Abstract
Sexual transmission risk occurs in the context of serodiscordant condomless anal intercourse (CAI) where the seropositive partner is virologically detectable (VL+) and/or seronegative partner is not on PrEP. We analyzed correlates of serodiscordant CAI among 688 VL+ young men who have sex with men (YMSM). In multivariable analyses, serodiscordant CAI was associated with a receiving a HIV diagnosis in the past 6 months, greater depressive symptoms, and cocaine use during the past 90 days. Although HIV+ YMSM currently experience disparities across the continuum of care, those new to care may need support adopting risk reduction strategies with their sexual partners.
Keywords: sexual risk behavior, HIV/AIDS, continuum of care, YMSM, serodiscordant
INTRODUCTION
Young men who have sex with men (YMSM) continue to be overrepresented in the HIV epidemic in the U.S., constituting over 1 in 4 of all new infections; in particular, YMSM of color remain disproportionately impacted [1]. Compared to adult populations, young persons living with HIV experience significant disparities at each stage of the HIV care continuum. For instance, young people living with HIV are more likely than adults to have undiagnosed HIV infection and to face greater challenges with linkage and retention in care [2]. Furthermore, YMSM living with HIV (HIV+ YMSM), especially African American and Latino HIV+ YMSM, are less likely to achieve viral suppression due to drop-offs across every step of the care continuum [3].
Models estimating HIV prevalence, risk behavior, and viral suppression show that current disparities in prevalence and viral suppression will continue to drive the epidemic in MSM populations, with the highest transmission rate attributable to serodiscordant condomless anal intercourse (serodiscordant CAI) among persons who are aware of their status with unsuppressed viral load [4]. Successful antiretroviral treatment (ART) that suppresses the viral load of a person living with HIV is recognized as one strategy to reduce risk of HIV transmission, and has been shown to significantly reduce the risk of HIV transmission in clinical trials [5] and in studies of serodiscordant couples [6]. HIV+ YMSM who demonstrate optimal outcomes at points later in the continuum (being on ART, over 90% adherent to ART, as well as being virally suppressed) are less likely to engage in condomless anal intercourse [7]. At present, however, the degree to which virologically detectable YMSM (VL+YMSM) exhibit sexual risk at earlier continuum points is largely undocumented.
Under a treatment as prevention paradigm, sexual transmission risk occurs in the context of serodiscordant unprotected anal intercourse (i.e., condomless anal sex where the seropositive partner is virologically detectable (VL+) and/or seronegative partner is not on PrEP). To date, little analysis of serodiscordant risk behavior correlates among VL+ YMSM has been conducted. Substance misuse and mental health symptoms may increase the likelihood of engaging in unprotected anal intercourse as well as experiencing challenges with ART adherence. Previous research has found stimulant use (e.g., cocaine, amphetamines) to be associated with serodiscordant CAI among HIV+ adult MSM [8], and alcohol use to be associated with serodiscordant CAI among HIV+ YMSM [9].
Findings by Wilson, et al. [10] reported high rates of serodiscordant CAI associated with problematic substance use and depression among a national clinic-based sample of VL+ YMSM, although particular substances significantly associated with serodiscordant CAI were not identified. In order to target interventions to the specific needs of VL+ YMSM, more research is needed on transmission risk across stages of the HIV care continuum and the psychosocial contexts in which sexual risk occurs among patient populations. We conducted a post-hoc analysis of 688 VL+ YMSM [10] to identify specific substance use patterns and clinical continuum markers associated with serodiscordant CAI among VL+ YMSM. We focused on serodiscordant CAI as an outcome, as PrEP was not widely available at the time of data collection. We hypothesized that serodiscordant CAI would be associated with (1) alcohol use, marijuana use, and other drug use, and (2) an HIV diagnosis in the past 6 months, less retention in care, and not being on ART.
