Background
Experiences of HIV stigma and discrimination remain high in Canada, causing significant stress and negatively affecting the health and wellbeing of people living with HIV [
1]. Despite antiretroviral treatments (ART) that have improved the quality and quantity of life for people living with HIV [
2,
3], HIV-related stigma (HIV stigma) still can create a barrier preventing individuals from accessing healthcare and promoting their own wellness [
4,
5]. Rueda et al., Katz et al., and Chambers et al. have shown through meta-analyses that individuals who experience greater HIV stigma have higher viral loads, worse mental health, poorer quality of life, increased likelihood of alcohol and drug misuse, and have difficulty with treatment adherence and access to healthcare services [
6‐
8]. Increased HIV stigma is also associated with poorer self-rated health [
9,
10], however there is limited research on the mechanisms behind this effect. Understanding this interaction may help to inform the development of targeted intervention strategies aimed at overcoming or helping people manage the burden of HIV stigma on health.
While studies have demonstrated the negative impact of stigma on downstream health outcomes for years [
6‐
8], there is limited understanding regarding which aspects of stigma are linked to health and which interpersonal, psychological, or external factors may moderate or buffer these impacts [
11]. The HIV Stigma Framework was designed to address these issues by breaking down stigma into three distinct dimensions and examining how they may have different impacts on an individual’s health and wellness [
11‐
13]. These dimensions include “enacted stigma” which refers to experiences of discrimination, prejudice, or stereotyping, “internalized stigma” which involves the endorsement of negative thoughts and beliefs surrounding HIV and applying them to the self, and “anticipated stigma” or the expectation that other people will treat you negatively in the future because of your HIV status [
11‐
13]. Each dimension has been associated with various different health outcomes, with enacted stigma often being linked with physical health and heightened stress response [
11,
14,
15], internalized stigma being associated with mental health, poor affective and cognitive functioning, lack of psychological resources, and lower treatment adherence [
11,
13,
16,
17], and anticipated stigma being linked with HIV non-disclosure and increased incidence of having a chronic illness comorbidity [
11,
15,
18]. The conceptualization of internalized stigma as closely linked to, or in some cases synonymous with cognitive and psychological difficulties (e.g. depression) has driven the development of intervention strategies for HIV stigma so far, however these interventions have shown lackluster results [
19,
20]. A secondary function of this study is to examine whether internalized stigma and depression have independent and separate impacts on health.
The HIV Stigma Framework has helped to increase our understanding of stigma and health, however the impact of stigma on an individual’s self-rated health has gone largely uninvestigated. Incorporating self-rated health into the framework facilitates exploration of how living with HIV may impact an individual’s self-concept of health and how this interaction affects their real-life health outcomes. Focusing on self-reported overall health is especially relevant now that increased access to ART has resulted in a shift in focus for HIV research from survival rates to how people living with HIV can thrive.
Self-rated health has been measured in large scale epidemiological studies for decades due to its simplicity and robust ability to predict key health outcomes such as mortality, disability, objective health status, and use of healthcare services [
21‐
24]. It is most commonly assessed using one question that elicits a rating of a participant’s general perception of their health on a poor to excellent response scale [
25]. This makes the use of a subjective global health question an extremely efficient way to glean information about an individual’s health in a clinical or research setting. The predictive ability is generally high across genders, ethnic groups, socioeconomic statuses, and education levels which makes it an ideal outcome measure for the diverse HIV population [
26‐
32].
While objective health evaluation using signs, symptoms, and laboratory tests are the most common ways to quantify disease and their effects on health, subjective self-rated health is beneficial as it can account for the complex interaction of biological, psychological, and social implications of illness, and how these impact an individual’s wellbeing [
33]. The few studies that examine the relationship between HIV stigma and self-rated health show that greater stigma is associated with poorer self-rated health [
9,
10], however they do not explore whether the dimensions of stigma have different impacts on self-rated health or the mechanisms behind these effects.
