Abstract
Introduction
PrEP and Treatment-as-Prevention (TasP) are biomedical strategies to reduce HIV transmission. Some men who have sex with men (MSM) are combining biomedical strategies with HIV serosorting–termed “biomed matching” when both partners are either on PrEP or TasP, or “biomed sorting” when one partner is using PrEP and the other TasP. Nevertheless, there is limited data on the extent of biomed matching/sorting in large geographically diverse samples.
Method
In 2016-2017, 5,021 MSM from across the US were surveyed about their HIV status and HIV viral load/PrEP use, as well as that of their recent casual male partners. For each participant, we calculated the proportion of his partners who were (1) HIV-positive and undetectable, (2) HIV-positive and detectable/unknown, (3) HIV unknown/undiscussed, (4) HIV-negative on PrEP, (5) HIV-negative, not on PrEP.
Results
In total, 66.6% (n=3346) of participants were HIV-negative and not on PrEP, 11.9% (n=599) on PrEP, 14.1% (n=707) HIV-positive and undetectable, 1.1% (n=55) HIV-positive and viral load detectable/unknown, and 6.2% (n=313) HIV unsure/unknown. A participant’s own HIV and PrEP status/was significantly associated with that of his partners (all p<.001), evincing evidence of both serosorting and biomed matching. Among men on PrEP and those who were HIV-undetectable, there was also some evidence to suggest these participants dually engaged in biomed matching as well as biomed sorting.
Discussion
We found evidence of biomed matching and sorting, which may compound its effectiveness for those using it (i.e., both partners bring biomedical protection). Unintended consequences of biomed matching/sorting include that men not using a biomedical strategy may be less likely to benefit from a partner’s use of the strategy—potentially further driving disparities in HIV infections. Public health campaigns might be well served to highlight not only the benefits that biomedical HIV prevention strategies provide for their users (e.g., “being on PrEP protects me from getting HIV”), but also the benefits that a user brings to his partners (e.g., “my use of PrEP means my partners won’t get HIV”), and the benefits of being with a partner who is using a biomedical strategy (e.g., “my partner’s use of PrEP/TasP protects me from HIV”).
Keywords: Serosorting, men who have sex with men, Pre-Exposure Prophylaxis (PrEP), Treatment as prevention (TasP), HIV
INTRODUCTION
Gay, bisexual, and other men who have sex with men (MSM) remain a critical population at risk for HIV/AIDS1–4 with new infections on the rise.5–7 In 2016, the CDC noted that if current infection rates persist, one in six MSM will be diagnosed with HIV during their lifetimes, and, more specifically, one in two Black MSM and one in four Latino MSM.8 MSM have adopted a variety of strategies in the decades since HIV was discovered, broadly referred to as ‘seroadaption,’ to reduce the risk of transmission.
Seroadaption9–15 describes a diverse set of potentially harm-reducing behaviors that use HIV status to inform sexual decision making; examples include seropositioning/strategic positioning14,16–18 (selectively practicing insertive or receptive anal sex based on a partner’s HIV status), selectively having only oral sex or mutual masturbation,19–21 and serosorting.14,15,22–27 Serosorting, specifically, describes a person choosing partners of the same HIV serostatus, including to engage in sex without condoms.28–30
Data suggest a diverse set of MSM engage in seroadaptive behaviors, and that such behaviors may have increased over time.14,28–30 For example, one study of San Francisco MSM found that prevalence of seroadaptive behaviors increased from 36% in 2004 to 47% in 2011.31,32 HIV-positive men were more likely to report seroadaptive behavior patterns compared to HIV-negative men.14 Studies suggest that serosorting is not as effective at reducing HIV transmission as condom use, and some evidence suggests that serosorting may actually increase HIV acquisition, depending on community-level HIV prevalence.33 In settings with low HIV testing rates, serosorting can more than double the risk of HIV acquisition.33
In addition to behavioral strategies, biomedical strategies involving the use of antiretroviral medications, can also reduce the risk of HIV transmission. For HIV-positive individuals, using antiretroviral therapy (ART) to reduce viral load to undetectable levels greatly reduces infectiousness. One study34 found that reducing the burden of viral load in a given community through wide-scale treatment-as-prevention (TasP) could reduce HIV transmission at the population level.34,35 In 2016, the Prevention Access Campaign issued a consensus statement indicating that individuals with undetectable HIV viral loads present negligible risk for HIV transmission to their partners,36 and there has since been consistent increasing support that HIV undetectable individuals do not transmit HIV,37,38 including endorsement by the CDC.39 Meanwhile, for HIV-negative individuals, anti-retroviral drugs, in the form of once-daily Emtricitabine/Tenofovir, have been approved for use in the US as HIV pre-exposure prophylaxis (PrEP) since 2012.40–42 PrEP and TasP are among the most promising biomedical tools available to prevent HIV transmission.43–46
The extent to which MSM are currently employing combinations of biomedical and behavioral strategies to reduce HIV transmission risk has not been well described. Newcomb et al.47 introduced the term “biomed matching” to refer to individuals who seek out partners who are using the same biomedical prevention strategy (e.g., HIV-negative men on PrEP partnering with each other, or HIV-positive men seeking out other virally suppressed individuals). Whereas “biomed sorting” (a term that we do not believe has yet been used in the literature) more broadly describes individuals who seek out partners who are using a biomedical strategy, regardless of whether that strategy is PrEP or TasP (i.e., men on PrEP having sex with partners on PrEP or virally suppressed HIV-positive men, and vice versa).48 In contrast to biomed matching, one can biomed sort without using a biomedical strategy themselves (i.e., someone not on PrEP seeking out partners who are on PrEP or using TasP). Unintended consequences of biomed matching/sorting include that men not using a biomedical strategy may be less likely to benefit from a partner’s use of the strategy—potentially further driving disparities in HIV infections. Whereas, there are benefits to be gleaned when one’s partner uses a biomedical strategy (e.g., his partner is on PrEP or his partner his HIV-positive undetectable) even if he is HIV-negative and not using PrEP himself. To our knowledge, there have been no published studies explicitly estimating rates of biomed sorting and matching. Further, it is also unclear if the use or integration of biomedical and behavioral practices vary between HIV-positive and HIV-negative men. Such data would be essential to informing public health messages around the benefits that biomedical strategies bring to the users themselves (e.g., “PrEP protects me”), as well as their partners (“PrEP/TasP protects my partners”), and the benefits of having a partner who is using a strategy (“My partner’s use of PrEP/TasP protects me”).
Current Study
Although behavioral HIV risk reduction strategies such as serosorting have been described well in the literature, the combined use of seroadaptive and biomedical strategies among MSM has not.49–51 To address this gap, we implemented a brief self-administered survey in a variety of settings (online, in sexual health clinics, and community-based outreach). We report demographic and behavioral differences by HIV status and assess the prevalence of various bio-behavioral strategies employed by MSM that could reduce their HIV risk.
METHOD
Recruitment
Between May 2016 and March 2017, data were collected from participants recruited from six different settings. To be eligible, participants had to report being over the age of 18, cisgender male, and report sex with a man in the past 5 years.
Tablet devices with MSM in clinical settings (e.g., waiting area) of both HIV and sexual health clinics in NYC: A variety of methods were used to recruit MSM patients in clinical settings (n = 162). These included posted flyers in waiting areas, asking providers to refer their patients to the study, and directly approaching MSM patients in waiting areas and asking them if they were interested in completing an online survey. A privacy screen, which prevents the device from being viewed at an angle, was used and we had a separate private room available should participants have wanted to complete the survey alone. Participants were told that their responses on the survey as well as their participation in the project would not be disclosed to their provider.
