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Abstract Number: 2647

Predictors of Incident Seizure in Systemic Lupus Erythematosus

Xiangyang Huang1, Laurence S. Magder2 and Michelle Petri3, 1Sichuan University School of Medicine, Sichuan, China, 2Department of Epidemiology and Public Health, University of Maryland, Baltimore, MD, 3Johns Hopkins University School of Medicine, Baltimore, MD

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Systemic lupus erythematosus (SLE)

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Session Information

Title: Systemic Lupus Erythematosus - Clinical Aspects and Treatment: Epidemiology, Women's Health, Cardiovascular and CNS

Session Type: Abstract Submissions (ACR)

Background/Purpose: We identified the rate and risk factors for first occurrences of seizure based on a large closely followed longitudinal cohort of patients with systemic lupus erythematosus.

Methods: Rates of incident seizure were calculated overall and in subgroups defined by demographic and clinical variables.  Adjusted estimates of association of risk factors were derived using pooled logistic regression.

Results: Of 2203 patients with no history of seizure prior to SLE diagnosis, 157 (7.1%) had the first seizure occurrence at the time of (37 patients, 1.63%) or after the diagnosis of (120 patients, 5.44%) SLE.  The rate of incident seizure was 4.9 per 1000 person-years.  The risk of seizure occurring around the time of SLE diagnosis was higher in patients with a history of malar rash (p = 0.002), proteinuria (p = 0.004), and psychosis (p < 0.000).  Multivariable analysis of the first seizure occurring after the diagnosis of SLE showed that history of low C3 (RR = 1.763, p = 0.0078), psychosis (RR = 2.432, p < 0.0001), cranial or peripheral neuropathy (RR = 2.212, p = 0.0043), anti-Smith (RR = 1.518, p = 0.0551), renal involvement (urine dipstick protein positive 3+) (RR = 2.888, p = 0.0177) and current prednisone dose (RR = 9.960, p < 0.0001) were independently associated with a higher risk of incident seizure.  SELENA-SLEDAI was not predictive and hydroxychloroquine was not protective after adjusting for the other variables in the model.

Conclusion: Seizure in SLE is multi-factorial.  The risk of seizure in SLE is independently increased in those patients with prior psychosis, neuropathy, proteinuria, anti-Sm, low C3 and current corticosteroid use.  Anti-Sm is of particular interest as it has also been incriminated in other CNS-SLE syndromes.


Disclosure:

X. Huang,
None;

L. S. Magder,
None;

M. Petri,
None.

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