Abstract
IntroductionNeuropsychiatric manifestations are common in childhood-onset systemic lupus erythematosus (cSLE) and often include neurocognitive dysfunction (NCD). Functional magnetic resonance imaging (fMRI) can measure brain activation during tasks that invoke domains of cognitive function impaired by cSLE. This study investigates specific changes in brain function attributable to NCD in cSLE that have potential to serve as imaging biomarkers.MethodsFormal neuropsychological testing was done to measure cognitive ability and to identify NCD. Participants performed fMRI tasks probing three cognitive domains impacted by cSLE: visuoconstructional ability (VCA), working memory, and attention. Imaging data, collected on 3-Tesla scanners, included a high-resolution T1-weighted anatomic reference image followed by a T2*-weighted whole-brain echo planar image series for each fMRI task. Brain activation using blood oxygenation level-dependent contrast was compared between cSLE patients with NCD (NCD-group, n = 7) vs. without NCD (noNCD-group, n = 14) using voxel-wise and region of interest-based analyses. The relationship of brain activation during fMRI tasks and performance in formal neuropsychological testing was assessed.ResultsGreater brain activation was observed in the noNCD-group vs. NCD-group during VCA and working memory fMRI tasks. Conversely, compared to the noNCD-group, the NCD-group showed more brain activation during the attention fMRI task. In region of interest analysis, brain activity during VCA and working memory fMRI tasks was positively associated with the participants' neuropsychological test performance. In contrast, brain activation during the attention fMRI task was negatively correlated with neuropsychological test performance. While the NCD group performed worse than the noNCD group during VCA and working memory tasks, the attention task was performed equally well by both groups.ConclusionsNCD in patients with cSLE is characterized by differential activation of functional neuronal networks during fMRI tasks probing working memory, VCA, and attention. Results suggest a compensatory mechanism allows maintenance of attentional performance under NCD. This mechanism appears to break down for the VCA and working memory challenges presented in this study. The observation that neuronal network activation is related to the formal neuropsychological testing performance makes fMRI a candidate imaging biomarker for cSLE-associated NCD.
Highlights
Neuropsychiatric manifestations are common in childhood-onset systemic lupus erythematosus and often include neurocognitive dysfunction (NCD)
Site comparison for this study focused on calculations of signal-to-noise ratio (SNR) and signal-to-fluctuation noise ratio (SFNR)
We demonstrated greater activation in an insular/superior temporal region of interest (ROI) in the presence of clinically overt NCD compared to no NCD while continuous performance taskidentical pairs (CPT-IP) performance remained unaffected
Summary
Neuropsychiatric manifestations are common in childhood-onset systemic lupus erythematosus (cSLE) and often include neurocognitive dysfunction (NCD). Functional magnetic resonance imaging (fMRI) can measure brain activation during tasks that invoke domains of cognitive function impaired by cSLE. Studies suggest that neuropsychiatric systemic lupus erythematosus (NPSLE) is present in as many as 80% of adults with SLE [1,2,3] and may be even more common in childhood-onset SLE (cSLE) [3,4]. Neurocognitive dysfunction (NCD) is one of the many manifestations of NPSLE and is encountered in up to 59% of all children with cSLE, often impairing attention, visuoconstructional ability (VCA), and working memory [3], conventional structural brain imaging often fails to identify matching pathology. The objective of this study was to use fMRI to characterize differences in neuronal network activation that distinguish patients with cSLE-associated NCD from cSLE patients with normal cognition
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