| Literature DB >> 32471809 |
Lara C Foland-Ross1, Gabby Tong2, Nelly Mauras3, Allison Cato4, Tandy Aye5, Michael Tansey6, Neil H White7, Stuart A Weinzimer8, Kimberly Englert3, Hanyang Shen2, Paul K Mazaika2, Allan L Reiss.
Abstract
Glucose is a primary fuel source to the brain, yet the influence of dysglycemia on neurodevelopment in children with type 1 diabetes remains unclear. We examined brain activation using functional MRI in 80 children with type 1 diabetes (mean ± SD age 11.5 ± 1.8 years; 46% female) and 47 children without diabetes (control group) (age 11.8 ± 1.5 years; 51% female) as they performed a visuospatial working memory (N-back) task. Results indicated that in both groups, activation scaled positively with increasing working memory load across many areas, including the frontoparietal cortex, caudate, and cerebellum. Between groups, children with diabetes exhibited reduced performance on the N-back task relative to children in the control group, as well as greater modulation of activation (i.e., showed greater increase in activation with higher working memory load). Post hoc analyses indicated that greater modulation was associated in the diabetes group with better working memory function and with an earlier age of diagnosis. These findings suggest that increased modulation may occur as a compensatory mechanism, helping in part to preserve working memory ability, and further, that children with an earlier onset require additional compensation. Future studies that test whether these patterns change as a function of improved glycemic control are warranted.Entities:
Mesh:
Year: 2020 PMID: 32471809 PMCID: PMC7372069 DOI: 10.2337/db20-0123
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461