Online, with participants recruited via a sexual networking website or via porn websites: For a 30 day period, we hosted a banner advertising the survey on a popular men-for-men sexual networking website. The same banner was used on the porn websites for a period of 39 days. The ad was restricted to the U.S. Those clicking the banner were taken to a separate secure webpage where the survey was housed. We generated 934 responses from the sexual networking website and 454 from the porn websites.
Mobile devices, with participants recruited via a popular geo-social sexual networking app: We had one pop-up message that was displayed to participants when they opened the app for the first time during a given 12-hour window. We generated 1891 responses from eligible participants via this method.
Online, with MSM recruited via Facebook. We ran an ad on Facebook for 11 days. This method generated 454 responses.
Tablet devices with MSM recruited in gay neighborhood settings (e.g., gay bars, clubs): Teams of two project staff visited gay neighborhoods/spaces (e.g., gay bars) and approached patrons to see if they would be interested in completing a survey about sexual health. Those interested were handed a tablet device to complete the survey alone. This method generated 292 participants.
Online with participants from an ongoing cohort study of HIV-negative gay and bisexual men. The One Thousand Strong study is following a U.S. national sample of 1,071 gay and bisexual men for a period of 3 years. Enrollment for the cohort has been described in detail elsewhere,52 but sampling was targeted (using census data) such that the distribution of participants in the panel would closely mirror that of gay and bisexual men across the U.S, and all participants were confirmed to be HIV-negative at enrollment. Participants in One Thousand Strong complete online assessments annually; however, the study team also conducted check-in surveys half way between annual assessments to verify participant contact information. During the 18-month check-in survey participants were offered an opportunity to complete an additional brief online survey, in which the measures for this study were embedded. In total, 834 participants completed this assessment.
Across recruitment methods, participants were informed they were completing a sexual health survey. Recruitment materials and the informed consent did not market the study as one being about PrEP, serosorting, etc.
Incentives
As an incentive, participants from clinic settings were offered a gift certificate to see a movie at a local movie theater. Participants from online settings (adult websites, hook-up website, geosocial sexual networking app, Facebook, and the One Thousand Strong cohort) were entered into a raffle to win one of fifty $20 amazon gift cards. With the exception of the One Thousand Strong cohort, the survey in online settings was anonymous, but participants were told they would need to provide an email address if they wanted to be entered into the raffle for the gift card. Finally, participants surveyed in gay neighborhood settings were offered one scratch off lottery ticket valued at $1 each for completing the survey.
Measures
Participants completed a self-administered computerized survey that took approximately 10 minutes to complete. The survey itself assessed demographic characteristics as well as sexual behaviors for main and casual male partners in the prior three months using the Brief Seroadaptive Assessment Tool (B-SAT),53 a brief-intercept self-administered sexual behavior data collection method.14,54–57 The B-SAT first asks about sexual behavior with a main partner and then separately asks about sexual behavior with casual partners who were HIV-positive and undetectable, HIV-positive and not undetectable (or viral load was not discussed), HIV-negative and on PrEP, HIV-negative and not on PrEP (or PrEP was not discussed), and partners whose status was unknown/not discussed. The B-SAT also assesses participant’s HIV status and viral load (if HIV-positive) or PrEP use (if HIV-negative). Study procedures were approved by relevant organizational Institutional Review Boards.
Analysis plan
We report (1) demographic differences in the samples across the recruitment venues, followed by (2) demographic differences across participants’ HIV status. In so doing, we categorized participants’ HIV status into five mutually exclusive groups: HIV-positive and undetectable; HIV-positive and detectable or of unknown viral load; HIV-negative and on PrEP; HIV-negative and not on PrEP; and HIV status unsure/unknown. Finally, we report the extent to which participants were engaged in serosorting and biomed matching. In so doing, for each participant HIV-status, we report the proportion of his casual male partners from the past 3 months who were (1) HIV-positive and undetectable, (2) HIV-positive and detectable/unknown, (3) HIV unknown/undiscussed, (4) HIV-negative on PrEP, and (5) HIV-negative, not on PrEP. We also compared participants’ HIV status by the total number of casual male partners in the previous three months, as well as by the reported HIV status for participants’ main partner (for those in a relationship, n = 2,027). As appropriate, we used ANOVA, chi-squared, and Kruskal-Wallis tests. Statistical significance was set and α = 0.05 and all analyses were conducted in SPSS version 22.
RESULTS
Participants came from all 50 US states plus the District of Columbia and Puerto Rico (though the survey itself was in English). First, we report data on how the composition of our sample varied by recruitment source (see Table 1). All variables examined differed significantly by recruitment venue. Participants from the hook-up website were oldest on average (M = 46.1), whereas those via gay neighborhood settings in NYC were youngest on average (M = 32.3). Clinic settings had the highest proportion of men of color (84%) whereas One Thousand Strong had the lowest (29.1%). Participants recruited via Facebook and clinic settings tended to report the least amount of education and those from LGBT neighborhood settings tended to report the most education. Participants from the One Thousand Strong cohort were the most likely to identify as gay and those from the hookup website were the least (95% vs. 71.2%). Participants surveyed via the One Thousand Strong cohort (53.8%) and adult websites (52.2%) were among the most likely to report being in a relationship, whereas those surveyed via the geosocial sexual networking app were the least (30.1%). Finally, participants from clinic settings were the most likely to report being HIV-positive and undetectable (44.4%) or HIV-negative on PrEP (23.5%) (i.e., using a biomedical strategy).
Table 1.
