Three randomized controlled trials (RCTs) have confirmed that male circumcision (MC) significantly reduces acquisition of HIV-1 infection among men. The objective of this study was to perform a comprehensive, prospective evaluation of risk compensation, comparing circumcised versus uncircumcised controls in a sample of RCT participants.
Methods and Findings
Between March 2004 and September 2005, we systematically recruited men enrolled in a RCT of MC in Kenya. Detailed sexual histories were taken using a modified Timeline Followback approach at baseline, 6, and 12 months. Participants provided permission to obtain circumcision status and laboratory results from the RCT. We evaluated circumcised and uncircumcised men's sexual behavior using an 18-item risk propensity score and acquisition of incident infections of gonorrhea, chlamydia, and trichomoniasis. Of 1780 eligible RCT participants, 1319 enrolled (response rate = 74%). At the baseline RCT visit, men who enrolled in the sub-study reported the same sexual behaviors as men who did not. We found a significant reduction in sexual risk behavior among both circumcised and uncircumcised men from baseline to 6 (p<0.01) and 12 (p = 0.05) months post-enrollment. Longitudinal analyses indicated no statistically significant differences between sexual risk propensity scores or in incident infections of gonorrhea, chlamydia, and trichomoniasis between circumcised and uncircumcised men. These results are based on the most comprehensive analysis of risk compensation yet done.
Citation: Mattson CL, Campbell RT, Bailey RC, Agot K, Ndinya-Achola JO, Moses S (2008) Risk Compensation Is Not Associated with Male Circumcision in Kisumu, Kenya: A Multi-Faceted Assessment of Men Enrolled in a Randomized Controlled Trial. PLoS ONE3(6): e2443. https://doi.org/10.1371/journal.pone.0002443
Editor: Landon Myer, University of Cape Town, South Africa
Received: March 8, 2008; Accepted: May 1, 2008; Published: June 18, 2008
This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
Funding: This research was supported by grant number AI50440 from the Division of AIDS, National Institute of Allergies and Infectious Disease of the United States National Institutes of Health and by grant number HCT 44180 from the Canadian Institutes of Health Research (CIHR).
Competing interests: The authors have declared that no competing interests exist.
The results of three randomized controlled trials (RCTs) have demonstrated that male circumcision (MC) significantly reduces acquisition of heterosexually transmitted HIV-1 among men,– confirming observational evidence ,  and adding plausibility to previous immunohistochemistry studies of the foreskin. ,  All three trials were stopped prematurely by their respective Data and Safety Monitoring Boards when, at interim analyses, circumcision was found to be highly efficacious in reducing HIV incidence, indicating that it would be unethical to continue withholding circumcision from the control group. – The protective effect of male circumcision ranged from 51% to 60% in intent to treat analyses, and from 60% to 76% in as treated analyses. Despite these results, concern about how men perceive the protective effect of circumcision remains.  If circumcised men believe that circumcision confers substantial or complete protection against HIV infection, they may engage in increased risk behavior, commonly referred to as risk compensation or behavioral disinhibition.  Significant risk compensation could reduce the protective effect of circumcision and possibly result in increased rather than decreased incidence of HIV.
The empirical evidence regarding risk compensation in the context of male circumcision is inconsistent. Two cross-sectional studies have indicated that circumcised men engage in higher risk behaviors than uncircumcised men; however, given the observational nature of the studies, these results could reflect confounding. ,  In contrast, a prospective cohort study conducted in Siaya and Bondo Districts, Kenya found that circumcised men did not have more extra-marital sex partners than uncircumcised men.  Data from the RCTs of MC did not show consistent evidence of risk compensation; however, minimal increases in some risky behaviors were noted. – In the Orange Farm study, the following five variables were evaluated at baseline and at 3, 12, and 21 months later: at least one sexual contact without a condom, being married or living as married, more than 1 non-spousal partner, at least one sexual partnership with only one sexual contact, and more than 5 sexual contacts. Only differences in mean number of sexual contacts were statistically significant between 4–12 months after circumcision (5.9 versus 5.0, p<0.001) and 13–21 months (7.5 versus 6.4, p = 0.0015).  Controlling for behavioral differences between study groups altered the protective effect against HIV acquisition minimally from 60% (95% CI 32%–76%) to 61% (95% CI 34%–77%).  All other differences were non-significant.
The Ugandan trial found no consistent evidence of behavioral disinhibition.  In this study, the following sexual behaviors were evaluated: condom use (defined as none, inconsistent, or consistent), number of sexual partners (0, 1, 2, 3+), any non-marital partners, alcohol use with sexual intercourse (none versus any), and transactional sex (exchanging money or gifts for sex). There was no difference in the proportion of circumcised and uncircumcised men reporting consistent condom use at the 6, 12 and 24 month follow-up visit (p = 0.11, p = 0.6, p = 1.0, respectively). Inconsistent condom use was higher in the circumcised group (p = 0.0004) at the 6 month follow-up visit, but men in the control group were more likely to report no condom use compared to circumcised men (p = 0.0004).  At the 12 and 24 month follow-up visits, number of sexual partners, non-marital relationships, and condom use were similar in both groups. Alcohol use with sexual intercourse was the same at enrollment, but higher among uncircumcised men at the 6 month (p = 0.001), 12 month (p = 0.06), and 24 month follow-up visit (p = 0.02). Transactional sex did not differ between groups.
