Receipt of opioid agonist treatment halves the risk of HIV-1 RNA viral load rebound through improved ART adherence for HIV-infected women who use illicit drugs
•Most studies aren’t powered to examine risk factors for HIV viral rebound specifically for women.•Longitudinal analyses for a cohort of women living with HIV who use illicit drugs.•Opioid agonist treatment in the past six months halved the hazard of viral rebound.•Recent stimulant use more than dou...
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Published in | Drug and alcohol dependence Vol. 206; p. 107670 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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01.01.2020
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Abstract | •Most studies aren’t powered to examine risk factors for HIV viral rebound specifically for women.•Longitudinal analyses for a cohort of women living with HIV who use illicit drugs.•Opioid agonist treatment in the past six months halved the hazard of viral rebound.•Recent stimulant use more than doubled hazard of viral rebound.
Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound.
We used longitudinal data from 2006 to 2017 to evaluate the impact of sociodemographic, behavioral, social-structural, and clinical factors on the hazard of viral rebound for women enrolled in the ACCESS study, a prospective cohort with systematic VL monitoring. Women were included if they achieved VL suppression (<50 copies/mL) following antiretroviral therapy (ART) initiation and had more than one study interview. Sociodemographic as well as substance use, social-structural, addiction treatment, and HIV clinical factors were evaluated as predictors of viral rebound (VL > 1000 copies/mL). Cox regressions using a recurrent events framework, time-varying covariates, robust standard errors, and a frailty component were used.
Of the 185 women included, 62 (34%) experienced at least one viral rebound event over an 11-year period, accumulating a total of 87 viral rebound events. In adjusted analysis, stimulant use more than doubled the hazard of viral rebound (adjusted hazard ratio [AHR]: 2.35, 95% confidence interval [CI]: 1.07–5.14) while the only factor protective against viral rebound was receipt of opioid agonist treatment (OAT) in the past six months (AHR: 0.46, 95% CI: 0.26–0.81). After adjusting for ART adherence in the past six months, the effect of OAT was attenuated (AHR: 0.57, 95% CI: 0.32–1.02).
Efforts to improve access to and retention within OAT programs and decrease stimulant use may improve rates of viral suppression for HIV-positive women who use illicit drugs. |
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AbstractList | Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound.BACKGROUNDWomen living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound.We used longitudinal data from 2006 to 2017 to evaluate the impact of sociodemographic, behavioral, social-structural, and clinical factors on the hazard of viral rebound for women enrolled in the ACCESS study, a prospective cohort with systematic VL monitoring. Women were included if they achieved VL suppression (<50 copies/mL) following antiretroviral therapy (ART) initiation and had more than one study interview. Sociodemographic as well as substance use, social-structural, addiction treatment, and HIV clinical factors were evaluated as predictors of viral rebound (VL > 1000 copies/mL). Cox regressions using a recurrent events framework, time-varying covariates, robust standard errors, and a frailty component were used.METHODSWe used longitudinal data from 2006 to 2017 to evaluate the impact of sociodemographic, behavioral, social-structural, and clinical factors on the hazard of viral rebound for women enrolled in the ACCESS study, a prospective cohort with systematic VL monitoring. Women were included if they achieved VL suppression (<50 copies/mL) following antiretroviral therapy (ART) initiation and had more than one study interview. Sociodemographic as well as substance use, social-structural, addiction treatment, and HIV clinical factors were evaluated as predictors of viral rebound (VL > 1000 copies/mL). Cox regressions using a recurrent events framework, time-varying covariates, robust standard errors, and a frailty component were used.Of the 185 women included, 62 (34%) experienced at least one viral rebound event over an 11-year period, accumulating a total of 87 viral rebound events. In adjusted analysis, stimulant use more than doubled the hazard of viral rebound (adjusted hazard ratio [AHR]: 2.35, 95% confidence interval [CI]: 1.07-5.14) while the only factor protective against viral rebound was receipt of opioid agonist treatment (OAT) in the past six months (AHR: 0.46, 95% CI: 0.26-0.81). After adjusting for ART adherence in the past six months, the effect of OAT was attenuated (AHR: 0.57, 95% CI: 0.32-1.02).RESULTSOf the 185 women included, 62 (34%) experienced at least one viral rebound event over an 11-year period, accumulating a total of 87 viral rebound events. In adjusted analysis, stimulant use more than doubled the hazard of viral rebound (adjusted hazard ratio [AHR]: 2.35, 95% confidence interval [CI]: 1.07-5.14) while the only factor protective against viral rebound was receipt of opioid agonist treatment (OAT) in the past six months (AHR: 0.46, 95% CI: 0.26-0.81). After adjusting for ART adherence in the past six months, the effect of OAT was attenuated (AHR: 0.57, 95% CI: 0.32-1.02).Efforts to improve access to and retention within OAT programs and decrease stimulant use may improve rates of viral suppression for HIV-positive women who use illicit drugs.CONCLUSIONSEfforts to improve access to and retention within OAT programs and decrease stimulant use may improve rates of viral suppression for HIV-positive women who use illicit drugs. •Most studies aren’t powered to examine risk factors for HIV viral rebound specifically for women.