Background <p>High-risk human papillomavirus (hrHPV) is a leading cause of anogenital cancers and disproportionately affects men who have sex with men (MSM), particularly in low- and middle-income countries. Few studies in sub-Saharan Africa have concurrently examined penile and rectal hrHPV infection and their site-specific behavioral and biological correlates. We assessed the prevalence, genotype distribution, and behavioral factors associated with penile and rectal hrHPV among MSM in Kisumu, Kenya.</p> Methods <p>We conducted a cross-sectional analysis of baseline data from MSM aged 18–35 years. Clinician-collected penile and rectal swabs were tested for hrHPV using the ScreenFire HPV assay. Urine and rectal specimens were tested for <i>Chlamydia trachomatis</i> and <i>Neisseria gonorrhoeae</i> using GeneXpert, and HIV status was confirmed as per Kenyan national guidelines. hrHPV was analyzed separately by anatomical site. Log-binomial regression was used to estimate adjusted prevalence ratios (aPR) for associations with sociodemographic, behavioral, and biological factors.</p> Results <p>Penile hrHPV prevalence was 24.7% (39/158) and rectal hrHPV prevalence was 12.5% (22/176); 6.7% of participants tested at both sites had dual-site infection. Most infections at both sites involved a single genotype group. HPV-18/45 was the most common genotype group at both sites. Penile hrHPV was more likely among participants with HIV (aPR = 2.27, <i>p</i> = 0.050) and trended toward an association for those reporting insertive anal sex (aPR = 5.26, <i>p</i> = 0.062) and was less common among employed participants (aPR = 0.25, <i>p</i> = 0.048). Circumcision showed a protective trend (aPR = 0.52, <i>p</i> = 0.090). Rectal hrHPV was more common among participants with rectal chlamydia and/or gonorrhea infection (aPR = 3.34, <i>p</i> = 0.001), transgender or non-binary identity (aPR = 2.28, <i>p</i> = 0.036), with a possible association for those practicing receptive anal intercourse (aPR = 3.97, <i>p</i> = 0.062). Although HIV was associated with rectal hrHPV in unadjusted analyses, this relationship was attenuated after accounting for rectal bacterial STI infection.</p> Conclusions <p>hrHPV infection was common among MSM in Kisumu, Kenya, with distinct site-specific correlates. The strong association between rectal bacterial STIs and rectal hrHPV highlights the need for integrated HPV and STI screening. These findings support expansion of gender-neutral HPV vaccination and etiologic STI screening to reduce HPV-associated cancer risk among MSM in sub-Saharan Africa.</p> Clinical trial number <p>Not applicable.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Prevalence and behavioral factors associated with penile and rectal HPV infection among men who have sex with men in Kenya

  • Kate Klein,
  • Fredrick O. Otieno,
  • Walter Agingu,
  • Patriciah Wambua,
  • Felix Ochieng,
  • Minjee Lee,
  • Lyle R. McKinnon,
  • Lifang Hou,
  • Supriya D. Mehta

摘要

Background

High-risk human papillomavirus (hrHPV) is a leading cause of anogenital cancers and disproportionately affects men who have sex with men (MSM), particularly in low- and middle-income countries. Few studies in sub-Saharan Africa have concurrently examined penile and rectal hrHPV infection and their site-specific behavioral and biological correlates. We assessed the prevalence, genotype distribution, and behavioral factors associated with penile and rectal hrHPV among MSM in Kisumu, Kenya.

Methods

We conducted a cross-sectional analysis of baseline data from MSM aged 18–35 years. Clinician-collected penile and rectal swabs were tested for hrHPV using the ScreenFire HPV assay. Urine and rectal specimens were tested for Chlamydia trachomatis and Neisseria gonorrhoeae using GeneXpert, and HIV status was confirmed as per Kenyan national guidelines. hrHPV was analyzed separately by anatomical site. Log-binomial regression was used to estimate adjusted prevalence ratios (aPR) for associations with sociodemographic, behavioral, and biological factors.

Results

Penile hrHPV prevalence was 24.7% (39/158) and rectal hrHPV prevalence was 12.5% (22/176); 6.7% of participants tested at both sites had dual-site infection. Most infections at both sites involved a single genotype group. HPV-18/45 was the most common genotype group at both sites. Penile hrHPV was more likely among participants with HIV (aPR = 2.27, p = 0.050) and trended toward an association for those reporting insertive anal sex (aPR = 5.26, p = 0.062) and was less common among employed participants (aPR = 0.25, p = 0.048). Circumcision showed a protective trend (aPR = 0.52, p = 0.090). Rectal hrHPV was more common among participants with rectal chlamydia and/or gonorrhea infection (aPR = 3.34, p = 0.001), transgender or non-binary identity (aPR = 2.28, p = 0.036), with a possible association for those practicing receptive anal intercourse (aPR = 3.97, p = 0.062). Although HIV was associated with rectal hrHPV in unadjusted analyses, this relationship was attenuated after accounting for rectal bacterial STI infection.

Conclusions

hrHPV infection was common among MSM in Kisumu, Kenya, with distinct site-specific correlates. The strong association between rectal bacterial STIs and rectal hrHPV highlights the need for integrated HPV and STI screening. These findings support expansion of gender-neutral HPV vaccination and etiologic STI screening to reduce HPV-associated cancer risk among MSM in sub-Saharan Africa.

Clinical trial number

Not applicable.