ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meeting Abstracts
    • All Meetings
    • ACR Convergence 2026
    • PRSYM 2026
    • ACR Convergence 2025
    • Download Abstract Supplements
  • Keyword Index
  • My Favorites
    • View & print my favorites
  • Search

Home » Meeting Abstracts » Pediatric Rheumatology Symposium 2017

Abstract Number: 26

Gray Matter Volume Loss in Youth with SLE

Andrea Knight1, Michelle Vickery2, Arastoo Vossough3, Guray Erus4, Jimit Doshi5 and Susan Furth6, 1Center for Pediatric Clinical Effectiveness & PolicyLab, Philadelphia, PA, 2PolicyLab, Children's Hospital of Philadelphia, Philadelphia, PA, 3Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, 4Section on Biomedical Image Analysis, University of Pennsylvania, Philadelphia, PA, 5Section of Biomedical Image Analysis, University of Pennsylvania, Philadelphia, PA, 6Division of Nephrology, Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA

Share on X (Twitter) Share on Facebook Share on LinkedIn Share on Email
Print

Meeting: Pediatric Rheumatology Symposium 2017

Keywords: Lupus, Neuroimaging, neurologic involvement and pediatric rheumatology

Session Information

Date: Saturday, May 20, 2017

Title: Clinical and Therapeutic Poster Breakout II

Session Type: Abstract Submissions

Session Time: 5:15PM-5:45PM

Background/Purpose: Neuropsychiatric SLE in children and adolescents presents diagnostic challenge due to limitations of conventional magnetic resonance imaging (MRI) to detect clinically relevant brain changes. We examined structural brain abnormalities in pediatric-onset SLE (pSLE) utilizing advanced MRI techniques.

Methods: We conducted a cross-sectional analysis of clinically-obtained brain MRI images from subjects with pSLE, and compared them to existing brain MRI images from age and sex-matched controls from another study.  All images were obtained between 2007 and 2015 on the same scanner at 3T using a T1-weighted MPRAGE (magnetization-prepared rapid, acquisition gradient echo) protocol. We used an advanced multi-atlas segmentation algorithm to divide the brain into 154 anatomical regions of interest (ROIs), organized hierarchically within larger brain structures. We calculated volumes of individual ROIs and larger brain structures, and compared volumetric measurements from pSLE and control subjects using univariate paired t-tests. ROIs with significant group differences after Bonferroni correction for multiple comparisons (q<0.01, where q=p/#ROIs tested) were reported. A neuroradiologist, blinded to the volumetric results, performed conventional re-reads of MRIs for pSLE subjects.

Results: We matched 28 SLE adolescents to 28 controls, comprised of 89% females with a mean age of 15.9 (SD=3.6). Median disease duration for SLE subjects was 1.1 years (interquartile range, IQR 0.3, 2.9), and median SLEDAI score was 5 (IQR 1, 11). There was a history of nephritis in 12 (43%), seizures and/or stroke in 5 (18%), anti-phospholipid syndrome in 3 (11%), depression and/or anxiety in 18 (64%). Glucocorticoids were used by 89% of pSLE subjects at the time of MRI (median prednisone dose=5 mg, IQR=10,25). Conventional pSLE MRI reads indicated T2 hyperintensities in 48% and mild diffuse volume loss in 28%. Using advanced segmentation, total brain volume did not differ between groups, but volumes in specific gray matter ROIs were significantly decreased in pSLE subjects compared to controls (q<0.01). These ROIs are involved in: decision-making, memory, and social cognition (right medial frontal cortex); empathy, emotional memory and processing (right temporal pole, left anterior cingulate gyrus); topographical and facial recognition (right lingual gyrus); language processing (left parietal lateral cortex, bilateral planum polare, frontal operculum); visual and spatial attention (bilateral cuneus).

Conclusion: Compared to healthy peers, children and adolescents with SLE have decreased gray matter volumes in regions involved in executive function, social cognition, language and emotional processing. Future study should examine the functional correlates of these structural brain abnormalities.


Disclosure: A. Knight, None; M. Vickery, None; A. Vossough, None; G. Erus, None; J. Doshi, None; S. Furth, None.

To cite this abstract in AMA style:

Knight A, Vickery M, Vossough A, Erus G, Doshi J, Furth S. Gray Matter Volume Loss in Youth with SLE [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 4). https://acrabstracts.org/abstract/gray-matter-volume-loss-in-youth-with-sle/. Accessed .

ACR Meeting Abstracts - https://acrabstracts.org/abstract/gray-matter-volume-loss-in-youth-with-sle/

My Favorites

Save and print abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract (must have cookies enabled in browser). See saved favorites.

Abstract Policies

  • ACR Convergence Abstract Embargo Policies
  • ACR Convergence Abstract Permissions & Reprints
  • PRSYM Abstract Policies

ACR Convergence. Where Rheumatology Meets

ACR Convergence 2026

Join us November 6-11 in Orlando, Florida.
See Registration Information

  • Contact ACR
  • Privacy Policy
  • ACR Policies
  • Cookie Preferences

© Copyright 2026 American College of Rheumatology