The present study utilizes data from the Ontario implementation of the People Living with HIV Stigma Index to: (1) identify which dimensions of stigma have significant relationships with self-rated health and (2) examine the mechanisms by which stigma impacts self-rated health. To understand how stigma impacts health, we use a parallel mediation model which establishes pathways between an antecedent and an outcome through two or more mediating variables. Previous studies have demonstrated a link between experienced HIV stigma and internalized stigma as well as possible consequences for depressive symptoms [
15,
34,
35]. Another study has demonstrated that depression mediates the relationship between loneliness and self-rated health [
36]. Building on this knowledge and the HIV Stigma Framework, we hypothesize that enacted and internalized stigma will be significant predictors of self-rated health and that the relationship between enacted stigma and self-rated health is mediated in parallel by both internalized stigma and depression.
Methods
The People Living with HIV Stigma Index is the world’s largest social research project developed by and for people living with HIV to measure nuanced changes in stigma and discrimination [
37]. This global survey tool has been implemented in more than 100 countries and relies heavily on the Greater Involvement of People Living with HIV and AIDS (GIPA) principle [
38]. We utilize data from the Ontario implementation of the HIV Stigma Index which included additional externally validated scales to measure stigma and other health risks. The present analysis primarily uses data from these externally validated scales.
Trained peer research associates (PRAs) living with HIV were hired to recruit 724 people living with HIV and administer the Ontario HIV Stigma Index. Survey participants are a cross-section of people living with HIV from several regions across Ontario and include priority populations such as gay, bisexual, and other men who have sex with men (GBMSM), African/Caribbean/Black (ACB) individuals, women, youth, Aboriginal peoples, injection drug users, and individuals from rural communities. PRAs administered the HIV Stigma Index in their respective regions through face-to-face interviews lasting approximately two hours between September 2018 and August 2019. All adult participants were considered for enrollment if they were (1) HIV-positive, (2) able to adequately communicate in English or French for the duration of the interview process, and (3) willing and able to complete the interview process and provide informed consent. The study was approved by the Research Ethics Board of St. Michael’s Hospital, Unity Health Toronto.
Study participants
Various demographic data about each participant were collected at the beginning of the survey including age, years since HIV diagnosis, gender, sexual orientation, ethnicity, education, and employment status for use as potential covariates. For multivariable analyses, gender was dichotomized into male vs. non-male, sexual orientation into heterosexual vs. non-heterosexual, ethnicity into Caucasian vs. non-Caucasian, education into high school completion or less vs. greater than high school completion, and employment status into employed vs. not employed.
HIV stigma
To measure HIV stigma, we used the 32-item version of the HIV Stigma Scale which measures stigma using four subscales [
39,
40]. The enacted stigma subscale (formerly personalized stigma) examines personal experiences of rejection, the negative self-image subscale deals with feelings of guilt or shame around being HIV positive, the disclosure concerns subscale refers to the need to conceal information regarding one’s HIV status, and the concern with public attitudes subscale measures what a person with HIV believes other people may think of them because of their HIV status [
40]. The disclosure concerns and concern with public attitudes subscales were merged to form a single anticipated stigma subscale and the negative self-image subscale was renamed to internalized stigma to match the HIV Stigma Framework [
11,
41]. Participants were asked to respond to each item using a 4-point Likert scale ranging from “strongly disagree” to “strongly agree”. Factor analysis showed that all items loaded into the same dimensions as described during the development of the scale [
40]. Subscale scores were calculated by taking the mean of all items in the subscale with higher scores indicating greater stigma. Internal consistency was high for subscales with enacted stigma, internalized stigma, and anticipated stigma having Cronbach’s alphas of 0.940, 0.894, and 0.901 respectively.
Depression
We utilized the 9-item Patient Health Questionnaire (PHQ-9) to measure depression. The scale covers the domains of depression as defined in the DSM-IV (which remain the same in the DSM-V) and can provide both a provisional depression diagnosis and a grade of depression symptom severity [
42]. Participants were asked “over the past 2 weeks, how often have you been bothered by any of the following problems” and presented with a list of 9 depressive symptoms to respond to on a 0–3 scale from “not at all” to “nearly every day”. Total depression score was calculated by taking the sum of all items with higher scores indicating greater depression. Scores from 0 to 9 are classified as “none” or “mild” depression and scores from 10 to 27 are classified as “moderate”, “moderately severe”, or “severe” depression [
42]. Factor analysis demonstrated that items on the PHQ-9 loaded on one dimension and internal consistency was strong with a Cronbach’s alpha of 0.852.