Demographic differences by recruitment source
| Hook-up website N = 934 |
Facebook N = 454 |
NYC gay neighborhood settings N = 292 |
Geo-social App N = 1891 |
Adult websites N = 454 |
One Thousand Strong cohort N = 834 |
Clinic settings N = 162 |
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|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| n | % | n | % | n | % | n | % | n | % | n | % | n | % | χ2 or F | p | |
|
|
||||||||||||||||
| Age (M, SD) | 46.1 | 12.79 | 38.4 | 14.98 | 32.3 | 8.8 | 35.0 | 12.1 | 40.7 | 13.8 | 41.7 | 13.7 | 34.3 | 11.7 | 102.8 | < .001 |
| Race1 | 320.77 | < .001 | ||||||||||||||
| Black | 79 | 8.5 | 33 | 7.3 | 63 | 21.6 | 186 | 9.8 | 44 | 9.7 | 64 | 7.7 | 41 | 25.3 | ||
| Latino | 117 | 12.5 | 91 | 20.0 | 54 | 18.5 | 386 | 20.4 | 59 | 13.0 | 95 | 11.4 | 67 | 41.4 | ||
| White | 668 | 71.5 | 285 | 62.8 | 136 | 46.6 | 1077 | 57.0 | 312 | 68.7 | 600 | 71.9 | 26 | 16.0 | ||
| All other | 70 | 7.5 | 42 | 9.3 | 37 | 12.7 | 241 | 12.7 | 39 | 8.6 | 75 | 9.0 | 28 | 17.3 | ||
| Education | 250.93 | < .001 | ||||||||||||||
| High School | 154 | 16.5 | 103 | 22.7 | 30 | 10.3 | 259 | 13.7 | 59 | 13.0 | 47 | 5.6 | 48 | 29.6 | ||
| Some college | 359 | 38.4 | 196 | 43.2 | 58 | 19.9 | 729 | 38.6 | 161 | 35.5 | 258 | 34.2 | 71 | 43.8 | ||
| 4-year college degree | 237 | 25.4 | 101 | 22.2 | 131 | 44.9 | 549 | 29.0 | 122 | 26.9 | 259 | 31.1 | 32 | 19.8 | ||
| Graduate school | 184 | 19.7 | 54 | 11.9 | 73 | 25.0 | 355 | 18.8 | 112 | 24.7 | 243 | 29.1 | 11 | 6.8 | ||
| Sexual identity as gay3 | ||||||||||||||||
| No | 269 | 28.8 | 46 | 110.1 | 25 | 8.6 | 338 | 17.9 | 90 | 19.8 | 42 | 5.0 | – | – | 213.74 | < .001 |
| Yes | 665 | 71.2 | 408 | 89.9 | 267 | 91.4 | 1553 | 82.1 | 364 | 80.2 | 792 | 95.0 | – | – | ||
| Currently in a relationship | ||||||||||||||||
| No | 586 | 62.7 | 230 | 50.7 | 172 | 59.9 | 1321 | 69.9 | 217 | 47.8 | 385 | 46.2 | 82 | 50.6 | 195.83 | < .001 |
| Yes | 348 | 37.3 | 224 | 49.3 | 120 | 41.1 | 570 | 30.1 | 237 | 52.2 | 449 | 53.8 | 80 | 49.4 | ||
| HIV status2 | ||||||||||||||||
| HIV-Positive, undetectable | 192 | 20.6 | 74 | 16.3 | 24 | 8.2 | 274 | 14.5 | 71 | 15.6 | 0 | 0.0 | 72 | 44.4 | 545.01 | < .001 |
| HIV-positive, detectable or unknown viral load | 11 | 1.2 | 8 | 1.8 | 0 | 0.0 | 23 | 1.2 | 5 | 1.1 | 0 | 0.0 | 8 | 4.9 | ||
| HIV-negative on PrEP | 75 | 8.0 | 46 | 10.1 | 66 | 22.6 | 232 | 12.3 | 38 | 8.4 | 104 | 12.5 | 38 | 23.5 | ||
| HIV-negative | 585 | 62.6 | 297 | 65.4 | 191 | 65.4 | 1192 | 63.0 | 316 | 69.6 | 725 | 86.9 | 40 | 24.7 | ||
| Unknown/unsure | 71 | 7.6 | 29 | 6.4 | 11 | 3.8 | 170 | 9.0 | 24 | 5.3 | 4 | 0.5 | 4 | 2.5 | ||
| STI diagnosis in prior 6 months | ||||||||||||||||
| Chlamydia | 19 | 2.0 | 16 | 3.5 | 23 | 7.9 | 109 | 5.8 | 15 | 3.3 | 41 | 4.9 | 17 | 10.5 | 41.05 | < .001 |
| Gonorrhea | 27 | 2.9 | 15 | 3.3 | 21 | 7.2 | 114 | 6.0 | 8 | 1.8 | 34 | 4.1 | 17 | 10.5 | 41.91 | < .001 |
| Genital warts, anal warts, HPV | 13 | 1.4 | 11 | 2.4 | 5 | 1.7 | 40 | 2.1 | 4 | 0.9 | 40 | 4.8 | 7 | 4.3 | 32.9 | < .001 |
| Genital herpes, HSV1, HSV2 | 14 | 1.5 | 5 | 1.1 | 4 | 1.4 | 42 | 2.2 | 9 | 2.0 | 42 | 5.0 | 5 | 3.1 | 33.36 | < .001 |
| Syphilis | 21 | 2.2 | 14 | 3.1 | 10 | 3.4 | 62 | 3.3 | 7 | 1.5 | 23 | 2.8 | 24 | 14.8 | 77.79 | < .001 |
| Hepatitis C | 6 | 0.6 | 2 | 0.4 | 1 | 0.3 | 12 | 0.6 | 2 | 0.4 | 1 | 0.1 | 3 | 1.9 | – | |
| Hepatitis B | 4 | 0.4 | 7 | 1.5 | 1 | 0.3 | 7 | 0.4 | 3 | 0.7 | 8 | 1.0 | 2 | 1.2 | – | |
| Urethritis | 2 | 0.2 | 4 | 0.9 | 4 | 1.4 | 16 | 0.8 | 1 | 0.2 | 14 | 1.7 | 1 | 0.6 | – | |
Note:
n = 6 men did not provide responses on their race/ethnicity
n= 1 Participant in One Thousand Strong was HIV-positive, but his viral load was not asked.
Due to a programming error, sexual identity was not assessed in clinic settings; however, all participants were men who reported sex with men
Table 2 reports on demographic differences by participants’ HIV status, all of which were statistically significant. HIV-positive and undetectable participants were the oldest on average (M = 43.11) and those not knowing their status were the youngest on average (M = 33.8). HIV-positive and men who said they did not know their HIV status were among the most likely to be men of color (49% and 44.7% respectively). Men on PrEP tended to report more education than other groups (64.6% had completed college). Men who did not know their HIV status were the least likely to identify as gay and the least likely to be in a current relationship.
Table 2.
Demographic differences by participants’ HIV statusn
| Participant’s HIV status 1 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HIV-positive and undetectable Group A |
HIV-positive, but detectable (or “I do not know my viral load”) Group B |
HIV-negative, and on PrEP Group C |
HIV-negative, but not on PrEP Group D |
I do not know,or I am unsure Group E |
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| n | % | n | % | n | % | n | % | n | % | ||||
| 707 | 14.1 | 55 | 1.10 | 599 | 11.9 | 3346 | 66.6 | 313 | 6.2 | χ2 or F | p | Post hoc | |
|
|
|||||||||||||
| Age (M, SD) | 43.11 | 11.53 | 38.22 | 11.27 | 37.04 | 12.27 | 38.73 | 13.96 | 33.83 | 13.43 | 31.79 | < .001 | A ≠ C, D, E; C ≠ D, E; D ≠ E |
| Race | |||||||||||||
| Black | 139 | 19.7 | 18 | 32.7 | 66 | 11.1 | 259 | 7.7 | 28 | 8.9 | 152.07 | < .001 | A, B ≠ C, D, E; C ≠ D ≠ E |
| Latino | 142 | 20.1 | 10 | 18.2 | 97 | 16.3 | 546 | 16.3 | 74 | 23.6 | |||
| White | 360 | 51.0 | 21 | 38.2 | 370 | 62.1 | 2810 | 65.2 | 173 | 55.3 | |||
| All other | 65 | 9.2 | 6 | 10.9 | 63 | 10.6 | 359 | 10.7 | 38 | 12.1 | |||
| Education | |||||||||||||
| High School | 135 | 19.1 | 19 | 34.5 | 50 | 8.3 | 409 | 12.2 | 87 | 27.8 | 217.65 | < .001 | A ≠ B; B ≠ C, D; A ≠ C ≠ D ≠ E |
| Some college | 320 | 45.3 | 26 | 47.3 | 162 | 27 | 125 | 36.6 | 126 | 40.3 | |||
| 4-year college degree | 156 | 22.1 | 9 | 16.4 | 232 | 38.7 | 976 | 29.2 | 57 | 18.2 | |||
| Graduate school | 96 | 13.6 | 1 | 1.8 | 155 | 25.9 | 736 | 22 | 43 | 13.7 | |||
| Sexual identity as gay | |||||||||||||
| No | 45 | 7.0 | 5 | 10.6 | 60 | 10.6 | 618 | 18.7 | 86 | 27.8 | 96.139 | < .001 | E ≠ A, B, C, D; D ≠ A, C, E |
| Yes | 597 | 93.0 | 42 | 89.4 | 504 | 89.4 | 2694 | 81.3 | 223 | 72.2 | |||