In the Kenya trial, the following sexual behavior variables were evaluated: unprotected intercourse with any partner in the previous 6 months, last sexual relations with a casual partner, sexual abstinence in the last 6 months, consistent condom use in the previous 6 months, and 2 or more partners in the previous 6 months. There was a reduction in risk behavior among both circumcised and uncircumcised men from baseline to follow-up visits, except in the proportion of men reporting 2 or more sex partners, which progressively declined in the control group throughout the duration of follow-up, but declined and then stabilized after the 6 month follow-up visit in circumcised men.  At the 24 month follow-up visit, the proportion of circumcised men reporting unprotected sexual intercourse in the previous six months was greater than the control group (p = 0.03), and fewer circumcised men reported consistent condom use versus controls (p = 0.03), which could suggest that men's behavior became refractory to prevention messages.  It is notable that risk behaviors declined for both circumcised and uncircumcised men from baseline to 24 months of follow-up, which the authors attribute to the risk reduction counseling that participants received.  It was suggested that circumcised men not only did not increase their sexual risk behaviors after circumcision, they reduced their risk, but there were even greater reductions from baseline to month 24 in the control group. 
At most, 5 behaviors were evaluated in the context of the trials and the behaviors chosen to indicate sexual risk varied across studies. Measuring condom use and sex with multiple partners is conventional in studies of risk compensation, but how those variables are defined and what other behaviors are chosen to represent risk are not consistent. This is due, in part, to the lack of a consensus definition of “sexual risk,” as well as to the statistical challenges inherent in analyzing multiple, highly correlated behavioral variables.  It is possible that information obtained from relatively brief questionnaires lacks sufficient breadth to comprehensively address the issue of risk compensation. This study was specifically designed to measure and analyze a comprehensive set of sexual behaviors by applying a behavioral risk propensity scale developed to assess risk compensation in circumcised versus uncircumcised men participating in the circumcision trial in Kenya.
Design and Data Collection
The Kenyan RCT of MC enrolled men who were sexually active within the last 12 months, were HIV negative, uncircumcised at baseline, aged 18–24 years, and resident in Kisumu District. The men received HIV testing and counseling on risk reduction strategies following Kenyan National Guidelines at the following RCT visits: 1, 3, 6, and 12 month. All men who enrolled in the RCT between March 2004 and September 2005 were systematically invited to participate in the current study, which took place at a separate facility approximately 100 meters from the trial study site. The men received HIV testing and counseling on risk reduction strategies following Kenyan National Guidelines at the following RCT visits: 1, 3, 6, and 12 month. All men were informed that although there was some evidence of an association between circumcision and reduced HIV acquisition, the evidence was not conclusive. Participants provided written informed consent to undergo separate interviews for this study at baseline and at 6 and 12 month follow-up visits, and allowed us to obtain data from the RCT. The questionnaires and consent documents were developed in English and translated into Dholuo and Kiswahili (the predominant local languages) independently by two indigenous speakers, and discrepancies were resolved with assistance from a third individual. Interviews were conducted by male interviewers fluent in all three languages. Men were offered 150 Kenyan shillings (approximately $2.00 USD) for each scheduled visit to cover transport and loss of income. The research protocol was approved by the Kenyatta National Hospital Ethics and Research committee, the University of Illinois at Chicago's Institutional Review Board #3, and the University of Manitoba Biomedical Research Ethics Board.
To obtain sexual histories, we adapted the well-validated Timeline Followback approach  to collect information about every sexual relationship in the last 6 months for up to 12 partners at baseline (within 10 days of being randomized in the trial), and at 6 and 12 month follow up visits (plus or minus 3 months). Interviewers obtained the following information for each partner: age, gender, type of partner, dates of the relationship, length of time knowing the partner prior to sex, approximate number of sexual encounters, sexual practices (vaginal, oral, anal), exchange of sex for money or gifts, condom use (ever used a condom with the partner, used at the first encounter, at last encounter, and at every encounter), and clients' perception of their partners (e.g. if partners had other partners concurrently, engaged in transactional sex, or were thought to be HIV positive). Men were identified as having a concurrent partnership if the start and end dates of any two partners overlapped by at least one month. Men were also asked whether or not they thought circumcision reduced the risk of HIV. A priori power analyses indicated that 500 circumcised and 500 uncircumcised men would provide at least 80% power to detect an absolute difference of 7% among the proportion of men reporting unprotected sex with 2 or more partners between baseline and the 6 or 12 month follow-up visits with a base rate of .45 (paired proportion) among uncircumcised men with two-sided type 1 error of 0.05.
