Association of antiretroviral therapy with brain aging changes among HIV-infected adults

被引:0
|
作者
Soontornniyomkij, Virawudh [1 ,2 ]
Umlauf, Anya [1 ]
Soontornniyomkij, Benchawanna [2 ]
Gouaux, Ben [1 ]
Ellis, Ronald J. [1 ,3 ]
Levine, Andrew J. [4 ]
Moore, David J. [1 ,2 ]
Letendre, Scott L. [1 ,5 ]
机构
[1] Univ Calif San Diego, Sch Med, HIV Neurobehav Res Program, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Dept Psychiat, 9500 Gillman Dr, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sch Med, Dept Neurosci, La Jolla, CA 92093 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[5] Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
关键词
amyloidosis; gliosis; neurodegeneration; neuroinflammation; tauopathy; PROTEASE INHIBITOR RITONAVIR; ENDOTHELIAL DYSFUNCTION; DISEASE; BETA; NEUROPATHOLOGY; MECHANISMS; DEPOSITION; EFAVIRENZ; CELLS; METHAMPHETAMINE;
D O I
10.1097/QAD.0000000000001927
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: Antiretroviral therapy (ART) is currently recommended for all persons living with HIV (PLWH), regardless of their CD4(+) T-cell count, and should be continued throughout life. Nonetheless, vigilance of the safety of ART, including its neurotoxicity, must continue. We hypothesized that use of certain ART drugs might be associated with aging-related cerebral degenerative changes among PLWH. Design: Clinicopathological study of PLWH who were using ART drugs at the last clinical assessment. Methods: Using multivariable logistic regression, we tested associations between use of each specific ART drug (with reference to use of other ART drugs) and cerebral degenerative changes including neuronal phospho-tau lesions, beta-amyloid plaque deposition, microgliosis, and astrogliosis in the frontal cortex and putamen (immunohistochemistry), as well as cerebral small vessel disease (CSVD) in the forebrain white matter (standard histopathology), with relevant covariates being taken into account. The Bonferroni adjustment was applied. Results: Darunavir use was associated with higher likelihood of neuronal phospho-tau lesions in the putamen [odds ratio (OR) 15.33, n = 93, P = 0.005]. Ritonavir use was associated with marked microgliosis in the putamen (OR 4.96, n = 101, P = 0.023). On the other hand, use of tenofovir disoproxil fumarate was associated with lower likelihood of beta-amyloid plaque deposition in the frontal cortex (OR 0.13, n = 102, P = 0.012). There was a trend toward an association between emtricitabine use and CSVD (OR 13.64, n = 75, P = 0.099). Conclusion: Our findings suggest that PLWH treated with darunavir and ritonavir may be at increased risk of aging-related cerebral degenerative changes. Copyright (C) 2018 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:2005 / 2015
页数:11
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