Prediction of clinical depression scores and detection of changes in whole-brain using resting-state functional MRI data with partial least squares regression

Kosuke Yoshida; Yu Shimizu; Junichiro Yoshimoto; Masahiro Takamura; Go Okada; Yasumasa Okamoto; Shigeto Yamawaki; Kenji Doya

doi:10.1371/journal.pone.0179638

Abstract

In diagnostic applications of statistical machine learning methods to brain imaging data, common problems include data high-dimensionality and co-linearity, which often cause over-fitting and instability. To overcome these problems, we applied partial least squares (PLS) regression to resting-state functional magnetic resonance imaging (rs-fMRI) data, creating a low-dimensional representation that relates symptoms to brain activity and that predicts clinical measures. Our experimental results, based upon data from clinically depressed patients and healthy controls, demonstrated that PLS and its kernel variants provided significantly better prediction of clinical measures than ordinary linear regression. Subsequent classification using predicted clinical scores distinguished depressed patients from healthy controls with 80% accuracy. Moreover, loading vectors for latent variables enabled us to identify brain regions relevant to depression, including the default mode network, the right superior frontal gyrus, and the superior motor area.

Citation: Yoshida K, Shimizu Y, Yoshimoto J, Takamura M, Okada G, Okamoto Y, et al. (2017) Prediction of clinical depression scores and detection of changes in whole-brain using resting-state functional MRI data with partial least squares regression. PLoS ONE 12(7): e0179638. https://doi.org/10.1371/journal.pone.0179638

Editor: Dewen Hu, National University of Defense Technology College of Mechatronic Engineering and Automation, CHINA

Received: December 19, 2016; Accepted: June 1, 2017; Published: July 12, 2017

Copyright: © 2017 Yoshida et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: The original data for this study is confidential due to the involvement of patient data. It can be obtained upon request to the Department of Psychiatry and Neurosciences, Hiroshima University, Japan (primary contact: Shigeto Yamawaki, PhD, MD, yamawaki@hiroshima-u.ac.jp). IRB imposing these restrictions on our data is Ethical Committee for Epidemiology of Hiroshima University (contact: Shoji Karatsu kasumi-kenkyu@office.hiroshima-u.ac.jp). Additional contact information is available from: https://www.hiroshima-u.ac.jp/en/pharm/contact.

Funding: This research is supported by the Strategic Research Program for Brain Sciences from Japan Agency for Medical Research and development, AMED (http://www.amed.go.jp/en). All authors of this study are supported by this program. This program does not have a grant number. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors have declared that no competing interests exist.

Introduction

Advances in analyzing large datasets with machine learning algorithms promote their application in medical diagnosis. In particular, their use in objective diagnosis of psychiatric disorders using brain imaging and other biological data is now being actively studied [1]. A major challenge in applying statistical machine learning algorithms to brain imaging or genetic data is the high dimensionality of the input variables, such as the number of voxels and the number of possible genetic polymorphisms. Even though algorithms such as support vector machine (SVM) and L1-regularized classifiers (LASSO) manage the issue of high-dimensionality, the problem of co-linearity in brain imaging data remains. Neural activities in nearby voxels or in the same functional network are highly correlated, which makes the results of commonly used regression or classification tools unreliable. In this paper, we propose the use of partial least squares (PLS) regression [2–7] with multiple clinical measures to address this problem. We use resting-state functional magnetic resonance imaging (rs-fMRI) data and clinical measures from clinically depressed patients and healthy control subjects to obtain low-dimensional representations of symptoms and brain activities, and we use them to predict depression-related clinical measures and thereafter, to classify subjects.

Use of rs-fMRI is gaining attention in diagnosis of psychiatric disorders because it makes few cognitive demands in measurements and because it can be applied to multiple disorders [8]. In depressed patients, functional connectivities (FCs) between brain areas estimated using rs-fMRI show distributed changes throughout the entire brain [9–12]. Zeng et al. (2012) [13] demonstrated that ∼94% of 53 subjects could be correctly classified as patients or healthy controls using FCs and linear SVM, and they reported that the majority of discriminating FCs were distributed within or across the default mode network, the affective network, visual cortical areas, and the cerebellum. While the aforementioned study sought to discern differences between patients and healthy controls in a binary manner, Zhang et al. (2011) [14] tried to predict clinical measures of the Beck Depression Inventory II (BDI-II) [15] by regressing fMRI signals acquired during a face-watching task. They showed that true and predicted BDI-II were significantly correlated (r = 0.55) and using the standard threshold of 14 for the predicted BDI-II, 89% of the automated diagnoses agreed with those of psychiatrists.

Clinical depression is characterized by multiple, related symptoms [16]. There are various clinical measures for assessing symptoms, such as the Snaith-Hamilton Pleasure Scale (SHAPS) [17] for anhedonia and Positive and Negative Affect Schedule (PANAS) [18] for altered mood. In addition, the age of subjects is important for diagnosis since aging increases the risk of depression in general [19].

Here, we consider a two-step approach which predicts multiple measures of clinical depression from rs-fMRI in the first step, and then uses results of the first step for diagnosis. For the first step, we train a regression model to predict BDI-II, SHAPS, PANAS(n), and age from functional connectivity data. Although this could be done using ordinary least squares regression, in order to tackle the issue of high-dimensionality and co-linearity of the input, we explore the use of partial least squares (PLS) regression [2–7], which maps input and output variables to low-dimensional spaces so that the covariance of data in the latent spaces is maximized. We compare the classification performance of the two-step approach using PLS regression with other classification methods. Thereafter, we consider the use of subject age by testing (i) a model with age as a response variable (output-age model), (ii) a model with age as a predictor (input-age model), and (iii) a model that does not consider age (no-age model).

