PLoS Medicine (Dec 2019)

Executive task-based brain function in children with type 1 diabetes: An observational study.

  • Lara C Foland-Ross,
  • Bruce Buckingam,
  • Nelly Mauras,
  • Ana Maria Arbelaez,
  • William V Tamborlane,
  • Eva Tsalikian,
  • Allison Cato,
  • Gabby Tong,
  • Kimberly Englert,
  • Paul K Mazaika,
  • Allan L Reiss,
  • Diabetes Research in Children Network (DirecNet)

DOI
https://doi.org/10.1371/journal.pmed.1002979
Journal volume & issue
Vol. 16, no. 12
p. e1002979

Abstract

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BackgroundOptimal glycemic control is particularly difficult to achieve in children and adolescents with type 1 diabetes (T1D), yet the influence of dysglycemia on the developing brain remains poorly understood.Methods and findingsUsing a large multi-site study framework, we investigated activation patterns using functional magnetic resonance imaging (fMRI) in 93 children with T1D (mean age 11.5 ± 1.8 years; 45.2% female) and 57 non-diabetic (control) children (mean age 11.8 ± 1.5 years; 50.9% female) as they performed an executive function paradigm, the go/no-go task. Children underwent scanning and cognitive and clinical assessment at 1 of 5 different sites. Group differences in activation occurring during the contrast of "no-go > go" were examined while controlling for age, sex, and scan site. Results indicated that, despite equivalent task performance between the 2 groups, children with T1D exhibited increased activation in executive control regions (e.g., dorsolateral prefrontal and supramarginal gyri; p = 0.010) and reduced suppression of activation in the posterior node of the default mode network (DMN; p = 0.006). Secondary analyses indicated associations between activation patterns and behavior and clinical disease course. Greater hyperactivation in executive control regions in the T1D group was correlated with improved task performance (as indexed by shorter response times to correct "go" trials; r = -0.36, 95% CI -0.53 to -0.16, p ConclusionsThese data indicate that increased recruitment of executive control areas in pediatric T1D may act to offset diabetes-related impairments in the DMN, ultimately facilitating cognitive and behavioral performance levels that are equivalent to that of non-diabetic controls. Future studies that examine whether these patterns change as a function of improved glycemic control are warranted.