Key result
Youth with type 1 diabetes exhibited lower fractional anisotropy in the superior parietal lobule compared to healthy controls (0.435 vs 0.465, p=0.007), suggesting altered white matter integrity.
Why the study?
Does type 1 diabetes and exposure to glycemic extremes alter white matter microstructural integrity in youth?
Observational (n=103)
No
Does type 1 diabetes and exposure to glycemic extremes alter white matter microstructural integrity in youth?
Standardized Mean Difference: 0.6
Absolute Event Rate: 0.435% vs 0.465%
p-value: p=0.007
Youth with type 1 diabetes exhibit altered white matter microstructural integrity in specific brain regions, which is exacerbated by a history of severe hyperglycemic episodes.
Association with type 1 diabetes may signal early brain vulnerability; leaves open whether glycemic optimization preserves white matter integrity.
Decreased white and gray matter volumes have been reported in youth with type 1 diabetes mellitus (T1DM), but the effects of hyperglycemia on white matter integrity have not been quantitatively assessed during brain development. We performed diffusion tensor imaging, using two complimentary approaches--region-of-interest and voxelwise tract-based spatial statistics--to quantify white matter integrity in a large retrospective study of T1DM youth and control participants. Exposure to chronic hyperglycemia, severe hyperglycemic episodes, and severe hypoglycemia, as defined in the Diabetes Control and Complications Trial (DCCT), were estimated through medical records review, HbA(1c) levels, and interview of parents and youth. We found lower fractional anisotropy in the superior parietal lobule and reduced mean diffusivity in the thalamus in the T1DM group. A history of three or more severe hyperglycemic episodes was associated with reduced anisotropy and increased diffusivity in the superior parietal lobule and increased diffusivity in the hippocampus. These results add microstructural integrity of white matter to the range of structural brain alterations seen in T1DM youth and suggest vulnerability of the superior parietal lobule, hippocampus, and thalamus to glycemic extremes during brain development. Longitudinal analyses will be necessary to determine how these alterations change with age or additional glycemic exposure.
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Antenor‐Dorsey et al. (2012) conducted an observational in Type 1 Diabetes Mellitus (n=103). Type 1 Diabetes Mellitus vs. Healthy nondiabetic siblings was evaluated on Fractional anisotropy in the superior parietal lobule (Cohen's d 0.60, p=0.007). Youth with type 1 diabetes exhibited lower fractional anisotropy in the superior parietal lobule compared to healthy controls (0.435 vs 0.465, p=0.007), suggesting altered white matter integrity.
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