Recent studies in Puerto Rico have reported an increasing incidence of anal cancer in Puerto Rican men. The objective of this study was to determine the prevalence, genotype distribution and risk factors associated with anal HPV infection among men attending an STI clinic in Puerto Rico.
We conducted a cross-sectional study among 205 men 18 years and older. A comprehensive survey was administered that included a demographic and a behavioral assessment. Separate logistic regression models were performed to determine factors associated with any, high-risk (HR), and multiple anal HPV infection.
The mean age of the study sample was 38.0±13.5 years. The most common HR types were 58, 51 and 31. Overall, HR anal HPV infection was found in 53.5% of the participants. Multiple HPV types in the anal canal were found in 47.6% of the sample. A third (29.8%) of participants reported being men who had sex with men (MSM). MSM had a significantly higher prevalence of any, HR and multiple HPV infection (p-value<0.05). Separate multivariate logistic regression analyses showed that being MSM was associated with any (OR = 4.5; [95%CI: 1.9–10.7]), HR (OR = 3.4; [95%CI: 1.1–10.3) and multiple anal HPV infection (OR = 3.6; [95%CI: 1.5–9.1). HIV was marginally associated with multiple anal HPV infection in multivariate analysis (OR = 3.3; 95%CI = 1.0–11.0).
Citation: Colón-López V, Ortiz AP, Del Toro-Mejías L, Clatts MC, Palefsky JM (2014) Epidemiology of Anal HPV Infection in High-Risk Men Attending a Sexually Transmitted Infection Clinic in Puerto Rico. PLoS ONE 9(1): e83209. doi:10.1371/journal.pone.0083209
Editor: Xuefeng Liu, Georgetown University, United States of America
Received: August 3, 2013; Accepted: October 25, 2013; Published: January 6, 2014
Copyright: © 2014 Colón-López et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This project was fully supported by National Institutes of Health R03 DA027939-01, and AIDS-Science Track Award for Research Transition A-START 1R03DA031590-01 from NIDA. The project was also partially supported by Award Number U54 RR026139 from the National Center for Research Resources, and the Award Number 8U54MD 007587-03 from the National Institute on Minority Health and Health Disparities. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health or the PR Department of Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have the following interests: Dr. J. Palefsky has received research funding and travel support from Merck and Co. and research support from Hologic. Dr. Ortiz has a research contract with Merck and Co. There are no patents, products in development or marketed products to declare. This does not alter in any way the authors' adherence to all the PLOS ONE policies on sharing data and materials.
Human Papillomavirus (HPV) infection causes approximately 600,000 cases of cancer of the cervix, vulva, vagina, anus and oropharynx annually, as well as benign diseases such as genital warts and recurrent respiratory papillomatosis . HPV is responsible for 100% of the cervical cancer cases and more than 80% of anal cancer cases , . Increasing interest in understanding the burden of HPV in men has been documented recently, particularly since the incidence of anal cancer, for which there are no effective screening programs, has been rising over the last couple of decades . In the United States, anal cancer in men has increased from 0.5 per 100,000 in 1974 to 1.3 per 100,000 in 2004 . In Puerto Rico, an increase in percent change of 26.7% among men has been documented, with incidence rates ranging from 1.13 per 100,000 in the period of 1992–1996 to 1.43 per 100,000 in 2009 .
High-risk (HR) anal HPV infection, particularly genotypes 16 and 18, is a significant risk factor for the development of anal intraepithelial neoplasia (AIN) and anal cancer , . Although a high burden of HPV infection in men attending STI clinics has been documented , , there are only a small number of studies in these settings that describe the epidemiology of anal HPV, by HPV types. Since a critical first question is to identify which HPV types are prevalent in the anal canal in men attending these clinics, the purpose of this study is to determine the prevalence of anal HPV infection and identify risk factors associated with anal HPV-specific types (any type, HR, and multiple types) in a sample of high-risk men attending an STI clinic in Puerto Rico.