Using item response theory , , we developed an 18-item behavioral risk propensity scale to capture specific behaviors and practices that men reportedly engaged in with each partner discussed in their sexual histories (for up to 12 partners). Items were included in the scale if previous epidemiologic research demonstrated they were risk factors for HIV  and there was reason to believe the behavior may be affected by circumcision (e.g. condom use, multiple sex partners, transactional sex, etc). Count variables were created to summarize behaviors across 0–12 partnerships. Using differential item function analyses, we demonstrated that the scale performed consistently at all three time points, and whether interviews were conducted in English or not (Dholuo or Kiswahili). The resulting logit risk scores were transformed so that the lowest logit score (−4.62) was equal to zero. Transformed scores ranging from 0 to 9.24 were computed at baseline, 6 and 12 month follow-up visits. The scale demonstrated very good reliability (Cronbach's alpha of 0.87) and, based on assessments of monotonicity; it resulted in a unidimensional continuum to represent sexual risk propensity (e.g. sexual behavior).
The scale's construct validity (i.e. whether it does, indeed, measure risky sexual behavior) was established by demonstrating that men's scores on the risk scale were associated with the presence of an incident sexually transmitted infection (STI) of Neisseria gonorrhoeae, Chlamydia trachomatis, and Trichomonas vaginalis or incident HIV (in press). At both follow-up visits men diagnosed with an incident STI had higher risk scores than uninfected men, but the difference was only statistically significant at the 6 month follow-up visit (Wilcoxon two-sided probability p = 0.01), presumably due to the small number of respondents with STIs at the 12 month follow-up visit (n = 24). At the 6 and 12 month follow-up visits, 8 and 4 men respectively were diagnosed with incident HIV infection. Similar to the STI analyses, men who seroconverted throughout the study had higher risk scores than those who did not. The non-parametric Savage Two-Sample Test with one-sided probability was borderline at 6 months (p = 0.07) and statistically significant at 12 months (p = 0.01).
To corroborate self-reported risk behavior, we independently evaluated incident STIs as a secondary outcome variable. Because these infections occurred at a relatively high rate in our study population, ,  and are not generally considered to be associated with male circumcision, they provide ideal biologic markers of sexual risk behavior. ,  Also, since men received treatment for their infections, it was possible to distinguish prevalent from incident infections.  We used the following diagnostic criteria to identify infections: Neisseria gonorrhoeae and Chlamydia trachomatis: by polymerase chain reaction assay (AMPLICOR® CT/NG Test, Roche Diagnostics, Montreal Canada) and Trichomonas vaginalis: by culture (InPouch™ TV test, Biomed Diagnostics, Oregon, United States). Infections identified at baseline were considered prevalent. Since men identified with an STI at baseline were treated, infections subsequent to baseline were considered incident.
Data were entered into SPSS Version 10.0 (SPSS Inc., Chicago, IL). Approximately 30% of interviews were entered in duplicate to evaluate accuracy. The error rate was less than 1%. Further data management, descriptive analyses, and multivariable modeling were performed in SAS Version 8.2 (SAS Institute Inc., Cary, North Carolina, USA).
To compare men who enrolled in the sub-study to those who did not and to compare circumcised to uncircumcised men at baseline, we used Pearson Chi-Square tests for categorical variables, independent t-tests for normally distributed continuous variables and Wilcoxon's Two Sample Z Test for continuous variables that were not normally distributed. To evaluate whether circumcision altered men's sexual risk behavior, we used random effects regression models to deal with statistical dependence resulting from repeated observations. 
The primary outcome was the 18-item risk score, which had a “semi-continuous” or “mixed” distribution ranging from 0 to 9. – Men who had not engaged in any sexual activity in the past 6 months had scores of 0, but men who were sexually active in the 6 months prior to the interview had scores ranging from >0–9. We implemented a two-part random effects regression model to accommodate the “semi-continuous” distribution.  The first equation in the model evaluated whether or not men engaged in any activity in the last 6 months as a binary yes/no outcome (modeled as logistic) and the second equation modeled the positive sexual risk score as a continuous outcome (modeled as lognormal to account for the skewed distribution). The covariates were interpreted as if the two parts of the model were fit separately but the random effects in the two equations were allowed to correlate. Population-averaged rather than subject-specific odds ratios are reported.  The model was estimated using SAS Proc Mixed, implemented via a set of SAS macros developed by Tooze and Grunwald. , 
The independent variables of interest were: circumcision group (men randomized to receive circumcision versus those randomized to remain uncircumcised); time (indicator variables for 6 month and 12 month follow-up); and the interaction between circumcision group and time. Additional covariates included age, marital status, education, income and the belief that circumcision reduces risk of acquiring HIV.
The secondary outcome variable included information on whether or not men were diagnosed with an incident infection of Neisseria gonorrhoeae, Chlamydia trachomatis, or Trichomonas vaginalis within 3 months before or after the behavioral interview at the 6th and 12 month follow-up visit. Any incident STIs versus none were modeled using dichotomous random effects models using Proc NLMIXED. 
