Trends in use of genotypic resistance testing and frequency of major drug resistance among antiretroviral-naive persons in the HIV Outpatient Study, 1999–2011
Author:
Buchacz Kate1, Young Benjamin23, Palella Frank J.4, Armon Carl5, Brooks John T.1, Buchacz Kate, Brooks John T., Durham Marcus D., Hays Harlen, Wood Kathleen C., Hankerson Darlene, Hart Rachel, Subramanian Thilakavathy, Armon Carl, Dean Bonnie, Franklin Dana, Palella Frank J., Chmiel Joan S., Jahangir Saira, Flaherty Conor Daniel, Dixon-Evans Jerian Denise, Lichtenstein Kenneth A., Stewart Cheryl, Hammer John, Greenberg Kenneth S., Widick Barbara, Franklin Rosa, Yangco Bienvenido G., Chagaris Kalliope, Ward Doug, Fuhrer Jack, Ording-Bauer Linda, Kelly Rita, Esteves Jane, Tedaldi Ellen M., Christian Ramona A., Ruley Faye, Beadle Dania, Graham Princess, Novak Richard M., Wendrow Andrea, Smith Renata, Young Benjamin, Widick Barbara, Scott Mia,
Affiliation:
1. 1 Division of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA 2. 2 APEX Family Medicine, Denver, CO, USA 3. 3 International Association of Providers of AIDS Care, Washington, DC, USA 4. 4 Northwestern University, Chicago, IL, USA 5. 5 Cerner Corporation, Vienna, VA, USA
Abstract
Abstract
Background
Monitoring antiretroviral drug resistance can inform treatment recommendations; however, there are few such data from US patients before they initiate ART.
Methods
We analysed data from HIV Outpatient Study (HOPS) participants from nine US HIV clinics who were diagnosed with HIV infection during 1999–2011. Using the IAS-USA December 2010 guidelines, we assessed the frequency of major drug resistance mutations (mDRMs) related to antiretroviral agents in viral isolates from patients who underwent commercial genotypic testing (GT) for resistance before initiating ART. We employed general linear regression models to assess factors associated with having undergone GT, and then factors associated with having mDRM.
Results
Among 1531 eligible patients, 758 (49.5%) underwent GT before first ART, increasing from 15.5% in 1999–2002 to 75.9% in 2009–11 (P < 0.001). GT was carried out a median of 1.2 months after the diagnosis of HIV. In adjusted regression analyses, patients with pre-ART CD4+ T lymphocyte counts ≥200 cells/mm3 or with HIV RNA levels >5.0 log10 copies/mL and those with a first HOPS visit in 2006 or later were significantly (P < 0.05) more likely to have undergone GT. Of the 758 patients, 114 (15.0%) had mDRMs; mutations relating to NRTIs, NNRTIs and PIs were present in 8.0%, 7.1% and 2.6%, respectively. There was no temporal change in the frequency of mDRM, and mDRMs were associated with an HIV RNA level <4.0 log10 copies/mL.
Conclusions
During 1999–2011, GT use among antiretroviral-naive patients became more common, but a quarter of patients in recent years remained untested. The frequency of mDRMs remained stable over time at about 15%.
Funder
US Centers for Disease Control and Prevention
Publisher
Oxford University Press (OUP)
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)
Cited by
15 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|