Evidence map›Paper›PMID 38988673›Full record

ArticleJournal of virus eradication2024

Impact of interrupting antiretroviral therapy started during primary HIV-1 infection on plasma neurofilament light chain protein, a marker of neuronal injury: The SPARTAC trial.

Jasmini Alagaratnam, Wolfgang Stöhr, Elizabeth Hamlyn, Kholoud Porter, Jamie Toombs, Amanda Heslegrave, Henrik Zetterberg, Magnus Gisslén, Jonathan Underwood, Mauro Schechter and 10 more

Abstract read
In one paragraph

Article in Journal of virus eradication, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Jasmini AlagaratnamDepartment of Infectious Disease, Faculty of Medicine, Imperial College London, London, United Kingdom.
Wolfgang StöhrMedical Research Council Clinical Trials Unit at University College London, London, United Kingdom.
Elizabeth HamlynCaldecot Centre, Kings College Hospital NHS Foundation Trust, London, United Kingdom.
Kholoud PorterInstitute for Global Health, University College London, London, United Kingdom.
Jamie ToombsUK Dementia Research Institute at University College London, London, United Kingdom.
Amanda HeslegraveUK Dementia Research Institute at University College London, London, United Kingdom.
Henrik ZetterbergUK Dementia Research Institute at University College London, London, United Kingdom.
Magnus GisslénDepartment of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Jonathan UnderwoodDivision of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Mauro SchechterProjeto Praça Onze, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Pontiano KaleebuMedical Research Council/Uganda Virus Research Institute, Entebbe, Uganda.
Giuseppe TambussiSan Raffaele Scientific Institute, Milan, Italy.
Sabine KinlochDepartment of Infection and Immunity, Royal Free Hospital, Pond Street, London, United Kingdom.
Jose M MiroInfectious Diseases Service, Hospital Clinic - IDIBAPS. University of Barcelona, Barcelona, Spain.
Anthony D KelleherKirby Institute, UNSW Sydney, New South Wales, Australia.
Abdel BabikerMedical Research Council Clinical Trials Unit at University College London, London, United Kingdom.
John FraterPeter Medawar Building for Pathogen Research, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Alan WinstonDepartment of Infectious Disease, Faculty of Medicine, Imperial College London, London, United Kingdom.
Sarah FidlerDepartment of Infectious Disease, Faculty of Medicine, Imperial College London, London, United Kingdom.
SPARTAC Trial Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Antiretroviral therapy (ART)-conferred suppression of HIV replication limits neuronal injury and inflammation. ART interruption tests efficacy in HIV cure trials and viral rebound after ART interruption may induce neuronal injury. We investigated the impact of protocol-defined ART interruption, commenced during primary HIV-1 infection (PHI) on a biomarker of neuro-axonal injury (neurofilament light protein (NfL)), and its associations with inflammation (D-dimer and interleukin-6 (IL-6)) and HIV-1 reservoir size (total HIV-1 DNA). Design: Retrospective study measuring plasma NfL in 83 participants enrolled in SPARTAC randomised to receive 48-weeks ART initiated during PHI, followed by ART interruption. Methods: NfL (Simoa immunoassay, Quanterix™) was measured before ART, after 48 weeks on ART, and 12 weeks after stopping ART. Plasma D-dimer and IL-6, and total HIV-1 DNA in peripheral CD4 Results: NfL decreased following 48-weeks ART (geometric mean 6.9 to 5.8 pg/mL, p = 0.006) with no further significant change up to 12-weeks post-stopping ART despite viral rebound in the majority of participants (median 1.7 to 3.9 plasma HIV-1 RNA log Conclusions: Using plasma NfL as a surrogate marker, a decrease in neuro-axonal injury was observed in a cohort of participants following ART initiation during PHI, with no evidence of neuro-axonal injury rebound following ART interruption for up to 12 weeks, despite viral rebound in the majority of participants.

Indexed as

Anti-retroviral agentsHIV-1NeurofilamentsPrimary HIV infectionViral rebound

Identifiers

PMID38988673
PMCPMC11234014

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.