Between March 2004 and September 2005, 1780 men were enrolled in the RCT and therefore met eligibility criteria for this study. Of these, 1319 chose to participate in this study, yielding an overall response rate of 74%, which surpassed our target enrollment of 1000. Men who joined this sub-study were slightly more likely to have been randomized to the control (53%) versus circumcision (47%) arm (p<0.001), were younger (46% vs. 41% p = 0.03), more likely to have completed secondary school (58% vs. 52%, p = 0.03), and more likely to be unemployed (67% vs. 60%, p = 0.02) than those who did not enroll. There were no significant differences between the median number of lifetime sex partners (Wilcoxon Two Sample Z Test = 0.01, p = 0.95), number of sex partners in the last 6 months (χ2 = 0.53, p = 0.77), or occurrence of a prevalent sexually transmitted infection (χ2 = 0.17, p = 0.68) at baseline between the men who enrolled in this study versus those who did not.
Ten men with missing data on key outcome variables were eliminated from all subsequent analyses. The final sample included 1309 men, of whom 620 (47%) had been randomized to undergo circumcision and 689 (53%) were controls in the parent RCT. Table 1 compares the baseline characteristics of the enrolled circumcised and uncircumcised men. In general, the groups were similar, except that uncircumcised men were more likely to be unemployed (χ2 = 16.1, p = 0.01) and circumcised men were more likely to be diagnosed with a sexually transmitted infection (χ2 = 5.6, p = 0.02). In the main RCT, 11 men who were randomized to the control group became circumcised. Three of these men enrolled in this study. Of 57 men in the RCT who were randomized to receive circumcision never received the surgery, sixteen of these enrolled in this study. To investigate the effect of these crossovers, we performed an “as treated” analysis, which yielded the same conclusions as the “intent to treat” analysis, which we report here.
Of the 1309 men enrolled, 1001 (76%) returned for the 6 month follow-up and 1007 (77%) returned at 12 months. There was no differential loss to follow-up between study groups (χ2 = 0.02., p = 0.90). Men who were interviewed at all three time points (n = 873) had slightly higher sexual risk propensity scores ( = 3.4) than men interviewed at one ( = 3.0) or two ( = 3.3) time points indicating that men with less risky sexual behavior were more likely to be lost to follow-up than men with high risk behavior (Wilcoxon Two Sample Z Test with a continuity correction of .5 = −1.93, p = 0.054).
Table 2 shows the 18 risk scale items, the STI data, and the belief that circumcision reduces the risk of HIV by group and time. There were no statistically significant differences between the proportion of circumcised and uncircumcised men who engaged in any of the 18 behaviors at any time point. Moreover, both circumcised and uncircumcised men reported lower numbers of total sex partners and lower numbers of partners with whom they did not always use a condom at follow-up visits than they did at baseline. Of note, circumcised men were no more likely to report the belief that circumcision reduces the risk of acquiring HIV than uncircumcised men at any time point. At baseline, 57% of circumcised and 56% of uncircumcised men reported that they thought circumcision reduces the risk of HIV. However by the 12 month follow-up visit, endorsement of this belief rose to 75% of circumcised and 76% of uncircumcised men.
Both groups were diagnosed with fewer incident sexually transmitted infections at the 12 month follow-up visit compared to the 6 month visit. Because infections at baseline were considered prevalent and not incident, a direct comparison cannot be made from baseline to follow-up visits. However, when looking at the proportion of men diagnosed with an STI, circumcised men were more likely than uncircumcised men to be diagnosed with a prevalent infection at baseline (OR = 1.6, p = 0.02) and an incident infection at the 6 month follow-up visit (OR = 1.8, p = 0.05). At the 12 month follow-up visit, there were no significant differences between the proportions of circumcised and uncircumcised men diagnosed with incident STIs.
Median risk scores declined for all men (circumcised and uncircumcised) (Figure 1). Declining risk is confirmed by the two-part random effects regression models (Table 3). In the crude model evaluating circumcision and time, at the 6 month follow-up visit men were 57% less likely to engage in any sexual activity (OR = 0.43, 95% CI 0.34–0.54), and among men who had sex, there was a 12% decrease (expβ = 0.88, 95% CI 0.86–0.90) in risk scores compared to the baseline visit. Similarly, at the 12 month follow-up visit, men were 59% less likely to engage in any sex (OR = 0.41, 95% CI 0.33–0.51) and, of those who did, there was a 16% decrease in risk scores (expβ = 0.84, 95% CI 0.81–0.86) compared to baseline. There was no statistically significant difference in the risk scores of circumcised and uncircumcised men (OR = 1.09, 95% CI 0.86–1.38 for logistic and expβ = 1.02, 95% CI 0.99–1.01 for lognormal). Similarly, as shown in table 3, the interaction terms for circumcision group and time were not significant at the 6 month follow-up visit (OR = 1.27, 95% CI 0.83–1.95 for logistic and expβ = 1.01, 95% CI 0.96–1.06 for lognormal) or the 12 month follow-up visit (OR = 1.21, 95% CI 0.79–1.86 for logistic and expβ = 1.03, 95% CI 0.98–1.07 for lognormal). Thus, there was no evidence of differential risk according to circumcision group. Because it was not statistically significant, the interaction terms for circumcision status and visit were not included in the adjusted model. The random effects variance in both parts of the model was significant (p<0.01 for both) demonstrating that there was heterogeneity among men with respect to engaging in any sexual activity and in risk scores.
