Abstract

The Multi-Biomarker Disease Activity (MBDA) score is a validated rheumatoid arthritis (RA) disease activity measure based on 12 serum biomarkers. Here, we evaluate short-term biological variability of MBDA scores to determine the magnitude of change that might be considered clinically meaningful. Twenty-eight adult seropositive RA patients with clinically stable disease and no changes in RA medications for 4 weeks prior to study were enrolled. Nine serum samples were obtained over four consecutive days (non-fasting). MBDA score variation was assessed day-to-day (daily) and within 24 h (diurnal). The standard deviation (SD) of MBDA scores was calculated by a linear mixed model including random effects for patient, day, and time of day. The minimally important difference (MID) was calculated as {z}_{0.95}sqrt{2times mathrm{total} mathrm{variance} mathrm{of} mathrm{MBDAs}} . A subgroup analysis was performed for patients with active RA (moderate or high MBDA score). The SD of MBDA score change in the full cohort was 4.7 in a combined daily-diurnal variation analysis, which corresponds with an MID of 11. The SD of MBDA score change in the subset of patients with active RA (moderate/high MBDA scores) was 3.6. This corresponds with an MID of 8 units in patients with active RA for whom clinicians are most likely to need guidance with respect to therapeutic decisions. Changes in MBDA score ≥ 8 represent a change in RA disease activity that clinicians can use as a benchmark for therapeutic drug efficacy and can be incorporated into a treat-to-target strategy.

Highlights

  • Rheumatoid arthritis (RA) is a chronic inflammatory disease of unknown etiology in which joint damage and physical disability are major adverse outcomes resulting in poor quality of life and premature mortality

  • All categories of Multi-Biomarker Disease Activity (MBDA) disease activity scores were represented at baseline with 6 patients (21.4%) having a low MBDA score, 13 patients (46.4%) having a moderate MBDA score, and Baseline characteristic Age Sex Body mass index Race (Caucasian)

  • Formal joint counts are often not performed in routine clinical practice settings [23,24,25] and have been shown to be poorly reproducible [26, 27]

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Summary

Introduction

Rheumatoid arthritis (RA) is a chronic inflammatory disease of unknown etiology in which joint damage and physical disability are major adverse outcomes resulting in poor quality of life and premature mortality. An international rheumatology task force has recommended a Treat-to-Target approach to achieve optimal therapeutic outcomes by using defined measures of clinical disease activity to guide treatment in order to achieve remission or a low disease activity state [2]. Both the American College of Rheumatology (ACR) and the European Union League Against Rheumatism (EULAR) recommendations that the management of RA include systematic longitudinal and quantitative RA disease activity assessment [3, 4].

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