TY - JOUR
T1 - Impact of Type 1 Diabetes in the Developing Brain in Children
T2 - A Longitudinal Study
AU - Diabetes Research in Children Network (DirecNet)
AU - Mauras, Nelly
AU - Buckingham, Bruce
AU - White, Neil H.
AU - Tsalikian, Eva
AU - Weinzimer, Stuart A.
AU - Jo, Booil
AU - Cato, Allison
AU - Fox, Larry A.
AU - Aye, Tandy
AU - Arbelaez, Ana Maria
AU - Hershey, Tamara
AU - Tansey, Michael
AU - Tamborlane, William
AU - Foland-Ross, Lara C.
AU - Shen, Hanyang
AU - Englert, Kimberly
AU - Mazaika, Paul
AU - Marzelli, Matthew
AU - Reiss, Allan L.
N1 - Funding Information:
The authors thank all the children and their families for participating in these studies. The authors thank the clinical and imaging staff at all the investigator sites as well as external collaborators for the use of imaging facilities, including University of Florida Shands Jacksonville Medical Center, University of California at San Francisco, and El Camino Hospital (Mountain View, CA). The authors also thank Karen Winer, program officer at the Eunice Kennedy Shriver National Institute of Child Health and Human Development, for advice and support; Roy Beck and the Jaeb Center for Health Research for glucose analytics; and the data and safety monitoring board, including Mark Sperling (chair) (Emeritus University of Pittsburgh), Doro-thy M. Becker (University of Pittsburgh), Carla Greenbaum (Benaroya Research Institute), and Antoinette Moran (University of Minnesota). The authors are grateful to Medtronic for supplying the iPro2 CGM and to LifeScan for supplying the OneTouch Ultra 2 meter and test strips used in these studies. Funding. This research was supported by National Institutes of Health Eunice Kennedy Shriver National Institute of Child Health and Human Development grant R01-HD-078463 aswellasgrants U01-HD-41908, U01-HD-41915, U01-HD-41918, U01-HD-56526, and U01-HD-41906 (Washington University in St. Louis), and U.S. Department of Health and Human Services grants U54-HD-087011 (Washington University in St. Louis) and UL1-TR-001085 (Stanford University).
Publisher Copyright:
© 2021, American Diabetes Association Inc. All rights reserved.
PY - 2021/4
Y1 - 2021/4
N2 - OBJECTIVE To assess whether previously observed brain and cognitive differences between children with type 1 diabetes and control subjects without diabetes persist, worsen, or improve as children grow into puberty and whether differences are associated with hyperglycemia. RESEARCH DESIGN AND METHODS One hundred forty-four children with type 1 diabetes and 72 age-matched control subjects without diabetes (mean ± SD age at baseline 7.0 ± 1.7 years, 46% female) had unsedated MRI and cognitive testing up to four times over 6.4 ± 0.4 (range 5.3– 7.8) years; HbA1c and continuous glucose monitoring were done quarterly. Free-Surfer-derived brain volumes and cognitive metrics assessed longitudinally were compared between groups using mixed-effects models at 6, 8, 10, and 12 years. Correlations with glycemia were performed. RESULTS Total brain, gray, and white matter volumes and full-scale and verbal intelligence quotients (IQs) were lower in the diabetes group at 6, 8, 10, and 12 years, with estimated group differences in full-scale IQ of-4.15,-3.81,-3.46, and-3.11, respectively (P < 0.05), and total brain volume differences of-15,410,-21,159,-25,548, and-28,577 mm3 at 6, 8, 10, and 12 years, respectively (P < 0.05). Differences at baseline persisted or increased over time, and brain volumes and cognitive scores negatively correlated with a life-long HbA1c index and higher sensor glucose in diabetes. CONCLUSIONS Detectable changes in brain volumes and cognitive scores persist over time in children with early-onset type 1 diabetes followed longitudinally; these differences are associated with metrics of hyperglycemia. Whether these changes can be reversed with scrupulous diabetes control requires further study. These longitudinal data support the hypothesis that the brain is a target of diabetes complications in young children.
AB - OBJECTIVE To assess whether previously observed brain and cognitive differences between children with type 1 diabetes and control subjects without diabetes persist, worsen, or improve as children grow into puberty and whether differences are associated with hyperglycemia. RESEARCH DESIGN AND METHODS One hundred forty-four children with type 1 diabetes and 72 age-matched control subjects without diabetes (mean ± SD age at baseline 7.0 ± 1.7 years, 46% female) had unsedated MRI and cognitive testing up to four times over 6.4 ± 0.4 (range 5.3– 7.8) years; HbA1c and continuous glucose monitoring were done quarterly. Free-Surfer-derived brain volumes and cognitive metrics assessed longitudinally were compared between groups using mixed-effects models at 6, 8, 10, and 12 years. Correlations with glycemia were performed. RESULTS Total brain, gray, and white matter volumes and full-scale and verbal intelligence quotients (IQs) were lower in the diabetes group at 6, 8, 10, and 12 years, with estimated group differences in full-scale IQ of-4.15,-3.81,-3.46, and-3.11, respectively (P < 0.05), and total brain volume differences of-15,410,-21,159,-25,548, and-28,577 mm3 at 6, 8, 10, and 12 years, respectively (P < 0.05). Differences at baseline persisted or increased over time, and brain volumes and cognitive scores negatively correlated with a life-long HbA1c index and higher sensor glucose in diabetes. CONCLUSIONS Detectable changes in brain volumes and cognitive scores persist over time in children with early-onset type 1 diabetes followed longitudinally; these differences are associated with metrics of hyperglycemia. Whether these changes can be reversed with scrupulous diabetes control requires further study. These longitudinal data support the hypothesis that the brain is a target of diabetes complications in young children.
UR - http://www.scopus.com/inward/record.url?scp=85103305657&partnerID=8YFLogxK
U2 - 10.2337/DC20-2125
DO - 10.2337/DC20-2125
M3 - Article
C2 - 33568403
AN - SCOPUS:85103305657
SN - 0149-5992
VL - 44
SP - 983
EP - 992
JO - Diabetes care
JF - Diabetes care
IS - 4
ER -