TY - JOUR
T1 - Predictors of relapse and treatment outcomes in biopsy-proven giant cell arteritis
T2 - A retrospective cohort study
AU - Labarca, Cristian
AU - Koster, Matthew J.
AU - Crowson, Cynthia S.
AU - Makol, Ashima
AU - Ytterberg, Steven R.
AU - Matteson, Eric L.
AU - Warrington, Kenneth J.
N1 - Publisher Copyright:
© The Author 2015.
PY - 2015/10/5
Y1 - 2015/10/5
N2 - Objective. To evaluate characteristics of relapse, relapse rates, treatment and outcomes among patients with biopsy-proven GCA in a large, single-institution cohort. Methods. We conducted a retrospective review of all patients with biopsy-proven GCA from 1998 to 2013. Demographic, clinical, laboratory and treatment data at presentation and during follow-up were collected. Comparisons by relapse rate were performed using chi-square tests. Prednisone discontinuation by initial oral dose ≤40 and >40 mg/day was compared using Cox models. Results. The cohort included 286 patients [74% female, mean age at diagnosis 75.0 years (S.D. 7.6), median follow-up 5.1 years). During follow-up, 73 patients did not relapse, 80 patients had one relapse and 133 had two or more relapses. The first relapse occurred during the first year in 50% of patients, by 2 years in 68% and by 5 years in 79%. More patients with established hypertension (P = 0.007) and diabetes (P = 0.039) at GCA diagnosis were in the high relapse rate group (≥0.5 relapses/year) and more females were in the low or high relapse groups than in the no relapse group (P = 0.034). Patients receiving an initial oral prednisone dose>40 mg/day were able to reach a dose of<5 mg/day [hazard ratio (HR) 1.46 (95% CI 1.09, 1.96)] and discontinue prednisone [HR 1.56 (95% CI 1.09, 2.23)] sooner than patients receiving≤40 mg/day without an increase in observed glucocorticoid-associated adverse events. Conclusion. Females and patients with hypertension or diabetes at GCA diagnosis have more relapses during follow-up. Patients treated with an initial oral prednisone dose>40 mg/day achieved earlier prednisone discontinuation.
AB - Objective. To evaluate characteristics of relapse, relapse rates, treatment and outcomes among patients with biopsy-proven GCA in a large, single-institution cohort. Methods. We conducted a retrospective review of all patients with biopsy-proven GCA from 1998 to 2013. Demographic, clinical, laboratory and treatment data at presentation and during follow-up were collected. Comparisons by relapse rate were performed using chi-square tests. Prednisone discontinuation by initial oral dose ≤40 and >40 mg/day was compared using Cox models. Results. The cohort included 286 patients [74% female, mean age at diagnosis 75.0 years (S.D. 7.6), median follow-up 5.1 years). During follow-up, 73 patients did not relapse, 80 patients had one relapse and 133 had two or more relapses. The first relapse occurred during the first year in 50% of patients, by 2 years in 68% and by 5 years in 79%. More patients with established hypertension (P = 0.007) and diabetes (P = 0.039) at GCA diagnosis were in the high relapse rate group (≥0.5 relapses/year) and more females were in the low or high relapse groups than in the no relapse group (P = 0.034). Patients receiving an initial oral prednisone dose>40 mg/day were able to reach a dose of<5 mg/day [hazard ratio (HR) 1.46 (95% CI 1.09, 1.96)] and discontinue prednisone [HR 1.56 (95% CI 1.09, 2.23)] sooner than patients receiving≤40 mg/day without an increase in observed glucocorticoid-associated adverse events. Conclusion. Females and patients with hypertension or diabetes at GCA diagnosis have more relapses during follow-up. Patients treated with an initial oral prednisone dose>40 mg/day achieved earlier prednisone discontinuation.
KW - Adverse events
KW - Cohort
KW - Diabetes
KW - Giant cell arteritis
KW - Glucocorticoids
KW - Hypertension
KW - Relapse
KW - Retrospective
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U2 - 10.1093/rheumatology/kev348
DO - 10.1093/rheumatology/kev348
M3 - Article
C2 - 26385368
AN - SCOPUS:84961942710
SN - 1462-0324
VL - 55
SP - 347
EP - 356
JO - Rheumatology and Rehabilitation
JF - Rheumatology and Rehabilitation
IS - 2
ER -