Self-rated health
To measure self-rated health, we used the one-item self-report health question: “In general, how would you describe your health at the moment?”. Participants were asked to rate their health on a 1–5 scale from “poor” to “excellent”. This single item measure is often included in other popular validated measures on quality of life including the World Health Organization Quality of Life (WHOQOL) assessment, SF-36, and the QOL10 and allows participants to evaluate their health and life satisfaction as it relates to their own experience [
43‐
46].
Statistical analyses
All statistical analyses were conducted using IBM SPSS Statistics version 24 [
47]. Participants with no data for any demographic variables, depression, stigma, or self-rated health were removed from analyses (
n = 54) leaving a final sample of
N = 676. First, we conducted multiple regression analyses to examine which variables had a significant impact on self-rated health. Variables were entered in blocks to control for certain demographic variables and to examine whether variables of interest had a significant impact on the outcome. Demographic variables were entered first, then depression was added, followed by dimensions of stigma being added separately, and lastly all dimensions of stigma were added together. Results from the multiple regression guided the mediation analysis. The parallel mediation model was created using the PROCESS macro, a regression-based tool designed for conducting mediation, moderation, and conditional process analysis [
48]. The antecedent variable was enacted stigma, the mediating variables were internalized stigma and depression, and the outcome variable was self-rated health. Demographic variables were added as covariates to control for any possible confounding effect. Mediation was deemed significant if the bootstrap 95% confidence interval associated with the indirect effect did not include zero. Analysis of the indirect effect was conducted with 5000 bootstrap samples [
48]. Completely standardized indirect effects were computed to compare the effects of the mediators with each other by removing the scaling of antecedent and outcome variables.
Discussion
This study aims to identify which dimensions of stigma are most connected to an individual’s self-rated health and the mechanisms by which those dimensions impact the health and wellbeing of people living with HIV. Out of the types of stigma, feelings of guilt or shame around living with HIV (internalized stigma) had a significant impact on health. An individual’s mood state (depression) and employment status also had significant impact on health. While enacted stigma was not a significant predictor of health in the multiple regression analysis like we hypothesized, our mediation model demonstrated that there is a relationship between enacted stigma and self-rated health that is mediated in parallel by internalized stigma and depression.
Anticipated stigma did not show any significant relationship with self-rated health despite being highly endorsed. Anticipated stigma may manifest itself more as an external fear that influences social interactions and impacts disclosure behavior or engagement with the healthcare system rather than an individual’s self-rated health [
11‐
13,
15]. This may also indicate that the strength of the predictors which are already significant may overshadow any potential small effect of anticipated stigma.
These findings combine useful conceptualizations of stigma mechanisms from the HIV Stigma Framework [
11,
13] with research demonstrating the ability of self-rated health to translate into important real-life health outcomes [
21‐
24]. By incorporating self-rated health into the framework, we begin to understand how stigma impacts overall health and wellbeing. We found that experiences of stigma can lead to increased internalized stigma (a social process which manifests as a chronic stressor that develops over time) and depression (a low mood state that is evaluated over a shorter period of weeks or months). These are two possible pathways through which enacted stigma impacts health and wellbeing.
Our model suggests that addressing enacted stigma would improve self-rated health (possibly by reducing feelings of guilt, shame, and depression), however a proven intervention has yet to have been developed [
20,
49,
50]. Reducing instances of enacted stigma would likely require a combination of individual, community, and societal changes coupled with regional, national, and international policy changes and implementation strategies [
20,
51]. This is the goal we are all striving toward, but the scope of the work to be done may discourage individual people living with HIV who are struggling with experiences of discrimination, prejudice, or stereotyping on a day-to-day basis. Conceptually, it is difficult for an individual to reduce their own enacted stigma. Our mediation model suggests that addressing internalized stigma and depression may be an effective complement to reduce the impact of stigma on health if we cannot reduce enacted stigma itself.