METHODS
Study Procedures
From December 2009 to June 2012, 2,225 youth and young adults living with HIV/AIDS receiving primary care at clinics within the Adolescent Medicine Trials Network for HIV/AIDS Interventions (ATN) were recruited to participate in a cross-sectional survey. The 20 clinics were geographically representative of the HIV epidemic in the U.S. and Puerto Rico (see Acknowledgements for cities represented). To be eligible, youth had to be: 1) between 12 and 26 years of age (inclusive); 2) living with HIV/AIDS; 3) aware they were HIV-infected; 4) engaged in care in one of the ATN’s clinical sites or affiliates; and 5) able to understand English or Spanish. The study was approved by the Institutional Review Boards at each participating site as well as those from the members of the protocol team.
Research staff at the sites approached all youth meeting eligibility criteria during one of their scheduled clinic visits. After a thorough explanation of the study, staff obtained signed informed consent or assent from youth agreeing to participate. Participants completed audio-computer assisted self-interviews (ACASI) which took approximately 45 to 90 minutes. The ACASI included demographic information and several psychosocial domains, including substance use, mental health, sexual behavior and other behavioral health data. Participants were given a small incentive determined by the sites’ IRB as compensation for their time.
Medical charts of participants were abstracted by research staff at each site to extract ART regimen data and viral load (Plasma HIV-1 RNA) assay results obtained within the prior six months of study consent. Using the corresponding assay cutoff for the lower limit of HIV RNA detection (<200 copies/mL), we created a dichotomous variable to differentiate virally suppressed and unsuppressed participants. The current study focuses on a subsample of 688 participants ages 16–24 who identified their birth sex as male, reported sexual behavior with another male in the past 90 days, and were virologically detectable at time of study consent.
Measures
Sexual Behavior
Serodiscordant CAI during the past 90 days was assessed across (1) any insertive CAI with male HIV-negative partner(s) or partner(s) of unknown status, and (2) any receptive CAI with male HIV-negative partner(s) or partner(s) of unknown status. We transformed the two types of serodiscordant CAI into a combined “any serodiscordant CAI” variable.
Mental Health
Mental health symptoms were assessed with the Brief Symptom Inventory (BSI) which yields nine primary symptom scales, and a global severity index (GSI). For the purposes of descriptive and multivariate analyses, mean scores were calculated for the anxiety (α =.86; 6 items) and depression (α =.87; 6 items) subscales.
Substance Use
The Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST) was used to measure substance use behaviors. Frequency of alcohol, marijuana and other drug use (e.g., cocaine, heroin, hallucinogens, methamphetamine/amphetamines,) was assessed during the past 90 days.
HIV Continuum Indicators
Participants who reported confirmatory HIV diagnosis within the past 6 months were classified as “recently diagnosed.” We assessed retention in care by self-reported number of missed visits with an HIV care provider over the past 12 months, dichotomized as <1 vs. >1 missed appointments. Participants who self-reported being on ART and had a current regimen identified during medical chart review were classified as “currently on ART.”
Data Analysis
Serodiscordant CAI was modeled as the outcome in our regression analyses. We conducted bivariate logistic regression analysis of possible correlates of serodiscordant CAI, including demographic, mental health, substance use, and HIV continuum variables. Given the potential for site-level clustering, we examined the variance at Level 2 in a null hierarchical generalized linear model for our outcome yet found the Level 2 variance to be non-significant (p=.28). Mental health, substance use, and HIV continuum variables that approached statistical significance with the CAI variables in the bivariate analyses (p < .10) were entered into multivariate stepwise logistic regression equations to determine significant correlates of serodiscordant CAI while controlling for demographic factors. The BSI-anxiety score (p<.10 in the bivariate analysis) was not entered into the multivariate model due to its multicollinearity with the BSI-depression score.
RESULTS
Sample Characteristics
Demographic, biomedical, and psychosocial/behavioral variable frequencies for participants appear in Table 1. Slightly more than half of participants reported missing ≥2 appointments during the past 12 months, one-third were currently on ART, and 39.8% were diagnosed within the past 6 months. Slightly more than one-third reported serodiscordant CAI.
