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).

Highlights

  • Rheumatoid arthritis (RA) is a chronic inflammatory joint disease, leading to progressive clinical deformation, erosive radiographic changes and disability

  • Tocilizumab treatment in rheumatoid arthritis (RA) patients was associated with a significant increase in total and high molecular weight (HMW) adiponectin, especially at the onset of the treatment

  • Tocilizumab induced a significant gain in lean mass, while fat mass did not change

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Summary

Methods

Laboratory assessments Blood samples were obtained from each patient at each time point, in the morning (8.00 AM) after an overnight fast. Analyses that were performed on frozen serum samples were circulating IL-6, serum adipokines, insulinaemia and serum ghrelin, a gastric peptide involved in appetite regulation. These analyses were all analysed in a central laboratory (Medical biochemical laboratory, University Hospital of Besancon, France). Body composition was studied from the total body scan, with measurements of fat mass and lean mass. According to the low number of patients in specific patient subgroups and the non-normality of the distribution (using Shapiro-Wilk test), the variation of total and HMW adiponectin according to EULAR response was evaluated by Kruskall-Wallis test and Dwass-SteelCrichtlow-Fligner test for post hoc analysis.

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