| Currently in a relationship | |||||||||||||
| No | 436 | 61.7 | 30 | 54.5 | 371 | 61.9 | 1940 | 58.0 | 216 | 69.0 | 18.359 | 0.001 | D ≠ E |
| Yes | 271 | 38.3 | 25 | 45.5 | 228 | 38.1 | 1406 | 42.0 | 97 | 31.0 | |||
| STI diagnosis in prior 6 months | |||||||||||||
| Chlamydia | 40 | 5.7 | 6 | 10.9 | 85 | 14.2 | 104 | 3.1 | 5 | 1.6 | 149.76 | < .001 | A ≠ C, D, E; B ≠ E; C ≠ D, E |
| Gonorrhea | 47 | 6.6 | 6 | 10.9 | 71 | 11.9 | 103 | 3.1 | 8 | 2.6 | 102.391 | < .001 | A ≠ C, D, E; B ≠ E; C ≠ D, E |
| Genital warts, anal warts, HPV | 21 | 3 | 7 | 12.7 | 24 | 4.0 | 63 | 1.9 | 5 | 1.6 | 37.45 | < .001 | A ≠ B; B ≠ C, E; C ≠ D |
| Genital herpes, HSV1, HSV2 | 12 | 1.7 | 1 | 1.8 | 30 | 5.0 | 74 | 2.2 | 4 | 1.3 | 21.06 | < .001 | A ≠ C; C ≠ D, E |
| Syphilis | 48 | 6.8 | 9 | 16.4 | 40 | 6.7 | 60 | 1.8 | 4 | 1.3 | 108.43 | < .001 | A ≠ B, D, E; B ≠ C, E; C ≠ D, E |
| Hepatitis C | 8 | 1.1 | 1 | 1.8 | 5 | 0.8 | 10 | 0.3 | 3 | 1.0 | – | ||
| Hepatitis B | 9 | 1.3 | 0 | 0 | 8 | 1.3 | 14 | 0.4 | 1 | 0.3 | – | ||
| Urethritis | 5 | 0.7 | 0 | 0 | 12 | 2.0 | 23 | 0.7 | 2 | 0.6 | 11.48 | 0.02 | C ≠ D |
Note: n = 1 participant from One Thousand Strong indicated he was HIV-positive, but his viral load was not assessed
– Chi-Square could not be calculated due to low expected cell counts
Table 3 reports on HIV serosorting and biomed matching/sorting among participants in the sample. Among men who reported casual male sex partners in the prior 3 months, HIV-negative participants who were not on PrEP reported the fewest partners on average (Mdn = 3), whereas HIV-positive and undetectable participants and participants on PrEP reported the greatest, on average (Mdn = 6). By and large, participants tended to report partners whose HIV-status and biomedical strategy matched their own. For example, the proportion of casual partners who were HIV-positive and undetectable was significantly higher among participants who were themselves HIV-positive and undetectable at 0.28 (versus 0.20 for participants who were HIV-positive and detectable, 0.12 among those HIV-negative and on PrEP, 0.07 for those HIV-negative and not on PrEP, and 0.08 for participants who did not know their HIV status, p < 0.001). The proportion of partners HIV-positive and detectable was highest among those who were themselves HIV-positive and detectable at 0.16 (versus 0.06 for those HIV-positive and undetetable, 0.02 for those HIV-negative on PrEP, 0.01 for those HIV-negative and not on PrEP, and 0.02 for participants who did not know their HIV status, p < 0.001). This pattern of “matching” was observed for all five HIV status groups. Full results in Table 3.
Table 3.
HIV serosorting and biomed matching among gay and bisexual men
| Participant’s HIV status | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HIV-positive and undetectable Group A |
HIV-positive, but detectable (or “I do not know my viral load”) Group B |
HIV-negative, and on PrEP Group C |
HIV-negative, but not on PrEP Group D |
I do not know, or I am unsure Group E |
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|
|
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| Mdn | IQR | Mdn | IQR | Mdn | IQR | Mdn | IQR | Mdn | IQR | K-W | post hoc | ||
| Total Casual Male Partners < 3 months (Mdn, IQR), valid n = 36411 | 6.0 | 3 to 11 | 5.0 | 2.75 to 15 | 6.0 | 3 to 12 | 3.0 | 1 to 6 | 4.0 | 2 to 8 | 249.54 | < .001 | A, B, C # D, E |
|
|
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| M | SD | M | SD | M | SD | M | SD | M | SD | F | P | ||
| Sexual behavior with casual male partners, < 3 months | |||||||||||||
| Proportion that were HIV-positive and Undetectable | 0.28 | 0.28 | 0.20 | 0.27 | 0.12 | 0.18 | 0.07 | 0.19 | 0.08 | 0.18 | 109.6 | < .001 | A ≠ B ≠ C ≠ D; E ≠ A |
| Proportion that were HIV-positive and viral load was unknown or detectable | 0.06 | 0.13 | 0.16 | 0.20 | 0.02 | 0.07 | 0.01 | 0.07 | 0.02 | 0.07 | 64.8 | < .001 | A ≠ B, C, D, E; B ≠ C |
| Proportion that were on PrEP | 0.24 | 0.26 | 0.14 | 0.21 | 0.41 | 0.29 | 0.22 | 0.30 | 0.14 | 0.21 | 55.9 | < .001 | A ≠ C, E; B ≠ C; C ≠ D, |
| Proportion that were HIV-negative, but not on PrEP (or PrEP not discussed) | 0.15 | 0.23 | 0.21 | 0.35 | 0.28 | 0.28 | 0.44 | 0.38 | 0.28 | 0.32 | 86.3 | < .001 | A ≠ C, E, E; B ≠ D; C ≠ I |
| Proportion whose HIV status was unknown/not discussed | 0.27 | 0.33 | 0.28 | 0.29 | 0.17 | 0.25 | 0.26 | 0.36 | 0.48 | 0.39 | 34.8 | < .001 | A ≠ C, E; B ≠ E; C ≠ D, ] |
|
|
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| n | % | n | % | n | % | n | % | n | % | Chi-Sq | P | ||
| Sexual behavior2 with casual male partners, < 3 months | |||||||||||||
| Condomless anal sex (CAS) with HIV-positive and Undetectable, valid n = 1375 | 127 | 35.4 | 10 | 45.5 | 52 | 19.4 | 47 | 7.1 | 13 | 21.7 | 128.9 | < .001 | A, B ≠ C, D, E; C ≠ D; D ≠ |
| CAS with HIV-positive and viral load was unknown or detectable, valid n = 725 | 41 | 30.8 | 7 | 35.0 | 12 | 9.4 | 12 | 2.9 | 9 | 33.3 | 105.98 | < .001 | A, B ≠ C, D; C ≠ D, E; D ≠ |
| CAS with partners on PrEP, valid n = 2126 | 106 | 31.2 | 6 | 31.6 | 138 | 29.4 | 131 | 11.0 | 27 | 26.0 | 119.65 | < .001 | A, B, C, E ≠ D |
| CAS with HIV-negative, but not on PrEP (or PrEP not discussed), valid n = 2221 | 45 | 21.6 | 5 | 38.5 | 85 | 23.5 | 195 | 12.9 | 29 | 22.3 | 39.2 | < .001 | A, B, C, E ≠ D |
| CAS with partners whose HIV status was unknown/not discussed, valid n = 1901 | 70 | 24.0 | 8 | 36.4 | 37 | 12.2 | 90 | 8.2 | 30 | 16.6 | 68.98 | < .001 | A ≠ C, D; B ≠ C, D, E; C ≠ |
| Main partner’s HIV status, valid n = 2027 3 | |||||||||||||
| HIV-positive, undetectable | 96 | 35.4 | 5 | 20.0 | 51 | 22.4 | 57 | 4.1 | 4 | 4.1 | 866.07 | < .001 | A ≠ B ≠ C ≠ D ≠ E |
| HIV-positive, viral load detectable/unknown | 11 | 4.1 | 8 | 32.0 | 3 | 1.3 | 14 | 1.0 | 1 | 1.0 | |||
| HIV status uncertain or unknown | 35 | 12.9 | 2 | 8.0 | 18 | 7.9 | 197 | 14.0 | 39 | 40.2 | |||
| HIV-negative, on PrEP | 35 | 12.9 | 2 | 8.0 | 75 | 32.9 | 23 | 1.6 | 1 | 1.0 | |||
| HIV-negative, not on PrEP or PrEP unknown | 94 | 34.7 | 8 | 32.0 | 81 | 35.5 | 1115 | 79.3 | 52 | 53.6 | |||
n= 3641 (72.5%) participants reported at least one casual male sex partner in the 3 months prior.