After adjusting for age, marital status, education, income, and the belief that circumcision status reduces the risk of acquiring HIV, there was still a significant decline in risk scores at the 6 and 12 month follow-up visits compared to baseline. Circumcision group remained non-significant. Men who were married or cohabitating with a woman were more likely to engage in any sexual activity (OR = 10.29, 95% CI 4.19–25.5) and had slightly higher mean risk scores (expβ = 1.02, 95% CI 0.98–1.06) than single men. Similarly, men who earned less than 2000 ksh/month (approximately $27 US) were less likely to engage in any sexual activity (OR = 0.69, 95% CI 0.53–0.89) and had lower mean risk scores (expβ = 0.96, 95% CI 0.94–0.98). Of note, although the proportion of men reporting the belief that circumcision reduces the risk of acquiring HIV increased from baseline (57%) to the 12 month follow-up visit (76%), this belief was not associated with engaging in any sexual activity (OR 1.09, 95% CI 0.87–1.36) or in higher risk scores (expβ = 1.00, 95% CI 0.97–1.02).
Table 4 presents the results of the crude model with circumcision and time, the model including the interaction between circumcision and time, and the adjusted random effect regression models comparing incident STIs at the 12 month visit compared to the 6 month visit. Like risk scores, circumcision was not associated with a statistically significant increase in STIs in the crude (OR 1.28, 95% CI 0.82–2.00) or adjusted models (OR 1.25, 95% CI 0.79–2.00). Fewer men were diagnosed with incident STIs at the 12 month visit compared to the 6 month visit (adjusted OR 0.55, 95% CI 0.34–0.88). The interaction between circumcision status and time indicated that circumcised men were slightly less likely to be diagnosed with an STI at the 12 month visit than their uncircumcised counterparts, but the term was not statistically significant (OR = 0.49, 95% CI 0.21–1.21).
We used two different measures of sexual risk to evaluate risk compensation associated with male circumcision: an index based on 18 sexual behaviors and laboratory diagnosed STIs. We found no evidence to suggest that circumcised men engaged in increased risk behavior after the procedure. To the contrary, both circumcised and uncircumcised men significantly reduced their HIV risk behavior from baseline to the 6 and 12 month follow-up visits. This decline was evident when evaluating the overall risk score across time and by comparing the individual 18 behaviors at a given time point. There was also a decline in the number of incident infections of gonorrhea, chlamydia and trichomoniasis from the 6 month visit to the 12 month visit. The overall consistency of the self-reported sexual behavior data with the biologic indicator (STI) likely indicates a low degree of misreported sexual behavior.
Circumcised men were slightly more likely to be diagnosed with incident STIs than uncircumcised men at the 6 month visit (6% vs. 3%, p = 0.05). However, it is important to note that circumcised men were also more likely to be diagnosed with an STI at baseline (10% vs. 7%, p = 0.02). Even though all men received treatment and referrals for their partners to receive treatment, it is possible that sex partners did not receive treatment and potentially re-infected the men. Ideally, we would have compared incident infections at all three time points, but it was not possible to disentangle prevalent from incident infections at the baseline visit. Given that limitation, longitudinal analyses indicated that incident STIs declined from the 6 month to the 12 month visit and there was no interaction between circumcision and time.
In general, our findings are consistent with most empirical studies of behavioral disinhibition in the context of male circumcision. , ,  This sub-study included approximately half the participants enrolled in the RCT, but used a different methodology that was specifically designed to assess a comprehensive combination of risk behaviors. Instead of focusing on 5 sexual risk behaviors as was done in the RCT, we evaluated 18 risk behaviors/sexual practices and evaluated the occurrence of incident STIs. Similar to the conclusions drawn from the trials in Kenya and Uganda and a prospective study in Siaya and Bondo districts in Kenya, we found no compelling evidence of increased risk behavior among circumcised men. , ,  As was the case in the overall results from the Kenyan trial, we detected an equal reduction in risky sexual practices among both circumcised and uncircumcised men.  That the results from the RCT and from this study were consistent strengthens the conclusions of both studies. These are important results in the face of reluctance on the part of some in the international health community to endorse male circumcision.  The consistency and strength of the results presented in this study, the RCT, and in previous studies, –,  provide evidence that risk compensation is likely to be minimal or absent among circumcised men and, therefore, it should not a priori be considered a barrier to the promotion of male circumcision for HIV and STI prevention.
There were several limitations to this study. All the participants were from a narrow age range (18–24 years) and were enrolled in a RCT which accepted only healthy, sexually active HIV-uninfected individuals. When MC services are made widely available, it is likely that men and boys from a wide spectrum of ages will access the services and, in the absence of HIV testing, some may be HIV infected prior to circumcision. Of those eligible for this study, 74% enrolled. We found no differences in sexual behavior between those enrolled and those not enrolled but eligible. Nevertheless, there could have been differences that we were unable to measure. Further, because this was an observational study, we were unable to control for unknown confounders. In addition, the participants were followed for only twelve months. Although logically one might think that risk compensation would occur soon after wound healing in the circumcised men, it is possible that circumcised men become less sexually inhibited after they have been in their new status for more than one year. Finally, as with all studies that rely on participants' self-reports, misreporting of behaviors was possible. Study interviewers were carefully trained and the questionnaire using the Timeline Followback approach had many means of checking for inconsistencies. We also used biologic outcomes of risk (STIs), and these were consistent with the results from the self-reported behaviors.
