Evidence map›Paper›PMID 39538056›Full record

ArticleJournal of neurovirology2025

The incidence of symptomatic CSF viral escape in patients on antiretroviral therapy in western India: a retrospective cohort study.

Atul Patel, Ketan Patel, Niyati Patel, Kinjal Shah, Ambuj Kumar

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Article in Journal of neurovirology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Atul PatelInfectious Diseases Department, Sterling Hospital, Ahmedabad, 380052, India. atulpatel65@gmail.com.
Ketan PatelInfectious Diseases Department, Sterling Hospital, Ahmedabad, 380052, India.
Niyati PatelGMERS Medical College, Sola, Ahmedabad, 380060, India.
Kinjal ShahInfectious Diseases Department, Sterling Hospital, Ahmedabad, 380052, India.
Ambuj KumarResearch Methodology and Biostatistics Core, Office of Research, Department of Internal Medicine, Morsani College Of Medicine, University of South Florida, Tampa, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antiretroviral treatment (ART) effectively suppresses viral loads in both plasma and cerebrospinal fluid (CSF). Patients with discordant plasma and CSF viral loads may experience chronic-progressive or fluctuating neurocognitive dysfunctions. This study examined the incidence of symptomatic CSF viral escape (CSFVE) in patients receiving ART. This retrospective cohort study was conducted between 2000 and 2023. The primary outcome measure was the incidence of symptomatic CSFVE. Nonparametric Mann-Whitney U and Fisher exact/χ 2 tests were applied for continuous and categorical variables, respectively. The cumulative incidence function with Gray's test was used to compare the incidence of CSFVE across the treatment regimens. During the study period, 52 of the 8415 patients were diagnosed with CSFVE. The median duration of HIV diagnosis in patients with CSF VE was 150 (12-288) months, with a median nadir CD4 + T-cell count 96.5 (13-601 cells/L)], and 75% of the patients were on a ritonavir-boosted protease inhibitor (PI/r) regimen. The cumulative incidence of symptomatic CSFVE at a follow-up of 14 years was 1% (95% CI, 0-1%). PI/r (HR 34.73; 95% CI 13.5 to 89.4; p < 0.001) and integrase strand transfer inhibitor (INSTI) (HR 3.42; 95% CI 1.94 to 6.02; p < 0.001) regimens were significantly more likely to be associated with CSFVE than the Non-nucleoside reverse transcriptase inhibitors (NNRTIs) regimens. NNRTIs had the lowest risk of CSFVE compared to the PI/r and INSTI regimens. A rapid and complete recovery is possible with symptomatic CSFVE if it is diagnosed and treated early.

Indexed as

Anti-HIV AgentsHIV-1HIV InfectionsAdultCD4 Lymphocyte CountFemaleHIV Protease InhibitorsHumansIncidenceIndiaMaleMiddle AgedRetrospective StudiesRitonavirViral LoadAnti-HIV AgentsHIV Protease InhibitorsRitonavirCNS penetrationCSF viral escapeDolutegravirHANDHIV encephalitis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.