PLoS ONE (Jan 2013)

Recovery of adrenal function after long-term glucocorticoid therapy for giant cell arteritis: a cohort study.

  • Yvan Jamilloux,
  • Eric Liozon,
  • Gregory Pugnet,
  • Sylvie Nadalon,
  • Kim Heang Ly,
  • Stephanie Dumonteil,
  • Guillaume Gondran,
  • Anne-Laure Fauchais,
  • Elisabeth Vidal

DOI
https://doi.org/10.1371/journal.pone.0068713
Journal volume & issue
Vol. 8, no. 7
p. e68713

Abstract

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OBJECTIVES: Giant cell arteritis (GCA) is a chronic systemic vasculitis of large and medium-sized arteries, for which long-term glucocorticoid (GC) treatment is needed. During GC withdrawal patients can suffer adrenal insufficiency. We sought to determine the time until recovery of adrenal function after long-term GC therapy, and to assess the prevalence and predictors for secondary adrenal insufficiency. SUBJECTS AND DESIGN: 150 patients meeting the ACR criteria for GCA between 1984 and 2012 were analyzed. All received the same GC treatment protocol. The low-dose ACTH stimulation test was repeated annually until adrenal recovery. Biographical, clinical and laboratory data were collected prospectively and compared. RESULTS: At the first ACTH test, 74 (49%) patients were non-responders: of these, the mean time until recovery of adrenal function was 14 months (max: 51 months). A normal test response occurred within 36 months in 85% of patients. However, adrenal function never recovered in 5% of patients. GC of >15 mg/day at 6 months, GC of >9.5 mg/day at 12 months, treatment duration of >19 months, a cumulative GC dose of >8.5 g, and a basal cortisol concentration of <386 nmol/L were all statistically associated with a negative response in the first ACTH test (p <0.05). CONCLUSION: Adrenal insufficiency in patients with GCA, treated long-term with GC, was frequent but transitory. Thus, physicians' vigilance should be increased and an ACTH test should be performed when GC causes the above associated statistical factors.