Male circumcision and Neisseria gonorrhoeae, Chlamydia trachomatis and Trichomonas vaginalis: observations after a randomised controlled trial for HIV prevention
- 1INSERM U687, Hôpital Paul Brousse, Villejuif, France
- 2Progressus, Johannesburg, South Africa
- 3National Institute for Communicable Diseases, Johannesburg, South Africa
- 4INSERM U687, Assistance Publique-Hôpitaux de Paris, University of Versailles, France
- Dr Bertran Auvert, INSERM U687, 12 avenue Paul Vaillant-Couturier, 94804 Villejuif Cedex, France;
- Accepted 28 November 2008
- Published Online First 15 December 2008
Objective: To assess the association between male circumcision and Neisseria gonorrhoeae, Chlamydia trachomatis and Trichomonas vaginalis using data from a male circumcision randomised controlled trial.
Methods: We used data collected during the male circumcision trial conducted in Orange Farm (South Africa) among men aged 18–24 years. Altogether, 1767 urine samples collected during the final follow-up visit were analysed using PCR. Prevalence of N gonorrhoeae, C trachomatis and T vaginalis was assessed as a function of male circumcision using odds ratios (OR) given by univariate and multivariate logistic regression.
Results: In an intention-to-treat analysis, prevalence of N gonorrhoeae, C trachomatis and T vaginalis among intervention and control groups were 10.0% versus 10.3% (OR 0.97; p = 0.84), 2.1% versus 3.6% (OR 0.58; p = 0.065) and 1.7% versus 3.1% (OR 0.54; p = 0.062), respectively. The association between T vaginalis and male circumcision remained borderline when controlling for age, ethnic group, number of lifetime partners, marital status, condom use and HIV status (AOR 0.48; p = 0.069). In the as-treated analysis, this association became significant (OR 0.49, p = 0.030; AOR 0.41, p = 0.030).
Conclusions: This study demonstrates for the first time that male circumcision reduces T vaginalis infection among men. This finding explains why women with circumcised partners are less at risk for T vaginalis infection than other women. The protective effect on T vaginalis is an additional argument to recommend male circumcision in Africa where it is acceptable.
Trial registration number: NCT00122525.
Recent evidence has shown that male circumcision is a promising prevention approach for sexually transmitted infections (STIs): three randomised controlled trials (RCTs)1–3 have shown that male circumcision reduces HIV infection among young men in Africa. According to a meta-analysis published in 2006, circumcised men may be at lower risk of herpes simplex virus 2 (HSV-2) infection, chancroid and syphilis.4 However, there are conflicting results about the association of male circumcision and non-ulcerative STIs such as Neisseria gonorrhoeae, Chlamydia trachomatis5–11 and Trichomonas vaginalis infections among men.12–14
Infection with non-ulcerative STIs is major public health issue. There are about 62 million new cases of N gonorrhoeae annually worldwide, with an estimated incidence of 17 million in sub-Saharan Africa.15 N gonorrhoeae is asymptomatic in only 10% of men but primarily asymptomatic in women and its complications can be lethal.15 C trachomatis worldwide incidence has been estimated at 92 million annually, with about 16 million occurring in sub-Saharan Africa.15 It is a significant public health concern because C trachomatis infection is asymptomatic in over 50% of cases among men and women15 and it can lead to serious health complications if untreated.16 Finally, T vaginalis is the most common non-viral STI in the world, with 174 million new cases estimated in 1999.15 In sub-Saharan Africa, the incidence is estimated at 32 million.15 The infection is asymptomatic in about 50% of infected women and in over 90% of men;15 thus, re-infection and re-exposure is problematic.17 Furthermore, co-infections among these three STIs are common.18 19
The objective of this study was to analyse the effect of male circumcision on N gonorrhoeae, C trachomatis and T vaginalis prevalence using data collected during a male circumcision RCT conducted in Orange Farm, South Africa.1
Collection of data
The technical details of the trial (ANRS-1265 study), including the description of the population, has been published elsewhere.1 Between February 2002 and July 2004, 3274 uncircumcised male volunteers, aged 18 to 24 years, signed a consent form and were recruited, randomised into two groups and followed-up. Male circumcision was offered immediately after randomisation to the intervention group and after the end of the follow-up period to control group participants. During each follow-up visit at 3, 12 and 21 months, circumcision status was assessed by a nurse through genital examination, a blood sample was taken and information about sexual behaviour was collected.
For 318 consecutive days, between 10 January 2005 and 24 November 2005, a 10 ml sample of first-voided urine was collected from all participants coming for the 21-month visit during this period. These samples were analysed to assess the association between male circumcision and N gonorrhoeae, C trachomatis and T vaginalis prevalence.
