Evidence map›Paper›PMID 27819802›Full record

ArticleAIDS (London, England)2017

Immediate initiation of cART is associated with lower levels of cerebrospinal fluid YKL-40, a marker of microglial activation, in HIV-1 infection.

Michael J Peluso, Victor Valcour, Nittaya Phanuphak, Jintanat Ananworanich, James L K Fletcher, Thep Chalermchai, Shelly J Krebs, Merlin L Robb, Joanna Hellmuth, Magnus Gisslén and 3 more

Open access · greenAbstract read
In one paragraph

Article in AIDS (London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
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  8. Neuroimaging the Neuropathogenesis of HIV.Current HIV/AIDS reports · 2021
    Review
  9. Article
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  14. Review
  15. Article
  16. Applying fluid biomarkers to Alzheimer's disease.American journal of physiology. Cell physiology · 2017
    Review
  17. 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

13 authors at 1 institution in 2 countries.

Michael J PelusoaDepartment of Medicine, Brigham and Women's Hospital, Boston, Massachusetts bDepartment of Neurology, Memory and Aging Center, University of California, San Francisco, California, USA cSEARCH, The Thai Red Cross AIDS Research Center, Bangkok, Thailand dUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring eHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland , USA fDepartment of Infectious Diseases, Institute of Biomedicine, Gothenburg gDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden hUniversity College London Institute of Neurology, London, UK iYale University School of Medicine, New Haven, Connecticut, USA.
Victor Valcour
Nittaya Phanuphak
Jintanat Ananworanich
James L K Fletcher
Thep Chalermchai
Shelly J Krebs
Merlin L Robb
Joanna Hellmuth
Magnus Gisslén
Henrik Zetterberg
Serena Spudich
RV254SEARCH 010, RV304SEARCH 013, and SEARCH 011 Study Teams
University College London · GB

Funding

Long-Term CNS Consequences of Treatment During Acute InfectionR01MH095613 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SPUDICH, SERENA S, VALCOUR, VICTOR · 2011 to 2015
$3.1M
Therapeutic Interventions during Acute Infection to Address the CNS Reservoir forR01NS084911 · NINDS · YALE UNIVERSITY · PI ANANWORANICH, JINTANAT, SPUDICH, SERENA S · 2013 to 2017
$2.3M
NIMH NIH HHS R01 MH095613NINDS NIH HHS R01 NS084911
6 · The paper itself

Abstract

objectiveTo characterize cerebrospinal fluid (CSF) YKL-40, a unique biomarker that reflects activation of microglial cells, in acute (AHI) and chronic HIV-1 infection (CHI) and to determine the effect of treatment initiation on levels of this marker.

designA cross-sectional study of two groups of HIV-infected participants at baseline and follow-up timepoints.

methodsAHI (n = 33) and CHI (n = 34) participants underwent CSF and blood sampling before treatment initiation with combination antiretroviral therapy (cART) and at follow-up on cART in a subset of these individuals [6 months in AHI participants (n = 24), 1 year in CHI participants (n = 10)]. Measured parameters were analyzed at each timepoint. Analyses employed Mann-Whitney tests and Spearman correlations.

resultsBaseline median YKL-40 was higher in CHI than AHI (96844 versus 80754 ng/l; P = 0.011). Elevations in the CHI group relative to the AHI group persisted at follow-up despite treatment (87414 versus 66130 ng/l; P = 0.003). In untreated CHI, YKL-40 correlated with neopterin (r = 0.51, P = 0.0025), chemokine (CXC-motif) ligand-10 (r = 0.44, P = 0.011), and neurofilament light chain (r = 0.56, P = 0.0008) in CSF.

conclusionsThis study is the first to describe the dynamics of CSF YKL-40 in two groups of HIV-infected individuals before and after cART and demonstrates the value of this marker in understanding HIV neuropathogenesis. The results suggest the utility of further exploring the prognostic value of YKL-40, particularly in individuals with early HIV infection or those initiating treatment during CHI.

Indexed as

Secondary PreventionAdultAnti-Retroviral AgentsCerebrospinal FluidChitinase-3-Like Protein 1Cross-Sectional StudiesFemaleHIV InfectionsHumansMaleNeurocognitive DisordersYoung AdultAnti-Retroviral AgentsCHI3L1 protein, humanChitinase-3-Like Protein 1

Identifiers

PMID27819802
PMCPMC5844231
OpenAlexW2546572177

What OpenQuestion holds

Textmetadata
LicenceTDM
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.