Nested among men who reported that type of partner (e.g., CAS with partners on PrEP (yes/no), nested among the 2126 participants who reported having a partner on PrEP)
Nested among those with a main male partner
Values in bold indicate biomed matching. Values in italics indicate biomed sorting.
In contrast to the strong evidence that partcipants were engaging in biomed matching, there was some evidence of biomed sorting. In terms of proportions of partners, participants who were HIV-positive and undetectable said that 28% of their partners were HIV-positive and undetectable (i.e., biomed matched), 27% of their partners were HIV unknown/not discussed, and 24% were on PrEP (i.e., biomed sorted). Participants on PrEP said that 41% of their partners were on PrEP (i.e., biomed matched), 28% were HIV-negative not on PrEP, 17% were HIV unknown/not discussed, and 12% were HIV-positive undetectable (i.e., biomed sorted). HIV-negative men not on PrEP said that 44% of their partners were also HIV-negative and not on PrEP (i.e., serosorting), 26% were HIV unknown, 22% were on PrEP (i.e., biomed sorted), 7% were HIV undetectable (i.e., biomed sorted), and 1% were HIV-positive and detectable (or viral load not known).
We next examined whether participants had engaged in condomless anal sex (CAS) with partners across HIV categories. Overall, HIV-positive participants were more likely to engage in CAS than HIV-negative participants; however, HIV-positive participants tended to report engaging in CAS more so with HIV-positive partners than compared to HIV-negative participants—and HIV-negative participants tended to engage in CAS with other HIV-negative partners. See Table 3. There was stronger evidence of biomed sorting when it came to CAS. HIV-positive undetectable participants tended to report CAS more when their partners were also HIV-positive (i.e., biomed matched) as well as when their partners were on PrEP (CAS with 31.2% of partners on PrEP; i.e., biomed sorted), as opposed to when their partners were HIV-negative and not on PrEP (CAS with 21.6% of these partners) or when they did not know the status of their partners (CAS with 24% of these partners). Similarly for men on on PrEP, CAS was most common when partners were also on PrEP (CAS with 29.4% of these partners; i.e., biomed matched), HIV-negative and not on PrEP (CAS with 23.5% of these partners; i.e., serosorting), or HIV-positive and undetectable (CAS with 19.4% of these partners; i.e., biomed sorted). Whereas, among men on PrEP, CAS was least common when partners were HIV-positive and detectable (9.4%) or when partners status was unknown (12.2%). For HIV-negative men not on PrEP, CAS was most common when partners were also HIV-negative and not on PrEP (CAS with 12.9% of these partners; i.e., serosorting), followed by when partners were on PrEP (CAS with 11% of these partners; i.e., biomed sorted), when status was not discussed/unknown (CAS with 8.2% of these partners), when partners were HIV-positive undetectable (CAS with 7.1% of these partners; ie., biomed sorted), and when partners were HIV-positive but detectable/unknown (CAS with 2.9% of these partners).
As with casual male sex partners, there was strong evidence of biomed matching among participants in relationships (n = 2027). For example, 35.4% of HIV-positive and undetectable participants said their partner was HIV-positive and undetectable (versus 22.4% among HIV-negative men on PrEP, 20.0% among HIV-positive and detectable, 4.1% among HIV-negative men not on PrEP, and 4.1% among men who did not know their HIV status, p < .001). Similarly, 32.9% of men on PrEP said their partner was on PrEP (versus 12.9% among HIV-positive undetectable, 8.0% among HIV-positive and detetable men, 1.6% among HIV-negative men not on PrEP, and 1.0% among men who did not know their status). And 40.2% of men who said they were unsure of their status said their partner was also unsure of his status (versus 14.0% among men who were HIV-negative and not on PrEP, 12.9% among HIV-positive undetectable men, 8.0% among HIV-positive and detectable men, and 7.9% among HIV-negative men on PrEP). Full results are shown in Table 3.
DISCUSSION
We found strong evidence that not only were participants engaging in serosorting (having sex with partners of the same perceived HIV status), but also—for those taking advantage of a biomedical strategy—engaging in biomed matching. That is, HIV-positive undetectable participants comprised 14.1% of the sample, yet they indicated that 28% of their casual partners were HIV-positive undetectable. Meanwhille, 35% of HIV-positive undetectable participants who were in relationships said their partner was also HIV-positive undetectable. Similarly, men on PrEP comprised 11.9% of participants, yet reported that 41% of their casual male partners were on PrEP. And, 33% of the participants on PrEP who were in a relationship said their partner was also on PrEP. Meanwhile, compared with others, men not utilizing a biomedical strategy more often partnered with men also not using a biomedical strategy. Among men on PrEP and those who were HIV-undetectable, there was also some evidence to suggest these participants dually engaged in biomed matching as well as biomed sorting. Both biomed sorting and biomed matching may compound their effectiveness for those using it (i.e., both partners bring biomedical protection).47 However, this also means that men not using a biomedical strategy may be less likely to benefit from a partner’s use of the strategy—potentially further driving disparities in HIV infections in certain subpopulations with lower access to or uptake of biomedical prevention.
We also found that, in addition to partnering with men who shared the same HIV status, participants also tended to report engaging in CAS more so with partners who were believed to share the same HIV status. For men using a biomedical strategy, the risk for HIV transmission during these encounters may be negligible; however, for those not using a biomedical strategy, there may be additional risk for HIV transmission. Compared to other groups, HIV-negative men not on PrEP were the least likely to report CAS; however, when CAS did occur among these participants, it was most often with a partner believed to be HIV-negative and also not on PrEP. If undiagnosed and untreated HIV infection is higher among this group, this could significantly potentiate HIV transmission during CAS. Some research has suggested that serosorting is not as effective at reducing HIV transmission as condom use, and some evidence suggests that serosorting may actually increase HIV acquisition.33 This may be due to low HIV testing rates/frequency,33 yet partners still report they are HIV-negative.
We also reported demographic differences by the venue in which participants were surveyed. Similar to what others have reported,56,58–63 participant characteristics were associated with where participants were recruited. For both providers and researchers, these findings further highlight the need to focus efforts (whether for recruitment, interventions, health education messages) within different venues to reach diverse populations. In our study, men of color were most likely to have been identified via clinic settings (likely an artifact of who the clinics served), men via gay neighborhood settings (e.g., bars) were youngest on average, the greatest proportion of men who did not know their HIV status were identified via the social-sexual networking app, and the greatest proportion of men who did not identify as gay were enrolled via the hook-up website. Researchers and providers seeking to reach younger MSM might be well served to conduct outreach in gay neighborhood settings. Likewise, those seeking to engage with MSM who do not know their HIV status might be well served to conduct outreach via social-sexual networking apps, and those seeking to engage with non-gay-identified MSM might be well served to conduct outreach via hook-up websites. In addition to knowing which venue to go to in order to engage a particular population (e.g., where to go), these findings also inform the types of messages that might be more appropriate in different venues (e.g., how to market one’s message).
