Brain Function Differences in Children With Type 1 Diabetes: A Functional MRI Study of Working Memory

Author:

Foland-Ross Lara C.1,Tong Gabby1ORCID,Mauras Nelly2,Cato Allison3,Aye Tandy4,Tansey Michael5ORCID,White Neil H.6,Weinzimer Stuart A.7,Englert Kimberly2,Shen Hanyang1,Mazaika Paul K.1ORCID,Reiss Allan L.148,Tsalikian Eva,Tansey Michael J.,Coffey Julie,Cabbage Joanne,Salamat Sara,Bisbee Rachel,Mauras Nelly,Fox Larry A.,Cato Allison,Englert Kim,Sikes Kaitlin,Ewen Tina,Bird Keisha,Buckingham Bruce A.,Wilson Darrell M.,Aye Tandy,Kingman Ryan S.,Weinzimer Stuart A.,Tamborlane William V.,Ambrosino Jodie,Steffen Amy,Weyman Kate,Zgorski Melinda,White Neil H.,Arbelaez Ana Maria,Levandoski Lucy,Starnes Angie,Hershey Tamara,Reiss Allan L.,Foland-Ross Lara,Marzelli Matthew J.,Mazaika Paul K.,Tong Gabby,Sperling Mark,Becker Dorothy M.,Cleary Patricia,Greenbaum Carla,Moran Antoinette,

Affiliation:

1. Center for Interdisciplinary Brain Sciences Research, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA

2. Division of Endocrinology, Diabetes and Metabolism, Nemours Children’s Health System, Jacksonville, FL

3. Division of Neurology, Nemours Children’s Health System, Jacksonville, FL

4. Department of Pediatrics, Stanford University School of Medicine, Stanford, CA

5. Department of Pediatrics, The University of Iowa, Iowa City, IA

6. Department of Pediatrics, Washington University in St. Louis and the St. Louis Children’s Hospital, St. Louis, MO

7. Pediatric Endocrinology, Yale University, New Haven, CT

8. Department of Radiology, Stanford University School of Medicine, Stanford, CA

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.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Center for Advancing Translational Sciences

National Center for Research Resources

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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