Safety of glucocorticoid dose reduction in microscopic polyangiitis: a multicentre REVEAL cohort study

Hirofumi Miyake1, Takuya Kotani2, Shogo Matsuda2

  • 1Department of General Internal Medicine, Tenri Hospital, Tenri, Japan.

Modern Rheumatology
|June 9, 2025
PubMed
Abstract

Insights

Reducing glucocorticoids (GCs) in microscopic polyangiitis patients to 10 mg/day at 6 months did not increase mortality or relapse risks. This suggests a feasible target for GC tapering in managing this autoimmune condition.

Area of Science:

  • Rheumatology
  • Clinical Immunology
  • Pharmacology

Background:

  • Microscopic polyangiitis (MPA) is a rare autoimmune vasculitis often treated with glucocorticoids (GCs).
  • Long-term GC use is associated with significant adverse events.
  • Optimizing GC tapering strategies is crucial for improving patient outcomes in MPA.

Purpose of the Study:

  • To evaluate the safety and efficacy of reducing glucocorticoids (GCs) in patients diagnosed with microscopic polyangiitis (MPA).
  • To determine if a 6-month GC dose target of ≤10 mg/day prednisolone-equivalent is associated with adverse outcomes.

Main Methods:

  • Retrospective analysis of 223 MPA patients from the REVEAL cohort (2005-2023).
  • Patients were stratified by 6-month GC dose (≤10 vs. >10 mg/day).
  • Overlap weighting balanced baseline characteristics; Cox models assessed 10-year outcomes; logistic regression identified predictors of GC dose.

Main Results:

  • Reducing GCs to ≤10 mg/day at 6 months showed no increased risk of all-cause mortality, infection-related mortality, or hospitalised infections.
  • No significant increase in all relapses or major relapses was observed with lower GC doses.
  • Treatment initiation from 2020 onwards was associated with achieving a ≤10 mg/day GC dose at 6 months (OR 5.54).

Conclusions:

  • A 6-month GC target of ≤10 mg/day appears safe in MPA patients, not increasing mortality or relapse risks.
  • While a feasible intermediate target, more aggressive GC reduction may be necessary for optimal infection risk reduction.
  • Individualized GC tapering and close patient monitoring remain essential for managing MPA effectively.

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