This paper further develops the basic idea presented in [20] to overcome limitations of linear methods and perform objective diagnosis. In section 2, we illustrate the details of rs-fMRI and clinical measures for subjects. Section 3 provides the mathematical basis of PLS and its kernel variants. In addition, it is extended to classification models for the purpose of objective diagnosis. In section 4, we illustrate the efficacy of our application in predicting clinical measures, discriminating between patients and healthy controls, and interpreting derived coefficients. Finally, we offer our conclusions and discuss future work in section 5.

Data set

This study was approved by the Human Subjects Research Review Committee at the Okinawa Institute of Science of Technology, as well as the Research Ethics Committee of Hiroshima University (permission nr. 172). Written and informed consent was obtained from all subjects participating in the study.

Subjects

58 patients (age 26–73, average 42.8 ± 11.9, 33 female) with major depression disorder were recruited by the Psychiatry Department of Hiroshima University and collaborating medical institutions, based on the Mini-international neuropsychiatric interview (M.I.N.I [21]), which enables doctors to identify psychiatric disorders, according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV [22]). As a healthy control group, 65 subjects (ages 20–66, average 34.8 ± 13.0, 28 female) with no history of mental or neurological disease, were recruited via advertisements in local newspapers.

Clinical measures

The following interview- and questionnaire-based measures are used for determination of disease presence and quantification of the severity of two primary symptoms we wish to predict, namely, anhedonia (loss of motivation, loss of pleasure, etc.) and negative mood (low mood, guilty feelings, suicidal thoughts, etc.).

Beck Depression Inventory II (BDI-II).

This measure evaluates the presence and severity of depression based on a self-report questionnaire [15]. Subjects are asked to answer 21 questions about feelings of punishment or guilt, suicidal thoughts, etc. Each answer is scored with a value between 0 and 3, with 3 being the most serious. High scores indicate severe symptoms. The standardized score of ≥14 indicates that a subject is suffering from depression.

Snaith-Hamilton Pleasure Scale (SHAPS).

This measure was developed to evaluate the level of anhedonia [17]. Subjects are asked to answer 14 questions about hedonic capacity, with scores between 1 and 4. High scores indicate more severe anhedonia.

Positive and Negative Affect Schedule (PANAS).

This widely used measure evaluates positive and negative moods of subjects [18, 23]. In this study, we considered only scores related to negative mood items. This measure is generally known as PANAS(n). Subjects are asked to respond to 10 questions about their moods, with answers between 0 and 5. The sum of all scores indicates the strength of their negative moods. Due to an evaluation issue, one subject’s response could not be assessed, so that score was replaced with the mean of the remaining subjects.

Table 1 summarizes scores exhibited for each measure by each group in our study [20]. Although most patients showed both anhedonia and negative mood, some exhibited only one trait. Correspondingly, the scores of the BDI-II, SHAPS, and PANAS(n) are highly, but not completely correlated. As decreased mental function results from aging, the age of the subjects is expected to correlate with BDI-II, SHAPS, and PANAS(n) as well.

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Table 1. Mean (± standard deviation) of clinical measures [20].

https://doi.org/10.1371/journal.pone.0179638.t001

We verified these correlations by calculating the correlation coefficients (Table 2) [20]. Strong correlations between clinical measures are reflected in coefficients above 0.7. Weaker correlations between age and individual clinical measures were around 0.3. In our regression model, BDI-II, SHAPS, PANAS(n), and age of each subject are considered as responses in order to correct for their natural correlation, resulting from functional connectivity. We will show that the introduction of subject age as an output rather than as an input is beneficial with respect to classification accuracy.

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Table 2. The Pearson’s correlation coefficients between the clinical measures and the subjects’ age [20].

https://doi.org/10.1371/journal.pone.0179638.t002

Functional connectivity of resting-state fMRI

Functional MRI measurements were acquired on a 3T GE Signa HDx scanner with a 2D EP/GR (TR = 3s, TE = 27ms, FA = 90deg, matrix size 64x64x32, voxel size 4x4x4 mm, no gap, interleaved). Subjects were instructed to lie with their eyes open, to think of nothing in particular, and to remain awake. They are also instructed to refrain from taking caffeine, nicotine, and alcohol in the day of experiment.

For each subject, acquired images were processed with SPM8 (Wellcome Trust Centre for Neuroimaging, UCL, London) following standard procedures. We first perform slice timing correction, motion correction, co-registration to anatomical MRI, normalization with standard brain and smoothing (Gaussian of full-width at half-maximum 8mm). We confirmed that there were no significant differences in six motion parameters between two diagnostic groups in order to reject a possible effect of spurious functional connectivity due to head motion [24, 25]. Voxels were assigned to 116 brain regions, according to the automatic anatomical labeling atlas (AAL) [26]. Mean activation time series in each brain region were obtained by averaging MRI signal time series over all voxels assigned to each region. Finally, functional connectivity between each pair of regions was computed as the cross correlation of the corresponding time-series.

Methods

Partial least squares (PLS) regression is a method for modeling a relationship between two sets of multivariate data via a latent space, and of performing least squares regression in that space. PLS can handle high-dimensional co-linear datasets because of its underlying assumption that the two datasets are generated by a small number of latent components. In this process, latent components are formed by maximizing the covariance between the two datasets.

