen M, et al. Age-specific prevalence of and risk factors for anal human papillomavirus (HPV) among men who have sex with women and men who have sex with men: the HPV in men (HIM) study. J Infect Dis. 2011;203(1):49–57 pmid:21148496
  35. 35. Glick SN, Feng Q, Popov V, Koutsky LA, Golden MR. High rates of incident and prevalent anal human papillomavirus infection among young men who have sex with men. J Infect Dis. 2014;209(3):369–76. pmid:23956439
  36. 36. Geskus RB, González C, Torres M, Del Romero J, Viciana P, Masiá M, et al. Incidence and clearance of anal high-risk human papillomavirus in HIV-positive men who have sex with men: estimates and risk factors. AIDS. 2016;30(1):37–44. pmid:26355673
  37. 37. Sonnex C, Strauss S, Gray JJ. Detection of human papillomavirus DNA on the fingers of patients with genital warts. Sex Transm Infect. 1999;75(5):317–9. pmid:10616355
  38. 38. Jaspal R. 'I never faced up to being gay': sexual, religious and ethnic identities among British Indian and British Pakistani gay men. Cult Health Sex. 2012;14(7):767–80. pmid:22651130
  39. 39. Jaspal R, Cinnirella M. Coping with potentially incompatible identities: accounts of religious, ethnic, and sexual identities from British Pakistani men who identify as Muslim and gay. Br J Soc Psychol. 2010; 49(Pt 4):849–70. pmid:20170600
  40. 40. Pan SW, Zhang Z, Li D, Carpiano RM, Schechter MT, Ruan Y, et al. Religion and HIV Sexual Risk Among Men Who Have Sex With Men in China. J Acquir Immune DeficSyndr. 2016;73(4):463–474.