•Longitudinal analyses for a cohort of women living with HIV who use illicit drugs.•Opioid agonist treatment in the past six months halved the hazard of viral rebound.•Recent stimulant use more than doubled hazard of viral rebound. Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound. We used longitudinal data from 2006 to 2017 to evaluate the impact of sociodemographic, behavioral, social-structural, and clinical factors on the hazard of viral rebound for women enrolled in the ACCESS study, a prospective cohort with systematic VL monitoring. Women were included if they achieved VL suppression (<50 copies/mL) following antiretroviral therapy (ART) initiation and had more than one study interview. Sociodemographic as well as substance use, social-structural, addiction treatment, and HIV clinical factors were evaluated as predictors of viral rebound (VL > 1000 copies/mL). Cox regressions using a recurrent events framework, time-varying covariates, robust standard errors, and a frailty component were used. Of the 185 women included, 62 (34%) experienced at least one viral rebound event over an 11-year period, accumulating a total of 87 viral rebound events. In adjusted analysis, stimulant use more than doubled the hazard of viral rebound (adjusted hazard ratio [AHR]: 2.35, 95% confidence interval [CI]: 1.07–5.14) while the only factor protective against viral rebound was receipt of opioid agonist treatment (OAT) in the past six months (AHR: 0.46, 95% CI: 0.26–0.81). After adjusting for ART adherence in the past six months, the effect of OAT was attenuated (AHR: 0.57, 95% CI: 0.32–1.02). Efforts to improve access to and retention within OAT programs and decrease stimulant use may improve rates of viral suppression for HIV-positive women who use illicit drugs. Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound. We used longitudinal data from 2006 to 2017 to evaluate the impact of sociodemographic, behavioral, social-structural, and clinical factors on the hazard of viral rebound for women enrolled in the ACCESS study, a prospective cohort with systematic VL monitoring. Women were included if they achieved VL suppression (<50 copies/mL) following antiretroviral therapy (ART) initiation and had more than one study interview. Sociodemographic as well as substance use, social-structural, addiction treatment, and HIV clinical factors were evaluated as predictors of viral rebound (VL > 1000 copies/mL). Cox regressions using a recurrent events framework, time-varying covariates, robust standard errors, and a frailty component were used. Of the 185 women included, 62 (34%) experienced at least one viral rebound event over an 11-year period, accumulating a total of 87 viral rebound events. In adjusted analysis, stimulant use more than doubled the hazard of viral rebound (adjusted hazard ratio [AHR]: 2.35, 95% confidence interval [CI]: 1.07-5.14) while the only factor protective against viral rebound was receipt of opioid agonist treatment (OAT) in the past six months (AHR: 0.46, 95% CI: 0.26-0.81). After adjusting for ART adherence in the past six months, the effect of OAT was attenuated (AHR: 0.57, 95% CI: 0.32-1.02). Efforts to improve access to and retention within OAT programs and decrease stimulant use may improve rates of viral suppression for HIV-positive women who use illicit drugs. Background: Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound. Methods: We used longitudinal data from 2006 to 2017 to evaluate the impact of sociodemographic, behavioral, social-structural, and clinical factors on the hazard of viral rebound for women enrolled in the ACCESS study, a prospective cohort with systematic VL monitoring. Women were included if they achieved VL suppression (<50 copies/mL) following antiretroviral therapy (ART) initiation and had more than one study interview. Sociodemographic as well as substance use, social-structural, addiction treatment, and HIV clinical factors were evaluated as predictors of viral rebound (VL > 1000 copies/mL). Cox regressions using a recurrent events framework, time-varying covariates, robust standard errors, and a frailty component were used. Results: Of the 185 women included, 62 (34%) experienced at least one viral rebound event over an 11-year period, accumulating a total of 87 viral rebound events. In adjusted analysis, stimulant use more than doubled the hazard of viral rebound (adjusted hazard ratio [AHR]: 2.35, 95% confidence interval [CI]: 1.07–5.14) while the only factor protective against viral rebound was receipt of opioid agonist treatment (OAT) in the past six months (AHR: 0.46, 95% CI: 0.26–0.81). After adjusting for ART adherence in the past six months, the effect of OAT was attenuated (AHR: 0.57, 95% CI: 0.32–1.02). Conclusions: Efforts to improve access to and retention within OAT programs and decrease stimulant use may improve rates of viral suppression for HIV-positive women who use illicit drugs. |
