Quantitative detection of posterior cingulate gyrus injuries and correlation with cognitive function in patients with type 2 diabetes mellitus based on 1H-MRS combined with DTI
10.13929/j.1003-3289.201810110
- Author:
Qing CAI
1
Author Information
1. Department of Radiology, Affiliated Zhongshan Hospital of Dalian University
- Publication Type:Journal Article
- Keywords:
Diabetes mellitus, type 2;
Diffusion tensor imaging;
Gyrus cinguli;
Magnetic resonance spectroscopy
- From:
Chinese Journal of Medical Imaging Technology
2019;35(6):812-817
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To detect and evaluate brain metabolism abnormalities and white matter changes of posterior cingulate cortex (PCC) in type 2 diabetes mellitus (T2DM) patients with 1H-MRS combined with DTI, and to explore the correlation between the changes and cognitive impairment. Methods: Single-voxel 1H-MRS and DTI in PCC were performed in 43 patients with T2DM (21 with cognitive impairment [T2DM+CD group], 22 without cognitive impairment [T2DM group] ) and 23 healthy volunteers (HC group). The integral value of related crest area and fractional anisotropy (FA), mean diffusivity (MD) values were calculated, and their correlation with cognitive function indicators were analyzed. Results: The value of myo-inositol/creatine (mI/Cr) in PCC region of T2DM+CD group was higher than that of T2DM and HC groups, and the value of glutamate+glutamine/creatine (Glx/Cr) value was lower than that of T2DM and HC groups (all P<0.05). Glx/Cr was significantly positively correlated with Montreal cognitive assessment score (MoCA; r=0.59, P<0.01). FA values in the whole brain and PCC regions of T2DM+CD group were lower than those of T2DM and HC groups, and the MD values were higher than those of T2DM and HC groups (all P<0.05). FA value was significantly positively correlated with the score of MoCA (r=0.57, P=0.01). Conclusion: The combination of 1H-MRS and DTI with PCC as ROI can be used to quantitatively reflect and mutually confirm the neuropathological basis of cognitive impairment induced by T2DM, which is expected to be a clinical indicator of early warning.
