Journal of affective disorders · 2019
Fusion analysis of gray matter and white matter in bipolar disorder by multimodal CCA-joint ICA.
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Tang Fei, Yang Haichen, Li Linling, Ji Erni, Fu Zening, Zhang Zhiguo
Аннотация
BACKGROUND: Bipolar disorder (BD) patients show morphological abnormalities in gray matter (GM) and white matter (WM), which can be revealed by structure MRI (sMRI) and diffusion tensor imaging (DTI) respectively. However, previous studies on BD mainly relied on separated analysis of single neuroimaging modality, and it remains unclear how GM and WM covary to the abnormal brain structures of BD patients.
METHODS: We recorded multimodal sMRI-DTI data of 35 BD patients and 30 healthy controls (HC) and used multimodal canonical component analysis and joint independent component analysis (mCCA-jICA) to identify altered covariant structures in GM and WM of BD. Group-discriminative and joint group-discriminative independent components (ICs) were identified between BD and HC. Correlation analysis was performed between the mixing coefficients and behavioral index.
RESULTS: For BD patients, experiments results revealed that the GM atrophy in inferior frontal gyrus, right anterior cingulate gyrus and left superior frontal gyrus are associated with the WM integrity reduction in corticospinal tract and superior longitudinal fasciculus. Further, compared with HC, different correlation between mixing coefficients of ICs and age was observed for BD patients.
LIMITATIONS: The number of participants needs to be increased to more rigorously validate the results of this study, ideally from multiple sites. Functional imaging data could be utilized to explore structural-functional covariant pattern in BD. Possible confounding effect of medication.
CONCLUSIONS: We performed fusion analysis of sMRI and DTI and revealed covariant (GM-WM) structural patterns of BD patients. This study could be useful for developing more reliable neural biomarkers of BD.
METHODS: We recorded multimodal sMRI-DTI data of 35 BD patients and 30 healthy controls (HC) and used multimodal canonical component analysis and joint independent component analysis (mCCA-jICA) to identify altered covariant structures in GM and WM of BD. Group-discriminative and joint group-discriminative independent components (ICs) were identified between BD and HC. Correlation analysis was performed between the mixing coefficients and behavioral index.
RESULTS: For BD patients, experiments results revealed that the GM atrophy in inferior frontal gyrus, right anterior cingulate gyrus and left superior frontal gyrus are associated with the WM integrity reduction in corticospinal tract and superior longitudinal fasciculus. Further, compared with HC, different correlation between mixing coefficients of ICs and age was observed for BD patients.
LIMITATIONS: The number of participants needs to be increased to more rigorously validate the results of this study, ideally from multiple sites. Functional imaging data could be utilized to explore structural-functional covariant pattern in BD. Possible confounding effect of medication.
CONCLUSIONS: We performed fusion analysis of sMRI and DTI and revealed covariant (GM-WM) structural patterns of BD patients. This study could be useful for developing more reliable neural biomarkers of BD.