Elsevier

Addictive Behaviors

Volume 83, August 2018, Pages 109-115
Addictive Behaviors

Situational HIV stigma and stimulant use: A day-level autoregressive cross-lagged path model among HIV-positive gay and bisexual men

https://doi.org/10.1016/j.addbeh.2018.01.003Get rights and content

Highlights

  • Internalized HIV stigma was associated with subsequent increases in emotion dysregulation.

  • Internalized HIV stigma was associated with later use of stimulant drugs.

  • Emotion dysregulation was not associated with stimulant use.

  • Emotion dysregulation did not explain the link between internalized stigma and drugs.

Abstract

Background

Data on the association between HIV stigma and drug use are scarce, but some research suggests that internalized HIV stigma may be associated with increased drug use and that this association may be at least partially mediated by emotion dysregulation. We sought to test this hypothesis with event-level data to more accurately tease out the co-occurrence of these phenomena.

Methods

We conducted a 21-day, twice-daily ecological momentary assessment study with a sample of 52 HIV-positive gay and bisexual men. We utilized multivariate multilevel path analysis to test an autoregressive cross-lagged model of the direct and indirect effects of situational-level internalized HIV stigma and emotion dysregulation on non-prescription stimulant drug use.

Results

As hypothesized, we observed significant concurrent effects of internalized HIV stigma on emotion dysregulation as well as autoregressive associations of internalized HIV stigma and emotion dysregulation with themselves across the day. Furthermore, findings revealed direct effects of internalized HIV stigma on later emotion dysregulation and increased likelihood of stimulant use, but no direct effect of emotion dysregulation on stimulant use.

Conclusions

Situational increases in internalized HIV stigma appear to exert a direct risk-enhancing effect on the likelihood of daily stimulant drug use and do not appear to do so through emotion dysregulation. Future research is needed to more carefully examine distinct affective experiences and regulation strategies to better understand what mechanism links internalized HIV stigma with drug use behaviors.

Introduction

HIV stigma has several well-documented associations with adverse mental health outcomes for people living with HIV, including depression (Chaudoir et al., 2012, Rao et al., 2012, Wright et al., 2007), anxiety (Tomassilli et al., 2013, Varni et al., 2012), general distress (Miller et al., 2016), and low self-esteem (Turan, Budhwani, Fazeli, et al., 2017). Internalized HIV stigma, whereby negative societal attitudes become directed towards oneself, has been shown to be particularly problematic for its effects on mental health and health behaviors among both general samples of HIV-positive individuals (Katz et al., 2013, Rueda et al., 2016, Sayles et al., 2008, Sweeney and Vanable, 2016, Turan et al., 2017, Turan et al., 2016) and among HIV-positive gay and bisexual men (GBM), specifically (Berg et al., 2017, Dowshen et al., 2009, Hatzenbuehler et al., 2011, Rendina et al., 2017, Rendina et al., 2012, Wohl et al., 2013). In particular, rates of drug use and related problems are disproportionately higher for GBM in general as compared to their heterosexual peers (Green and Feinstein, 2012, McCabe et al., 2013) and, among GBM, disproportionately higher among HIV-positive compared to HIV-negative individuals (Schmidt, Bourne, Weatherburn, et al., 2016). Among GBM, non-prescription stimulant drugs such as cocaine/crack and crystal methamphetamine are among the most frequently reported illicit drugs used (Carrico et al., 2007, Grov et al., 2006, Lea et al., 2013, McCabe et al., 2009, Skinner, 1994), and consequences of their use have included greater HIV transmission risk behavior and lower antiretroviral medication adherence (Lelutiu-Weinberger et al., 2013, Li and McDaid, 2014, Parsons et al., 2013, Rendina et al., 2015). Furthermore, stimulants such as cocaine/crack and crystal methamphetamine are known to have significant HIV-related health consequences, such as increased viral replication (Baum et al., 2009, Massanella et al., 2015, Shoptaw et al., 2012), inflammation (Roth, Whittaker, Choi, Tashkin, & Baldwin, 2005), and quickened progression to AIDS (Carrico, Shoptaw, Cox, et al., 2014).

One prominent model for understanding the disproportionate burden of negative health outcomes observed among GBM is the minority stress model (Hatzenbuehler, 2009, Hatzenbuehler et al., 2008, Meyer, 1995, Meyer, 2003). In both theoretical and empirical work, the link between sexual minority stress and behavioral outcomes such as drug use among GBM has been posited to operate through the mediating factor of emotion dysregulation (Feinstein and Newcomb, 2016, Hatzenbuehler, 2009, Lelutiu-Weinberger et al., 2013, McCabe et al., 2010). Prior research has shown consistent effects of both sexual minority and HIV-related stigma on emotion dysregulation for HIV-positive GBM (Rendina et al., 2017), and that emotion dysregulation mediates the effect of these forms of stigma on negative mental health, sexual risk behavior, and substance use outcomes (Hatzenbuehler et al., 2008, Pachankis et al., 2015, Rendina et al., 2017). As such, there is a growing empirical basis for theorizing that stigma may lead to behaviors such as drug use through emotion dysregulation, whereby an individual experiences both behavioral disinhibition as well as a drive to seek such behavioral experiences in order to improve positive mood or distract from negative mood.

