Abstract
Biomarker composites (BCs) that objectively quantify psychosocial stress independent of self report could help to identify
those at greatest risk for negative health outcomes and elucidate mechanisms of stress-related processes. Here, BCs are examined
in the context of existing disease progression among HIV-positive African American men who have sex with men and women (MSMW)
with high stress histories, including childhood sexual abuse. Participants (N = 99) collected 12-h overnight and morning urine samples for assay of cortisol and catecholamines (primary BC) and neopterin
(an indicator of HIV disease progression). Data on cumulative psychosocial trauma history (severity, types, frequency, age
at first incident), posttraumatic stress disorder (PTSD) symptoms, sexual risk behaviors, and a secondary BC consisting of
routine health indicators (heart rate, blood pressure, body mass index, waist-to-hip ratio) were also collected. Lifetime
trauma exposure was highly pervasive and significantly greater among those meeting a standard cutoff for PTSD caseness (24 %).
After controlling for HIV factors (neopterin levels and years with disease), PTSD was a significant (p < .05) predictor of the primary, but not secondary BC. Those with PTSD also had significantly more sexual partners, sex without
a condom, and exchange sex for money or drugs than those without PTSD. Specific trauma characteristics predicted PTSD severity
and caseness independently and uniquely in regression models (p’s < .05–.001). A primary BC appears sensitive to cumulative trauma burden and PTSD in HIV-positive African American MSMW,
providing support for the use of BCs to quantify psychosocial stress and inform novel methods for examining mechanisms of
stress influenced health behaviors and disease outcomes in at-risk populations.
those at greatest risk for negative health outcomes and elucidate mechanisms of stress-related processes. Here, BCs are examined
in the context of existing disease progression among HIV-positive African American men who have sex with men and women (MSMW)
with high stress histories, including childhood sexual abuse. Participants (N = 99) collected 12-h overnight and morning urine samples for assay of cortisol and catecholamines (primary BC) and neopterin
(an indicator of HIV disease progression). Data on cumulative psychosocial trauma history (severity, types, frequency, age
at first incident), posttraumatic stress disorder (PTSD) symptoms, sexual risk behaviors, and a secondary BC consisting of
routine health indicators (heart rate, blood pressure, body mass index, waist-to-hip ratio) were also collected. Lifetime
trauma exposure was highly pervasive and significantly greater among those meeting a standard cutoff for PTSD caseness (24 %).
After controlling for HIV factors (neopterin levels and years with disease), PTSD was a significant (p < .05) predictor of the primary, but not secondary BC. Those with PTSD also had significantly more sexual partners, sex without
a condom, and exchange sex for money or drugs than those without PTSD. Specific trauma characteristics predicted PTSD severity
and caseness independently and uniquely in regression models (p’s < .05–.001). A primary BC appears sensitive to cumulative trauma burden and PTSD in HIV-positive African American MSMW,
providing support for the use of BCs to quantify psychosocial stress and inform novel methods for examining mechanisms of
stress influenced health behaviors and disease outcomes in at-risk populations.
- Content Type Journal Article
- Pages 1-12
- DOI 10.1007/s10865-012-9421-5
- Authors
- Dorie A. Glover, Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, 760 Westwood Plaza, 68-237 NPI, Los Angeles, CA 90024-1759, USA
- John K. Williams, Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, 760 Westwood Plaza, 28-259 NPI, Los Angeles, CA 90024-1759, USA
- Kimberly A. Kisler, Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, 760 Westwood Plaza, 28-259 NPI, Los Angeles, CA 90024-1759, USA
- Journal Journal of Behavioral Medicine
- Online ISSN 1573-3521
- Print ISSN 0160-7715