| Literature DB >> 26257686 |
Yingchao Shi1, Weiming Zeng1, Nizhuan Wang1, Shujiang Wang1, Zhijian Huang1.
Abstract
Effective mental sub-health early warning mechanism is of great significance in the protection of individual mental health. The traditional mental health assessment method is mainly based on questionnaire surveys, which may have some uncertainties. In this study, based on the relationship between the default mode network (DMN) and the mental health status, we proposed a human mental sub-health early warning method by utilizing two-fold support vector machine (SVM) model, where seafarers' fMRI data analysis was utilized as an example. The method firstly constructed a structural-functional DMN template by combining the anatomical automatic labeling template with the functional DMN extracted by independent component analysis. Then, it put forward a two-fold SVM-based classifier, with one-class SVM utilized for the training of the initial classifier and two-class SVM utilized to refine the classification performance, to identify seafarers' mental health status by utilizing the correlation coefficients (CCs) among the areas of structural-functional DMN as the features. The experimental results showed that the proposed model could discriminate the seafarers with DMN function alteration from the healthy control (HC) effectively, and further the results demonstrated that when compared with the HC group, the brain functional disorders of the mental sub-healthy seafarers mainly manifested as follows: the functional connectivity of DMN had obvious alteration; the CCs among the different DMN regions were significant lower; the regional homogeneity decreased in parts of the prefrontal cortex and increased in multi-regions of the parietal, temporal and occipital cortices; the fractional amplitude of low-frequency fluctuation decreased in parts of the prefrontal cortex and increased in parts of the parietal cortex. All of the results showed that fMRI-based analysis of brain functional activities could be effectively used to distinguish the mental health and sub-health status.Entities:
Keywords: default mode network; fMRI; mental; seafarer; support vector machine
Year: 2015 PMID: 26257686 PMCID: PMC4511829 DOI: 10.3389/fpsyg.2015.01030
Source DB: PubMed Journal: Front Psychol ISSN: 1664-1078
Information and scan-parameters of healthy control datasets.
| Milwankee_b | 39 | 2000 | 175 | 64 | 36×64 | 4×3.75 | 3.75 |
| New_York_a | 8 | 2000 | 192 | 39 | 64×64 | 3×3 | 3 |
| New_York_b | 7 | 2000 | 175 | 33 | 64×80 | 3×3 | 4 |
| SKLMR | 20 | 2000 | 160 | 36 | 64×64 | 3.75×3.75 | 4 |
Figure 1Implementation diagram of the classification process: OCSVM provides an initial classifier, which is used to predict the class labels of seafarers. The negative-class samples are selected, together with the healthy control samples whose class labels are set to “1,” as the training data with the class labels are set to “-1.” The TCSVM training process can be repeated to further refine the classifier.
Figure 2The distributions of CCs among different DMN regions of the HC group, the mental sub-healthy seafarers, and the mental healthy seafarers. The CCs of the mental sub-healthy seafarers were significant lower than that of the HC group; the distribution of the CCs of the mental healthy seafarers was similar to that of the HC group.
Figure 3DMN areas with decreased functional connectivity in mental sub-healthy seafarers. (A) Regard the prefrontal cortex as seed point with FC decreased in multi-regions of DMN; (B) regard the parietal as seed point with FC decreased in the prefrontal and parietal cortices.
Prefrontal cortex based DMN areas with decreased functional connectivity in mental sub-healthy seafarers comparing with healthy controls.
| Prefrontal | Frontal_Sup_Medial_L | 132 | −10, 58, 22 | −3.9472 |
| Cingulum_Ant_L | ||||
| Frontal_Sup_L | ||||
| Parietal/ | Angular_L | 345 | −52, −68, 26 | −5.6042 |
| Parietal cortex | Precuneus_L/R | 226 | −4, −56, 46 | −4.4093 |
R, right; L, left; AAL, Anatomical Automatic Labeling atlas; MNI, Montreal Neurological Institute.
Parietal cortex based DMN areas with decreased functional connectivity in mental sub-healthy seafarers comparing with healthy controls.
| Prefrontal cortex | Frontal_Sup_Medial_L/R | 451 | −6, 46, 0 | −5.2889 |
| Cingulum_Ant_L/R | ||||
| Frontal_Sup_L/R | ||||
| Parietal cortex | Precuneus_L/R | 183 | 8, −66, 40 | −4.7463 |
| Parietal cortex | Angular_R | 220 | 50, −58, 30 | −6.6391 |
| Parietal cortex | Cingulum_Post_L/R | 179 | −4, −56, 44 | −3.4711 |
| Precuneus_L/R | ||||
| Cingulum_Mid_R | ||||
| Prefrontal | Frontal_Sup_Medial_L/R | 366 | 8, 58, 38 | −6.3596 |
R, right; L, left; AAL, Anatomical Automatic Labeling atlas; MNI, Montreal Neurological Institute.
Figure 4DMN areas with decreased and increased regional homogeneity in multi-regions of DMN regarding to the mental sub-healthy seafarers.
DMN areas with decreased or increased regional homogeneity in mental sub-healthy seafarers comparing with healthy controls.
| Prefrontal cortex | Frontal_Sup_Medial_L | 239 | −8, 54, 2 | −6.3117 |
| Parietal/temporal cortex | Temporal_Mid_L | 235 | −48, −54, 22 | 4.9141 |
| parietal cortex | Precuneus_L/R | 922 | −12, −54, 18 | 5.309 |
| Cingulum_Post_L/RCingulum_Mid_RCuneus_L/R | ||||
| parietal/temporal cortex | Angular_R | 304 | 36, −74, 50 | 4.2039 |
| parietal/occipital cortex | Angular_L | 141 | −46, −60, 42 | 3.3074 |
R, right; L, left; AAL, Anatomical Automatic Labeling atlas; MNI, Montreal Neurological Institute.
Figure 5DMN areas with decreased fractional amplitude of low-frequency fluctuation (fALFF) in the prefrontal cortex, and increased fALFF in the parietal cortex regarding to the mental sub-healthy seafarers.
DMN areas with decreased or increased fractional amplitude of low-frequency fluctuation (fALFF) in negative-class seafarers comparing with healthy controls.
| Prefrontal cortex | Frontal_Sup_Medial_L/R | 120 | −4, 58, 2 | −4.2828 |
| Parietal cortex | Precuneus_L/R | 217 | 0, −68, 28 | 4.4146 |
R, right; L, left; AAL, Anatomical Automatic Labeling atlas; MNI, Montreal Neurological Institute.