While a growing body of evidence has shown the links between HIV stigma and emotion dysregulation as cited above, research on HIV stigma's direct association with substance use has been relatively scarce and has focused mostly on heterosexual samples (Edelman et al., 2017, Lunze et al., 2017, Wolitski et al., 2009, Wright et al., 2007). We are aware of only two studies looking at the association between HIV stigma and substance use in GBM: one that demonstrated a non-significant association between HIV stigma and alcohol dependency (Berg et al., 2017), and another that showed that, among young Black GBM, those with greater HIV stigma reported higher odds of having sex while high or intoxicated (Radcliffe et al., 2010). Further investigation in this area is therefore needed, especially given the elevated rates of drug use among HIV-positive GBM, the link between emotion dysregulation and stimulant use (Carrico et al., 2007), and the detrimental effects of use on various HIV-related health outcomes (Carrico et al., 2007, Tucker et al., 2003).

Most of the aforementioned research on the mental and behavioral health effects of HIV stigma has focused on links between global or enduring levels of HIV stigma and aggregate outcomes (e.g., depression, substance use dependency). However, a more temporally-precise understanding of the co-occurrence of HIV stigma and health outcomes has been provided by two recent studies looking at day-level associations. In the first study, Fazeli et al. showed a positive association between enacted and internalized HIV stigma using a 7-day experience sampling design (Fazeli, Turan, Budhwani, et al., 2016). In the second study, Rendina et al. showed a positive effect of situationally-fluctuating levels of internalized HIV stigma measured once daily on negative affect and emotion dysregulation using a 21-day ecological momentary assessment (EMA) design (Rendina, Millar, & Parsons, 2018). No study of which we aware has yet looked at event-level associations between HIV stigma and drug use, though three recent daily diary studies on sexual minority stigma among GBM—one showing that daily sexual minority stigma was associated with increased negative affect (Eldahan et al., 2016), one showing that individual-level sexual minority stigma was associated with increased odds of alcohol and tobacco use on a given day (Pachankis, Hatzenbuehler, & Starks, 2014), and another showing that daily sexuality-based discrimination was associated with both daily nicotine and substance use (Livingston, Flentje, Heck, Szalda-Petree, & Cochran, 2017)—further support the possibility that daily fluctuations in levels of internalized HIV stigma may be associated at an event-level with the experience of emotion dysregulation and drug use.

Building upon the existing data, the purpose of the present study was to examine an event-level, autoregressive cross-lagged path model of internalized HIV stigma, emotion dysregulation, and use of non-prescription stimulant drugs among HIV-positive GBM participating in a twice-daily, 21-day EMA study. As depicted in Fig. 1, we hypothesized the following: (1) concurrent effects whereby afternoon levels of internalized HIV stigma would be positively associated with afternoon levels of emotion dysregulation (curved Path A) and the same would be true for the nighttime measurements (curved Path F); (2) autoregressive effects whereby afternoon levels of internalized HIV stigma would be positively associated with nighttime levels of internalized HIV stigma (Path B) and the same would be true for emotion dysregulation (Path C); (3) a positive cross-lagged effect of afternoon levels of internalized HIV stigma on nighttime levels of emotion dysregulation (Path E); (4) a positive direct effect of nighttime levels of emotion dysregulation on subsequent stimulant drug use (Path H); and (5) positive indirect effects (i.e., mediation) of afternoon internalized HIV stigma on stimulant drug use through nighttime emotion dysregulation (Path E–H). Based on the proposed theoretical model, we expected that internalized HIV stigma would be associated with higher levels of subsequent emotion dysregulation, but that the reverse would not be true—that is, that earlier experiences of emotion dysregulation would not be associated with later experiences of internalized HIV stigma (Path D). Similarly, based on prior work, we expected the effect of internalized HIV stigma on stimulant drug use would be through emotion dysregulation, so we expected no direct effect of internalized HIV stigma on stimulant drug use (Path G). However, this was not tested as formal hypotheses due to the fact that a null hypothesis cannot be supported.

Section snippets

Method

Data for this paper were drawn from 52 participants enrolled in the day2day pilot study, a 21-day twice-daily EMA study of HIV-positive GBM in New York City that was conducted in late 2015 and early 2016.

Results

One of the 53 men in the study was missing demographic data and excluded from analyses, resulting in an analytic sample of 52 participants. The median number of surveys completed per participant was 35 (83.3% of sent)—median completion for both the afternoon and nighttime surveys was 17, and we analyzed a total of 784 days' worth of data. Table 1 reports on the demographic characteristics of the sample, showing that most were men of color, gay-identified, single, and unemployed, and had

Discussion

We examined an autoregressive cross-lagged path model of internalized HIV stigma, emotion dysregulation, and drug use within a twice-daily EMA study with HIV-positive GBM. In doing so, we found the following: (1) there were significant and positive concurrent associations between internalized HIV stigma and levels of emotion dysregulation measured at the same time, which was true at both time points examined; (2) there were significant autoregressive effects of internalized HIV stigma in the

Role of funding sources

This work was funded by a career development award from the National Institute on Drug Abuse (K01-DA039030, PI: Rendina). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Contributors

HJR was responsible for study design, data collection, data analysis, interpreting the results, and drafting of the manuscript. BMM was responsible for drafting of the manuscript. JTP was responsible for study design and revising the manuscript. All three authors read, revised, and approved a final version of the manuscript.

Conflict of interest

None.

Acknowledgments

The authors would like to acknowledge the mentorship provided to the first author by the mentors and collaborators on his K01 award: Dr. John Pachankis, Dr. Steven Safren, Dr. Sarah Feldstein Ewing, Dr. Christina Meade, and Dr. Brian Mustanski. The authors also acknowledge the contributions of the day2day Research Team: Sitaji Gurung, Ruben Jimenez, Douglas Keeler, Jonathan Lopez Matos, Chloe Mirzayi, and Laurie Spacek. Finally, the authors would like to thank the CHEST staff, particularly

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