Partial Least Squares Regression (PLS)

PLS models a linear relationship between two blocks of variables and . In the following parts, X = (x₁, …, x_n)^T represents the (n × p) predictor matrix and Y = (y₁, …, y_n)^T represents the (n × q) response matrix. This procedure obtains L latent components as and . This technique assumes following decomposition: (1) (2) where both T = (t₁, …, t_L) and U = (u₁, …, u_L) are the (n × L) matrices of L latent components corresponding to X and Y, respectively. The (p × L) matrix P and the (q × L) matrix Q are loadings and the (n × p) matrix F_x and the (n × q) matrix F_y are the matrices of residuals. Since our objective is to perform least squares regression in a low-dimensional latent space, the underlying assumption is that the latent component u_i can be well predicted from t_i from a relation such as: (3) where D is the (L × L) matrix. We need to maximize the covariance between t_i and u_i to satisfy the above assumption.

Our objective criterion is (4) where and are weight vectors for projection into the latent components.

After extracting the latent component, the observation matrices X and Y are deflated by subtracting their rank-one approximation. It is important to stress the asymmetry scheme, i.e. that Y is deflated based on t, in the case of regression. By repeating the above procedures L times, we obtain the weight matrices W = (w₁, …, w_L) and C = (c₁, …, c_L).

Finally, the relation in the original data space is expressed by (5) where B is the (p × q) matrix of regression coefficients and E is the (n × q) matrix of residuals.

Plugging the relationship B = W(P^TW)⁻¹C^T [27, 28] into Eq (5), we obtain a different representation of Y as: (6) (7) (8) The final transformation is derived from the following equalities [29], (9) (10) (11) Note that (the Kronecher delta) takes the values 1 for i = j and 0 for i ≠ j as a consequence of the algorithm.

In general, B is obtained from a centered training dataset. The response y_new for a new subject x_new, referred to as test dataset, is then estimated as follows: (12) where and represent the mean predictor and response in the training dataset, respectively. A schematic outline of PLS is illustrated in Fig 1 and S1 Appendix.

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Fig 1. Schematic illustration of partial least squares regression.

Two blocks of data, X and Y, are projected by w and c onto latent components, t and u, and least squares regression is performed. p and q represent loading vectors.

https://doi.org/10.1371/journal.pone.0179638.g001

Kernel Partial Least Squares Regression (KPLS)

Linear PLS is easily extended to nonlinear regression using a kernel trick [28, 30].

Let be a nonlinear transformation of the predictor, , into a feature vector, , where is a high-dimensional feature space. Define a Gram matrix K as inner products of points in feature space, i.e., K = ΦΦ^T, where Φ = (ϕ(x₁), …, ϕ(x_n))^T represents the predictor matrix in feature space. In general, the number of columns of Φ is so large that with the explicit form of Φ, we can not perform the same procedure as in the linear case. However, due to the kernel trick, the explicit form of Φ becomes unnecessary.

The deflation procedure is performed as follows: (13) (14) where I_n represents an n-dimensional identity matrix.

We obtain the prediction on the training data from: (15) (16) (17)

To exclude the bias term, we assume that the responses and the predictors are set to have zero mean in the feature space by applying the following procedure to test kernel K_t and training kernel K [31]: (18) (19) where 1_n represents the n-length vector whose n elements are 1. Note that n and n_t represent the number of training and test samples, respectively.

In the following section of this paper, we investigate three kernel functions: 1) a second order polynomial kernel k(x, x′) = (x^Tx′ + 1)², referred to as KPLS-Poly(2), 2) a third order polynomial kernel k(x, x′) = (x^Tx′ + 1)³, referred to as KPLS-Poly(3), 3) a Gaussian kernel k(x, x′) = exp(−γ||x − x′||)²), referred to as KPLS-Gauss, where γ is a hyper parameter and set to the inverse of the median of the Euclidian distance of data points.

Classification

In addition to predicting clinical measures, our aim is to classify subjects into depressed patients and healthy controls using the predicted value of clinical measures for objective diagnosis. We evaluate generalization of binary classifiers using linear discriminant analysis (LDA). Given the training data and test data , , , and z ∈ {0, 1} represent functional connectivity as predictors, clinical measures as responses, and binary labels (i.e. 0 is patients and 1 is healthy controls), respectively. In the prediction phase, our objective is to learn the function , which, given predictors, x_tr, and responses, y_tr, assigns predictors to the most probable values of y. The prediction on the training dataset is . In the next classification phase, our objective is to learn the classifier , which, given predicted responses, , and binary labels, z_tr, assigns predicted responses to the most probable labels. Assigned labels on the test dataset are obtained as . It is important to stress that the binary classifier is not trained on actual clinical measures, y_tr, but on predicted values of .

In a previous study [13], the authors only identified the binary classifier , which, given functional connectivity, x_tr, and binary labels, z_tr, assigns functional connectivity directly to binary labels. By exploiting the predicted result of clinical measures, it may be possible to improve classification performance. We compared two scenarios, i.e. i) classification of patients and healthy controls using LDA from predicted clinical measures with KPLS (with KPLS-Gauss, KPLS-Poly(3), and KPLS-Poly(2)), PLS, and ordinary least squares regression (OLS), ii) classification of patients and healthy controls by means of LDA and SVM from functional connectivity directly. Note that we perform feature selection before scenario 2) by calculating connection-wise t-tests to determine the connections with different group means, represented by t-scores. We select the M functional connections with the highest absolute t-scores. M is optimized by cross validations.

Pre-screening

Even though PLS can cope with high-dimensional, co-linear datasets, we prescreened variables depending on their relevance to responses in the following way.

Based on Pearson correlation coefficients, ρ_rl, between the r-th functional connection and the l-th clinical measures, we define the empirical relevance of the r-th functional connection as (20) where p is the total number of functional connections.

These functional connections are ranked according to their empirical relevance, , and only M relevant functional connections are used in following procedure. The optimal number for M was determined through nested leave-one-out cross-validation.