Limitations
The findings of this study should be understood in light of its limitations. The B-SAT is a self-administered assessment tool that can be used in both research and clinical settings to assess for HIV risk among MSM. However, it focuses on sexual behavior in the prior 3 months, whereas CDC recommendations for PrEP indication assesses for sexual behavior over the prior 6 months.64 Thus although the B-SAT could be used to identify men who would be appropriate candidates for PrEP, it is limited in that there could be men whose behavior between 3 and 6 months ago would suggest PrEP is indicated, but their more recent behavior (within the last 3 months, as captured on the B-SAT) could suggest that PrEP is not indicated. In addition, the B-SAT does not capture motivation or intent, only past behavior. In an effort to be brief, it also does not capture withdrawal before ejaculation during CAS, nor does it capture behavior with female or transgender partners.
Responses on our survey were self-report and, for many of our participants, anonymous. We believe we found evidence of serosorting as well as biomed matching, both of which have been documented in prior research.9–14,22–27,47 However, we do not know the actual HIV statuses of participants’ partners, and it may be that participants believed their partners shared the same status. In online venues, our ads were targeted to reach MSM, but it is possible that some responses were collected from participants who might have misrepresented their data. Our survey was programmed to record IP address as well as block multiple submissions from a given IP address and our incentives were low and not guaranteed (i.e., a raffle) such to disincentivize fraudulent participants. Next, our analyses did not control for confounders. Finally, we are unable to calculate a response rate for our survey and cannot attest as to whether those who chose to participate characteristically differed from those who did not.
Conclusion
As opposed to picking partners at random (i.e., regardless of a partners’ HIV status/biomedical strategy), our findings indicate that participants gravitated toward partners who share the same HIV status and—in the case of those using a biomedical prevention strategy—the same biomedical HIV prevention or treatment strategy. Furthermore, CAS events were also more common when a partner shared the same HIV status. When two partners both use a biomedical HIV prevention strategy, its effectiveness could be compounded (i.e., both partners bring biomedical protection). One consequence of biomed matching, however, is that men not using a biomedical strategy would be less likely to benefit from the protection that a partner using a biomedical strategy would bring to the sexual encounter. With the continued rollout of PrEP as well as the dissemination of new data regarding untransmisibility of HIV among HIV-positive and undetectable individuals,36,39 our findings highlight the need for researchers to investigate both serosorting and biomedical sorting/matching as well as their impact on ongoing HIV disparities. That is, an unintended consequence of biomedical prevention strategies is that they may further contribute to racial disparities in HIV. Public health campaigns might be well served to highlight not only the benefits that biomedical HIV prevention strategies provide for their users (e.g., “being on PrEP protects me from getting HIV”), but also the benefits that a user brings to his partners (e.g., “my use of PrEP means my partners are protected from HIV”), and the benefits of being with a partner who is using a biomedical strategy (e.g., “my partner’s use of PrEP/TasP protects me from HIV”).
Acknowledgments
Support for this manuscript was provided by the Centers for Disease Control and Prevention-funded NYU-CUNY Prevention Research Center (U48DP005008) Special Interest Project (SIP 15-009: Christian Grov/Simona Kwon - MPI) and the Einstein-Rockefeller-CUNY Center for AIDS Research (P30-AI-124414). H. Jonathon Rendina was supported by a Career Development Award from the National Institute on Drug Abuse (K01-DA039030; H. Jonathon Rendina, PI). One Thousand Strong was supported by the National Institute on Drug Abuse of the National Institutes of Health (R01-DA036466; Jeffrey T. Parsons & Christian Grov, MPI). Dr. Patel was also supported by a Career Development Award from the National Institute of Mental Health (K23-MH102118; Viraj V. Patel, PI). Special thanks to members of the team at CHEST (Chris Murphy, Carlos Ponton, Chris Hietikko, Mark Pawson, Lamar Lewis, Desmond Dutcher, Andrew Cortopassi, Chloe Mirzayi, Demetria Cain, Darren Agboh), Albert Einstein (Shirlyn Charles, Zoe Ginsburg), and NYU (Smiti Nadkarni). Finally thank you to Virginia “Ginny” Bowen and Kyle Bernstein at the CDC and the many participants who gave their time. The content is solely the responsibility of the authors and does not necessarily represent the official views of the Centers for Disease Control or National Institutes for Health.
References
- 1.Ostrow DG, et al. Specific sex drug combinations contribute to the majority of recent HIV seroconversions among MSM in the MACS. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2009;51(3):349–355. doi: 10.1097/QAI.0b013e3181a24b20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Ostrow DG, Stall R. Unequal opportunity: health disparities affecting gay and bisexual men in the United States. In: Wolitski RJ, Stall R, Valdiserri RO, editors. Alcohol, Tobacco, and Drug Use among Gay and Bisexual Men. New York: Oxford University Press; 2008. pp. 121–158. [Google Scholar]
- 3.Plankey MW, et al. The relationship between methamphetamine and popper use and risk of HIV seroconversion in the multicenter AIDS cohort study. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2007;45(1):85–92. doi: 10.1097/QAI.0b013e3180417c99. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Sullivan PS, Wolitski RJ. HIV infection among gay and bisexual men. In: Wolitski RJ, Stall R, Valdisem RO, editors. Unequal Opportunity: health disparities affecting gay and bisexual men in the United States. New York: Oxford University Press; 2008. pp. 220–247. [Google Scholar]
- 5.Ackers ML, Greenberg AE, Lin CY, et al. High and Persistent HIV Seroincidence in Men Who Have Sex with Men across 47 U.S. Cities. PLoS ONE. 2012;7(4):e34972. doi: 10.1371/journal.pone.0034972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Satcher Johnson A, Hall HI, Hu X, Lansky A, Holtgrave DR, Mermin M. Trends in Diagnoses of HIV Infection in the United States, 2002-2011. JAMA. 2014;312(4):432–434. doi: 10.1001/jama.2014.8534. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.CDC. HIV Surveillance Report. Atlanta: US Department of Health and Human Services; 2010. Diagnoses of HIV infection and AIDS in the United States and dependent areas, 2009. [Google Scholar]
- 8.CDC. Half of black gay men and a quarter of Latino gay men projected to be diagnosed within their lifetime. :2016. http://www.cdc.gov/nchhstp/newsroom/2016/croi-press-release-risk.html. Accessed April 26, 2016.
