Age of Childhood Onset in Type 1 Diabetes and Functional Brain Connectivity in Midlife
- PMID: 26163816
- PMCID: PMC4503367
- DOI: 10.1097/PSY.0000000000000206
Age of Childhood Onset in Type 1 Diabetes and Functional Brain Connectivity in Midlife
Erratum in
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Age of Childhood Onset in Type 1 Diabetes and Functional Brain Connectivity in Midlife: Erratum.Psychosom Med. 2016 Sep;78(7):886. doi: 10.1097/PSY.0000000000000396. Psychosom Med. 2016. PMID: 27574889 No abstract available.
Abstract
Objectives: The development of Type 1 diabetes mellitus (T1DM) within the first 7 years of life has been linked to poorer cognitive performance. Adults with T1DM have altered functional brain connectivity, but no studies have examined whether earlier age of T1DM onset is associated with functional connectivity later in life. Accordingly, we tested the relationship between age of onset and resting state functional connectivity in a cohort of middle-aged adults with childhood-onset T1DM.
Methods: Participants were from a subsample of the Pittsburgh Epidemiology of Diabetes Complications cohort and included 66 adults (mean age = 47.54 years, 32 men). Resting state blood oxygen level-dependent activity was used to calculate mean connectivity for eight functional brain networks. A multivariate analysis of variance examined associations between age of onset and network connectivity. Diffusion tensor and fluid-attenuated inversion recovery images were analyzed to identify microstructural alterations and white-matter hyperintensity volumes.
Results: Later childhood onset of T1DM was associated with lower connectivity (F(8,57) = 2.40, p = .026). A significant interaction was present for current age such that an inverse association with age of onset for functional connectivity was present in older individuals (F(8,55) = 2.88, p = .035). Lower connectivity was associated with older age, increased white-matter hyperintensity volume, and lower microstructural integrity.
Conclusions: Diagnosis of T1DM later in childhood may be associated with lower brain functional connectivity, particularly in those surviving into older ages. These alterations may be an early marker for subsequent cognitive decrements. Future studies are warranted to understand the pathways underlying these associations.
Conflict of interest statement
The authors declare no conflicts of interest
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