Table I.
Virally unsuppressed HIV+ YMSM (n=688) | Virally suppressed HIV+ YMSM (N=288) | p- value | Univariate analysis of serodiscordant CAI among VL+ YMSM | Final multivariate model of serodiscordant CAI among VL+YMSM | |||||
---|---|---|---|---|---|---|---|---|---|
M | SD | M | SD | OR | 95% CI | OR | 95% CI | ||
BSI Depression Score | 7.39 | 6.24 | 6.17 | 5.80 | <.05 | 1.04** | 1.01– 1.07 | 1.03* | 1.00– 1.06 |
BSI Anxiety Score | 5.73 | 5.45 | 4.65 | 5.13 | <.05 | 1.02 | .99– 1.05 | ||
Age | 21.0 | 1.99 | 21.7 | 1.93 | N/S | 1.00 | .99– 1.01 | 1.00 | .99– 1.01 |
n | % | n | % | ||||||
HIV diagnosis within past 6 mos. | 272 | 39.8 | 20 | 7.0 | <.001 | 1.44* | 1.04– 1.98 | 1.56* | 1.11– 2.19 |
≥2 Missed appointments, past 12 mos. | 355 | 51.6 | 90 | 31.5 | N/S | .92 | .67– 1.27 | ||
Currently on ART | 232 | 33.7 | 281 | 98.2 | <.001 | .94 | .67– 1.31 | ||
Any alcohol use, past 90 days | 599 | 87.6 | 248 | 86.1 | N/S | 2.11** | 1.22– 3.65 | 1.70 | .96– 3.01 |
Any marijuana use, past 90 days | 429 | 62.7 | 168 | 58.3 | N/S | 1.14 | .82– 1.58 | ||
Any cocaine use, past 90 days | 92 | 13.4 | 37 | 12.8 | N/S | 2.15** | 1.38– 3.36 | 1.68* | 1.02– 2.81 |
Any amphetamine use, past 90 days | 142 | 20.6 | 40 | 13.9 | <.05 | 1.80** | 1.23– 2.62 | 1.24 | .79– 1.95 |
Any opioid use, past 90 days | 24 | 3.5 | 6 | 2.1 | N/S | 1.39 | .61– 3.19 | ||
Any hallucinogen use, past 90 days | 43 | 6.3 | 8 | 2.8 | <.05 | 1.03 | .54– 1.98 | ||
White/Caucasian | 99 | 14.5 | 39 | 13.6 | N/S | Ref. | Ref. | ||
Black/African American | 437 | 63.9 | 179 | 62.6 | N/S | .58* | .37– .90 | .67 | .41– 1.10 |
Mixed Race/Biracial/Other | 131 | 19.1 | 58 | 20.3 | N/S | .64 | .52– 1.45 | .17 | .02– 1.56 |
Asian American/Pacific Islander | 8 | 1.2 | 5 | 1.7 | N/S | .73 | .17– 3.39 | .87 | .48– 1.60 |
Native American/American Indian | 7 | 1.0 | 3 | 1.0 | N/S | .22 | .03– 2.27 | .69 | .14– 3.39 |
Hispanic/Latino | 147 | 21.5 | 67 | 23.4 | N/S | 1.14 | .92– 1.40 | 1.03 | .79– 1.33 |
Gay | 514 | 75.1 | 219 | 76.6 | N/S | Ref. | |||
Bisexual | 114 | 16.7 | 43 | 15.0 | N/S | 1.50 | .98– 2.28 | 1.52 | .98– 2.35 |
Other sexual orientation | 55 | 7.3 | 23 | 8.0 | N/S | 1.06 | .59– 1.90 | 1.18 | .63– 2.21 |
Transgender | 34 | 4.9 | 11 | 3.8 | N/S | .47 | .20– 1.09 | .44 | .18– 1.10 |
Post High School education | 251 | 36.7 | 146 | 51.0 | <.001 | 1.27 | .92– 1.76 | 1.28 | .89– 1.83 |
Current employment | 281 | 41.1 | 146 | 51.0 | <.01 | .94 | .70– 1.24 | .84 | .61– 1.15 |
Current unstable housing | 43 | 6.3 | 9 | 3.1 | <.05 | 1.56 | .83– 2.91 | 1.30 | .66– 2.56 |
Ever incarcerated | 262 | 38.3 | 90 | 31.5 | <.05 | 1.18 | .89– 1.55 | 1.21 | .88– 1.64 |
Any serodiscordant CAI, past 90 days | 235 | 34.4 | 71 | 24.8 | <.01 | --- | --- | --- | --- |
p<.05
p<.01
