4.7 Article

Four-way multimodal fusion of 7T imaging data using an mCCA plus jICA model in first-episode schizophrenia

期刊

HUMAN BRAIN MAPPING
卷 39, 期 4, 页码 1475-1488

出版社

WILEY
DOI: 10.1002/hbm.23906

关键词

amplitude of low frequency fluctuations; first-episode schizophrenia; joint independent component analysis; multimodal fusion; resting-state fMRI; 7 Tesla

资金

  1. National Institute of Mental Health [R01 MH102951]
  2. Civitan International Research Center
  3. UAB Center for Clinical and Translational Science (CCTS)
  4. National Institute of Biomedical Imaging and Bioengineering [R01EB006841]
  5. National Institute of General Medical Sciences [P20GM103472]
  6. National Science Foundation [IOS 0622318]
  7. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH102951] Funding Source: NIH RePORTER
  8. Office Of The Director [1539067] Funding Source: National Science Foundation

向作者/读者索取更多资源

Acquisition of multimodal brain imaging data for the same subject has become more common leading to a growing interest in determining the intermodal relationships between imaging modalities to further elucidate the pathophysiology of schizophrenia. Multimodal data have previously been individually analyzed and subsequently integrated; however, these analysis techniques lack the ability to examine true modality inter-relationships. The utilization of a multiset canonical correlation and joint independent component analysis (mCCA+jICA) model for data fusion allows shared or distinct abnormalities between modalities to be examined. In this study, first-episode schizophrenia patients (n(SZ)=19) and matched controls (n(HC)=21) completed a resting-state functional magnetic resonance imaging (fMRI) scan at 7 T. Grey matter (GM), white matter (WM), cerebrospinal fluid (CSF), and amplitude of low frequency fluctuation (ALFF) maps were used as features in a mCCA+jICA model. Results of the mCCA+jICA model indicated three joint group-discriminating components (GM-CSF, WM-ALFF, GM-ALFF) and two modality-unique group-discriminating components (GM, WM). The joint component findings are highlighted by GM basal ganglia, somatosensory, parietal lobe, and thalamus abnormalities associated with ventricular CSF volume; WM occipital and frontal lobe abnormalities associated with temporal lobe function; and GM frontal, temporal, parietal, and occipital lobe abnormalities associated with caudate function. These results support and extend major findings throughout the literature using independent single modality analyses. The multimodal fusion of 7T data in this study provides a more comprehensive illustration of the relationships between underlying neuronal abnormalities associated with schizophrenia than examination of imaging data independently.

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