- 9.McConnell JJ, Bragg L, Shiboski S, Grant RM. Sexual Seroadaptation: Lessons for Prevention and Sex Research from a Cohort of HIV-Positive Men Who Have Sex with Men. PLoS ONE. 2010;5(1):e8831. doi: 10.1371/journal.pone.0008831. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Wei C, Raymond HF, Guadamuz TE, et al. Racial/Ethnic Differences in Seroadaptive and Serodisclosure Behaviors Among Men Who Have Sex with Men. AIDS Behav. 2010 Mar 9; doi: 10.1007/s10461-010-9683-2. [DOI] [PubMed] [Google Scholar]
- 11.McFarland W, Chen Y-H, Raymond HF, et al. HIV seroadaptation among individuals, within sexual dyads, and by sexual episodes, men who have sex with men, San Francisco, 2008. AIDS Care. 2011;23(3):261–268. doi: 10.1080/09540121.2010.507748. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Wei C, Raymond HF, Guadamuz TE, et al. Racial/Ethnic differences in seroadaptive and serodisclosure behaviors among men who have sex with men. AIDS Behav. 2011 Jan;15(1):22–29. doi: 10.1007/s10461-010-9683-2. [DOI] [PubMed] [Google Scholar]
- 13.Vallabhaneni S, Li X, Vittinghoff E, Donnell D, Pilcher CD, Buchbinder SP. Seroadaptive Practices: Association with HIV Acquisition among HIV-Negative Men Who Have Sex with Men. PLoS ONE. 2012;7(10):e45718. doi: 10.1371/journal.pone.0045718. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Grov C, Rendina HJ, Moody RL, Ventuneac A, Parsons JT. HIV serosorting, status disclosure, and strategic positioning among highly sexually active gay and bisexual men. AIDS Patient Care STDS. 2015;29:559–568. doi: 10.1089/apc.2015.0126. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Card KG, Lachowsky NJ, Cui Z, et al. A Latent Class Analysis of seroadaptation among gay and bisexual men. Arch Sex Behav. 2016;47:95–106. doi: 10.1007/s10508-016-0879-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Marks G, Millett GA, Bingham T, Lauby J, Murrill CS, Stueve A. Prevalence and protective value of serosorting and strategic positioning among Black and Latino men who have sex with men. Sex Transm Dis. 2010 Jan 14; doi: 10.1097/OLQ.0b013e3181c95dac. [DOI] [PubMed] [Google Scholar]
- 17.Van de Ven P, Kippax S, Crawford J, et al. In a minority of gay men, sexual risk practice indicates strategic positioning for perceived risk reduction rather than unbridled sex. AIDS Care. 2002 Aug;14(4):471–480. doi: 10.1080/09540120208629666. [DOI] [PubMed] [Google Scholar]
- 18.Dubois-Arber F, Jeannin A, Lociciro S, Balthasar H. Risk reduction practices in men who have sex with men in Switzerland: serosorting, strategic positioning, and withdrawal before ejaculation. Arch Sex Beh. 2011 Nov 15; doi: 10.1007/s10508-011-9868-4. [DOI] [PubMed] [Google Scholar]
- 19.Cassels S, Katz DA. Seroadaptation among men who have sex with men: emerging research themes. Curr HIV/AIDS Rep. 2013;10(4):305–313. doi: 10.1007/s11904-013-0188-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.McFarland W, Chen YH, Nguyen B, et al. Behavior, intention or chance? A longitudinal study of HIV seroadaptive behaviors, abstinence and condom use. AIDS Behav. 2012 Jan;16(1):121–131. doi: 10.1007/s10461-011-9936-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Parsons JT, Schrimshaw EW, Bimbi DS, Wolitski RJ, Gomez CA, Halkitis PN. Consistent, inconsistent, and non-disclosure to casual sexual partners among HIV-seropositive gay and bisexual men. AIDS. 2005;19(Suppl. 1):S87–S97. doi: 10.1097/01.aids.0000167355.87041.63. [DOI] [PubMed] [Google Scholar]
- 22.Hopkins E, Rietmeijer CA. Exploring HIV serosorting as a preventive behavior among men who have sex with men: using a comprehensive approach to behavioral science theory. In: Ajzen I, Albarracin D, Hornik R, editors. Prediction and Change of Health Behavior: Applying the Reasoned Action Approach. Mahwah: Lawrence Erlbaum Associates Publishers; 2007. pp. 211–221. [Google Scholar]
- 23.Truong HHM, Kellogg T, Klausner JD, et al. Increases in sexually transmitted infections and sexual risk behavior without a concurrent increase in HIV incidence among men who have sex with men in San Francisco: A suggestion of HIV serosorting? Sex Transm Infect. 2007;82:461–466. doi: 10.1136/sti.2006.019950. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Berry M, Raymond HF, Kellogg T, McFarland W. The Internet, HIV serosorting and transmission risk among men who have sex with men, San Francisco. AIDS. 2008 Mar 30;22(6):787–789. doi: 10.1097/QAD.0b013e3282f55559. [DOI] [PubMed] [Google Scholar]
- 25.Zablotska IB, Imrie J, Prestage G, et al. Gay men’s current practice of HIV seroconcordant unprotected anal intercourse: Serosorting or seroguessing? AIDS Care. 2009;21(4):501–510. doi: 10.1080/09540120802270292. [DOI] [PubMed] [Google Scholar]
- 26.Hart GJ, Elford J. Sexual risk behaviour of men who have sex with men: Emerging patterns and new challenges. Curr Opin Infect Dis. 2010;23:39–44. doi: 10.1097/QCO.0b013e328334feb1. [DOI] [PubMed] [Google Scholar]
- 27.Chen YH, Vallabhaneni S, Raymond HF, McFarland W. Predictors of serosorting and intention to serosort among men who have sex with men, San Francisco. AIDS Educ Prev. 2012 Dec;24(6):564–573. doi: 10.1521/aeap.2012.24.6.564. [DOI] [PubMed] [Google Scholar]
- 28.Van der Bij AK, Kolader ME, de Vries HJ, Prins M, Coutinho RA, Dukers NH. Condom use rather than serosorting explains differences in HIV incidence among men who have sex with men. J Acquir Immune Defic Syndr. 2007 Aug 15;45(5):574–580. doi: 10.1097/QAI.0b013e3180959ab7. [DOI] [PubMed] [Google Scholar]
- 29.Golden MR, Stekler J, Hughes JP, Wood RW. HIV serosorting in men who have sex with men: Is it safe? JAIDS Journal of Acquired Immune Deficiency Syndromes. 2008;49(2):212–218. doi: 10.1097/QAI.0b013e31818455e8. [DOI] [PubMed] [Google Scholar]
- 30.Morin SF, Shade SB, Steward WT, et al. A behavioral intervention reduces HIV transmission risk by promoting sustained serosorting practices among HIV-infected men who have sex with men. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2008;49(5):544–551. doi: 10.1097/QAI.0b013e31818d5def. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Snowden J, Raymond HF, McFarland W. Prevalence of seroadaptive behaviors of men who have sex with men, San Francisco, 2004. Sex Transm Infect. 2009;85:439–476. doi: 10.1136/sti.2009.036269. [DOI] [PubMed] [Google Scholar]
- 32.Snowden JM, Wei C, McFarland W, Raymond HF. Prevalence, correlates and trends in seroadaptive behaviours among men who have sex with men from serial cross-sectional surveillance in San Francisco, 2004–2011. Sex Transm Infect. 2014 doi: 10.1136/sextrans-2013-051368. sextrans-2013-051368. [DOI] [PubMed] [Google Scholar]
- 33.Wilson DP, Regan DG, Heymer K-J, Fengyi J, Prestage GP, Grulich AE. Serosorting may increase the risk of HIV acquisition among men who have sex with men. Sex Transm Dis. 2010;37(1):13–17. doi: 10.1097/OLQ.0b013e3181b35549. [DOI] [PubMed] [Google Scholar]
- 34.Das M, Chu PL, Santos GM, et al. Decreases in community viral load are accompanied by reductions in new HIV infections in San Francisco. PLoS ONE. 2010;5(6):e11068. doi: 10.1371/journal.pone.0011068. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Attia S, Egger M, Müller M, Zwahlen M, Low N. Sexual transmission of HIV according to viral load and antiretroviral therapy: systematic review and meta-analysis. AIDS. 2009;23(11):1397–1404. doi: 10.1097/QAD.0b013e32832b7dca. [DOI] [PubMed] [Google Scholar]
- 36.Prevention Access Campaign. What is Undetectable = Untransmittable? 2016 https://www.preventionaccess.org/undetectable. Accessed March 3, 2017.
