Tenofovir disoproxil fumarate and coronavirus disease 2019 outcomes in men with HIV

被引:19
|
作者
Li, Guilin [1 ,2 ]
Park, Lesley S. [3 ]
Lodi, Sara [1 ,4 ]
Logan, Roger W. [1 ,2 ]
Cartwright, Emily J. [5 ,6 ]
Aoun-Barakat, Lydia [7 ]
Casas, Juan P. [8 ,9 ,10 ]
Dickerman, Barbra A. [1 ,2 ]
Rentsch, Christopher T. [11 ,12 ,13 ]
Justice, Amy C. [12 ,14 ,15 ]
Hernan, Miguel A. [1 ,2 ,16 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, CAUSALab, Boston, MA USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[3] Stanford Univ, Sch Med, Stanford Ctr Populat Hlth Sci, Palo Alto, CA 94304 USA
[4] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[5] Emory Univ, Dept Med, Div Infect Dis, Atlanta, GA 30322 USA
[6] Atlanta VA Med Ctr, North Druid Hills, GA USA
[7] Yale Sch Med, Dept Internal Med, Sect Infect Dis, New Haven, CT USA
[8] VA Boston Healthcare Syst, Massachusetts Vet Epidemiol Res & Informat Ctr Ma, Boston, MA USA
[9] Brigham & Womens Hosp, Dept Med, Div Aging, 75 Francis St, Boston, MA 02115 USA
[10] Harvard Med Sch, Dept Med, Boston, MA 02115 USA
[11] Yale Sch Med, Dept Internal Med, New Haven, CT USA
[12] US Dept Vet Affairs, VA Connecticut Healthcare Syst, Washington, DC USA
[13] London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, London, England
[14] Yale Sch Med, Dept Med, New Haven, CT USA
[15] Yale Sch Publ Hlth, Div Hlth Policy & Management, New Haven, CT USA
[16] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
基金
美国国家卫生研究院;
关键词
antiretroviral therapy; coronavirus disease 2019; HIV; severe acute respiratory syndrome coronavirus 2; tenofovir; COHORT; RISK;
D O I
10.1097/QAD.0000000000003314
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To compare the risk of coronavirus disease 2019 (COVID-19) outcomes by antiretroviral therapy (ART) regimens among men with HIV. Design: We included men with HIV on ART in the Veterans Aging Cohort Study who, between February 2020 and October 2021, were 18 years or older and had adequate virological control, CD4(+) cell count, and HIV viral load measured in the previous 12 months, and no previous COVID-19 diagnosis or vaccination. Methods: We compared the adjusted risks of documented severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, COVID-19-related hospitalization, and intensive care unit (ICU) admission by baseline ART regimen: tenofovir alafenamide (TAF)/emtricitabine (FTC), tenofovir disoproxil fumarate (TDF)/FTC, abacavir (ABC)/lamivudine (3TC), and other. We fit pooled logistic regressions to estimate the 18-month risks standardized by demographic and clinical factors. Results: Among 20 494 eligible individuals, the baseline characteristics were similar across regimens, except that TDF/FTC and TAF/FTC had lower prevalences of chronic kidney disease and estimated glomerular filtration rate <60 ml/min. Compared with TAF/FTC, the estimated 18-month risk ratio (95% confidence interval) of documented SARS-CoV-2 infection was 0.65 (0.43, 0.89) for TDF/FTC, 1.00 (0.85, 1.18) for ABC/3TC, and 0.87 (0.70, 1.04) for others. The corresponding risk ratios for COVID-19 hospitalization were 0.43 (0.07, 0.87), 1.09 (0.79, 1.48), and 1.21 (0.88, 1.62). The risk of COVID-19 ICU admission was lowest for TDF/FTC, but the estimates were imprecise. Conclusion: Our study suggests that, in men living with HIV, TDF/FTC may protect against COVID-19-related events. Randomized trials are needed to investigate the effectiveness of TDF as prophylaxis for, and early treatment of, COVID-19 in the general population.
引用
收藏
页码:1689 / 1696
页数:8
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