Amanda J Steiman1, Murray B Urowitz1, Dominique Ibañez1, Anjali Papneja1, Dafna D Gladman2. 1. From the Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital; University of Toronto, Toronto, Ontario, Canada.A.J. Steiman, MD, FRCPC, Rheumatology Fellow; M.B. Urowitz, MD, FRCPC, Professor of Medicine, Director; D.D. Gladman, MD, FRCPC, Professor of Medicine, University of Toronto, and the Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital; D. Ibañez, MSc, Biostatistician, Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital; A. Papneja, Medical Student, Toronto Western Hospital Research Institute, University Health Network. 2. From the Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital; University of Toronto, Toronto, Ontario, Canada.A.J. Steiman, MD, FRCPC, Rheumatology Fellow; M.B. Urowitz, MD, FRCPC, Professor of Medicine, Director; D.D. Gladman, MD, FRCPC, Professor of Medicine, University of Toronto, and the Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital; D. Ibañez, MSc, Biostatistician, Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital; A. Papneja, Medical Student, Toronto Western Hospital Research Institute, University Health Network. dafna.gladman@utoronto.ca.
Abstract
OBJECTIVE: Systemic lupus erythematosus (SLE) is typically a relapsing/remitting disease. However, some patients experience prolonged remission. These patients may provide further insights into SLE pathophysiology. In this study we characterize their clinical course. METHODS: Prolonged remission was defined as Systemic Lupus Erythematosus Disease Activity Index (SLEDAI-2K) = 0, = 2, or = 4 (based on serology) for ≥ 5 consecutive years, with visits ≤ 18 months apart. The patients could be taking antimalarials, but not corticosteroids or immunosuppressives. Flare was defined as clinical activity on SLEDAI-2K, or by corticosteroid/immunosuppressive initiation. Each patient's preremission course was classified as monophasic, relapsing/remitting, or chronic active. These patients were compared to matched SLE controls and patients achieving remission on medications. RESULTS: A total of 38/1613 (2.4%) patients achieved prolonged remission while taking no medications. The mean duration was 11.5 ± 6.4 years. Twenty-seven patients (71.0%) had relapsing/remitting disease, 11 (28.9%) had monophasic illness, and none had chronic active disease prior to remission. They differed from matched controls in ethnicity, disease activity at first visit, and cumulative organ damage. There were 34/1613 patients (2.1%) who achieved prolonged remission while taking steroids and/or immunosuppressives, with mean duration 8.5 ± 2.9 years. Twelve patients (35.3%) experienced disease flare. They were younger at diagnosis, with more disease activity prior to remission than patients taking no medications. CONCLUSION: Prolonged remission is an infrequent outcome among patients and is preceded by an atypically monophasic clinical course in a significant minority. Those taking medications represent a heterogeneous group: those who will tolerate eventual taper, and those whose disease activity was merely suppressed by ongoing immunosuppression. Prolonged remission may reflect unique pathophysiologic mechanisms, and warrants further investigation.
OBJECTIVE:Systemic lupus erythematosus (SLE) is typically a relapsing/remitting disease. However, some patients experience prolonged remission. These patients may provide further insights into SLE pathophysiology. In this study we characterize their clinical course. METHODS: Prolonged remission was defined as Systemic Lupus Erythematosus Disease Activity Index (SLEDAI-2K) = 0, = 2, or = 4 (based on serology) for ≥ 5 consecutive years, with visits ≤ 18 months apart. The patients could be taking antimalarials, but not corticosteroids or immunosuppressives. Flare was defined as clinical activity on SLEDAI-2K, or by corticosteroid/immunosuppressive initiation. Each patient's preremission course was classified as monophasic, relapsing/remitting, or chronic active. These patients were compared to matched SLE controls and patients achieving remission on medications. RESULTS: A total of 38/1613 (2.4%) patients achieved prolonged remission while taking no medications. The mean duration was 11.5 ± 6.4 years. Twenty-seven patients (71.0%) had relapsing/remitting disease, 11 (28.9%) had monophasic illness, and none had chronic active disease prior to remission. They differed from matched controls in ethnicity, disease activity at first visit, and cumulative organ damage. There were 34/1613 patients (2.1%) who achieved prolonged remission while taking steroids and/or immunosuppressives, with mean duration 8.5 ± 2.9 years. Twelve patients (35.3%) experienced disease flare. They were younger at diagnosis, with more disease activity prior to remission than patients taking no medications. CONCLUSION: Prolonged remission is an infrequent outcome among patients and is preceded by an atypically monophasic clinical course in a significant minority. Those taking medications represent a heterogeneous group: those who will tolerate eventual taper, and those whose disease activity was merely suppressed by ongoing immunosuppression. Prolonged remission may reflect unique pathophysiologic mechanisms, and warrants further investigation.
Authors: Vera Golder; Rangi Kandane-Rathnayake; Alberta Yik-Bun Hoi; Molla Huq; Worawit Louthrenoo; Yuan An; Zhan Guo Li; Shue Fen Luo; Sargunan Sockalingam; Chak Sing Lau; Alfred Lok Lee; Mo Yin Mok; Aisha Lateef; Kate Franklyn; Susan Morton; Sandra Teresa V Navarra; Leonid Zamora; Yeong-Jian Wu; Laniyati Hamijoyo; Madelynn Chan; Sean O'Neill; Fiona Goldblatt; Eric Francis Morand; Mandana Nikpour Journal: Arthritis Res Ther Date: 2016-11-09 Impact factor: 5.156
Authors: Pintip Ngamjanyaporn; Eoghan M McCarthy; Jamie C Sergeant; John Reynolds; Sarah Skeoch; Benjamin Parker; Ian N Bruce Journal: Lupus Sci Med Date: 2017-06-29