Nested leave-one-out cross validation

Conventionally, cross validation is employed to assure generalization ability of a model or to evaluate optimal parameters. Since we have to account for both generalization ability and parameter optimization, we made use of nested leave-one-out cross validation (LOOCV), which consisted of outer and inner LOOCV. The outer LOOCV repeats iterations that split the whole set of samples into a single outer validation sample used to evaluate the generalization ability, and an outer training set for model estimation. The inner loop of LOOCV is performed on the outer training set to optimize two parameters, M and L, the number of selected predictor variables and the number of components, respectively. The pair of parameters that achieves the lowest root mean squared error based on the inner validation sample are adopted as optimal parameters and used to evaluate the model using the outer LOOCV. These steps are repeated until each sample has served as the validation sample.

Age

Age is significantly correlated with three clinical measures (Table 2). In general, age matching performed on different diagnostic groups reduces sample size, causing poor performance. To avoid this problem, we investigated three models, i.e. (i) a model with age as a response (denoted by output-age), (ii) a model with age as a predictor (denoted by input-age), and (iii) a model without age (denoted by no-age). By incorporating age into our model, we can cope with age differences among subjects and can fairly evaluate prediction performance.

Interpretation

Interpretation of each latent component projected from input and output data gives novel insights into the relationship between functional connectivity and clinical measures. In the framework of PLS, loading matrices, P and C, indicate contributions from predictor variables and response variables to each latent component (see Eqs (10) and (11)). The (i, j)-element of the loading matrix, P, represents the contribution of the i-th functional connection to the j-th latent component. Similarly, the (i, j)-element of the loading matrix, C, represents the contribution of the i-th clinical measure to the j-th latent component. Note that due to subject variability, values of P_ij and C_ij vary depending on the training set used.

Results

Regression performance

We compared the prediction performance of PLS, its kernel variants, and other methods by means of the root mean squared error (RMSE) of the predicted clinical measures in nested leave-one-out cross validation (see Methods). Kernel PLS with a second-order polynomial kernel (KPLS-Poly(2)) achieved the lowest RMSE (9.56 for BDI-II, 6.11 for SHAPS, and 7.29 for PANAS(n)) (Fig 2). This performance was significantly better than that of ordinary least squares regression (OLS) (11.6 for BDI-II, 7.33 for SHAPS, and 8.91 for PANAS(n)) and comparable to that of other variants of PLS applied in our study, suggesting that projection of data into a low-dimensional space was beneficial to regression performance. All statistical comparisons were adjusted for multiplicity using the Bonferroni-Holm method with significance level, α = 0.05.

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Fig 2. Comparison of predicted performance by means of the root mean squared errors.

Linear and kernel variants of PLS achieved significantly better performance than did OLS in all clinical scores. Subject age was used as the output along with clinical scores (output-age model).

https://doi.org/10.1371/journal.pone.0179638.g002

Next, to evaluate the best way of incorporating age into our regression models, we compared RMSE of the output-age, input-age, and no-age models. In our study, incorporating age into our regression model as a response (output-age) achieved significantly better performance than that of the input-age and no-age models (Fig 3). The details were listed in Supporting Information (S1, S2 and S3 Tables). All statistical comparisons were adjusted for multiplicity using the Bonferroni-Holm method with significance level, α = 0.05.

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Fig 3. Root mean squared errors in KPLS-Poly(2).

KPLS-Poly(2) achieved significantly better performance in output-age model than in other models.

https://doi.org/10.1371/journal.pone.0179638.g003

The correlation coefficient of actual and predicted values for BDI-II, SHAPS, and PANAS(n) in the case of KPLS-Poly(2) were r = 0.541, 0.591, 0.563, respectively. The relationship between predicted and actual values of BDI-II for KPLS-Poly(2) was exemplified (Fig 4). This result was comparable to that of Zhang et al. (2011) [14]; however, the number of subjects in our study was larger than in theirs, reconfirming validity of the results.

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Fig 4. Actual and predicted values of BDI-II.

BDI-II were well predicted by KPLS-Poly(2) with RMSE = 9.56 and r = 0.541 (p < 10⁻¹⁰). Red and blue points represent patients and healthy controls, respectively.

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The optimal number of retained features M* identified by pre-screening and using the latent component L* identified with nested LOOCV were 40 and 3, respectively, suggesting that reduction of feature size was relevant for improvement of PLS prediction accuracy.

Classification performance

Projecting the original data onto a low-dimensional space was expected to improve classification accuracy. To verify the benefit of projection, several classification methods were performed and evaluated using accuracy, sensitivity, and specificity (Fig 5). The details were listed in Supporting Information (S4 and S5 Tables). In our study, KPLS-Poly(2) followed by LDA achieved the best accuracy 80.5% (sensitivity 81.0% and specificity 80.0%), which is significantly better than the 57.7% accuracy of direct LDA (sensitivity 53.4%, and specificity 61.5%) and 69.1% accuracy of direct SVM (sensitivity 69.0%, and specificity 69.2%). This result indicates that it was beneficial to exploit the prediction model for clinical measures in order to build a classification model. In addition, KPLS-Poly(2) followed by LDA also achieved significantly better accuracy than the 62.6% accuracy of OLS followed by LDA (sensitivity 62.1% and specificity 63.1%), indicating that considering a latent space in a regression model was beneficial to final classification. Accuracy did not differ significantly between PLS and kernel variants. All statistical tests were based on approximation with the normal and adjusted for multiplicity using the Bonferroni-Holm method with significance level α = 0.05.

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Fig 5. Classification accuracy, sensitivity, and specificity.

KPLS-Poly(2) followed by LDA achieves the best performance (accuracy = 80.5%, sensitivity = 81.0%, and specificity = 80.0%).