Participation in the main RCT and in this study entailed repeated HIV testing and individually-tailored risk reduction counseling at the baseline, 6 month, and 12 month study visits, and participants were informed that the evidence for MC having a protective effect against HIV acquisition was inconclusive. Conditions under which MC is provided widely are likely to be different. Consequently, despite there now being consistent findings from five studies that risk compensation is essentially absent after circumcision, –,  it will be necessary to further evaluate the possibility that men increase their HIV risk behavior after circumcision is offered in more naturalistic public health and medical settings. Alternatively and preferably, until further evidence becomes available, as MC services are introduced and promoted, the HIV prevention community should ensure that MC services are integrated with a full package of HIV prevention measures including HIV testing, STI diagnosis and treatment, condom provision, and risk reduction counseling. The results of this study suggest that, under such conditions, HIV risk behaviors after circumcision are unlikely to increase. Indeed, they may well decline.
We thank all of the participants, without whom this work would not have been possible. We are grateful to Evans Otieno, Nicholas Ouma, Bob Ogollah, Kevine Kamollah, and the entire UNIM Project staff for their assistance in data collection and recruitment efforts and to Dr. Donald Hedeker, Dr. Ronald Hershow, Dr. George Karabatsos and Nelli Westercamp for their helpful comments on the manuscript and on statistical analyses.
Conceived and designed the experiments: RB SM CM. Performed the experiments: RB CM KA. Analyzed the data: CM RC. Contributed reagents/materials/analysis tools: RB JN. Wrote the paper: RB SM CM RC KA JN.
- 1. Auvert B, Taljaar D, Lagarde E, Sobngwi-Tambekou J, Sitta R, et al. (2005) Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: the ANRS 1265 trial. PLoS Medicine 2: e298.B. AuvertD. TaljaarE. LagardeJ. Sobngwi-TambekouR. Sitta2005Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: the ANRS 1265 trial.PLoS Medicine2e298
- 2. Bailey R, Moses S, Parker CB, Agot K, Maclean I, et al. (2007) Male circumcision for HIV prevention in young men in Kisumu, Kenya: a randomised controlled trial. The Lancet 369: 643–656.R. BaileyS. MosesCB ParkerK. AgotI. Maclean2007Male circumcision for HIV prevention in young men in Kisumu, Kenya: a randomised controlled trial.The Lancet369643656
- 3. Gray RH, Kigozi G, Serwadda D, Makumbi F, Watya S, et al. (2007) Male circumcision for HIV prevention in men in Rakai, Uganda: a randomised trial. The Lancet 369: 657–666.RH GrayG. KigoziD. SerwaddaF. MakumbiS. Watya2007Male circumcision for HIV prevention in men in Rakai, Uganda: a randomised trial.The Lancet369657666
- 4. Siegfried N, Muller M, Deeks J, Volmink J, Egger M, et al. (2005) HIV and male circumcision–a systematic review with assessment of the quality of studies. The Lancet Infectious Diseases 5: 165–173.N. SiegfriedM. MullerJ. DeeksJ. VolminkM. Egger2005HIV and male circumcision–a systematic review with assessment of the quality of studies.The Lancet Infectious Diseases5165173
- 5. Weiss HA, Quigley MA, Hayes RJ (2000) Male circumcision and risk of HIV infection in sub-Saharan Africa: a systematic review and meta-analysis. AIDS 14: 2361–2370.HA WeissMA QuigleyRJ Hayes2000Male circumcision and risk of HIV infection in sub-Saharan Africa: a systematic review and meta-analysis.AIDS1423612370
- 6. Donoval BA, Landay AL, Moses S, Agot K, Ndinya-Achola JO, et al. (2006) HIV-1 target cells in foreskins of African men with varying histories of sexually transmitted infections. American Journal of Clinical Pathology 125: 386–391.BA DonovalAL LandayS. MosesK. AgotJO Ndinya-Achola2006HIV-1 target cells in foreskins of African men with varying histories of sexually transmitted infections.American Journal of Clinical Pathology125386391
- 7. McCoombe SG, Short RV (2006) Potential HIV-1 target cells in the human penis. AIDS 20: 1491–1495.SG McCoombeRV Short2006Potential HIV-1 target cells in the human penis.AIDS2014911495
- 8. NIH/NIAID (2006) Adult Male Circumcision Significantly Reduces Risk of Acquiring HIV. Trials Kenya and Uganda Stopped Early. NIH/NIAID2006Adult Male Circumcision Significantly Reduces Risk of Acquiring HIV. Trials Kenya and Uganda Stopped Early.