The study was conducted from 2009 to 2011, as part of an ongoing epidemiological study among patients attending a public STI/HIV screening and treatment center in Puerto Rico. This study was previously approved by University of Puerto Rico Medical Sciences Campus (UPR MSC) Institutional Review Board (IRB). The design and methods of the parent epidemiological study have been described elsewhere , . Briefly, men and women aged 16 years or older were selected from the clinic waiting room and screened for eligibility (including age and capacity for consent). Participants provided a signed written informed consent for the study procedures and for extraction of selected clinical data from their medical chart. They participated in a face-to-face interview that included demographic, behavioral, history of health services utilization and self-reported STIs.
Following the completion of the behavioral survey, all male participants were invited to participate in the HPV sub-study , . In this sub study, men older aged 16 years or older were eligible to participate. Participation involved an additional supplemental survey related to HPV, including assessments of HPV transmission knowledge, perceived susceptibility of HPV-related cancers (penile, anal and oral) and vaccine acceptability. Overall, 206 participants were recruited to participate. Separate informed consents were signed by the study participants after a detailed explanation of the sub-study was provided by research assistants.
Variables of Interest
A man was considered to have HR HPV infection if he was positive for one or more HR genotypes, whether or not he was also positive for one or more LR HPV genotypes. On the other hand, a man was considered to have LR HPV infection if he was positive only to LR HPV genotypes. Finally, multiple HPV types to HPV were identified if study participant was positive for two or more HR or LR HPV genotypes. Sociodemographic variables included age, education, current employment, annual income and marital status. A man was considered MSM if the participant reported having had sex (anal or oral sex) with another man in his lifetime. Use of cigarettes, alcohol and marihuana during the past 90 days was collected as well. Sexual behaviors included lifetime sexual partners (female and male), lifetime anal sex partners (female and male) and condom use in the last sexual event. Self-reported STIs included HIV and syphilis.
Genital Specimen Collection
For the anal sample collection, trained clinicians moistened a Dracon swab with tap water and inserted it into the anal canal as far as it would go. Applying gentle pressure to the walls of the anal canal, the physician removed the swab with spiral motion over a 30-second period, and immediately inserted it in a vial containing sample transport medium. After collection, specimens were frozen at the core lab at the Puerto Rico Clinical and Translational Research Consortium (PRCTRC), at the UPRMSC, where they were stored at −70°C; and shipped on dry ice to Dr. Palefsky's laboratory at the University of California at San Francisco (UCSF) for anal HPV typing.
DNA extraction/HPV detection and typing
DNA was prepared from each STM sample and frozen until the specimens were batched for analysis. To prepare DNA, after the samples were thawed they were heated at 56°C for 1 hour. After cooling, 25 µl of 10 mg/ml proteinase K, (Invitrogen, 250 µg/ml final concentration) were added. The samples were vortexed and digested at 50°C in a waterbath overnight and heated at 95°C for 10 minutes to inactivate PK. After DNA purification, PCR was performed using a modified pool of MY09/MY11 consensus HPV L1 primers as well as primers for amplification of the human beta-globin gene. Five microliters of sample were used for PCR amplification using a 40-cycle protocol. After PCR, 6 µL of amplification mixture were applied to a nylon membrane and probed with a biotin-labeled HPV consensus probe mixture containing HPV 11, 16, 18 and 51 L1 DNA. A separate membrane was probed with a biotin-labeled probe to the human beta-globin gene. Each specimen was also studied for the presence of specific HPV types by preparing membranes as described above with 6 µL of specimen. HPV genotypes sought included HR-HPV types (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, and 66), LR types (6/11, 32/42, 54, 57/2/27, 61, 62, 71, 72, 81, 83, 84, 86/87, 90/106, and 102/89, as well as 2 separate mixtures, mix1 containing 7/13/40/43/44/55/74/91, and mix2 containing 3/10/28/29/77/78/94) and types that are of unknown risk (26/69, 30, 34, 53, 67, 68, 70, 73, 82, 85, 97) . The biological specimen was considered HPV-positive when it was positive with the consensus probes or with one or more probes for specific HPV types. Specimens negative for beta-globin gene amplification were excluded from analysis. Negative controls for each experiment consisted of amplification of solution containing all of the above components except for sample DNA. Positive controls included amplification of cloned HPV DNA and HPV positive cell lines.