Bivariate analyses indicated serodiscordant CAI was associated with having received an HIV diagnosis in the past 6 months (OR=1.44, 95% CI: 1.04–1.98), greater depressive symptoms (OR=1.04, 95% CI: 1.01–1.07), and past 90 day use of alcohol (OR=2.11, 95% CI: 1.22=−3.65), cocaine (OR=2.15, 95% CI: 1.38–3.36), or methamphetamine (OR=1.80, 95% CI: 1.23–2.62). Black VL+ YMSM were less likely to engage in serodiscordant UAI (OR=.58, 95% CI: .37–.90). In multivariable analyses, serodiscordant CAI was associated with having received an HIV diagnosis in the past 6 months (OR=1.56, 95% CI: 1.11–2.19), greater depressive symptoms (OR= 1.03, 95% CI: 1.01–1.06) and cocaine use (OR=1.68. 95% CI: 1.02–2.81). We found no association between serodiscordant CAI and other HIV continuum of care stages or with other demographic or behavioral in the multivariable analysis.
DISCUSSION
This post-hoc analysis of a national sample of VL+ YMSM identified recent HIV diagnosis, cocaine use, and depressive symptomology as significant correlates of serodiscordant CAI. We found no significant associations between serodiscordant CAI and missed appointments or being on ART. Our findings point to the period immediately post-diagnosis as a period of heightened transmission risk among groups of VL+ YMSM compared to points later in the continuum of care. Youth newly diagnosed with HIV experience multiple stressors and are in need of developmentally appropriate health services to reduce risk and promote health [11]. While previous studies have shown reductions in mental health symptomology and sexual risk behavior over time among persons in HIV care [12], the period immediately post-diagnosis may involve challenges to adjustment among subsets of YMSM. These findings collectively highlight the importance of providing targeted interventions and support services at the initial stage of the care continuum.
Although alcohol, methamphetamine, and cocaine use were all associated with serodiscordant CAI in the birvariate analyses, participants reporting cocaine use during the past 90 days were more likely to report serodiscordant CAI than other VL+ YMSM in care in the multivariate analysis. While much of the research on stimulant use and CAI among HIV-positive MSM has focused on methamphetamine use, cocaine use among HIV-positive adult MSM has been found previously to be associated with CAI in conjunction with higher sexual compulsivity [13] and other stimulant use [14]. Among HIV-negative YMSM, cocaine use has also been associated with CAI in the context of other stimulant use [15–16]. Screening and interventions that contextualize stimulant use and sexual behavior among VL+YMSM are urgently needed.
Our study has several limitations deserving mention. We used a convenience sample of VL+ YMSM currently in care; therefore, rates of serodiscordant CAI among the VL+ YMSM population may be underestimated. We did not utilize a probability sample, which limits generalizability; however, our sample roughly mirrors the current HIV epidemic in the U.S. among YMSM proportionally in terms of racial/ethnic groups represented. Our cross-sectional design of this study does not allow for any establishment of causality. All data in the study were self-reported and as such potentially subject to social desirability or recall bias, but the use of ACASI may mitigate the perceived need to report socially desirable answers to potentially sensitive or stigmatizing questions.