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Interpretation

In our study, three clinical scores showed almost equally positive influences on the first component, and age also had a positive influence as well. However, age showed a strong negative influence on the second component, in contrast to the clinical scores (Fig 6).

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Fig 6. Loading matrix C.

The matrix indicates contributions of each clinical measure to the first two latent components. Age has a negative influence on the second latent component. Error bars indicate the standard deviation.

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Latent space representation of subjects showed that the first component explained most depression severity in comparison with the second component (Fig 7). This is consistent with the results of loading matrix C. Note that since the optimal number of latent components, in terms of minimizing regression error, was 3, the second and the third components are thought to contain some information about scores.

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Fig 7. Scatter plot of the latent variables in the first two latent components generated from KPLS-Poly(2).

Red and blue dots represent patients and healthy controls, respectively. The two groups are separated mainly by the first latent component.

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In order to validate the effect of age, especially in the second component, all subjects were grouped into young (age 20–31, 41 subjects), middle (age 31–43, 41 subjects), and old (age 44–73, 41 subjects) groups. Note we simply divided the subjects in three equal-sized groups for convenience, “young”, “middle”, and “old”. They are relative, not absolute age classes. Latent variables of old subjects in the second component were significantly lower than those of young and middle subjects (p < 10⁻⁵ by Wilcoxon Rank-Sum Test), suggesting that old patients have distinctive patterns in the second latent space [5] (Fig 8).

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Fig 8. Scatter plot of subjects separated on the basis of the two latent components generated from KPLS-Poly(2) for young, middle, and old subjects.

Old subjects have significantly lower values in the second component (p < 10⁻⁵ by Wilcoxon Rank-Sum Test).

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Evaluation of loading matrix, P, reveals functional connections relevant to each latent component. Especially, the first column of P, corresponding to the first component responsible for discrimination of each diagnostic group, is expected to reveal useful insights about the effect of functional connections on depression symptoms. Even though the performance of KPLS-Poly(2) in prediction and classification was comparable to or better than that of linear PLS, patterns of significant loadings were consistent in our experiments. For reasons of interpretation, we therefore focus on the loading matrix of the linear terms in following sections.

BrainNet Viewer [32] (http://www.nitrc.org/projects/bnv/) was used to visualize the top 10 connections with positive and negative loadings for the first component (Figs 9 and 10). In this figure, many regions involved in the default mode network (DMN), as well as the left supplementary motor area, the right superior frontal gyrus, and the insula, were relevant. In addition, some functional connectivity between the right cuneus and regions involved in the cerebellum were negatively correlated with the first component.

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Fig 9. Contributing functional connectivity in first latent component.

Red and blue lines represent positive and negative loadings, respectively. SFGdor.R: right superior frontal gyrus, INS: insula, SMA.L: left supplementary motor area, CUN.R:right cuneus.

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Fig 10. Contributing functional connectivity in first latent component.

Purple and yellow nodes represent brain areas within the default mode network and cerebellum, respectively. SFGdor.R: right superior frontal gyrus, INS: insula, SMA.L: left supplementary motor area, CUN.R:right cuneus.

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Discussion

MacIntosh et al. (1996) first introduced PLS analysis into the field of neuroimaging in order to extract common information between brain activity and exogenous information, such as experimental or behavioral data [3, 4]. In particular, behavioral data are increasingly used to extract associated brain activity patterns for various types of psychological diseases, such as Alzheimer’s disease [33], obsessive-compulsive disorder [34], and schizophrenia [35]. In these studies, neuropsychological test scores are used as behavioral data, in addition to the labels that represent diagnostic groups and age. To the best of our knowledge, this is the first study to investigate associations between functional connectivity in the whole brain and multiple clinical measures for depressed patients, using PLS and its kernel variants.

Diagnosis based on resting-state functional connectivity is a challenging task due to the high-dimensionality and co-linearity of data. Recent studies have demonstrated that depressed patients can be distinguished from healthy controls by means of their functional connectivity by applying conventional methods, such as support vector machine [9, 13]. Since binary labels are ultimately abstracted information about depression that ignores the severity of symptoms, it is worth considering more detailed information, such as BDI-II, SHAPS, and PANAS(n) to build more sophisticated models. Our study demonstrated that projecting functional connectivity data into a low-dimensional latent space, can predict clinical measures, and can also improve depression diagnostic accuracy.

To separately identify neural circuits associated with anhedonia and negative mood is a challenging task. A psychopathological study suggests that these primary symptoms result from different neural circuits and from alternation of different neurotransmitters [16]. Our results show that SHAPS and PANAS(n) are highly correlated and contributed quite similarly to each latent component (Fig 6), suggesting that further investigation and different approaches may be required to support psychopathological studies from the point of data driven analysis.

We also evaluated extended AAL generated by subdividing standard AAL into 600 regions to examine if the finer atlas could be used to improve the prediction of the clinical scores [36]. The performance was significantly worse than that of standard AAL (S6 Table) and the selected functional connections were inconsistent. Since analysis of brain imaging data with limited sample size highly depends on the choice of ROI, the finer atlas does not necessarily provide better prediction performance. Therefore, it is fare to note that further research is required to validate the best atlas.

Contributing brain regions

Identification of relevant brain regions in functional connectivity analysis yielded the following three observations: (1) connections between the default mode network and other regions, such as the right superior frontal gyrus and the left supplementary motor area are relevant (2) the left and right insulas in both hemispheres are relevant, (3) connections between the cerebellum and the right cuneus are relevant.

