Abstract

Anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive dermatomyositis (DM)-associated interstitial lung disease (ILD) may progress rapidly and lead to high mortality within 6 or 12 months. Except for reported prognostic factors, simple but powerful prognostic biomarkers are still in need in practice. In this study, we focused on circulating monocyte and lymphocyte counts and their variation tendency in the early stage of ILD. A total of 351 patients from two inception anti-MDA5 antibody-positive cohorts were included in this study, with various treatment choices. Lymphocyte count remained lower in the first month after admission in the non-survivor patients. Although baseline monocyte count showed no significant differences, average monocyte count in the following 4 weeks was also lower in the non-survivor group. Based on the C-index and analysis by the “survminer” R package in the discovery cohort, we chose 0.24 × 109/L as the cutoff value for Mono W0-2, 0.61 × 109/L as the cutoff value for lymph W0-2, and 0.78 × 109/L as the cutoff value for peripheral blood mononuclear cell (PBMC) W0-2, to predict the 6-month all-cause mortality. The Kaplan–Meier survival curves and adjusted hazard ratio with age, gender, and the number of immunosuppressants used all validated that patients with lower average monocyte count, lower average lymphocyte count, or lower average PBMC count in the first 2 weeks after admission had higher 6-month death risk, no matter in the validation cohort or in the pooled data. Furthermore, flow cytometry figured out that non-classical monocytes in patients with anti-MDA5 antibody-positive DM were significantly lower than healthy controls and patients with DM without anti-MDA5 antibodies. In conclusion, this study elucidated the predictive value of monocyte and lymphocyte counts in the early stage and may help rheumatologists to understand the possible pathogenesis of this challenging disease.

Highlights

  • Antimelanoma differentiation-associated gene 5 (MDA5) antibody-positive dermatomyositis (DM) is characterized by typical DM rashes, amyopathic or minimal muscle involvement, and rapid progressive interstitial lung disease (RPILD) [1]

  • According to a previous study [10, 11], complete blood counts analysis revealed that lymphocytopenia was correlated with poor outcomes of clinically amyopathic dermatomyositis (CADM)-associated RPILD

  • While monocytes of healthy controls (HCs) contain more ncMon and less cMon relatively, monocytes of patients with MDA5+ contain less ncMon and more cMon in their Peripheral Blood Mononuclear Cell (PBMC). This retrospective cohort study found that lower monocyte count and lymphocyte count collected from complete blood counts per week in the early course of ILD can predict poor outcomes in anti-MDA5 antibody-positive DM

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Summary

Introduction

Antimelanoma differentiation-associated gene 5 (MDA5) antibody-positive dermatomyositis (DM) is characterized by typical DM rashes, amyopathic or minimal muscle involvement, and rapid progressive interstitial lung disease (RPILD) [1]. According to a previous study [10, 11], complete blood counts analysis revealed that lymphocytopenia was correlated with poor outcomes of clinically amyopathic dermatomyositis (CADM)-associated RPILD. A recent study [11] reported that lower lymphocyte count at baseline was associated with higher mortality in anti-MDA5-associated RPILD. With the limited case number, there was no significant difference between baseline lymphocyte count in anti-MDA5 antibody-positive patients with DM with or without ILD. It is difficult for clinicians to identify the patients who will progress rapidly at diagnosis

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