Evidence map›Paper›PMID 38608008›Full record

ArticleAIDS (London, England)2024

Plasma galectin-9 relates to cognitive performance and inflammation among adolescents with vertically acquired HIV.

Preeti Moar, Kyaw Linn, Thomas A Premeaux, Scott Bowler, Urvinder Kaur Sardarni, Bindu Parachalil Gopalan, Ei E Shwe, Thidar San, Haymar Han, Danielle Clements and 12 more

Open access · greenAbstract read
In one paragraph

Article in AIDS (London, England), 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
1.2field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 10 institutions in 3 countries.

Preeti MoarDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, USA.
Kyaw LinnDepartment of Pediatrics, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Thomas A PremeauxDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, USA.
Scott BowlerDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, USA.
Urvinder Kaur SardarniDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, USA.
Bindu Parachalil GopalanDivision of infectious diseases, St. John's Research Institute, Bengaluru, India.
Ei E ShweDepartment of Pathology, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Thidar SanDepartment of Pathology, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Haymar HanDepartment of Pediatrics, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Danielle ClementsDepartment of Tropical Medicine, Medical Microbiology & Pharmacology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu.
Chaw S HlaingDepartment of Pediatrics, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Ei H KyuDepartment of Pediatrics, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Cho ThairDepartment of Pediatrics, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Yi Y MarDepartment of Pediatrics, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Nway NwayDepartment of Pediatrics, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Julie MannarinoMissouri Institute of Mental Health, University of Missouri-St. Louis, Missouri.
Jacob BolzeniusMissouri Institute of Mental Health, University of Missouri-St. Louis, Missouri.
Soe MarDepartment of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
Aye Mya M AyeDepartment of Pediatrics, Yangon Children's Hospital, University of Medicine 1, Yangon, Myanmar.
Ravi TandonLaboratory of AIDS Research and Immunology, School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.
Robert PaulMissouri Institute of Mental Health, University of Missouri-St. Louis, Missouri.
Lishomwa C NdhlovuDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, USA.
Yangon Children's Hospital · MMCornell University · USMissouri Institute of Mental Health · USWeill Cornell Medicine · USJawaharlal Nehru University · INNational Institutes of Health · USUniversity of Hawaiʻi at Mānoa · USUniversity of Missouri–St. Louis · USUniversity of Nebraska Medical Center · USWashington University in St. Louis · US

Funding

Viral and Host Determinants of Cognitive Status in Vertically Transmitted HIVR01MH108559 · NIMH · UNIVERSITY OF MISSOURI-ST. LOUIS · PI PAUL, ROBERT HARRIS · 2017 to 2021
$3.4M
Effects of Human Galectin-9 on the CNS HIV ReservoirR01MH112457 · NIMH · VITALANT · PI NDHLOVU, LISHOMWA C, PILLAI, SATISH KUMAR · 2016 to 2020
$2.0M
NIMH NIH HHS R01 MH108559NIMH NIH HHS R01 MH112457
6 · The paper itself

Abstract

objectiveAdolescents with perinatally acquired HIV (AWH) are at an increased risk of poor cognitive development yet the underlying mechanisms remain unclear. Circulating galectin-9 (Gal-9) has been associated with increased inflammation and multimorbidity in adults with HIV despite antiretroviral therapy (ART); however, the relationship between Gal-9 in AWH and cognition remain unexplored.

designA cross-sectional study of two independent age-matched cohorts from India [AWH on ART ( n  = 15), ART-naive ( n  = 15), and adolescents without HIV (AWOH; n  = 10)] and Myanmar [AWH on ART ( n  = 54) and AWOH ( n  = 22)] were studied. Adolescents from Myanmar underwent standardized cognitive tests.

methodsPlasma Gal-9 and soluble mediators were measured by immunoassays and cellular immune markers by flow cytometry. We used Mann-Whitney U tests to determine group-wise differences, Spearman's correlation for associations and machine learning to identify a classifier of cognitive status (impaired vs. unimpaired) built from clinical (age, sex, HIV status) and immunological markers.

resultsGal-9 levels were elevated in ART-treated AWH compared with AWOH in both cohorts (all P  < 0.05). Higher Gal-9 in AWH correlated with increased levels of inflammatory mediators (sCD14, TNFα, MCP-1, IP-10, IL-10) and activated CD8 + T cells (all P  < 0.05). Irrespective of HIV status, higher Gal-9 levels correlated with lower cognitive test scores in multiple domains [verbal learning, visuospatial learning, memory, motor skills (all P  < 0.05)]. ML classification identified Gal-9, CTLA-4, HVEM, and TIM-3 as significant predictors of cognitive deficits in adolescents [mean area under the curve (AUC) = 0.837].

conclusionOur results highlight a potential role of Gal-9 as a biomarker of inflammation and cognitive health among adolescents with perinatally acquired HIV.

Indexed as

GalectinsHIV InfectionsInflammationAdolescentBiomarkersChildCognitionCross-Sectional StudiesFemaleFlow CytometryHumansImmunoassayIndiaInfectious Disease Transmission, VerticalMalePlasmaBiomarkersGalectinsLGALS9 protein, human

Identifiers

PMID38608008
PMCPMC11239096
OpenAlexW4394743668

What OpenQuestion holds

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Registered trials

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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.