First, the default mode network (DMN) shows synchronized deactivation during cognitive tasks and is thought to be related to major depressive disorder [37–40]. Our study supports these results, indicating that many relevant connections are related to the DMN, such as the right posterior cingulum, the right precuneus, and the superior parietal gyrus. The DMN contributes positive connections with the right superior frontal gyrus and the left supplementary motor area. The superior frontal gyrus, as a critical region in cognitive tasks, was previously reported to be associated with depression [41]. While the supplementary motor area is known to be responsible for motor control, it is also reportedly related to some subtype of depression [42]. Our results support these results.

Second, our results suggest that the insula is associated with depression. Some meta-analysis of PET and fMRI studies revealed that the insula plays an important role in regulation of emotion [43, 44]. Similarly, resting-state fMRI studies have indicated that the insula is directly associated with depression [45, 46].

Finally, we showed that three connections between the right cuneus, located in the visual cortical area, and the cerebellum, negatively influence depression. While visual processing is believed not to be affected in depression, some previous studies have suggested that it is associated with bipolar disorder [47]. Moreover, regional homogeneity (ReHo) interpreted as a measure of localized synchrony in resting-state fMRI was decreased [48]. The cerebellum is usually considered to be responsible for motion control, but our results indicate that it may also be involved in regulation of mood and cognitive processing associated with symptoms of depression. Some fMRI studies demonstrate that this area is responsible for various types of information processing [49, 50], and resting-state functional connectivity studies imply that the cerebellum may be critical for the distinction between depressed patients and healthy controls [13, 51].

Conclusion

In summary, we employed partial least squares regression and its kernel variants to predict clinical measures of subjects using resting-state functional connectivity. Diagnosis of depression based on predicted clinical scores performed better than classification algorithms attempting diagnoses directly from functional connectivity. Moreover, analysis of latent variables identified functional networks relevant to the diagnosis of depression. These results suggest that a low-dimensional representation derived using PLS is beneficial for objective diagnosis. Further investigations are required to separate the two neural circuits associated with two primary symptoms, anhedonia and negative mood.

Supporting information

S1 Appendix. Partial least squares regression.

https://doi.org/10.1371/journal.pone.0179638.s001

(PDF)

S1 Table. Root mean squared errors in output-age.

Bold figures represent the best achievement.

https://doi.org/10.1371/journal.pone.0179638.s002

(PDF)

S2 Table. Root mean squared errors in input-age.

https://doi.org/10.1371/journal.pone.0179638.s003

(PDF)

S3 Table. Root mean squared errors in no-age.

https://doi.org/10.1371/journal.pone.0179638.s004

(PDF)

S4 Table. Classification performance.

KPLS-Poly(2) followed by LDA significantly outperformed direct LDA, SVM, and OLS followed by LDA in accuracy (adjusted for multiplicity using the Bonferroni-Holm method with significance level α = 0.05).

https://doi.org/10.1371/journal.pone.0179638.s005

(PDF)

S5 Table. Classification performance without subjects over 60.

KPLS-Poly(2) followed by LDA significantly outperformed direct LDA and OLS followed by LDA in accuracy (adjusted for multiplicity using the Bonferroni-Holm method with significance level α = 0.05).

https://doi.org/10.1371/journal.pone.0179638.s006

(PDF)

S6 Table. Root mean squared errors in extended AAL.

Performance with the standard AAL outperformed extended AAL significantly. (adjusted for multiplicity using the Bonferroni-Holm method with significance level α = 0.05).

https://doi.org/10.1371/journal.pone.0179638.s007

(PDF)

Acknowledgments

This research is supported by the Strategic Research Program for Brain Sciences from Japan Agency for Medical Research and development, AMED. Thanks to Dr. Steven D. Aird, technical editor of the Okinawa Institute of Science and Technology, for editing.

Author Contributions

Conceptualization: KY YS JY KD.
Data curation: MT GO YO SY.
Formal analysis: KY.
Funding acquisition: SY KD.
Investigation: KY.
Methodology: KY.
Project administration: KD.
Resources: MT GO YO SY.
Software: KY.
Supervision: KD.
Validation: KY.
Visualization: KY.
Writing – original draft: KY.
Writing – review & editing: YS JY MT GO YO SY.

