3.8 Article

Initial validation of the pediatric automated neuropsychological assessment metrics for childhood-onset systemic lupus erythematosus

Journal

ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH
Volume 57, Issue 7, Pages 1174-1182

Publisher

WILEY-LISS
DOI: 10.1002/art.23005

Keywords

cognitive functioning; systemic lupus erythematosus; children; automated neuropsychological assessment metrics

Categories

Funding

  1. NCRR NIH HHS [M01-RR-08084] Funding Source: Medline
  2. NIAMS NIH HHS [P60-AR-47784] Funding Source: Medline

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Objective. To evaluate the concurrent validity and diagnostic accuracy of the pediatric Automated Neuropsychological Assessment Metrics (Ped-ANAM) when used in childhood-onset systemic lupus erythematosus (SLE). Methods. Formal neuropsychological testing and the Ped-ANAM were performed on 27 children with SLE who had not been previously diagnosed with neuropsychiatric SLE. Performance when completing the 10 Ped-ANAM tests was based on accuracy (AC), mean time to correct response, coefficient of variation of the time required for a correct response (CVc), and throughput. Formal neuropsychological testing was used as a criterion standard for diagnosing neurocognitive dysfunction (NCD; yes/no). Results. NCD was common and present in 16 (59%) of 27 participants. Ped-ANAM performance parameters were often moderately correlated with the Z scores on formal neuropsychological testing. The NCD group differed significantly (P < 0.05) from the normal cognition group in 3 Ped-ANAM tests: CVc with mathematical processing (MTH-CVc), AC with continuous performance test (CPT-AC), and CVc with spatial processing (SPD-CVc). Areas under the receiver operating curves (AUCs) ranged between 0.75 and 0.84 when each of these parameters (CPT-AC, MTH-CVc, SPD-CVc) was used to identify NCD independently. The AUC was improved to 0.96 for the combined assessment. Conclusion. The Ped-ANAM has concurrent validity when used in children with SLE. Initial validation suggests that the Ped-ANAM could be a useful screening tool for NCD in children with SLE.

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