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


Journal

Arthritis research & therapy
ISSN: 1478-6362
Titre abrégé: Arthritis Res Ther
Pays: England
ID NLM: 101154438

Informations de publication

Date de publication:
29 09 2020
Historique:
received: 01 03 2020
accepted: 24 08 2020
entrez: 30 9 2020
pubmed: 1 10 2020
medline: 22 6 2021
Statut: epublish

Résumé

Patients 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. Patients 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. One 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. Tocilizumab 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. The 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).

Sections du résumé

BACKGROUND
Patients 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.
METHODS
Patients 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.
RESULTS
One 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.
CONCLUSIONS
Tocilizumab 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 REGISTRATION
The 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).

Identifiants

pubmed: 32993784
doi: 10.1186/s13075-020-02297-7
pii: 10.1186/s13075-020-02297-7
pmc: PMC7523335
doi:

Substances chimiques

Adiponectin 0
Antibodies, Monoclonal, Humanized 0
Leptin 0
tocilizumab I031V2H011

Banques de données

ClinicalTrials.gov
['NCT02843789']

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

224

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Auteurs

Eric Toussirot (E)

INSERM CIC-1431, CHU de Besançon, Centre d'Investigation Clinique Biothérapie, Pôle Recherche, 25000, Besançon, France. etoussirot@chu-besancon.fr.
Fédération Hospitalo-Universitaire INCREASE, CHU de Besançon, 25000, Besançon, France. etoussirot@chu-besancon.fr.
CHU de Besançon, Rhumatologie, Pôle PACTE (Pathologies Aiguës Chroniques Transplantation Éducation), 25000, Besançon, France. etoussirot@chu-besancon.fr.
Université de Bourgogne Franche-Comté, Département Universitaire de Thérapeutique, Besançon, France. etoussirot@chu-besancon.fr.
INSERM UMR1098 « Relations Hôte Greffon Tumeurs, ingénierie cellulaire et génique », Université de Bourgogne Franche-Comté, 25000, Besançon, France. etoussirot@chu-besancon.fr.

Hubert Marotte (H)

INSERM 1059, Université de Lyon, Saint-Etienne; Rhumatologie CHU de Saint-Etienne; CIC-1408, CHU de Saint-Etienne, Saint-Etienne, France.

Denis Mulleman (D)

Rhumatologie CHU de Tours, Tours, France.

Grégoire Cormier (G)

Rhumatologie Centre Hospitalier Départemental Vendée, La Roche sur Yon, France.

Fabienne Coury (F)

Rhumatologie Hospices Civils de Lyon, INSERM UMR1033, Université Lyon 1, Lyon, France.

Philippe Gaudin (P)

Rhumatologie CHU de Grenoble, Grenoble, France.

Emmanuelle Dernis (E)

Rhumatologie Centre Hospitalier, Le Mans, France.

Christine Bonnet (C)

Rhumatologie CHU de Limoges, Limoges, France.

Richard Damade (R)

Rhumatologie Centre Hospitalier, Chartres, France.

Jean-Luc Grauer (JL)

Rhumatologie Centre Hospitalier, Montélimar, France.

Tassadit Ait Abdesselam (TA)

Rhumatologie Centre Hospitalier, Meaux, France.

Caroline Guillibert-Karras (C)

Rhumatologie Hôpital St Joseph, Marseille, France.

Frédéric Lioté (F)

Rhumatologie Hôpital Lariboisière AP-HP Paris, Université de Paris, Paris, France.

Pascal Hilliquin (P)

Rhumatologie Centre Hospitalier Sud Francilien, Corbeil-Essonnes, France.

Antoinette Sacchi (A)

Rhumatologie Centre hospitalier Mantes la Jolie, Mantes-la-Jolie, France.

Daniel Wendling (D)

CHU de Besançon, Rhumatologie, Pôle PACTE (Pathologies Aiguës Chroniques Transplantation Éducation), 25000, Besançon, France.

Benoît Le Goff (B)

Rhumatologie CHU de Nantes, Nantes, France.

Marc Puyraveau (M)

INSERM CIC-1431, CHU de Besançon, Centre d'Investigation Clinique Biothérapie, Pôle Recherche, 25000, Besançon, France.
Unité de méthodologie uMETh, INSERM CIC-1431, Centre d'Investigation Clinique, CHU de Besançon, Besançon, France.

Gilles Dumoulin (G)

Laboratoire 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.

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