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Identifying Opportunities to Intervene in Reducing Risk of Sexual Transmission of Antiretroviral Drug Resistance among HIV-Infected Patients in Care Heidi M. Soeters , Christopher B. Hurt , Sonia Napravnik 1 2 1,2,3 , Oksana M. Zakharova , Joseph J. Eron, Jr. 2,3 2,3 Department of Epidemiology, 2Division of Infectious Diseases, and 3Center for AIDS Research University of North Carolina at Chapel Hill, Chapel Hill, NC USA 1 INTRODUCTION METHODS •Primary acquisition of drug-resistant HIV, called transmitted drug resistance (TDR), is detected in 10-15% of newly diagnosed individuals in the United States1-2 and Europe.3-4 •A subject was included if s/he was a participant in the UCHCC and had completed a comprehensive, standardized, face-to-face interview exploring HIV-related behaviors. •“Donors” for TDR may have been infected with drug-resistant HIV themselves,5 or have acquired drug resistance through suboptimal adherence to antiretroviral (ARV) therapy.6 •Clinical variables were obtained from medical records, and demographic and behavioral data were obtained from the in-person interview. •Patients who engage in ongoing risk behavior following their HIV diagnosis tend to be less adherent to prescribed ARV regimens,7-8 providing a pathway for TDR to occur. •Risk of TDR was defined as having unprotected sex in the 6 months prior to interview, HIV RNA ≥400 copies/mL, and ≥1 surveillance drug resistance mutation (SDRM).10 •We sought to characterize opportunities for TDR using cross-sectional clinical and behavioral data from the UNC CFAR HIV Clinical Cohort Study (UCHCC).9 •Multivariable log-linear binomial regression was used to identify predictors of TDR risk. 8.3 years 6.7 years RESULTS 595 Interviews included in analyses, by year 482 21% 100 Interviews included in analyses 2000 2005 2010 Median CD4 count at interview (cells/µL) Dual-class n=61 24% 10% NRTI & NNRTI n=33 (54%) NRTI & PI n=25 (41%) NNRTI & PI n=3 (5%) 478 None n=129 38% 62% 100% 38% No n=204 19% 0 n=194 <400 27% 58% 68% 42% Yes 40% Zero One ≥2 68% 24% One 2 to 4 Sexual Activity 8% Condom Use HIV RNA* ARV Resistance† n=353 n=239 Heterosexual n=180 1500- >10,000 10,000 Risks for transmitting resistant HIV among 244 interviewees with genotyping Number of partners MSM 4001499 0 Unprotected sex n=298 60% 50% 20% Yes Men Missed ARV doses in prior 4 days 60% Sexual activity in prior six months Women Range, 9-1998 Interquartile range, 256-704 HIV RNA (copies/mL) at time of interview Range, 19-82 Interquartile range, 38-50 Gender & sexual orientation n=118 n=85 n=290 78% 60% Non-White 40% n=377 Yes (n=30, 12%) No (n=14, 6%) Inconsistent (n=94, 39%) Yes (n=23, 9%) Undetectable (n=50, 20%) ≥1 partner (n=172, 70%) No (n=27, 11%) Yes (n=13, 5%) Detectable (n=27, 11%) No (n=14, 6%) Always (n=78, 32%) Yes (n=30, 12%) Undetectable (n=51, 21%) Yes, using Other 90% No (n=22, 9%) Detectable (n=44, 18%) Cannabis n=107 Crack n=96 Alcohol n=50 Cocaine n=27 Opiates n=14 Other n=12 Injection n=3 None Yes (n=22, 9%) Undetectable (n=44, 18%) Active substance use 22% No (n=15, 6%) No partners (n=72, 30%) More than 4 Race & ethnicity Yes (n=13, 5%) Detectable (n=28, 11%) n=29 n=339 47% of interviewees were ARV-naïve 40% Black 18% 0 43 n=105 NRTI n=28 (61%) NNRTI n=15 (33%) PI n=3 (7%) Triple-class n=26 Interviewees had genotypic resistance tests White n=117 7% of interviewees had a history of AIDS (n=101) Single-class n=46 50 250 n=184 No SDRMs Median time since first ARV regimen initiated 150 Face-to-face interviews between 2000-2011 Median age Median time from HIV diagnosis to interview Surveillance drug resistance mutations n=192 No (n=21, 9%) n=16 (4.2%) Hispanic n=7 (1.9%) Native American * The cutoff for “detectable” RNA was defined as ≥400 copies/mL. † Resistance was defined as having ≥1 surveillance drug resistance mutation (SDRM) from the 2009 WHO list.10 n=15 (4%) Bivariate and multivariate associations between demographic and clinical characteristics and having a high risk for transmitting drug-resistant HIV Race Education (Black = referent) Male Prevalence Ratio 1.95 Age (10Y) 1.00 White 1.05 Other 0.37 Years since HIV diagnosis (High school grad = referent) MSM 1.89 Substance Use† Depression * 1.42 3.86 Some College 2.03 (3-10 years = referent) College or Homeless- History of Less than Higher ness‡ AIDS 3 years 0.63 2.82 1.50 0.20 11-15 years 1.54 16 years or more 0.57 Adjusted Prevalence Ratios MSM 1.75 Substance HomelessUse ness 3.12 2.20 10 1 0.1 0.01 * Depression was defined as any diagnosis of depression in subject’s medical record prior to interview. † Substance use was defined as drinking alcohol ≥4 days per week, or regular consumption of any illicit substances in the year prior to interview. ‡ Homeless at any time since HIV diagnosis. LIMITATIONS CONCLUSIONS •Cohort members who participated in the interview represent a subset of the overall clinic population. Generalizability to other clinical settings may be limited. •A small but significant proportion (12%) of patients in the cohort are at risk of transmitting drug-resistant HIV to sexual partners. •Social desirability bias may have influenced subjects’ responses during the face-to-face interview, which would tend to underestimate risk behaviors. •Active substance use, a history of homelessness since HIV diagnosis, and being a man who has sex with men had the strongest associations with risk of transmitting drugresistant virus to sexual partners. •We did not quantitate the number of sexual encounters per partner, only the number of partners. Low average per-encounter risk may be compounded with regular partner(s). REFERENCES •Improved efforts in secondary prevention may have an impact on TDR prevalence. ACKNOWLEDGMENTS 1 Wheeler, et al. AIDS 2010;24(8):1203 6 Bangsberg, et al. Curr HIV/AIDS Rep 2007;4(2):65 2 Ross, et al. HIV Clin Trials 2007;8(1):1 7 Kozal, et al. AIDS 2004;18(16):2185 3 Wensing, et al. J Infect Dis 2005;192(6):958 8 Kalichman. Psychosom Med 2008;70(5):593 4 Masquelier, et al. JAIDS 2005;40(5):505 9 Howe, et al. AIDS Res Hum Retrov 2010;26(8):875 5 Brenner, et al. AIDS 2008;22(18):2509 10 Bennett, et al. PLoS ONE 2009;4(3):e4724 The authors thank Liz Yanik, Sam Stinnette, Brant Stalzer, and Luca Vernazza for their assistance. Funding for this project was provided by the Social and Behavioral Science Research Core of the University of North Carolina Center for AIDS Research (CFAR). HMS (2 T32 AI070114 06), CBH (8 KL2 TR000084 05), SN (5 R01 HS018731 03), and JJE (2 P30 AI50410 14) are supported by funding from the National Institutes of Health. XIX INTERNATIONAL AIDS CONFERENCE – JULY 22-27, 2012 – WASHINGTON DC