Frequency distributions and descriptive statistics were used to characterize the study sample. Prevalence estimates and 95% confidence intervals (95% CI) for any HPV, HR, LR, and multiple HPV types in the anal canal were calculated. Descriptive statistics were calculated to describe the most prevalent genotypes in this sample. Chi-square analysis or Fisher exact tests were used to evaluate differences in categorical outcome measures. Sociodemographic characteristics were stratified by sexual behavior (MSM vs. Non-MSM). Sexual practices were presented separately by these two groups.
Factors significantly associated with HPV (p<0.05) in the bivariate analysis were included in crude and age-adjusted logistic regression models to identify risk factors associated with anal HPV infection in four separately models: 1) any type, 2) HR, and 3) multiple types as dependent variables). Then, multivariate logistic regression model was performed among all variables that remained significant after adjusting for age. Statistical analyses were performed using SAS (Version 9.1.3, Cory, NC). The 95%CI for prevalence estimations were performed using the Binomial CI calculator from Stata Statistical Software (Release 11, College Station, TX).
Approximately a third of the study participants visited the clinic for the first time at the time of the interview (28.1%). The principal reasons for which study participants were attending the clinic were evaluation/screening for an STI (not HIV) (61.3%) and HIV screening (32.7%) (data not shown).
Demographic characteristics of the total sample overall and stratified by sexual behavior MSM vs. Non-MSM are shown in Table 1. A third (29.8%) of the study sample reported being MSM. The mean age of the study sample was (38.0±13.5) and (37.7±13.0) years for MSM and Non-MSM, respectively. Bivariate analysis showed significant differences by sexual identity in educational level, employment and annual income (p<0.05).
Sexual behaviors and other practices
Among Non-MSM, the mean age of sexual onset was 15.5±2.6 and the mean number of female sexual partners in their lifetime was 19.3±22.4. More than half (81.0%) reported having had anal sex in their lifetime (receptive or insertive), in which 0.7% reporting having had anal sex in the last 90 days. No condom use in the last sexual event was reported in 43.3% of the non MSM participants (data not shown).
Among MSM, 5.9% reported having had sex with women in their lifetime and only 3.4% reporting having vaginal sex with women in the last 90 days. More than half (61.0%) reported having anal sex with a men in their lifetime, with 37.9% reported having had receptive anal sex in the last 90 days. More than half (64.3%) reported having had insertive anal sex with a man during the same period of time. None of the MSM interviewed reported any condom use in the last sexual event (data not shown).
Overall, the prevalence of HIV in this sample was 42.2% [95%CI: 35.3%-49.4%]. Self-reported lifetime prevalence of syphilis was 16.1% [95%CI: 11.3–22.0%]. When stratified by sexual behavior, a higher prevalence of HIV and syphilis was observed among MSM when compared with Non-MSM (p<0.0001) (Table 1).
Anal HPV Prevalence
From the 205 participants from which anal samples were obtained, beta-globin was detected in 192 (93.7%) of the specimens, and thus these are included in this analysis. Table 2 shows the prevalence of anal HPV infection genotypes. In this sample, 57.8% [95%CI: 50.5%–64.9%] of participants tested positive for any type of HPV. The prevalence of HR anal HPV types was 53.5% [95%CI: 43.0%–65.0%]. The most prevalent HR types were 58, 31 and 51. LR-HPV types were found in 68.6% [95%CI: 57.2%–77.2%] of study participants; the most prevalent LR types were 6/11, 84 and 62. Meanwhile, multiple types were found in 47.6% [95%CI: 36.8–58.7%] of the sample and almost a half (42.7%) of the sample was positive for current HPV vaccine types 6/11, 16 and 18 HPV types.
