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Comparative Study
. 2011 Aug;63(8):1178-87.
doi: 10.1002/acr.20489.

Neurocognitive impairment in childhood-onset systemic lupus erythematosus: measurement issues in diagnosis

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Comparative Study

Neurocognitive impairment in childhood-onset systemic lupus erythematosus: measurement issues in diagnosis

Tricia S Williams et al. Arthritis Care Res (Hoboken). 2011 Aug.

Abstract

Objective: To assess the prevalence of neurocognitive impairment (NCI) in childhood-onset systemic lupus erythematosus (cSLE) by comparing published classification criteria, and to examine associations between NCI, disease characteristics, psychosocial well-being, and intelligence.

Methods: cSLE patients and ethnicity- and age-matched healthy controls completed a neuropsychological research battery, and results were categorized by 3 different NCI classification criteria with different cutoff scores (e.g., >2, 1.5, or 1 SD below the mean) and the number of required abnormal tests or domains.

Results: Forty-one cSLE subjects and 22 controls were included. Subjects were predominantly female (~70%) and Hispanic (∼70%). Executive functioning, psychomotor speed, and fine motor speed were most commonly affected. Method 1 classified 34.1% of cSLE subjects with NCI compared to method 2 (14.6% with decline and 7.3% with NCI) and method 3 (63.4% with NCI). The prevalence of NCI was not significantly different between the controls and patients using any of the categorization methods. NCI was not associated with SLE disease activity or characteristics or with depression. Using method 3, patients in the cognitive impairment group reported significantly lower quality of life estimates (69.7 versus 79.3; P = 0.03). Below average intellectual functioning (intelligence quotient <90) differentiated the number of test scores >1 and >1.5 SDs, but not >2 SDs below the mean.

Conclusion: NCI was prevalent in cSLE, but varied according to the chosen categorization method. A similar proportion of cSLE patients and controls had NCI, reinforcing the importance of studying an appropriate control group. Categorical classification (i.e., impaired/nonimpaired) may oversimplify the commonly observed deficits in cSLE.

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Figure 1
Figure 1
Test Results by Intelligence Level SD = standard deviation; *p<.01; #p<.05; Average IQ defined as Intelligence Quotient ≥ 90; Below Average IQ defined as Intelligence Quotient <89

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References

    1. The American College of Rheumatology nomenclature and case definitions for neuropsychiatric lupus syndromes. Arthritis Rheum. 1999;42:599–608. - PubMed
    1. Benseler SM, Silverman ED. Review: Neuropsychiatric involvement in pediatric systemic lupus erythematosus. Lupus. 2007;16:564–571. - PubMed
    1. Kozora E, Hanly JG, Lapteva L, Filley CM. Cognitive dysfunction in systemic lupus erythematosus: past, present, and future. Arthritis Rheum. 2008;58:3286–3298. - PubMed
    1. Levy DM, Ardoin SP, Schanberg LE. Neurocognitive impairment in children and adolescents with systemic lupus erythematosus. Nat Clin Pract Rheumatol. 2009;5:106–114. - PMC - PubMed
    1. Brunner H, Ruth N, German A, et al. Initial validation of the Pediatric Automated Neuropsychological Assessment Metrics for childhood-onset systemic lupus erythematosus. Arthritis Rheum. 2007;75:1174–1182. - PubMed

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