References

1. Shimizu Y, Yoshimoto J, Toki S, Takamura M, Yoshimura S, Okamoto Y, et al. Toward probabilistic diagnosis and understanding of depression based on functional MRI data analysis with logistic group LASSO. PLoS ONE. 2015;10(5):e0123524. pmid:25932629
- View Article
- PubMed/NCBI
- Google Scholar
2. Wold H, et al. Soft modeling by latent variables: the nonlinear iterative partial least squares approach. Perspectives in Probability and Statistics, papers in honour of MS Bartlett. 1975; p. 520–540.
- View Article
- Google Scholar
3. McIntosh A, Bookstein F, Haxby JV, Grady C. Spatial pattern analysis of functional brain images using partial least squares. NeuroImage. 1996;3(3):143–157. pmid:9345485
- View Article
- PubMed/NCBI
- Google Scholar
4. McIntosh AR, Lobaugh NJ. Partial least squares analysis of neuroimaging data: applications and advances. NeuroImage. 2004;23:S250–S263. pmid:15501095
- View Article
- PubMed/NCBI
- Google Scholar
5. Chen K, Reiman EM, Huan Z, Caselli RJ, Bandy D, Ayutyanont N, et al. Linking functional and structural brain images with multivariate network analyses: a novel application of the partial least square method. NeuroImage. 2009;47(2):602–610. pmid:19393744
- View Article
- PubMed/NCBI
- Google Scholar
6. Ziegler G, Dahnke R, Winkler AD, Gaser C. Partial least squares correlation of multivariate cognitive abilities and local brain structure in children and adolescents. NeuroImage. 2013;82:284–294. pmid:23727321
- View Article
- PubMed/NCBI
- Google Scholar
7. Giessing C, Fink GR, Rösler F, Thiel CM. fMRI data predict individual differences of behavioral effects of nicotine: a partial least square analysis. Journal of Cognitive Neuroscience. 2007;19(4):658–670. pmid:17381256
- View Article
- PubMed/NCBI
- Google Scholar
8. Yahata N, Morimoto J, Hashimoto R, Lisi G, Shibata K, Kawakubo Y, et al. A small number of abnormal brain connections predicts adult autism spectrum disorder. Nature Communications. 2016;7. pmid:27075704
- View Article
- PubMed/NCBI
- Google Scholar
9. Craddock RC, Holtzheimer PE, Hu XP, Mayberg HS. Disease state prediction from resting state functional connectivity. Magnetic Resonance in Medicine. 2009;62(6):1619–1628. pmid:19859933
- View Article
- PubMed/NCBI
- Google Scholar
10. Greicius MD, Flores BH, Menon V, Glover GH, Solvason HB, Kenna H, et al. Resting-state functional connectivity in major depression: abnormally increased contributions from subgenual cingulate cortex and thalamus. Biological Psychiatry. 2007;62(5):429–437. pmid:17210143
- View Article
- PubMed/NCBI
- Google Scholar
11. Veer IM, Beckmann CF, Van Tol MJ, Ferrarini L, Milles J, Veltman DJ, et al. Whole brain resting-state analysis reveals decreased functional connectivity in major depression. Frontiers in Systems Neuroscience. 2010;4. pmid:20941370
- View Article
- PubMed/NCBI
- Google Scholar
12. Zhang J, Wang J, Wu Q, Kuang W, Huang X, He Y, et al. Disrupted brain connectivity networks in drug-naive, first-episode major depressive disorder. Biological Psychiatry. 2011;70(4):334–342. pmid:21791259
- View Article
- PubMed/NCBI
- Google Scholar
13. Zeng LL, Shen H, Liu L, Wang L, Li B, Fang P, et al. Identifying major depression using whole-brain functional connectivity: a multivariate pattern analysis. Brain. 2012;135(5):1498–1507. pmid:22418737
- View Article
- PubMed/NCBI
- Google Scholar
14. Zhang X, Yaseen ZS, Galynker II, Hirsch J, Winston A. Can depression be diagnosed by response to mother’s face? A personalized attachment-based paradigm for diagnostic fMRI. PLoS ONE. 2011;6(12):e27253. pmid:22180777
- View Article
- PubMed/NCBI
- Google Scholar
15. Beck AT, Steer RA, Ball R, Ranieri WF. Comparison of Beck Depression Inventories-IA and-II in psychiatric outpatients. Journal of Personality Assessment. 1996;67(3):588–597. pmid:8991972
- View Article
- PubMed/NCBI
- Google Scholar
16. Hasler G, Northoff G. Discovering imaging endophenotypes for major depression. Molecular Psychiatry. 2011;16(6):604–619. pmid:21602829
- View Article
- PubMed/NCBI
- Google Scholar
17. Snaith R, Hamilton M, Morley S, Humayan A, Hargreaves D, Trigwell P. A scale for the assessment of hedonic tone the Snaith-Hamilton Pleasure Scale. The British Journal of Psychiatry. 1995;167(1):99–103. pmid:7551619
- View Article
- PubMed/NCBI
- Google Scholar
18. Watson D, Clark LA, Tellegen A. Development and validation of brief measures of positive and negative affect: the PANAS scales. Journal of Personality and Social Psychology. 1988;54(6):1063. pmid:3397865
- View Article
- PubMed/NCBI
- Google Scholar
19. Katona CL, Watkin V. Depression in old age. Reviews in Clinical Gerontology. 1995;5(04):427–441.
- View Article
- Google Scholar
20. Yoshida K, Shimizu Y, Yoshimoto J, Toki S, Okada G, Takamura M, et al. Resting state functional connectivity explains individual scores of multiple clinical measures for major depression. In: Bioinformatics and Biomedicine (BIBM), 2015 IEEE International Conference on. IEEE; 2015. p. 1078–1083.
21. Lecrubier Y, Sheehan DV, Weiller E, Amorim P, Bonora I, Harnett Sheehan K, et al. The Mini International Neuropsychiatric Interview (MINI). A short diagnostic structured interview: reliability and validity according to the CIDI. European Psychiatry. 1997;12(5):224–231.
- View Article
- Google Scholar
22. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR). American Psychiatric Association; 2000.
23. Ehring T, Tuschen-Caffier B, Schnülle J, Fischer S, Gross JJ. Emotion regulation and vulnerability to depression: spontaneous versus instructed use of emotion suppression and reappraisal. Emotion. 2010;10(4):563. pmid:20677873
- View Article
- PubMed/NCBI
- Google Scholar
