Treatment of Central Nervous System Manifestations of HIV in the Current Era

被引:8
作者
Handoko, Ryan [1 ]
Spudich, Serena [1 ,2 ]
机构
[1] Yale Univ, Dept Neurol, Sch Med, 300 George St Room 8300c, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Ctr Neuroepidemiol & Clin Neurol Res, New Haven, CT 06510 USA
关键词
central nervous system HIV; HIV comorbidities; chronic central nervous system infections; HIV-associated neurocognitive disorder; antiretroviral therapy; ONCE-DAILY DOLUTEGRAVIR; COMBINATION ANTIRETROVIRAL THERAPY; PROTEASE INHIBITOR MONOTHERAPY; CNS PENETRATION-EFFECTIVENESS; DARUNAVIR PLUS RITONAVIR; CEREBROSPINAL-FLUID; INFECTED PATIENTS; NAIVE ADULTS; POSITIVE PATIENTS; OPEN-LABEL;
D O I
10.1055/s-0039-1688915
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Treatment of neurological, neurocognitive, and neuropsychiatric impairment in the setting of human immunodeficiency virus (HIV) infection remains a complex problem, given several possible mechanisms of pathogenesis. The etiology must be determined based on clinical judgment and objective evidence, including cerebrospinal fluid (CSF) data from lumbar puncture and neuroimaging information from magnetic resonance imaging, when available and indicated. Other neuroinfectious etiologies must be ruled out, including central nervous system (CNS) opportunistic infections. HIV replication in the CNS (including CSF escape) should be evaluated for and excluded. If CSF HIV is detected, we recommend a treatment switch to antiretrovirals (ARVs) targeted to address any CSF HIV resistance mutations identified, or empiric treatment intensification using ARVs with high CNS penetration. If CSF HIV is not detected, treatment intensification with CCR5 inhibitors may be considered as an adjunct to reduce neuroinflammation. Finally, the current ARV regimen must be examined for possible neurotoxicity. Efavirenz has been well-recognized for its neuropsychiatric adverse effects and potential for causing sleep disturbances. Similar concerns have recently been raised with integrase inhibitors, especially dolutegravir and raltegravir, although further studies are needed to determine the risks for clinically relevant neuropsychiatric side effects from these medications, given their overall high potency and proven success in treating systemic HIV.
引用
收藏
页码:391 / 398
页数:8
相关论文
共 75 条
[1]   Neurological and Psychiatric Adverse Effects of Antiretroviral Drugs [J].
Abers, Michael S. ;
Shandera, Wayne X. ;
Kass, Joseph S. .
CNS DRUGS, 2014, 28 (02) :131-145
[2]   Week 48 efficacy and central nervous system analysis of darunavir/ritonavir monotherapy versus darunavir/ritonavir with two nucleoside analogues [J].
Antinori, Andrea ;
Clarke, Amanda ;
Svedhem-Johansson, Veronika ;
Arribas, Jose R. ;
Arenas-Pinto, Alejandro ;
Fehr, Jan ;
Gerstoft, Jan ;
Horban, Andrzej ;
Clotet, Bonaventura ;
Ripamonti, Diego ;
Girard, Pierre-Marie ;
Hill, Andrew M. ;
Moecklinghoff, Christiane .
AIDS, 2015, 29 (14) :1811-1820
[3]   Evaluation of cerebrospinal fluid virological escape in patients on long-term protease inhibitor monotherapy [J].
Arenas-Pinto, Alejandro ;
Stohr, Wolfgang ;
Clarke, Amanda ;
Williams, Ian ;
Beeching, Nicholas J. ;
Minton, Jane ;
Lee, Vincent ;
Paton, Nicholas, I .
ANTIVIRAL THERAPY, 2017, 22 (06) :535-538
[4]   Neurocognitive Function and Neuroimaging Markers in Virologically Suppressed HIV-positive Patients Randomized to Ritonavir-boosted Protease Inhibitor Monotherapy or Standard Combination ART: A Cross-sectional Substudy From the PIVOT Trial [J].
Arenas-Pinto, Alejandro ;
Stohr, Wolfgang ;
Jager, Hans Rolf ;
Haddow, Lewis ;
Clarke, Amanda ;
Johnson, Margaret ;
Chen, Fabian ;
Winston, Alan ;
Godi, Claudia ;
Thust, Steffi ;
Trombin, Rita ;
Cairns, Janet ;
Solanky, Bhavana S. ;
Golay, Xavier ;
Paton, Nicholas I. .
CLINICAL INFECTIOUS DISEASES, 2016, 63 (02) :257-264
[5]   Efficacy of protease inhibitor monotherapy vs. triple therapy: meta-analysis of data from 2303 patients in 13 randomized trials [J].
Arribas, J. R. ;
Girard, P-M ;
Paton, N. ;
Winston, A. ;
Marcelin, A-G ;
Elbirt, D. ;
Hill, A. ;
Hadacek, M. B. .
HIV MEDICINE, 2016, 17 (05) :358-367
[6]   The Effect of Central Nervous System Penetration Effectiveness of Highly Active Antiretroviral Therapy on Neuropsychological Performance and Neuroimaging in HIV Infected Individuals [J].
Baker, Laurie M. ;
Paul, Robert H. ;
Heaps-Woodruff, Jodi M. ;
Chang, Jee Yoon ;
Ortega, Mario ;
Margolin, Zachary ;
Usher, Christina ;
Basco, Brian ;
Cooley, Sarah ;
Ances, Beau M. .
JOURNAL OF NEUROIMMUNE PHARMACOLOGY, 2015, 10 (03) :487-492
[7]  
Bracchi M, 2016, J INT AIDS SOC
[8]  
Bumpus N, 2015, C RETR OPP INF
[9]   Antiretroviral penetration into the CNS and incidence of AIDS-defining neurologic conditions [J].
Caniglia, Ellen C. ;
Cain, Lauren E. ;
Justice, Amy ;
Tate, Janet ;
Logan, Roger ;
Sabin, Caroline ;
Winston, Alan ;
van Sighem, Ard ;
Miro, Jose M. ;
Podzamczer, Daniel ;
Olson, Ashley ;
Ramon Arribas, Jose ;
Moreno, Santiago ;
Meyer, Laurence ;
del Romero, Jorge ;
Dabis, Francois ;
Bucher, Heiner C. ;
Wandeler, Gilles ;
Vourli, Georgia ;
Skoutelis, Athanasios ;
Lanoy, Emilie ;
Gasnault, Jacques ;
Costagliola, Dominique ;
Hernan, Miguel A. .
NEUROLOGY, 2014, 83 (02) :134-141
[10]   Central nervous system penetration effectiveness of antiretroviral drugs and neuropsychological impairment in the Ontario HIV Treatment Network Cohort Study [J].
Carvalhal, Adriana ;
Gill, M. John ;
Letendre, Scott L. ;
Rachlis, Anita ;
Bekele, Tsegaye ;
Raboud, Janet ;
Burchell, Ann ;
Rourke, Sean B. .
JOURNAL OF NEUROVIROLOGY, 2016, 22 (03) :349-357