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Abstract Number: 1591

Monophasic Disease Course Pattern in Systemic Lupus Erythematosus

Konstantinos Tselios1, Dafna D Gladman2, Zahi Touma3, Jiandong Su4, Nicole Anderson2 and Murray Urowitz5, 1Medicine, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 3Rheumatology, University of Toronto, Division of Rheumatology, Institute of Health Policy, Management and Evaluation, Toronto, ON, Canada, 4University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 5Centre for Prognosis Studies in the Rheumatic Diseases, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: phenotypes and systemic lupus erythematosus (SLE)

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Session Information

Date: Monday, November 6, 2017

Title: Systemic Lupus Erythematosus – Clinical Aspects and Treatment Poster II: Damage and Comorbidities

Session Type: ACR Poster Session B

Session Time: 9:00AM-11:00AM

Background/Purpose: Disease course in systemic lupus erythematosus (SLE) is believed to follow three distinct patterns over time, namely relapsing-remitting, persistently active and prolonged quiescent. We recently showed that a small subgroup of patients might follow a course characterized by an initial active clinical presentation, followed by complete clinical remission, occasionally with no medications. The aim of the present study was to assess the prevalence, demographic, clinical and immunological characteristics of such patients.

Methods: The inception cohort a large lupus clinic (patients enrolled within 18 months from diagnosis) was investigated. Selected patients had a minimum follow-up of 10 years and no interval greater than 18 months between consecutive visits. Prolonged clinical remission was defined as clinical SLEDAI-2K=0 (serology excluded), achieved within the first five years since diagnosis and maintained for ≥10 years. Descriptive statistics were used.

Results: Of 883 inception patients, 382 met inclusion criteria. Twenty-seven (24 females, 21 Caucasians) achieved prolonged clinical remission (prevalence 7.1%) in 1.6 ± 1.3 years (median 1.2) since diagnosis. Mean age at diagnosis was 39±14.1 years. Clinical manifestations at diagnosis included mucocutaneous involvement in 19 (70.4%), arthritis in 16 (59.3%), serositis in 5 (18.5%), nephritis in 7 (25.9%), central nervous system in 2 (7.4%) and cytopenias in 15 (55.6%). Immunological and therapeutic characteristics are shown in Table 1.

Table 1. Clinical, immunological and therapeutic characteristics at enrollment and at 10 years

Variable

At enrollment

At 10 years

SLEDAI-2K (mean±SD)

10.7±11.6

1.19±1.59

Low C3/C4

9 (33.3%)

8 (29.6%)

Anti-dsDNA (+)

13 (48.1%)

6 (22.2%)

Anti-SSA/Ro (+)

8 (29.6%)

8 (29.6%)

Anti-SSB/La (+)

1 (3.7%)

2 (7.4%)

Anti-Sm (+)

1 (3.7%)

3 (11.1%)

Anti-RNP (+)

3 (11.1%)

5 (18.5%)

Antimalarials (n, %)

16 (59.3%)

11 (40.7%)

Glucocorticosteroids (n, %)

17 (63%)

6 (22.2%)

Mean prednisone dose (mg/day)

16.8±9.5

5.3±3.2

Immunosuppressives (n, %)

9 (33.3%)

3 (11.1%)

SLICC/DI (mean±SD)

0.26±0.53 *

0.96±1.06

* At one year after diagnosis, SLICC/DI: Systemic Lupus International Collaborating Clinics/Damage Index

Cumulative glucocorticosteroid dose over 10 years was 18.1±12.4grams. Beyond 10 years, 7 patients (25.9%) relapsed at a mean of 15.2±3.8 years since diagnosis (four with musculoskeletal and/or skin involvement). In the remaining three patients (two with nephritis and one with catastrophic antiphospholipid syndrome), the flare occurred during or shortly after pregnancy. Twenty of the 27 patients (5.2% of the entire cohort) sustained remission for the entire length of follow-up (17.8±6.7 years) and thus had pure monophasic disease. Twelve patients (44.4%) were not taking any medications after 10 years. Three patients died (11.1%), one from lung cancer and two from unknown cause.

Conclusion: A monophasic disease course was observed in 5.2% of our inception SLE patients, while approximately half of them maintained remission without any medications after 10 years from diagnosis.  


Disclosure: K. Tselios, None; D. D. Gladman, None; Z. Touma, None; J. Su, None; N. Anderson, None; M. Urowitz, GlaxoSmithKline, 5.

To cite this abstract in AMA style:

Tselios K, Gladman DD, Touma Z, Su J, Anderson N, Urowitz M. Monophasic Disease Course Pattern in Systemic Lupus Erythematosus [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/monophasic-disease-course-pattern-in-systemic-lupus-erythematosus/. Accessed .
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