Session Type: ACR Poster Session B
Session Time: 9:00AM-11:00AM
Background/Purpose: ANCA-associated vasculitides (AAVs) are potentially life-threatening diseases rarely observed in childhood. Whether AAVs in children (cAAVs) differ from adult-onset AAVs (aAAVs) is still not known. This study was undertaken to investigate differences in clinical presentations and disease outcomes between cAAV cases and matched aAAV controls.
Methods: Demographic and clinical data and disease outcomes of consecutive patients (age <18 years at diagnosis) with cAAVs satisfying ACR, PRINTO/EULAR classification criteria and/or the revised Chapel Hill Nomenclature for Vasculitides were compared to a randomly selected sample of aAAV patients from the French Vasculitis Study Group (FVSG) registry. Cases and controls were matched for the following features: AAV (granulomatosis with polyangiitis [GPA], microscopic polyangiitis [MPA] or eosinophilic granulomatosis with polyangiitis [EGPA]), sex, year of enrollment and duration of follow-up after diagnosis. Prospectively collected information included medications, and disease activity and damage as assessed by the Birmingham Vasculitis Activity Score (BVAS) and the Vasculitis Damage Index (VDI), respectively. Relapses, survival rates and causes of death were analyzed. Kaplan–Meier curves and the log-rank test were used to analyze predefined-outcome differences between cases and controls. STROBE guidelines for reporting observational studies were applied.
Results: Thirty-five cAAV cases (25 GPA, 4 MPA, 6 EGPA) were compared with 151 aAAV controls (106 GPA, 17 MPA, 28 EGPA). Respective median ages (range) were 14 (2–17) vs. 53 (18–87) years, with median AAV follow-up durations of 71 and 64 months (P=0.49), respectively. At study entry, children had less frequent myalgias (P=0.005) and peripheral neuropathy (P<0.001) but were more frequently febrile (P<0.05). Their respective rates of renal involvement were comparable (13 (37%) vs. 73 (48%); P=0.31). Initial GPA-associated ischemic abdominal pain and nasal cartilage damage were more common in cAAVs than aAAVs (P<0.05). Their first remission-induction regimens were comparable (P=0.13), most frequently combining glucocorticoids and an immunosuppressant. During follow-up, cAAV patients had a higher overall relapse rate (24.5 vs. 18.7 flares per 100 patient-years; P<0.05) and, at last visit, had accumulated more damage, mostly ENT sequelae (P=0.001), associated with longer maintenance therapy (P=0.03) than for aAAV controls. Four (11.4%) cAAV and 13 (8.6%) aAAV patients died (P=0.54).
Conclusion: cAAVs are severe diseases, characterized by a higher relapse rate, more accrued damage, mostly ENT sequelae, and longer maintenance therapy than aAAVs.
To cite this abstract in AMA style:Iudici M, Pagnoux C, Quartier P, Büchler M, Cevallos R, Cohen P, de Moreuil C, Guilpain P, Le Quellec A, Serratrice J, Terrier B, Le Jeunne C, Guillevin L, Mouthon L, Puéchal for the French Vasculitis Study Group X. Childhood- Vs. Adult-Onset ANCA-Associated Vasculitides: A Nested, Matched Case–Control Study from the French Vasculitis Study Group Registry [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/childhood-vs-adult-onset-anca-associated-vasculitides-a-nested-matched-case-control-study-from-the-french-vasculitis-study-group-registry/. Accessed July 6, 2020.
« Back to 2017 ACR/ARHP Annual Meeting
ACR Meeting Abstracts - https://acrabstracts.org/abstract/childhood-vs-adult-onset-anca-associated-vasculitides-a-nested-matched-case-control-study-from-the-french-vasculitis-study-group-registry/