ArticleNumber | 107670 |
Author | Milloy, M.-J. Mohd Salleh, Nur Afiqah Adams, Joëlla W. Barrios, Rolando Marshall, Brandon D.L. Nolan, Seonaid |
AuthorAffiliation | 2. British Columbia Centre on Substance Use, 400-1045 Howe Street, Vancouver, BC V6Z 2A9, Canada 4. British Columbia Centre for Excellence in HIV/AIDS, 608-1081 Burrad Street, Vancouver, BC V6Z 1Y6, Canada 3. Interdisciplinary Studies Graduate Program, University of British Columbia, 170-6371 Crescent Road, Vancouver, BC V6T 1Z2, Canada 5. Department of Medicine, University of British Columbia, 2775 Laurel Street, 10 th Floor, Vancouver, BC V5Z 1M9, Canada 1. Brown University School of Public Health, Department of Epidemiology, 121 South Main Street, Providence, RI 02903, United States |
AuthorAffiliation_xml | – name: 1. Brown University School of Public Health, Department of Epidemiology, 121 South Main Street, Providence, RI 02903, United States – name: 5. Department of Medicine, University of British Columbia, 2775 Laurel Street, 10 th Floor, Vancouver, BC V5Z 1M9, Canada – name: 4. British Columbia Centre for Excellence in HIV/AIDS, 608-1081 Burrad Street, Vancouver, BC V6Z 1Y6, Canada – name: 3. Interdisciplinary Studies Graduate Program, University of British Columbia, 170-6371 Crescent Road, Vancouver, BC V6T 1Z2, Canada – name: 2. British Columbia Centre on Substance Use, 400-1045 Howe Street, Vancouver, BC V6Z 2A9, Canada |
Author_xml | – sequence: 1 givenname: Joëlla W. surname: Adams fullname: Adams, Joëlla W. organization: Brown University School of Public Health, Department of Epidemiology, 121 South Main Street, Providence, RI 02903, United States – sequence: 2 givenname: Brandon D.L. orcidid: 0000-0002-0134-7052 surname: Marshall fullname: Marshall, Brandon D.L. organization: Brown University School of Public Health, Department of Epidemiology, 121 South Main Street, Providence, RI 02903, United States – sequence: 3 givenname: Nur Afiqah surname: Mohd Salleh fullname: Mohd Salleh, Nur Afiqah organization: British Columbia Centre on Substance Use, 400-1045 Howe Street, Vancouver, BC V6Z 2A9, Canada – sequence: 4 givenname: Rolando surname: Barrios fullname: Barrios, Rolando organization: British Columbia Centre for Excellence in HIV/AIDS, 608-1081 Burrad Street, Vancouver, BC V6Z 1Y6, Canada – sequence: 5 givenname: Seonaid surname: Nolan fullname: Nolan, Seonaid organization: British Columbia Centre on Substance Use, 400-1045 Howe Street, Vancouver, BC V6Z 2A9, Canada – sequence: 6 givenname: M.-J. orcidid: 0000-0003-3821-6221 surname: Milloy fullname: Milloy, M.-J. email: bccsu-mjsm@bccsu.ubc.ca organization: British Columbia Centre on Substance Use, 400-1045 Howe Street, Vancouver, BC V6Z 2A9, Canada |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31711873$$D View this record in MEDLINE/PubMed |
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Keywords | Women HIV-1 Medication assisted treatment of opioid use disorder Illicit drugs Opioid-related disorders |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Contributors. JWA, MJM, and BDLM conceptualized this specific analysis. JWA performed the formal analysis with guidance of MJM and BDLM. JWA wrote the resulting manuscript while MJM, BDLM, NA.MS, SN, and RB provided feedback and edits. All authors reviewed and approved submission. |
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Snippet | •Most studies aren’t powered to examine risk factors for HIV viral rebound specifically for women.•Longitudinal analyses for a cohort of women living with HIV... Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound. We used longitudinal data from 2006 to 2017 to... Background: Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound. Methods: We used longitudinal data... Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound.BACKGROUNDWomen living with HIV who use illicit... |
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SubjectTerms | Addictions Adult Agonists Analgesics, Opioid - therapeutic use Antiretroviral agents Antiretroviral drugs Antiretroviral therapy Antiretroviral Therapy, Highly Active - psychology Cohort Studies Confidence intervals Drug abuse Drugs Female Health risks HIV HIV Infections - complications HIV Infections - drug therapy HIV Infections - psychology HIV-1 HIV-1 - genetics Human immunodeficiency virus Humans Illicit drugs Illicit Drugs - adverse effects Male Medical treatment Medication Adherence - psychology Medication assisted treatment of opioid use disorder Middle Aged Narcotics Opioid-related disorders Opioids Patient compliance Prospective Studies Protective Agents - therapeutic use Recurrent Recurrent events Regression analysis Ribonucleic acid RNA Robustness (mathematics) Sociodemographics Substance abuse Substance use Substance-Related Disorders - complications Substance-Related Disorders - drug therapy Viral Load - drug effects Women |
Title | Receipt of opioid agonist treatment halves the risk of HIV-1 RNA viral load rebound through improved ART adherence for HIV-infected women who use illicit drugs |
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