Any anal HPV types
Table 3 shows correlates of any anal HPV infection. In age-adjusted models, men who reported having more than high school education were twice as likely to be positive for any anal HPV type as compared to those men who reported having less than a high school diploma at the time of the interview (age-adjusted OR = 2.1; [95%CI:1.1–3.7]). Those who identified themselves as MSM were more than 6 times more likely to be infected with any anal HPV type (age-adjusted OR = 6.3; 95%CI: 2.9–14.0]) as compared to those men who reported being heterosexual (Table 3). Finally, those participants who reported to be HIV+ were more than 3 times more likely to be infected with any HPV type (age-adjusted OR = 3.4; [95% CI: 1.6–7.4]) compared to HIV- subjects.
In multivariate logistic regression models, MSM had 4.49 higher odds of any anal HPV infection after adjusting for level of education and HIV status (OR = 4.5; [95%CI: 1.9–10.7]). No other variables achieved statistical significance in multivariate analysis (Data not shown).
HR HPV types
Participants who reported being MSM were more than 3 times more likely of having HR anal HPV (age-adjusted OR = 3.1; [95%CI: 1.2–8.1]) as compared with those who identified as non-MSM. On the other hand, those subjects who reported having had syphilis in their lifetime were almost 4 times more likely to be infected with HR HPV (age-adjusted OR = 3.8; [95%CI: 1.1–12.9]) as compared to those who have been never diagnosed with syphilis (Table 4).
In multivariate logistic regression models after adjusting for age, level of education and syphilis, MSM had higher odds of HR anal HPV infection (OR = 3.35; 95%CI = 1.1–10.3) (Data not shown).
Multiple HPV Infection
The prevalence of multiple HPV infection was higher among those men who identified as MSM as compared with those who identified as non-MSM (age-adjusted OR = 5.0; 95%CI: 2.1–11.9)]. Finally, those participants who self-reported as HIV+ had more than 2 times increased odds of being infected with multiple HPV types compared to HIV- men (age-adjusted OR = 2.8; [95%CI: 0.95–8.2] (Table 5). In multivariate logistic regression models, after adjusting for age and level of education a higher likelihood of multiple HPV infection were observed for MSM (OR = 3.70; 95%CI: 1.36–10.07) and HIV positive men (OR = 3.34; 95%CI = 1.02–10.97) (Data not shown).
To our knowledge, this is the first epidemiological study that reports the distribution and correlates of anal HPV infection in Puerto Rican men. In this group of high-risk men attending an STI clinic in Puerto Rico, in which the prevalence of HIV infection was high (42.2%), the prevalence of anal HPV infection (any type) was common (57.8%). HR HPV was also common in this sample (54.1%), with similar prevalence for HPV-16 (6.1%) and HPV-18 (6.1%). Similar findings were reported in other studies. For example, a study in Spain, in an STI clinic reported that the prevalence of any HPV type was similar to our study (49.6%) . In an STI unit in Italy, in which 89.4% of the men reported themselves as being MSM , the prevalence of any HPV type among men was 92.1% in the anal canal. As expected, a higher overall any HPV type prevalence has been observed among studies performed in STI clinics. However, comparisons with other studies show that findings of anal HPV infection in STI clinics are quite variable, primarily due to different anal sampling collection methods, such as the use of different sampling devices, as well as differences in the characteristics of the populations sampled (e.g. MSM, HIV+) which could account for the varying prevalence of anal HPV in STI settings , .
After multivariate logistic regression models, higher odds of any, HR and multiple anal HPV infection was reported among MSM. In a population-based study in Puerto Rico, it was documented that MSM have significant higher sexual risk practices as compared to Non-MSM . Since recent reports have highlighted that this group had also higher odds of HIV infection , this group might be at increased risk of HPV associated diseases such as anal dysplasia and anal cancer . In our study, multivariate logistic regression analysis showed a marginal association between multiple HPV infection and HIV. However, our study did not found a significant association between HIV and any, or HR anal HPV infection in multivariate analysis. This might be due to the lack of heterogeneity in our sample, in which a high prevalence of HIV was reported.
