TY - JOUR
T1 - Antiretroviral Therapy Intensification for Neurocognitive Impairment in Human Immunodeficiency Virus
AU - the A5324 Study Team
AU - Letendre, Scott L.
AU - Chen, Huichao
AU - Mckhann, Ashley
AU - Roa, Jhoanna
AU - Vecchio, Alyssa
AU - Daar, Eric S.
AU - Berzins, Baiba
AU - Hunt, Peter W.
AU - Marra, Christina M.
AU - Campbell, Thomas B.
AU - Coombs, Robert W.
AU - Ma, Qing
AU - Swaminathan, Shobha
AU - Macatangay, Bernard J.C.
AU - Morse, Gene D.
AU - Miller, Thomas
AU - Rusin, David
AU - Greninger, Alexander L.
AU - Ha, Belinda
AU - Alston-Smith, Beverly
AU - Robertson, Kevin
AU - Paul, Robert
AU - Spudich, Serena
N1 - Publisher Copyright: © 2023 The Author(s). Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved.
PY - 2023/9/15
Y1 - 2023/9/15
N2 - Background: Neurocognitive impairment (NCI) in people with HIV (PWH) on antiretroviral therapy (ART) is common and may result from persistent HIV replication in the central nervous system. Methods: A5324 was a randomized, double-blind, placebo-controlled, 96-week trial of ART intensification with dolutegravir (DTG) + MVC, DTG + Placebo, or Dual - Placebo in PWH with plasma HIV RNA <50 copies/mL on ART and NCI. The primary outcome was the change on the normalized total z score (ie, the mean of individual NC test z scores) at week 48. Results: Of 357 screened, 191 enrolled: 71% male, 51% Black race, 22% Hispanic ethnicity; mean age 52 years; mean CD4+ T-cells 681 cells/μL. Most (65%) had symptomatic HIV-associated NC disorder. Study drug was discontinued due to an adverse event in 15 (8%) and did not differ between arms (P =. 17). Total z score, depressive symptoms, and daily functioning improved over time in all arms with no significant differences between them at week 48 or later. Adjusting for age, sex, race, study site, efavirenz use, or baseline z score did not alter the results. Body mass index modestly increased over 96 weeks (mean increase 0.32 kg/m2, P =. 006) and did not differ between arms (P >. 10). Conclusions: This is the largest, randomized, placebo-controlled trial of ART intensification for NCI in PWH. The findings do not support empiric ART intensification as a treatment for NCI in PWH on suppressive ART. They also do not support that DTG adversely affects cognition, mood, or weight.
AB - Background: Neurocognitive impairment (NCI) in people with HIV (PWH) on antiretroviral therapy (ART) is common and may result from persistent HIV replication in the central nervous system. Methods: A5324 was a randomized, double-blind, placebo-controlled, 96-week trial of ART intensification with dolutegravir (DTG) + MVC, DTG + Placebo, or Dual - Placebo in PWH with plasma HIV RNA <50 copies/mL on ART and NCI. The primary outcome was the change on the normalized total z score (ie, the mean of individual NC test z scores) at week 48. Results: Of 357 screened, 191 enrolled: 71% male, 51% Black race, 22% Hispanic ethnicity; mean age 52 years; mean CD4+ T-cells 681 cells/μL. Most (65%) had symptomatic HIV-associated NC disorder. Study drug was discontinued due to an adverse event in 15 (8%) and did not differ between arms (P =. 17). Total z score, depressive symptoms, and daily functioning improved over time in all arms with no significant differences between them at week 48 or later. Adjusting for age, sex, race, study site, efavirenz use, or baseline z score did not alter the results. Body mass index modestly increased over 96 weeks (mean increase 0.32 kg/m2, P =. 006) and did not differ between arms (P >. 10). Conclusions: This is the largest, randomized, placebo-controlled trial of ART intensification for NCI in PWH. The findings do not support empiric ART intensification as a treatment for NCI in PWH on suppressive ART. They also do not support that DTG adversely affects cognition, mood, or weight.
KW - HIV
KW - antiretroviral therapy
KW - brain
KW - cognition
UR - https://www.scopus.com/pages/publications/85171806552
U2 - 10.1093/cid/ciad265
DO - 10.1093/cid/ciad265
M3 - Article
C2 - 37183889
SN - 1058-4838
VL - 77
SP - 866
EP - 874
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 6
ER -