Cerebral Venous Oxygen Saturation in Hypoperfusion Regions May Become a New Imaging Indicator to Predict the Clinical Outcome of Stroke.

To automatically and quantitatively evaluate the venous oxygen saturation (SvO2) in cerebral ischemic tissues and explore its value in predicting prognosis. A retrospective study was conducted on 48 AIS patients hospitalized in our hospital from 2015−2018. Based on quantitative susceptibility mapping and perfusion-weighted imaging, this paper measured the cerebral SvO2 in hypoperfusion tissues and its change after intraarterial rt-PA treatment. The cerebral SvO2 in different hypoperfusion regions between the favorable and unfavorable clinical outcome groups was analyzed using an independent t-test. Relationships between cerebral SvO2 and clinical scores were determined using the Pearson correlation coefficient. The receiver operating characteristic process was conducted to evaluate the accuracy of cerebral SvO2 in predicting unfavorable clinical outcomes. Cerebral SvO2 in hypoperfusion (Tmax > 4 and 6 s) was significantly different between the two groups at follow-up (p < 0.05). Cerebral SvO2 and its changes before and after treatment were negatively correlated with clinical scores. The positive predictive value, negative predictive value, accuracy, and area under the curve of the cerebral SvO2 were higher than those predicted by the ischemic core. Therefore, the cerebral SvO2 of hypoperfusion regions was a stronger imaging predictor of unfavorable clinical outcomes after stroke.

Quantitative Distribution of Cerebral Venous Oxygen Saturation and Its Prognostic Value in Patients with Acute Ischemic Stroke.

This study investigated the quantitative distribution of cerebral venous oxygen saturation (SvO2) based on quantitative sensitivity mapping (QSM) and determined its prognostic value in patients with acute ischemic stroke (AIS). A retrospective study was conducted on 39 hospitalized patients. Reconstructed QSM was used to calculate the cerebral SvO2 of each region of interest (ROI) in the ischemic hemisphere. The intraclass correlation coefficient (ICC) and Bland−Altman analysis were conducted to define the best resolution of the distribution map. The correlation between the cerebral SvO2 in hypoxic regions (SvO2ROI < 0.7) and clinical scores was obtained by Spearman and power analysis. The associations between cerebral SvO2 and unfavorable prognosis were analyzed using multivariate logistic regression. Excellent agreement was found between the cerebral SvO2 in hypoxic regions with a resolution of 7.18 × 7.18 × 1.6 mm3 and asymmetrically prominent cortical veins regions (ICC: 0.879 (admission), ICC: 0.906 (discharge)). The cerebral SvO2 was significantly negative with clinical scores (all |r| > 0.3). The cerebral SvO2 and its changes at discharge were significantly associated with an unfavorable prognosis (OR: 0.812 and 0.866). Therefore, the cerebral SvO2 in hypoxic regions measured by the quantitative distribution map can be used as an indicator for evaluating the early prognosis of AIS.

Deep symmetric three-dimensional convolutional neural networks for identifying acute ischemic stroke via diffusion-weighted images.

BACKGROUND: Acute ischemic stroke (AIS) results in high morbidity, disability, and mortality. Early and automatic diagnosis of AIS can help clinicians administer the appropriate interventions. OBJECTIVE: To develop a deep symmetric 3D convolutional neural network (DeepSym-3D-CNN) for automated AIS diagnosis via diffusion-weighted imaging (DWI) images. METHODS: This study includes 190 study subjects (97 AIS and 93 Non-AIS) by collecting both DWI and Apparent Diffusion Coefficient (ADC) images. 3D DWI brain images are split into left and right hemispheres and input into two paths. A map with 125×253×14×12 features is extracted by each path of Inception Modules. After the features computed from two paths are subtracted through L-2 normalization, four multi-scale convolution layers produce the final predation. Three comparative models using DWI images including MedicalNet with transfer learning, Simple DeepSym-3D-CNN (each 3D Inception Module is replaced by a simple 3D-CNN layer), and L-1 DeepSym-3D-CNN (L-2 normalization is replaced by L-1 normalization) are constructed. Moreover, using ADC images and the combination of DWI and ADC images as inputs, the performance of DeepSym-3D-CNN is also investigated. Performance levels of all three models are evaluated by 5-fold cross-validation and the values of area under ROC curve (AUC) are compared by DeLong's test. RESULTS: DeepSym-3D-CNN achieves an accuracy of 0.850 and an AUC of 0.864. DeLong's test of AUC values demonstrates that DeepSym-3D-CNN significantly outperforms other comparative models (p < 0.05). The highlighted regions in the feature maps of DeepSym-3D-CNN spatially match with AIS lesions. Meanwhile, DeepSym-3D-CNN using DWI images presents the significant higher AUC than that either using ADC images or using DWI-ADC images based on DeLong's test (p < 0.05). CONCLUSIONS: DeepSym-3D-CNN is a potential method for automatically identifying AIS via DWI images and can be extended to other diseases with asymmetric lesions.

Alterations of default mode functional connectivity in individuals with end-stage renal disease and mild cognitive impairment.

BACKGROUND: Mild cognitive impairment (MCI) occurs frequently in many end stage renal disease (ESRD) patients, may significantly worsen survival odds and prognosis. However, the exact neuropathological mechanisms of MCI combined with ESRD are not fully clear. This study examined functional connectivity (FC) alterations of the default-mode network (DMN) in individuals with ESRD and MCI. METHODS: Twenty-four individuals with ESRD identified as MCI patients were included in this study; of these, 19 and 5 underwent hemodialysis (HD) and peritoneal dialysis (PD), respectively. Another group of 25 age-, sex- and education level-matched subjects were recruited as the control group. All participants underwent resting-state functional MRI and neuropsychological tests; the ESRD group underwent additional laboratory testing. Independent component analysis (ICA) was used for DMN characterization. With functional connectivity maps of the DMN derived individually, group comparison was performed with voxel-wise independent samples t-test, and connectivity changes were correlated with neuropsychological and clinical variables. RESULTS: Compared with the control group, significantly decreased functional connectivity of the DMN was observed in the posterior cingulate cortex (PCC) and precuneus (Pcu), as well as in the medial prefrontal cortex (MPFC) in the ESRD group. Functional connectivity reductions in the MPFC and PCC/Pcu were positively correlated with hemoglobin levels. In addition, functional connectivity reduction in the MPFC showed positive correlation with Montreal Cognitive Assessment (MoCA) score. CONCLUSION: Decreased functional connectivity in the DMN may be associated with neuropathological mechanisms involved in ESRD and MCI.