In Puerto Rico, a 26.9% increase in anal cancer incidence rates has been documented for men . Also, it has been documented that Hispanics with AIDS in Puerto Rico consistently showed a greater risk of AIDS and non-AIDS related cancers compared to the general population of Puerto Rico, and that has not changed over time . Therefore, this information along with the present report merits the development of further investigation in the area of anal HPV infection, anal intraepithelial lesions, and anal cancer, primarily among MSM. Finally, research efforts need to be aligned with capacity building efforts, primarily among health care professionals in STI clinics. Capacity building activities in HPV associated diseases and long-term sequelae needs to be developed among physicians who routinely treat men in STI clinics.
Our findings need to be interpreted with caution. Since this study was done in an STI clinic setting, our findings are not generalizable to the general population of PR. Finally, due to our small sample size and since little variability regarding sexual practices was observed, the lack of identification of well-known predictors of HPV infection (such as HIV infection) were not reported in this sample as an independent predictor of anal HPV infection after multivariate analysis. Also, other clinical factors such as HIV plasma viral load, CD4+ count, were not collected as part of this study. Regarding the HPV laboratory analysis, it is always possible that some infections were missed using one set of primers and probes. This might be possible for all HPV types. Despite these limitations, our study documents for the first time evidence of the high prevalence of anal HPV infection in a clinic-based sample of men in Puerto Rico. Efforts in primary and secondary prevention should target high-risk men in STI clinics, primarily MSM.
We wish to express our gratitude to the undergraduate and graduate students from the University of Puerto Rico who participated as part of their research experience as well as the study participants. We will also like to thank the clinical staff faculty for their help and support. The manuscript's contents are solely the responsibility of the authors and do not necessarily represent the official view of the sponsors, the NIH, or the PR Department of Health. Sponsors of neither this study nor the PR Department of Health had no part in the design, data collection, analysis, or interpretation of the findings of this study and did not take part in the writing of or decision to publish this manuscript.
Conceived and designed the experiments: VCL APO MCC JMP. Performed the experiments: VCL APO MCC JMP. Analyzed the data: VCL APO LDTM MCC JMP. Contributed reagents/materials/analysis tools: JMP. Wrote the paper: VCL APO LDTM MCC JMP.
- 1. Arbyn M, de Sanjosé S, Saraiya M, Sideri M, Palefsky J, et al. (2012) EUROGIN 2011 roadmap on prevention and treatment of HPV-related disease. Int J Cancer 131: 1969–1982.
- 2. De Vuyst H, Clifford GM, Nascimento MC, Madeleine MM, Franceschi S (2009) Prevalence and type distribution of human papillomavirus in carcinoma and intraepithelial neoplasia of the vulva, vagina and anus: a meta-analysis. Int J Cancer 124: 1626–1636.
- 3. Machalek DA, Grulich AE, Jin F, Templeton DJ, Poynten IM (2012) The epidemiology and natural history of anal human papillomavirus infection in men who have sex with men. Sex Health 9: 527–537.
- 4. Jemal A, Simard EP, Dorell C, Noone AM, Markowitz LE, et al. (2013) Annual Report to the Nation onthe Status of Cancer, 1975–2009, featuring the burden and trends in human papillomavirus (HPV)-associated cancers and HPV vaccination coverage levels. J Natl Cancer Inst 105: 175–201.
- 5. Giuliano AR, Anic G, Nyitray AG (2010) Epidemiology and pathology of HPV disease in males. Gynecol Oncol 117: S15–19.
- 6. Colón-López V, Ortiz AP, Soto-Salgado M, Torres-Cintrón M, Mercado-Acosta JJ, et al. (2013) Anal Cancer Incidence and Mortality in Puerto Rico. PR Health Sci J 32: 76–81.
- 7. Yang Y, Li X, Zhang Z, Qian HZ, Ruan Y, et al. (2012) Association of Human Papillomavirus Infection and Abnormal Anal Cytology among HIV-Infected MSM in Beijing, China. PLoS One 7: e35983.
