Cytomegalovirus viremia as a risk factor for mortality in HIV-associated cryptococcal and tuberculous meningitis

被引:8
|
作者
Skipper, Caleb P. [1 ,2 ]
Hullsiek, Katherine Huppler [3 ]
Cresswell, Fiona V. [2 ,4 ,5 ]
Tadeo, Kiiza K. [2 ]
Okirwoth, Michael [2 ]
Blackstad, Mark [1 ]
Hernandez-Alvarado, Nelmary [1 ]
Fernandez-Alarcon, Claudia [1 ]
Walukaga, Stewart [1 ]
Martyn, Emily [2 ,4 ]
Ellis, Jayne [2 ,4 ]
Ssebambulidde, Kenneth [2 ]
Tugume, Lillian [2 ]
Nuwagira, Edwin [2 ,6 ]
Rhein, Joshua [1 ]
Meya, David B. [1 ,2 ]
Boulware, David R. [1 ]
Schleiss, Mark R. [1 ]
机构
[1] Univ Minnesota, Sch Med, Minneapolis, MN 55455 USA
[2] Makerere Univ, Infect Dis Inst, Kampala, Uganda
[3] Univ Minnesota, Div Biostat, Minneapolis, MN USA
[4] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Clin Res, London, England
[5] Brighton & Sussex Med Sch, Global Hlth & Infect, Brighton, E Sussex, England
[6] Mbarara Univ Sci & Technol, Dept Med, Mbarara, Uganda
基金
美国国家卫生研究院;
关键词
Cytomegalovirus; HIV; CMV; Cryptococcal meningitis; Tuberculous meningitis; INFECTED PATIENTS; ANTIRETROVIRAL THERAPY; DISEASE; SEROPREVALENCE; PREVALENCE; VALGANCICLOVIR; PERSISTENT; RECIPIENTS; RESPONSES; DEATH;
D O I
10.1016/j.ijid.2022.07.035
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: CMV viremia is associated with increased mortality in persons with HIV. We previously demonstrated that CMV viremia was a risk factor for 10-week mortality in antiretroviral therapy (ART)-naive persons with cryptococcal meningitis. We investigated whether similar observations existed over a broader cohort of patients with HIV-associated meningitis at 18 weeks. Methods: We prospectively enrolled Ugandans with cryptococcal or TB meningitis into clinical trials in 2015-2019. We quantified CMV DNA concentrations from stored baseline plasma or serum samples from 340 participants. We compared 18-week survival between those with and without CMV viremia. Results: We included 308 persons with cryptococcal meningitis and 32 with TB meningitis, of whom 121 (36%) had detectable CMV DNA. Baseline CD4(+) T-cell counts (14 vs. 24 cells/mu l; P = 0.07) and antiretroviral exposure (47% vs. 45%; P = 0.68) did not differ between persons with and without CMV viremia. The 18-week mortality was 50% (61/121) in those with CMV viremia versus 34% (74/219) in those without (P = 0.003). Detectable CMV viremia (adjusted hazard ratio [aHR] 1.60; 95% confidence interval [CI] 1.13-2.25; P = 0.008) and greater viral load (aHR 1.22 per log 10 IU/ml increase; 95% CI 1.09-1.35; P <0.001) were positively associated with all-cause mortality through 18 weeks. Conclusion: CMV viremia at baseline was associated with a higher risk of death at 18 weeks among persons with HIV-associated cryptococcal or TB meningitis, and the risk increased as the CMV viral load increased. Further investigation is warranted to determine whether CMV is a modifiable risk contributing to deaths in HIV-associated meningitis or is a biomarker of immune dysfunction. (c) 2022 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:785 / 792
页数:8
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