Evidence map›Paper›PMID 27428436›Full record

ArticleEBioMedicine2016

One of the immune activation profiles observed in HIV-1-infected adults with suppressed viremia is linked to metabolic syndrome: The ACTIVIH study.

Christina Psomas, Mehwish Younas, Christelle Reynes, Renaud Cezar, Pierre Portalès, Edouard Tuaillon, Adeline Guigues, Corinne Merle, Nadine Atoui, Céline Fernandez and 9 more

Erratum issued Registry-linked trialAbstract read
In one paragraph

Article in EBioMedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT04028882 (Immune Activation as a Cause of Insulin Resistance in Adults Living With HIV-1 on Effective Antiretroviral Therapy), which is not on this map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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.

NCT04028882 terminatednot on this mapstarted 2020, after this paper: background citation

Immune Activation as a Cause of Insulin Resistance in Adults Living With HIV-1 on Effective Antiretroviral Therapy

TypeobservationalSponsorUniversity Hospital, MontpellierRan2020 to 2024Enrolled148ConditionsHIV InfectionsArmsSignaling, metabolomic and transcriptomic analysis
3 · Its place in the literature

Who cites it

26 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Christina PsomasInstitute for Human Genetics, CNRS UPR1142, 141 rue de la Cardonille, 34396, Montpellier cedex 5, France; Infectious Diseases Department, University Hospital, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France.
Mehwish YounasInstitute for Human Genetics, CNRS UPR1142, 141 rue de la Cardonille, 34396, Montpellier cedex 5, France.
Christelle ReynesInstitute for Functional Genomics, Montpellier University, UMR5203, 141 rue de la Cardonille, 34396 Montpellier cedex 5, France.
Renaud CezarImmunology Department, University Hospital, Place du Pr Debré, 30029 Nîmes cedex, France.
Pierre PortalèsImmunology Department, University Hospital, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France.
Edouard TuaillonMicrobiology Department, University Hospital, 371 Av. du Doyen Gaston Giraud, 34295 Montpellier cedex 5, France.
Adeline GuiguesInstitute for Human Genetics, CNRS UPR1142, 141 rue de la Cardonille, 34396, Montpellier cedex 5, France.
Corinne MerleInfectious Diseases Department, University Hospital, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France.
Nadine AtouiInfectious Diseases Department, University Hospital, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France.
Céline FernandezInfectious Diseases Department, University Hospital, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France.
Vincent Le MoingInfectious Diseases Department, University Hospital, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France; IRD UMI 233, INSERM U1175, Montpellier University, 911 avenue Agropolis, 34294 Montpellier cedex 5, France; Montpellier University, 5 Boulevard Henri IV, 34967 Montpellier cedex 2, France.
Claudine BarbuatInfectious Diseases Department, University Hospital, Place du Pr Debré, 30029 Nîmes cedex, France.
Grégory MarinMedical Informatics Department, University Hospital, 39 Avenue Charles Flahault, 34090 Montpellier cedex 5, France.
Nicolas NagotMedical Informatics Department, University Hospital, 39 Avenue Charles Flahault, 34090 Montpellier cedex 5, France.
Albert SottoMontpellier University, 5 Boulevard Henri IV, 34967 Montpellier cedex 2, France; Infectious Diseases Department, University Hospital, Place du Pr Debré, 30029 Nîmes cedex, France.
Jean-François EliaouImmunology Department, University Hospital, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France; Montpellier University, 5 Boulevard Henri IV, 34967 Montpellier cedex 2, France.
Robert SabatierInstitute for Functional Genomics, Montpellier University, UMR5203, 141 rue de la Cardonille, 34396 Montpellier cedex 5, France.
Jacques ReynesInfectious Diseases Department, University Hospital, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France; IRD UMI 233, INSERM U1175, Montpellier University, 911 avenue Agropolis, 34294 Montpellier cedex 5, France; Montpellier University, 5 Boulevard Henri IV, 34967 Montpellier cedex 2, France.
Pierre CorbeauInstitute for Human Genetics, CNRS UPR1142, 141 rue de la Cardonille, 34396, Montpellier cedex 5, France; Immunology Department, University Hospital, Place du Pr Debré, 30029 Nîmes cedex, France; Montpellier University, 5 Boulevard Henri IV, 34967 Montpellier cedex 2, France. Electronic address: pcorbeau@igh.cnrs.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune activation in HIV-1-infected individuals is reduced under antiretroviral therapies, but persists, resulting in various morbidities. To better characterize this phenomenon, using a panel of 68 soluble and cell surface markers, we measured the level of activation in circulating CD4+ and CD8+ T cells, B cells, monocytes, NK cells, polynuclear and endothelial cells as well as of inflammation and fibrinolysis in 120 virologic responders over 45years of age. As compared with age- and sex-matched uninfected individuals, we observed a persistence of activation in all the cell subpopulations analyzed, together with marks of inflammation and fibrinolysis. Two independent hierarchical clustering analyses allowed us to identify five clusters of markers that varied concurrently, and five patient groups, each with the same activation profile. The five groups of patients could be characterized by a marker of CD4+ T cell, CD8+ T cell, NK cell, monocyte activation or of inflammation, respectively. One of these profiles was strongly associated with marks of metabolic syndrome, particularly with hyperinsulinemia (OR 12.17 [95% CI 1.79-82.86], p=0.011). In conclusion, our study unveils biomarkers linked to metabolic syndrome that could be tested as predictive markers, and opens the way to new therapeutic approaches tailored to each patient group.

Indexed as

ViremiaAgedAntiretroviral Therapy, Highly ActiveBiomarkersBlood CoagulationCD4 Lymphocyte CountCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCoinfectionCross-Sectional StudiesEndothelial CellsFemaleHIV-1HIV InfectionsHumansKiller Cells, NaturalBiomarkersCell activationCoagulationEndotheliumHyperinsulinemiaInflammation

Identifiers

PMID27428436
PMCPMC4919610

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Registered trials

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.