- 8. De Pokomandy A, Rouleau D, Ghattas G, Vézina S, Coté P, et al. (2009) Prevalence, clearance, and incidence of anal human papillomavirus infection in HIV-infected men: the HIPVIRG cohort study. J Infect Dis 199: 965–973.
- 9. Svare EI, Kjaer SK, Worm AM, Osterlind A, Meijer CJ, et al. (2002) Risk factors for genital HPV DNA in men resemble those found in women: a study of male attendees at a Danish STD clinic. Sex Transm Infect 3: 215–218.
- 10. Álvarez-Argüelles ME, Melón S, Junquera ML, Boga JA, Villa L, et al. (2013) Human papillomavirus infection in a male population attending a sexually transmitted infection service. PLoS One 1: e54375.
- 11. Clatts MC, Rodríguez-Díaz CE, García H, Vargas-Molina RL, et al. (2011) Sexually transmitted infections clinics as strategic venues for targeting high risk populations for HIV research and sexual health interventions. P R HealthSci J 3: 101–108.
- 12. Colón-López V, Del Toro-Mejías LM, Ortiz AP, Tortolero-Luna G, Palefsky JM (2012) HPV awareness and willingness to HPV vaccination among high-risk men attending an STI clinic in Puerto Rico. P R Health Sci J 4: 227–231.
- 13. Colón-López V, Ortiz AP, Del Toro-Mejías LM, García H, Clatts MC, et al. (2012) Awareness and knowledge of human papillomavirus (HPV) infection among high-risk men of Hispanic origin attending a sexually transmitted infection (STI) clinic. BMC Infect Dis 12: 346–352.
- 14. Colón-López V, Del Toro-Mejías LM, Ortiz AP, Tortolero G, Palefsky JM (2012) HPV awareness and willingness to HPV vaccination among high-risk men attending an STI clinic in Puerto Rico. P R Health Sci J 4: 227–231.
- 15. IARC (2012). Human papillomaviruses. IARC Monogr Eval Carcinog Risks Hum, Vol 100B. Available: http://monographs.iarc.fr/ENG/Monographs/vol100B/mono100B-11.pdf. Accessed February 20 2013.
- 16. Álvarez-Argüelles ME, Melón S, Junquera ML, Boga JA, Villa L, et al. (2013) Human papillomavirus infection in a male population attending a sexually transmitted infection service. PLoS One 1: e54375.
- 17. Orlando G, Tanzi E, Beretta R, Amendola A, Fasolo MM, et al. (2008) Human papillomavirus genotypes and anal-related lesions among HIV-1-infected men in Milan, Italy. J Acquir Immune Defic Syndr 1: 129–131.
- 18. Strand A, Rylander E, Evander M, Wadell G (1993) Genital human papillomavirus infection among patients attending an STD clinic. Genitourin Med 6: 446–449.
- 19. Nyitray AG, Carvalho da Silva RJ, Baggio ML, Lu B, Smith D (2011) 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 1: 49–57.
- 20. Colón-López V, Rodríguez-Díaz CE, Ortiz AP, Soto-Salgado M, Suárez E, et al. (2011) HIV-related risk behaviors among a sample of men who have sex with men in Puerto Rico: an overview of substance use and sexual practices. P R Health Sci J 2: 65–68.
- 21. Colón-López V, Ortiz AP, Banerjee G, Gertz AM, García H (2013) HIV and syphilis infection among men attending a sexually transmitted infection clinic in Puerto Rico. PR Health Sci J 1: 8–13.
- 22. Piketty C, Darragh TM, Da Costa M, Bruneval P, Heard I, et al. (2003) High prevalence of anal human papillomavirus infection and anal cancer precursors among HIV-infected persons in the absence of anal intercourse. Ann Intern Med 6: 453–459.
- 23. Ramírez-Marrero FA, Smit E, De La Torre-Feliciano T, Pérez-Irizarry J, Miranda S, et al. (2010) Risk of cancer among Hispanics with AIDS compared with the general population in Puerto Rico: 1987–2003. P R Health Sci J 3: 256–264.