- 9. UNAIDS/WHO/UNFPA/UNICEF (2005) Press statement: UNAIDS statement on South African trial findings regarding male circumcision and HIV. UNAIDS/WHO/UNFPA/UNICEF2005Press statement: UNAIDS statement on South African trial findings regarding male circumcision and HIV.Rio de Jeneiro: UNAIDS, World Health Organization, United Nations Population Fund, United Nations Children's Fund. Rio de Jeneiro: UNAIDS, World Health Organization, United Nations Population Fund, United Nations Children's Fund.
- 10. World Health Organization (WHO), the United Nations Population Fund (UNFPA), the United Nations Children's Fund (UNICEF), the World Bank, the UNAIDS Secretariat (2006) Statement on Kenyan and Ugandan trial findings regarding male circumcision and HIV.World Health Organization (WHO), the United Nations Population Fund (UNFPA), the United Nations Children's Fund (UNICEF), the World Bank, the UNAIDS Secretariat2006Statement on Kenyan and Ugandan trial findings regarding male circumcision and HIV.Statement developed by the World Health Organization (WHO), the United Nations Population Fund (UNFPA), the United Nations Children's Fund (UNICEF), the World Bank and the UNAIDS Secretariat. http://wwwwhoint/mediacentre/news/statements/2006/s18/en/indexhtml, Accessed on December 13, 2006. Statement developed by the World Health Organization (WHO), the United Nations Population Fund (UNFPA), the United Nations Children's Fund (UNICEF), the World Bank and the UNAIDS Secretariat. http://wwwwhoint/mediacentre/news/statements/2006/s18/en/indexhtml, Accessed on December 13, 2006.
- 11. World Health Organization (2005) UNAIDS statement on South African trial findings regarding male circumcision and HIV Statement developed by the World Health Organization (WHO), the United Nations Population Fund (UNFPA,) the United Nations Children's Fund (UNICEF) and the UNAIDS Secretariat, 26 July 2005.World Health Organization2005UNAIDS statement on South African trial findings regarding male circumcision and HIV Statement developed by the World Health Organization (WHO), the United Nations Population Fund (UNFPA,) the United Nations Children's Fund (UNICEF) and the UNAIDS Secretariat, 26 July 2005.http://www.who.int/mediacentre/news/releases/2005/pr32/en/. http://www.who.int/mediacentre/news/releases/2005/pr32/en/.
- 12. Cassell M, Halperin DT, Shelton JD, Stanton D (2006) Risk compensation: the Achilles' heel of innovations in HIV prevention. British Medical Journal 332: 605–607.M. CassellDT HalperinJD SheltonD. Stanton2006Risk compensation: the Achilles' heel of innovations in HIV prevention.British Medical Journal332605607
- 13. Bailey RC, Neema S, Othieno R (1999) Sexual behaviors and other HIV risk factors in circumcised and uncircumcised men in Uganda. Journal of Acquired Immune Deficiency Syndrome 22: 294–301.RC BaileyS. NeemaR. Othieno1999Sexual behaviors and other HIV risk factors in circumcised and uncircumcised men in Uganda.Journal of Acquired Immune Deficiency Syndrome22294301
- 14. Seed J, Allen S, Mertens T, Hudes E, Serufilira A, et al. (1995) Male circumcision, sexually transmitted disease, and risk of HIV. Journal of Acquired Immune Deficiency Syndromes & Human Retrovirology 8: 83–90.J. SeedS. AllenT. MertensE. HudesA. Serufilira1995Male circumcision, sexually transmitted disease, and risk of HIV.Journal of Acquired Immune Deficiency Syndromes & Human Retrovirology88390
- 15. Agot KE, Kiarie JN, Nguyen HQ, Odhiambo JO, Onyango TM, et al. (2007) Male Circumcision in Siaya and Bondo Districts, Kenya: Prospective Cohort Study to Assess Behavioral Disinhibition Following Circumcision. Journal of Acquired Immune Deficiency Syndromes: JAIDS 44: 66–70.KE AgotJN KiarieHQ NguyenJO OdhiamboTM Onyango2007Male Circumcision in Siaya and Bondo Districts, Kenya: Prospective Cohort Study to Assess Behavioral Disinhibition Following Circumcision.Journal of Acquired Immune Deficiency Syndromes: JAIDS446670
- 16. Carey MP, Carey KB, Maisto SA, Gordon CM, Weinhardt LS (2001) Assessing sexual risk behaviour with the Timeline Followback (TLFB) approach: continued development and psychometric evaluation with psychiatric outpatients. International Journal of STD & AIDS 12: 365–375.MP CareyKB CareySA MaistoCM GordonLS Weinhardt2001Assessing sexual risk behaviour with the Timeline Followback (TLFB) approach: continued development and psychometric evaluation with psychiatric outpatients.International Journal of STD & AIDS12365375
- 17. Junker B, Sijtsma K (2001) Nonparametric item response theory in action: an overview of a special issue. Applied Psychological Measurement 25: 211–220.B. JunkerK. Sijtsma2001Nonparametric item response theory in action: an overview of a special issue.Applied Psychological Measurement25211220
