Effect of age and HAART regimen on clinical response in an urban cohort of HIV-infected individuals

dc.contributor.authorGreenbaum, Adena H
dc.contributor.authorWilson, Lucy E
dc.contributor.authorKeruly, Jeanne C
dc.contributor.authorMoore, Richard D
dc.contributor.authorGebo, Kelly A
dc.date.accessioned2023-08-04T18:55:19Z
dc.date.available2023-08-04T18:55:19Z
dc.date.issued2008-08-03
dc.description.abstractObjectives: The prevalence of HIV infection in older patients (≥50 years) is increasing due to HAART, and new HIV infections in older patients. Some earlier studies suggest that older patients respond differently to HAART than younger patients. The objective of this study is to compare the effectiveness of HAART in older and younger HIV patients. Design: Retrospective analysis of an observational clinical cohort. Methods: Virologic and immunologic response, progression to AIDS and mortality were compared between 670 younger patients (<40 years) and 149 older patients (≥50 years) by t-test, Kaplan–Meier methods, and multivariate Cox proportional hazards analysis. Results: Compared with younger patients, older patients were more likely to be on nonnucleoside reverse transcriptase inhibitors based versus protease inhibitor based regimens (42 vs. 29%, P < 0.01). Time to HIV-1 RNA virologic suppression was less in older than in younger patients (3.2 vs. 4.4 months, P < 0.01). Immunologic response did not differ by age. Older patients had fewer AIDS-defining opportunistic infections (22 vs. 31%, P < 0.01), but higher mortality (36 vs. 27%, P = 0.04) and shorter survival (25th percentile survivor function 36.2 vs. 58.5 months, P = 0.02) than younger patients. Older age was associated with more rapid virologic suppression [adjusted hazard ratio = 1.33 (1.09–1.63)] and earlier mortality [adjusted hazard ratio = 1.56 (1.14–2.14)]. Nonnucleoside reverse transcriptase inhibitors based regimens were associated with more rapid virologic suppression [adjusted hazard ratio = 1.22 (1.03–1.44)]. Conclusion: Time to virologic suppression after HAART initiation was shorter in older patients, although CD4 response did not differ by age. Older patients had fewer opportunistic infections, but survival was shorter. Our data suggest a need to better understand causes of mortality in older patients.en_US
dc.description.sponsorshipSupported by the National Institutes of Aging (R01 AG026250) and Drug Abuse, NIH (K23-DA00523, K24-DA00432, and R01-DA-11602). Dr Gebo also received support from the Johns Hopkins University Richard S. Ross Clinician Scientist Award. Dr Greenbaum received support from the Johns Hopkins Medical Student Research Fund and T32 Predoctoral Clinical Research Training Program.en_US
dc.description.urihttps://journals.lww.com/aidsonline/Fulltext/2008/11120/Effect_of_age_and_HAART_regimen_on_clinical.12.aspxen_US
dc.genrejournal articlesen_US
dc.identifierdoi:10.13016/m2mkxv-jn60
dc.identifier.citationGreenbaum, Adena H; Wilson, Lucy E; Keruly, Jeanne C; Moore, Richard D; Gebo, Kelly A. Effect of age and HAART regimen on clinical response in an urban cohort of HIV-infected individuals. AIDS 22(17):p 2331-2339, November 12, 2008. DOI: 10.1097/QAD.0b013e32831883f9en_US
dc.identifier.urihttps://doi.org/10.1097/QAD.0b013e32831883f9
dc.identifier.urihttp://hdl.handle.net/11603/29089
dc.language.isoen_USen_US
dc.publisherWolters Kluweren_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Emergency Health Services Department Collection
dc.relation.ispartofA. All Hilltop Institute (UMBC) Works
dc.relation.ispartofUMBC School of Public Policy
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.en_US
dc.subjectagingen_US
dc.subjectCD4en_US
dc.subjectHAARTen_US
dc.subjectHIV/AIDSen_US
dc.subjectHIV-1 RNAen_US
dc.titleEffect of age and HAART regimen on clinical response in an urban cohort of HIV-infected individualsen_US
dc.typeTexten_US

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