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Page 6 of 8  Original Research





                                                     321 pa ents with baseline hrHPV
                                                            tes ng


                                                                                     241 hrHPV
                                80 hrHPV posi ve                                     nega ve

                                               73 Followed up                                       235 Followed Up for
                     7 Excluded from follow up                        6 Excluded from follow up
                    4 Concurrent VIA posi vity at  (median 2 years)  3 Concurrent VIA posi vity at   (median 2 years)
                   HPV tes ng (3 CINS, 1 cervici s)               HPV tes ng (all treated with cryotherapy)
                       2 Lost to follow up
                                                                            1 VIN3
                        1 Vulva HGSIL                                   2 Lost to follow up        4 Incident VIA posi vity
                                               14 Incident VIA
                                                 pos vity
                                                                                                     4 cryotherapy


                                                                  1 cryotherapy
                              2 cauteriza on of
                             transforma on zone    11 LEEP





                                                      9 HGSIL
                                                      1 LGSIL
                                                  1 chronic inflamma on

              HPV, human papillomavirus; hrHPV, high-risk HPV; VIA, visual inspection with acetic acid; LEEP, loop electrical excision procedure; HGSIL, high grade squamous intraepithelial neoplasia; LGSIL, low
              grade squamous intraepithelial neoplasia; VIN3, vulva intraepithelial neoplasia; CIN3, cervical intraepithelial neioplasia 3.
              FIGURE 2: Visual inspection with acetic acid follow-up outcomes after baseline high-risk human papillomavirus testing.


              following  exposure to  the  bivalent  vaccine  in  a cohort  of   Despite most women in our study being on first-line ART and
              young Dutch women.  In view of the dominance of subtypes   95% having  Viral load (VL) < 1000 copies/mL, women on
                               33
              other than HPV 16 or HPV 18/45, it is unclear whether   second-line therapy were twice as likely to test positive for
              the  bivalent vaccine currently being administered in the   hrHPV. In a systematic review of the association between
              Zimbabwe national programme will provide cross protection   HPV  infection and  ART, Menon et al. indicate that severe
                                                                                                            3
              against these subtypes. An understanding of the degree of   immuno-suppression of CD4 counts < 200 cells/mm  increases
              cross protection from context-specific data is warranted. This   the risk of hrHPV infection.  In our context, women on second-
                                                                                         38
              can be achieved through country-specific vaccine evaluation   line ART often have a history of severe immunosuppression
              studies in the vaccinated cohort.                     necessitating the switch to second-line ART.

              Early sexual debut and younger age were significant   After a median of 2 years follow-up, the incident rates for
              predictors of hrHPV infection in our cohort. Women with an   both VIA positivity and HGSIL were significantly higher
              early sexual debut (13–16 years) were at least three times   in  the women with hrHPV infection. No cases of HGSIL
              more likely to test positive for hrHPV when compared with   were  observed in hrHPV-negative women. These data are
              those whose sexual debut was after 21 years. In keeping with   consistent with findings from large longitudinal studies.
              these  findings,  a cohort  analysis  of  1445 urban  women in   Data from the Kaiser Portland cohort of over 20 000 women
              South Africa showed a peak in hrHPV prevalence in women   and more than 15 years of follow-up demonstrate a low risk
              younger than 25 years and a gradual decrease of hrHPV   of precancer or cancer in HIV-negative women with a single
              infection with increasing age of women.  Van Aardt et al.   negative hrHPV result. The high negative predictive value of
                                               34
              postulate  that  the  higher  hrHPV  prevalence  in  younger   HPV DNA testing is now well established, hence the adoption
              women may be partially explained by the lack of natural   by  many  global  cervical  screening  programmes  as  the
              immunity in the initial stages of sexual activity.  Literature   primary screening tool. 10,39  In low-income countries, less-
                                                    35
              also provides evidence  that over 35% of women contract   frequent  cervical  cancer  screening, once every  3 years, for
              HPV within the first 2 years of sexual debut  and that early   hrHPV-negative  WLHIV  will  have both  the potential  to
                                                 8
              sexual debut is also associated with a greater number of   reduce costs and divert scarce resources to hrHPV-positive
              sexual partners and an increased risk of STI infection. 36,37    women who are at higher risk of developing cervical cancer
              Research to further elucidate clearance and progression to   and in women who have never been screened. This resource
              cervical dysplasia in younger women is also necessary.   optimisation may translate to greater screening potential in

                                           http://www.sajhivmed.org.za 360  Open Access
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