Internalized stigma has historically been linked with adverse psychological and mental health outcomes, especially depression [
11,
13]. However, conceptualizing internalized stigma as so closely related to depression may discount the full impact it has on health and wellbeing and place the onus on the person feeling the stigma to overcome it. Thus far, intervention strategies for internalized stigma have focused on mental health-related intervention including psycho-education, increasing self-esteem, and personal empowerment, however these have shown suboptimal results [
19,
20]. Despite this conceptual conflation, our multiple regression model shows that both internalized stigma and depression have significant impacts on self-rated health, even when included together in the model. This led us to assess them both as mediators in our mediation model to determine if they provided separate pathways for the effect of enacted stigma on self-rated health. Our parallel mediation model indeed demonstrated that, while they may be related, internalized stigma is a distinct factor from depression. This suggests that there may be different factors that impact internalized stigma and depression even though both may be consequences of enacted stigma and contribute to worse overall health. Our findings shift the conceptualization of internalized stigma away from being synonymous with depression and invite further research to investigate internalized stigma through a social and structural lens in addition to understanding important psychological contributors.
Given the persistently high level of stigma among people living with HIV in Ontario, identifying internalized stigma and depression as major contributing factors could be key in designing interventions for stigma reduction. There are already many proven effective interventions for depression that could reduce the negative impact of experiencing stigma on health [
52‐
54]. Current internalized stigma interventions mostly focus on individual-level factors, however these have shown limited efficacy [
19,
20]. Future research could include the development and evaluation of evidence-based interventions designed to reduce levels of internalized stigma. This includes expanding beyond psychology-based interventions and incorporating social and structural forces that play a large role in internalized stigma [
19]. Developing internal and external resources such as resiliency, self-efficacy, and social support may also be helpful in overcoming the burden of stigma and improve the overall health and wellbeing of people living with HIV.
The findings from this study should be interpreted in light of some limitations. Mediation is ultimately a causal explanation which assumes that the mediator is located causally between the antecedent and the outcome [
48]. The cross-sectional nature of this study means that we cannot make conclusions about the directionality and causal nature of these relationships, however this does not preclude the use of mediation and we conduct these analyses based on previous research and logical relationships between variables. Future longitudinal research must be done to examine whether stigma impacts health in the direction conceptualized here. The study is also limited by how well the sample represents all people living with HIV. While the study team made a concerted effort at recruiting participants from various regions, socioeconomic statuses, and ethnicities to adequately represent people living with HIV in Canada, there will inevitably be gaps, leaving a subset of people living with HIV that are unrepresented in the data. We also do not account for other types of non-HIV stigma such as stigma associated with gender, sexual orientation, and race/ethnicity which have been associated with key health outcomes including depression and low treatment adherence [
55‐
57]. These are sure to be present in such a diverse sample and future research must examine how these intersectional stigmas interact with each other to influence health and wellbeing of people living with HIV. Lastly, while self-rated health has been shown to predict real-life health outcomes [
21‐
24], we did not directly measure these outcomes, so the connection in this study is purely implied. Future work must be done to explore whether the impact of stigma through these pathways can be extended to real-life health outcomes that have been linked with self-rated health in the literature.
Acknowledgements
The study team wishes to acknowledge and thank the people living with HIV who conducted and participated in this study. A special thank you to the Peer Researchers (Antoine, Fred Young, George Da Silva, James Gough, Keith Showers, Lynne Cioppa, Maria M., Michael Murphy, Murray, Monisola Ajiboye, R. K, S. Smith, Wayne Bristow). In addition, the team also wants to recognize the expertise of the Ontario Regional Advisory Committee (Ana Sophia Demetrakopoulos, Apondi Judith Odhiambo, Bridget Hall, Carlisle Robinson, Evana Ortigoza, Jasmine Cotnam, Joanne Lindsay, Joanne Lush, Michelle Sumner-Williams, Molly Bannerman, Muluba Habanyama, Phillip Banks, Rene Boucher, Sean LeBlanc, Ted Geatros, Trevor Stratton).
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