- 18. Sjitsma K, Emons WHM, Bouwmeester SB, Nycliček I, Roorda LD (2008) Nonparametric IRT analysis of quality of life scales and its application to the World Health Organization quality of life scale (WHOQOQ-Bref). Quality of Life Research 17: 275–290.K. SjitsmaWHM EmonsSB BouwmeesterI. NycličekLD Roorda2008Nonparametric IRT analysis of quality of life scales and its application to the World Health Organization quality of life scale (WHOQOQ-Bref).Quality of Life Research17275290
- 19. Mattson C, Bailey RC, Agot K, Ndinya-Achola JO, Moses S (2007) A nested case-control study of sexual practices and risk factors for prevalent HIV-1 infection among young men in Kisumu, Kenya. Sexually Transmitted Diseases 34: 731–736.C. MattsonRC BaileyK. AgotJO Ndinya-AcholaS. Moses2007A nested case-control study of sexual practices and risk factors for prevalent HIV-1 infection among young men in Kisumu, Kenya.Sexually Transmitted Diseases34731736
- 20. Buve A, Weiss HA, Laga M, Van Dyck E, Musonda R, et al. (2001) The epidemiology of trichomoniasis in women in four African cities. AIDS 15: Suppl 4S89–96.A. BuveHA WeissM. LagaE. Van DyckR. Musonda2001The epidemiology of trichomoniasis in women in four African cities.AIDS15Suppl 4S8996
- 21. Buve A, Weiss HA, Laga M, Van Dyck E, Musonda R, et al. (2001) The epidemiology of gonorrhoea, chlamydial infection and syphilis in four African cities. AIDS 15: Suppl 4S79–88.A. BuveHA WeissM. LagaE. Van DyckR. Musonda2001The epidemiology of gonorrhoea, chlamydial infection and syphilis in four African cities.AIDS15Suppl 4S7988
- 22. Gray Ra, Azire Jb, Serwadda Dc, Kiwanuka Nb, Kigozi Gb, et al. (2004) Male circumcision and the risk of sexually transmitted infections and HIV in Rakai, Uganda. AIDS December 18: 2428–2430.Ra GrayJb AzireDc SerwaddaNb KiwanukaGb Kigozi2004Male circumcision and the risk of sexually transmitted infections and HIV in Rakai, Uganda.AIDS December1824282430
- 23. Reynolds SJ, Shepherd ME, Risbud AR, Gangakhedkar RR, Brookmeyer RS, et al. (2004) Male circumcision and risk of HIV-1 and other sexually transmitted infections in India. Lancet 363: 1039–1040.SJ ReynoldsME ShepherdAR RisbudRR GangakhedkarRS Brookmeyer2004Male circumcision and risk of HIV-1 and other sexually transmitted infections in India.Lancet36310391040
- 24. Pequegnat W, Fishbein M, Celentano D, Ehrhardt A, Garnett G, et al. (2000) NIMH/APPC workgroup on behavioral and biological outcomes in HIV/STD prevention studies: a position statement. Sexually Transmitted Diseases 27: 127–132.W. PequegnatM. FishbeinD. CelentanoA. EhrhardtG. Garnett2000NIMH/APPC workgroup on behavioral and biological outcomes in HIV/STD prevention studies: a position statement.Sexually Transmitted Diseases27127132
- 25. Hu F, Goldberg JG, Hedeker D, Flay BR, Pentz M (1998) Comparison of population-averaged and subject-specific approaches for analyzing repeated binary outcomes. American Journal of Epidemiology 147: 694–703.F. HuJG GoldbergD. HedekerBR FlayM. Pentz1998Comparison of population-averaged and subject-specific approaches for analyzing repeated binary outcomes.American Journal of Epidemiology147694703
- 26. Olsen M, Schafer JL (2001) A two-part random-effects model for semicontinuous longitudinal data. Journal of the American Statistical Association 96: 730–745.M. OlsenJL Schafer2001A two-part random-effects model for semicontinuous longitudinal data.Journal of the American Statistical Association96730745
- 27. Tooze J, Grunwald GK, Jones R (2002) Analysis of repeated measures data with clumping at zero. Statistical Methods in Medical Research 11: 341–355.J. ToozeGK GrunwaldR. Jones2002Analysis of repeated measures data with clumping at zero.Statistical Methods in Medical Research11341355
- 28. Xie H, McHugo G, Sengupta A, Clark R, Drake R (2004) A method for analyzing longitudinal outcomes with many zeros. Mental Health Services Research 6: 239–246.H. XieG. McHugoA. SenguptaR. ClarkR. Drake2004A method for analyzing longitudinal outcomes with many zeros.Mental Health Services Research6239246
- 29. SAS Version 8.2 & 9.1 (2002, 2004) Cary, NC, SAS Institute.SAS Version 8.2 & 9.12002, 2004Cary, NC, SAS Institute.
- 30. Klausner J, Wamai RG, Bowa K, Agot K, Kagimba J, et al. (2008) Is male circumcision as good as the HIV vaccine we've been waiting for? Future Medicine 2: 1–7.J. KlausnerRG WamaiK. BowaK. AgotJ. Kagimba2008Is male circumcision as good as the HIV vaccine we've been waiting for?Future Medicine217