Evidence map›Paper›PMID 32993784›Full record

ArticleArthritis research & therapy2020

Increased high molecular weight adiponectin and lean mass during tocilizumab treatment in patients with rheumatoid arthritis: a 12-month multicentre study.

Eric Toussirot, Hubert Marotte, Denis Mulleman, Grégoire Cormier, Fabienne Coury, Philippe Gaudin, Emmanuelle Dernis, Christine Bonnet, Richard Damade, Jean-Luc Grauer and 9 more

Registry-linked trialOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in Arthritis research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02843789 (Evolution of Adipokines and Body Composition in Rheumatoid Arthritis Patients Receiving Tocilizumab Therapy), which is not on this map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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.

NCT02843789 phase4completednot on this map

Evolution of Adipokines and Body Composition in Rheumatoid Arthritis Patients Receiving Tocilizumab Therapy

TypeinterventionalSponsorCentre Hospitalier Universitaire de BesanconRan2013 to 2017Enrolled109ConditionsArthritis, RheumatoidArmsTocilizumab
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

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  12. IL-6 and diabetic kidney disease.Frontiers in immunology · 2024
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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

19 authors at 14 institutions in 1 country.

Eric ToussirotINSERM CIC-1431, CHU de Besançon, Centre d'Investigation Clinique Biothérapie, Pôle Recherche, 25000, Besançon, France. etoussirot@chu-besancon.fr.ORCID 0000-0002-6228-1464
Hubert MarotteINSERM 1059, Université de Lyon, Saint-Etienne; Rhumatologie CHU de Saint-Etienne; CIC-1408, CHU de Saint-Etienne, Saint-Etienne, France.
Denis MullemanRhumatologie CHU de Tours, Tours, France.
Grégoire CormierRhumatologie Centre Hospitalier Départemental Vendée, La Roche sur Yon, France.
Fabienne CouryRhumatologie Hospices Civils de Lyon, INSERM UMR1033, Université Lyon 1, Lyon, France.
Philippe GaudinRhumatologie CHU de Grenoble, Grenoble, France.
Emmanuelle DernisRhumatologie Centre Hospitalier, Le Mans, France.
Christine BonnetRhumatologie CHU de Limoges, Limoges, France.
Richard DamadeRhumatologie Centre Hospitalier, Chartres, France.
Jean-Luc GrauerRhumatologie Centre Hospitalier, Montélimar, France.
Tassadit Ait AbdesselamRhumatologie Centre Hospitalier, Meaux, France.
Caroline Guillibert-KarrasRhumatologie Hôpital St Joseph, Marseille, France.
Frédéric LiotéRhumatologie Hôpital Lariboisière AP-HP Paris, Université de Paris, Paris, France.
Pascal HilliquinRhumatologie Centre Hospitalier Sud Francilien, Corbeil-Essonnes, France.
Antoinette SacchiRhumatologie Centre hospitalier Mantes la Jolie, Mantes-la-Jolie, France.
Daniel WendlingCHU de Besançon, Rhumatologie, Pôle PACTE (Pathologies Aiguës Chroniques Transplantation Éducation), 25000, Besançon, France.
Benoît Le GoffRhumatologie CHU de Nantes, Nantes, France.
Marc PuyraveauINSERM CIC-1431, CHU de Besançon, Centre d'Investigation Clinique Biothérapie, Pôle Recherche, 25000, Besançon, France.
Gilles DumoulinLaboratoire de Biochimie Médicale, UF de Biochimie Endocrinienne et Métabolique, CHU de Besançon; EA 3920 Marqueurs pronostiques et facteurs de régulation des pathologies cardiaques et vasculaires, Université de Bourgogne Franche Comté, Besançon, France.
Inserm · FRUniversité Claude Bernard Lyon 1 · FRCentre Hospitalier Départemental Vendée · FRCentre Hospitalier du Mans · FRCentre Hospitalier Sud Francilien · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Limoges · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Tours · FRHôpital Saint Joseph · FRLaboratoire Pacte · FRLes Hôpitaux de Chartres · FRUniversité de Bourgogne · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with rheumatoid arthritis (RA) have an increased risk of cardiovascular (CV) disease. Adiponectin is involved in the metabolism of glucose and lipids with favourable effects on CV disease, especially its high molecular weight (HMW) isoform. Body composition changes are described in RA with various phenotypes including obesity. The effects of tocilizumab on serum adiponectin and body composition, especially fat mass, in patients with RA are not well determined.

methodsPatients with active RA despite previous csDMARDs and/or bDMARDs and who were tocilizumab naïve were enrolled in a multicentre open-label study. They were evaluated at baseline, 1, 3, 6 and 12 months. Clinical assessment included body mass index (BMI) and anthropometric measurements. Lipid and metabolic parameters, serum adiponectin (total and HMW), leptin, resistin and ghrelin were measured at each time point. Body composition (lean mass, fat mass, % fat, fat in the android and gynoid regions) was evaluated at baseline, 6 and 12 months.

resultsOne hundred seven patients were included. Both total and HMW adiponectin significantly increased from baseline to month 3, peaking respectively at month 3 (p = 0.0105) and month 1 (p < 0.0001), then declining progressively until month 6 to 12 and returning to baseline values. Significant elevation in HMW adiponectin persisted at month 6 (p = 0.001). BMI and waist circumference significantly increased at month 6 and 12, as well as lean mass at month 6 (p = 0.0097). Fat mass, percentage fat and android fat did not change over the study period. Lipid parameters (total cholesterol and LDL cholesterol) increased while glycaemia, insulin and HOMA-IR remained stable. Serum leptin, resistin and ghrelin did not change during follow-up.

conclusionsTocilizumab treatment in RA patients was associated with a significant increase in total and HMW adiponectin, especially at the onset of the treatment. Tocilizumab also induced a significant gain in lean mass, while fat mass did not change. These variations in adiponectin levels during tocilizumab treatment could have positive effects on the CV risk of RA patients. In addition, tocilizumab may have an anabolic impact on lean mass/skeletal muscle.

trial registrationThe ADIPRAT study was a phase IV open-label multicentre study retrospectively registered on ClinicalTrials.gov under the number NCT02843789 (date of registration: July 26, 2016).

Indexed as

Arthritis, RheumatoidInsulin ResistanceAdiponectinAntibodies, Monoclonal, HumanizedBody Mass IndexHumansLeptinMolecular WeightAdiponectinAntibodies, Monoclonal, HumanizedLeptintocilizumabAdiponectinBody compositionCardiovascular riskRheumatoid arthritisTocilizumab

Identifiers

PMID32993784
PMCPMC7523335
OpenAlexW3090245197

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.