Urine samples were frozen at −20°C immediately after collection and kept frozen until processing. N gonorrhoeae and C trachomatis testing was performed using the COBAS Amplicor detection kit (Roche Molecular Diagnostics, Pleasanton, California, USA). For the detection of T vaginalis, a qualitative FRET-based real-time PCR diagnostic test (Roche Molecular Diagnostics) was used based on previous published literature and validated using characterised specimens.20 21 PCR has been shown to identify significantly more trichomoniasis cases than culture.22
Categorical data of the control and intervention groups were compared using χ2 or Fisher exact test when appropriate and numerical data were compared using the Kruskal-Wallis test. N gonorrhoeae, C trachomatis and T vaginalis positive samples were analysed using intention-to-treat and as-treated analyses with univariate logistic regression. These analyses were repeated multivariately to control for ethnic group, education, age, number of lifetime partners, marital status, condom use and HIV status. To assess whether the effect of male circumcision on T vaginalis was independent of HIV infection, which is reduced by male circumcision1–3 and associated with T vaginalis infection,23 the analysis of the association between T vaginalis and male circumcision was repeated a) among those who remained HIV negative during follow-up and b) excluding those who were HIV positive at recruitment. To evaluate the effect of an imbalance between the groups, analyses of significant results were repeated when controlling for the propensity score coded in quintiles.24
The baseline characteristics of the participants who were tested for C trachomatis, N gonorrhoeae and T vaginalis by randomisation group are reported in table 1. The characteristics of those who did not attend follow-up visits during which biological samples were collected but who came for the last follow-up visit are also reported in table 1. Randomisation groups differed according to their ethnic distribution, the number of sex acts and HIV status. When compared with study participants, those not tested for C trachomatis, N gonorrhoeae and T vaginalis had a higher number of lifetime partners and a higher HIV prevalence.
Tables 2–4 present the univariate and multivariate association between male circumcision and N gonorrhoeae, C trachomatis and T vaginalis, respectively. It was found that there was no effect of male circumcision on N gonorrhoeae, as demonstrated by the odds ratio (OR) values close to 1 in table 2. The borderline association between male circumcision and C trachomatis in the intention-to-treat analysis disappeared in the as-treated analysis. The borderline association between male circumcision and T vaginalis in the intention-to-treat analysis became significant in the univariate and multivariate as-treated analysis. The adjusted ORs were slightly lower than the corresponding univariate ORs with values close to 0.5.
When excluding those who HIV seroconverted during follow-up, the OR values reported in table 4 remained almost unchanged with relative variation between −7.3% and +3.7% (results not shown). This indicates that the effect of male circumcision on T vaginalis is independent of the effect of male circumcision on HIV.
When excluding those who were HIV positive at recruitment, the OR values and p values reported in table 4 became slightly lower. The OR and adjusted OR (AOR) associated with randomisation groups were 0.45 (95% CI 0.22 to 0.89; p = 0.023) and 0.39 (95% CI 0.19 to 0.80; p = 0.0098), respectively. The OR and AOR associated with circumcision status were 0.34 (95% CI 0.14 to 0.82; p = 0.016) and 0.39 (95% CI 0.18 to 0.76; p = 0.065), respectively. The AORs of table 4 were almost identical when the analyses were adjusted for the propensity score in addition to the other covariates.
This study demonstrates that male circumcision does not have a protective effect on C trachomatis acquisition in men, which concurs with the findings from most studies exploring this association whether assessed in cross-sectional studies5 8 25 26 or in cohort studies.8–11 27 Only one multi-site study pooling cross-sectional data of 305 couples from Thailand, the Philippines, Brazil, Colombia and Spain found that when controlling for the number of sexual partners of the couple, male circumcision was associated with an 82% reduction in the risk of C trachomatis infection in female partners (OR 0.18, 95% CI 0.05 to 0.58). However, C trachomatis infection was not ascertained in the men themselves in that study and the authors admit that it is possible that male circumcision reduces the risk of transmission of the infection to the partner without reducing the risk of C trachomatis acquisition in the men themselves.16 In fact, two studies seem to suggest that C trachomatis prevalence is higher among circumcised men and their partners.9 27
This study has some limitations. Biological samples were not collected throughout the follow-up period, so the C trachomatis, N gonorrhoeae and T vaginalis statuses at inclusion are unknown. As a result, some T vaginalis infections may have predated the intervention. Thus, we report the effect of male circumcision on T vaginalis prevalence and not T vaginalis incidence. Only participants coming for the last follow-up visit and during a specified time period were tested for C trachomatis, N gonorrhoeae and T vaginalis. This may have introduced some bias. Indeed, we found that those having undergone STIs testing were slightly different from those who had not. However, this difference was not expected to change the association between male circumcision and the C trachomatis, N gonorrhoeae and T vaginalis statuses. Lastly, the slight difference between circumcised and uncircumcised participants, which may be partly explained by a differential follow-up, may also have interfered with the result of this study. Hence, the fact that the results were not changed when adjusting on the propensity score is reassuring. Nevertheless, the results of this study have to be confirmed using the data of the two other male circumcision trials conducted in Kenya and Uganda.2 3
No evidence of a protective effect of male circumcision on N gonorrhoeae infection was found. Previous studies have suggested that results will vary according to the population assessed: four studies among male attendees of STI clinics in developed countries found that uncircumcised men were up to twice as likely to develop N gonorrhoeae infection than circumcised men (OR of 1.6 to 2.0).7 8 26 28 However, none of the studies conducted in developing countries found evidence of such an effect.6 9 27 29
The study demonstrated a borderline protection effect of male circumcision on T vaginalis infection by young men in the intention-to-treat analysis and a significant effect in the as-treated analysis. The difference between the two analyses may have been caused by the high proportion of cross-over in this RCT,1 which diluted the effect observed in the intention-to-treat analysis. The fact that the protective effect became slightly stronger in the multivariate analysis, which includes HIV status, also suggests a protective independent effect of male circumcision on T vaginalis acquisition.
