Persistence of abnormalities in white matter in children with type 1 diabetes

被引:38
|
作者
Fox, Larry A. [1 ]
Hershey, Tamara [2 ,3 ]
Mauras, Nelly [1 ]
Arbelaez, Ana Maria [2 ,3 ]
Tamborlane, William V. [4 ]
Buckingham, Bruce [5 ]
Tsalikian, Eva [6 ]
Englert, Kim [1 ]
Raman, Mira [7 ]
Jo, Booil [7 ]
Shen, Hanyang [7 ]
Reiss, Allan [5 ,7 ,8 ]
Mazaika, Paul [7 ]
机构
[1] Nemours Childrens Hlth Syst, Pediat Endocrinol, 807 Childrens Way, Jacksonville, FL 32207 USA
[2] Washington Univ St Louis, Dept Psychiat & Radiol, St Louis, MO USA
[3] St Louis Childrens Hosp, St Louis, MO 63178 USA
[4] Yale Univ, Pediat Endocrinol, New Haven, CT USA
[5] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
[6] Univ Iowa, Dept Pediat Endocrinol, Iowa City, IA USA
[7] Stanford Univ, Dept Psychiat & Behav Sci, Interdisciplinary Brain Sci Res, Stanford, CA 94305 USA
[8] Stanford Univ, Sch Med, Dept Radiol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
Brain development; Paediatric diabetes; White matter; YOUNG-CHILDREN; BRAIN VOLUME; DIFFUSION; AGE; MICROSTRUCTURE; HYPERGLYCEMIA; PEPTIDE; GENDER; YOUTH; MRI;
D O I
10.1007/s00125-018-4610-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis Prior studies suggest white matter growth is reduced and white matter microstructure is altered in the brains of young children with type 1 diabetes when compared with brains of non-diabetic children, due in part to adverse effects of hyperglycaemia. This longitudinal observational study examines whether dysglycaemia alters the developmental trajectory of white matter microstructure over time in young children with type 1 diabetes. Methods One hundred and eighteen children, aged 4 to <10 years old with type 1 diabetes and 58 age-matched, non-diabetic children were studied at baseline and 18 months, at five Diabetes Research in Children Network clinical centres. We analysed longitudinal trajectories of white matter using diffusion tensor imaging. Continuous glucose monitoring profiles and HbA(1c) levels were obtained every 3 months. Results Axial diffusivity was lower in children with diabetes at baseline (p = 0.022) and at 18 months (p = 0.015), indicating that differences in white matter microstructure persist over time in children with diabetes. Within the diabetes group, lower exposure to hyperglycaemia, averaged over the time since diagnosis, was associated with higher fractional anisotropy (p = 0.037). Fractional anisotropy was positively correlated with performance (p < 0.002) and full-scale IQ (p < 0.02). Conclusions/interpretation These results suggest that hyperglycaemia is associated with altered white matter development, which may contribute to the mild cognitive deficits in this population.
引用
收藏
页码:1538 / 1547
页数:10
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