Despite these limitations, these findings add to the emergent literature of sexual risk behavior among VL+ YMSM engaged in care, and they point to the importance of behavioral interventions that address adjustment to diagnosis. Although HIV+ YMSM currently experience disparities across the continuum of care, those new to care may be particularly in need of support for risk reduction strategies. Interventions are needed for recently diagnosed YMSM to support risk reduction strategies with sexual partners, and to address stimulant use and depressive symptomology to reduce the likelihood of transmission behaviors among VL+MSM.
Acknowledgments
This study was funded under a cooperative agreement [U01 HD 040533 and U01 HD 040474] from the National Institutes of Health, the Eunice Kennedy Shriver National Institute of Child Health and Human Development (B. Kapogiannis, S. Lee), the National Institute on Drug Abuse (K. Davenny, S. Kahana), and the National Institute of Mental Health (P. Brouwers, S. Allison). Additional funding from the National Institute on Drug Abuse under grant R03DA041908 aided in the development of this paper. At the time of the development of this paper, Dr. Kahana was a NIDA research scientist with the ATN. The contents of this report are solely the responsibilities of the authors and do not necessarily represent the official views of the NIH.
The study was provided scientific and logistical support by the ATN Coordinating Center (C. Wilson, C. Partlow) at The University of Alabama at Birmingham. Network operations and data management support was provided by the ATN Data and Operations Center at Westat, Inc. (J. Korelitz, B. Driver). We acknowledge the contribution of the investigators and staff at the following sites that participated in this study: The following ATN sites participated in this study: University of South Florida, Tampa, FL (Emmanuel, Lujan-Zilbermann, Julian), Children’s Hospital of Los Angeles (Belzer, Flores, Tucker), Children’s National Medical Center, Washington, DC (D’Angelo, Hagler, Trexler), Children’s Hospital of Philadelphia (Douglas, Tanney, DiBenedetto), John H. Stroger Jr. Hospital of Cook County and the Ruth M. Rothstein CORE Center, Chicago, IL (Martinez, Bojan, Jackson), University of Puerto Rico (Febo, Ayala-Flores, Fuentes-Gomez), Montefiore Medical Center, Bronx, NY (Futterman, Enriquez-Bruce, Campos), Mount Sinai Medical Center, New York, NY (Steever, Geiger), University of California-San Francisco (Moscicki, Auerswald, Irish), Tulane University Health Sciences Center, New Orleans, LA (Abdalian, Kozina, Baker), University of Maryland, Baltimore, MD (Peralta, Gorle), University of Miami School of Medicine, Miami, FL (Friedman, Maturo, Major-Wilson), Children’s Diagnostic and Treatment Center, Fort Lauderdale, FL (Puga, Leonard, Inman), St. Jude’s Children’s Research Hospital, Memphis, TN (Flynn, Dillard), Children’s Memorial Hospital, Chicago, IL (Garofalo, Brennan, Flanagan), Baylor College of Medicine, Houston, TX (Paul, Calles, Cooper), Wayne State University, Detroit, MI (Secord, Cromer, Green-Jones), Johns Hopkins University School of Medicine, Baltimore, MD (Agwu, Anderson, Park), The Fenway Institute, Boston, MA (Mayer, George, Dormitzer), and University of Colorado, Denver (Reirden, Hahn, Witte). The investigators are grateful to the members of the local youth Community Advisory Boards for their insight and counsel.
Our deep gratitude goes to the youth who participated in this study, and whose time and thoughtful input made it possible.
The views and opinions expressed in this report are those of the authors and should not be construed to represent the views of the National Institutes of Health or any of the sponsoring organizations, agencies, or the U.S. government.
Footnotes
Ethical approval: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Conflict of Interest: The authors have no conflicts of interest to report.
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