This finding is noteworthy because very few studies have investigated this association in men—probably due to diagnostic limitations.14 17–19 Nevertheless, the size of the protective effect obtained in this study is consistent with what has been estimated by observational studies. A cross-sectional investigation conducted among men from the general population of Mwanza, Tanzania, found that male circumcision status was significantly associated with T vaginalis infection (OR 0.37, 95% CI 0.19 to 0.72) when adjusting for age.12 In their prospective study among US male partners of women infected with T vaginalis, Seña and colleagues found that uncircumcised men were almost twice as likely to be infected with T vaginalis (unadjusted OR 1.8, 95% CI 1.10 to 3.20).14
The fact that N gonorrhoeae and C trachomatis are almost exclusively urethral pathogens may explain why male circumcision has no protective effect against them. In contrast, the protective effect against T vaginalis may indicate that T vaginalis is both a sub-preputial and a urethral pathogen.
There is also evidence that male circumcision reduces T vaginalis acquisition by female partners. A recent randomised study conducted in Rakai, Uganda, among HIV discordant heterosexual couples indicated that the rate of T vaginalis infection among partners of participants from the intervention arms was reduced by almost half (adjusted risk ratio 0.52, 95% CI 0.05 to 0.98).13 Hence, our study illustrates why male circumcision is protective against T vaginalis infection among women having circumcised partners. Indeed, as shown in our study, male circumcision reduces the risk of T vaginalis infection among men and consequently reduces the exposure of women to T vaginalis. Thus, the risk of T vaginalis infection is lowered among women.
Some studies have suggested that T vaginalis facilitates the spread of HIV by up to twofold.15 23 30 31 Thus, the effect of male circumcision on HIV acquisition in young men may partly be due to its effect on T vaginalis. If the results of this study are confirmed by those of the male circumcision trials conducted in Uganda and Kenya, the findings of this study will reinforce the WHO-UNAIDS statement recommending the implementation of male circumcision programmes in African countries with low male circumcision prevalence and a high male circumcision acceptability.32
Male circumcision protects men against Trichomonas vaginalis infection, which is the most common non-viral sexually transmitted infection in the world.
T vaginalis infection causes severe morbidity among women. Male circumcision indirectly benefits women by reducing their exposure to T vaginalis.
Male circumcision does not provide protection against Neisseria gonorrhoeae or Chlamydia trachomatis.
The authors would like to thank all the volunteers who agreed to take part in this study, answer the questions put to them and provide swab samples. G Sipho Phatedi for his management of the recruitment process and Y de La Soudière for his help in the management of the data set. Dr B Gwala, Dr G Shilaluke and Dr D Zulu who performed the male circumcisions for the study. G Gumede for the clinical investigation and Z Nkosi for interviewing all the respondents. They would also like to thank B Klaas for the data capture, as well as M Hunter, the recruitment staff and all the assistants (C Dlamini, S Dumisi, B Masitenyane, R Matodzi, T Mbuso, A Motha, S Mpetsheni, J Nhlapo, J Ntsele, MChakela, A Tshabalala, D Mashamba, N Nhlapo) for their cooperation and support. L Short, M Mashiloane, B Miller, B Singh, S Hloma and the HIV serology laboratory of the National Institute for Communicable Diseases, Johannesburg, South Africa, provided technical assistance with the laboratory testing.
Funding: This study was supported by ANRS (France) grant 1265, NICD (South Africa), Gates Foundation (USA) grant 33759 and INSERM (France).
Competing interests: None.
Ethics approval: The research protocol was reviewed and approved by the University of Witwatersrand Human Research Ethics Committee (Medical) (protocol study number M020104). The trial was also approved by the Scientific Commission of the French National Agency for AIDS Research (ANRS, protocol study numbers 1265, 2002, decision number. 50) and authorisation was obtained from the City of Johannesburg, Region 11.
Contributors: JT and BA analysed the data and wrote the first draft. DT organised the collection of the samples. MN and AP analysed the samples. All authors contributed to the writing of the paper.
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