- 37.Bavinton BR, Grinsztej B, Phanuphak N, et al. HIV treatment prevents HIV transmission in male serodiscordant couples in Australia, Thailand and Brazil. International AIDS Society; Paris: 2017. Jul, [Google Scholar]
- 38.Bavinton B, Grinsztejn B, Phanuphak N, et al. HIV treatment prevents HIV transmission in male serodiscordant couples in Australia, Thailand and Brazil. International AIDS Society; Paris: 2017. [Google Scholar]
- 39.McCray E, Mermin JH. Dear Colleague: Information from the CDC’s division of HIV/AIDS Prevention. 2017 https://www.cdc.gov/hiv/library/dcl/dcl/092717.html. Accessed January 16, 2018.
- 40.Centers for Disease C, Prevention. Interim guidance: preexposure prophylaxis for the prevention of HIV infection in men who have sex with men. MMWR Morbidity and mortality weekly report. 2011 Jan 28;60(3):65–68. [PubMed] [Google Scholar]
- 41.Centers for Disease C, Prevention. Interim guidance for clinicians considering the use of preexposure prophylaxis for the prevention of HIV infection in heterosexually active adults. MMWR Morbidity and mortality weekly report. 2012 Aug 10;61(31):586–589. [PubMed] [Google Scholar]
- 42.Centers for Disease C, Prevention. Update to Interim Guidance for Preexposure Prophylaxis (PrEP) for the Prevention of HIV Infection: PrEP for injecting drug users. MMWR Morbidity and mortality weekly report. 2013 Jun 14;62(23):463–465. [PMC free article] [PubMed] [Google Scholar]
- 43.Peabody R. CROI 2016: Rapid Rise in PrEP Awareness in US Gay Men, But Only 5% Have Used PrEP. 2016 http://hivandhepatitis.com/hiv-prevention/hiv-prep/5646-croi-2016-rapid-rise-in-prep-awareness-in-us-gay-men-but-only-5-have-used-prep. Accessed March 17, 2016.
- 44.Grov C, Rendina HJ, Whitfield THF, Ventuneac A, Parsons JT. Changes in familiarity with- and willingness to take- PrEP: Results from a longitudinal study of gay and bisexual men. LGBT Health. 2016;3:252–257. doi: 10.1089/lgbt.2015.0123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Poz.com. PrEP is on the upswing among young New York City gay men, with higher-risk guys more incliend toward its use. 2016 https://www.poz.com/article/prep-upswing-among-young-new-york-city-gay-men-higherrisk-guys-inclined-toward-use. Accessed March 11, 2016.
- 46.Bush S, Magnuson D, Rawlings MK, Hawkins T, McCallister S, Mera Giler R. American Society for Microbiology: ICAAC. Boston, MA: 2016. Jun 16–20, Racial characteristics of FTC/TDF for pre-exposure prophylaxis (PrEP) users in the US #2651. [Google Scholar]
- 47.Newcomb ME, Mongrella MC, Weis B, McMillen SJ, Mustanski BS. Partner disclosure of PrEP use and undetectable viral load on geosocial networking apps: frequency of disclosure and decisions about condomless sex. JAIDS Journal of Acquired Immune Deficiency Syndromes. doi: 10.1097/QAI.0000000000000819. in press. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Grov C, Rendina HJ, Parsons JT. How different are men who do not know their HIV status from those who do? Results from an U.S. online study of gay and bisexual men. AIDS Behav. 2016;20(1989–1999) doi: 10.1007/s10461-015-1284-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Elford J. Changing patterns of sexual behaviour in the era of highly active antiretroviral therapy. Curr Opin Infect Dis. 2006 Feb;19(1):26–32. doi: 10.1097/01.qco.0000199018.50451.e1. [DOI] [PubMed] [Google Scholar]
- 50.Prestage G, Mao L, Kippax S, et al. Use of viral load to negotiate condom use among gay men in Sydney, Australia. AIDS Behav. 2009;13(4):645–651. doi: 10.1007/s10461-009-9527-0. [DOI] [PubMed] [Google Scholar]
- 51.Jin F, Prestage GP, Mao L, et al. “Any condomless anal intercourse” is no longer an accurate measure of HIV sexual risk behavior in gay and other men who have sex with men. Frontiers in immunology. 2015:6. doi: 10.3389/fimmu.2015.00086. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Grov C, Cain D, Whitfield THF, et al. Recruiting a U.S. national sample of HIV-negative gay and bisexual men to complete at-home self-administered HIV/STI testing and surveys: Challenges and opportunities. Sexuality Research & Social Policy. 2016;13(1–21) doi: 10.1007/s13178-015-0212-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Grov C, Pawson M, Rendina HJ, Parsons JT. The brief seroadaptive assessment tool (B-SAT) for men who have sex with men. In: Milhausen R, Fisher T, Davis C, Yarber B, Sakaluk J, editors. Handbook of Sexuality-Related Measures. 4th. New York: Taylor and Francis; in press. [Google Scholar]
- 54.Miller KW, Wilder LB, Stillman FA, Becker DM. The feasibility of a street-intercept survey method in an African-American community. Am J Public Health. 1997;87:655–658. doi: 10.2105/ajph.87.4.655. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Parsons JT, Grov C, Golub SA. Sexual compulsivity, co-occurring psychosocial health problems, and HIV risk among gay and bisexual men: Further evidence of a syndemic. Am J Public Health. 2012;102:156–162. doi: 10.2105/AJPH.2011.300284. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Grov C, Golub SA, Parsons JT. HIV status differences in venues where highly-sexually active gay and bisexual men meet sex partners: Results from a pilot study. AIDS Educ Prev. 2010;22:496–508. doi: 10.1521/aeap.2010.22.6.496. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Pantalone DW, Tomassilli JC, Starks TJ, Golub SA, Parsons JT. Unprotected anal intercourse with casual male partners in urban gay, bisexual, and other men who have sex with men. Am J Pub Health. 2015;105(1):103–110. doi: 10.2105/AJPH.2014.302093. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Grov C, Hirshfield S, Remien RH, Humberstone M, Chiasson MA. Exploring the venue’s role in risky sexual behavior among gay and bisexual men: An event-level analysis from a national online survey in the U.S. Arch Sex Behav. 2013;42:297–302. doi: 10.1007/s10508-011-9854-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Grov C, Rendina HJ, Parsons JT. Comparing three cohorts of MSM sampled from sex parties, bars/clubs, and Craigslist.org: Implications for researchers and providers. AIDS Educ Prev. 2014;26(4):362–382. doi: 10.1521/aeap.2014.26.4.362. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Grov C, Rendina HJ, Jimenez R, Parsons JT. Using online settings to identify gay and bisexual men willing to take or with experience taking PrEP: Implications for researchers and providers. AIDS Educ and Prev. 2016;28 doi: 10.1521/aeap.2016.28.5.378. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Merchant RC, Romanoff J, Clark MA, et al. Variations in Recruitment Yield and Characteristics of Participants Recruited Across Diverse Internet Platforms in an HIV Testing Study of Young Adult Men-Who-Have-Sex-With-Men (YMSM) American Journal of Men’s Health. 2017;11:1342–1357. doi: 10.1177/1557988317717383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Vial AC, Starks TJ, Parsons JT. Finding and recruiting the highest risk HIV-negative men who have sex with men. AIDS Educ and Prev. 2014;26(1):56–67. doi: 10.1521/aeap.2014.26.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Parsons JT, Vial AC, Starks TJ, Golub SA. Recruiting drug using men who have sex with men in behavioral intervention trials: A comparison of Internet and field-based strategies. AIDS Behav. 2013 Jun 10;17:688–699. doi: 10.1007/s10461-012-0231-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.CDC. PreExposure Prophylaxis for the Prevention of HIV infection in the United States - 2014: A clinical practice guideline. 2014 http://www.cdc.gov/hiv/pdf/guidelines/PrEPguidelines2014.pdf. Accessed April 14, 2016.