24. Van Dijk KR, Sabuncu MR, Buckner RL. The influence of head motion on intrinsic functional connectivity MRI. NeuroImage. 2012;59(1):431–438. pmid:21810475
- View Article
- PubMed/NCBI
- Google Scholar
25. Zeng LL, Wang D, Fox MD, Sabuncu M, Hu D, Ge M, et al. Neurobiological basis of head motion in brain imaging. Proceedings of the National Academy of Sciences. 2014;111(16):6058–6062.
- View Article
- Google Scholar
26. Tzourio-Mazoyer N, Landeau B, Papathanassiou D, Crivello F, Etard O, Delcroix N, et al. Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. NeuroImage. 2002;15(1):273–289. pmid:11771995
- View Article
- PubMed/NCBI
- Google Scholar
27. Manne R. Analysis of two partial-least-squares algorithms for multivariate calibration. Chemometrics and Intelligent Laboratory Systems. 1987;2(1):187–197.
- View Article
- Google Scholar
28. Rosipal R, Trejo LJ. Kernel partial least squares regression in reproducing kernel hilbert space. Journal of Machine Learning Research. 2002;2:97–123.
- View Article
- Google Scholar
29. Rännar S, Lindgren F, Geladi P, Wold S. A PLS kernel algorithm for data sets with many variables and fewer objects. Part 1: Theory and algorithm. Journal of Chemometrics. 1994;8(2):111–125.
- View Article
- Google Scholar
30. Bennett K, Embrechts M. An optimization perspective on kernel partial least squares regression. NATO Science Series sub series III Computer and Systems Sciences. 2003;190:227–250.
- View Article
- Google Scholar
31. Schölkopf B, Smola A, Müller KR. Nonlinear component analysis as a kernel eigenvalue problem. Neural Computation. 1998;10(5):1299–1319.
- View Article
- Google Scholar
32. Xia M, Wang J, He Y. BrainNet Viewer: a network visualization tool for human brain connectomics. PLoS ONE. 2013;8(7):e68910. pmid:23861951
- View Article
- PubMed/NCBI
- Google Scholar
33. Price J, Ziolko S, Weissfeld L, Klunk W, Lu X, Hoge J, et al. Quantitative and statistical analyses of PET imaging studies of amyloid deposition in humans. In: Nuclear Science Symposium Conference Record, 2004 IEEE. vol. 5. IEEE; 2004. p. 3161–3164.
34. Menzies L, Achard S, Chamberlain SR, Fineberg N, Chen CH, Del Campo N, et al. Neurocognitive endophenotypes of obsessive-compulsive disorder. Brain. 2007;130(12):3223–3236. https://doi.org/10.1093/brain/awm205 pmid:17855376
35. Nestor PG, O’Donnell BF, McCarley RW, Niznikiewicz M, Barnard J, Shen ZJ, et al. A new statistical method for testing hypotheses of neuropsychological/MRI relationships in schizophrenia: partial least squares analysis. Schizophrenia Research. 2002;53(1):57–66. pmid:11728838
- View Article
- PubMed/NCBI
- Google Scholar
36. Hermundstad AM, Bassett DS, Brown KS, Aminoff EM, Clewett D, Freeman S, et al. Structural foundations of resting-state and task-based functional connectivity in the human brain. Proceedings of the National Academy of Sciences. 2013;110(15):6169–6174.
- View Article
- Google Scholar
37. Zhu X, Wang X, Xiao J, Liao J, Zhong M, Wang W, et al. Evidence of a dissociation pattern in resting-state default mode network connectivity in first-episode, treatment-naive major depression patients. Biological Psychiatry. 2012;71(7):611–617. pmid:22177602
- View Article
- PubMed/NCBI
- Google Scholar
38. Zeng LL, Shen H, Liu L, Hu D. Unsupervised classification of major depression using functional connectivity MRI. Human Brain Mapping. 2014;35(4):1630–1641. pmid:23616377
- View Article
- PubMed/NCBI
- Google Scholar
39. Kaiser RH, Andrews-Hanna JR, Wager TD, Pizzagalli DA. Large-scale network dysfunction in major depressive disorder: a meta-analysis of resting-state functional connectivity. JAMA psychiatry. 2015;72(6):603–611. pmid:25785575
- View Article
- PubMed/NCBI
- Google Scholar
40. Mulders PC, van Eijndhoven PF, Schene AH, Beckmann CF, Tendolkar I. Resting-state functional connectivity in major depressive disorder: A review. Neuroscience and Biobehavioral Reviews. 2015;56:330–344. pmid:26234819
- View Article
- PubMed/NCBI
- Google Scholar
41. Fitzgerald PB, Laird AR, Maller J, Daskalakis ZJ. A meta-analytic study of changes in brain activation in depression. Human Brain Mapping. 2008;29(6):683–695. pmid:17598168
- View Article
- PubMed/NCBI
- Google Scholar
42. Exner C, Lange C, Irle E. Impaired implicit learning and reduced pre-supplementary motor cortex size in early-onset major depression with melancholic features. Journal of Affective Disorders. 2009;119(1-3):156–62. pmid:19345999
- View Article
- PubMed/NCBI
- Google Scholar
43. Phan KL, Wager T, Taylor SF, Liberzon I. Functional neuroanatomy of emotion: a meta-analysis of emotion activation studies in PET and fMRI. NeuroImage. 2002;16(2):331–348. pmid:12030820
- View Article
- PubMed/NCBI
- Google Scholar
44. Hamilton JP, Etkin A, Furman DJ, Lemus MG, Johnson RF, Gotlib IH. Functional neuroimaging of major depressive disorder: a meta-analysis and new integration of baseline activation and neural response data. American Journal of Psychiatry. 2012;. pmid:22535198
- View Article
- PubMed/NCBI
- Google Scholar
45. Yao Z, Wang L, Lu Q, Liu H, Teng G. Regional homogeneity in depression and its relationship with separate depressive symptom clusters: a resting-state fMRI study. Journal of Affective Disorders. 2009;115(3):430–438. pmid:19007997
- View Article
- PubMed/NCBI
- Google Scholar
46. Liu Z, Xu C, Xu Y, Wang Y, Zhao B, Lv Y, et al. Decreased regional homogeneity in insula and cerebellum: a resting-state fMRI study in patients with major depression and subjects at high risk for major depression. Psychiatry Research: Neuroimaging. 2010;182(3):211–215. pmid:20493670
- View Article
- PubMed/NCBI
- Google Scholar
47. Haldane M, Cunningham G, Androutsos C, Frangou S. Structural brain correlates of response inhibition in Bipolar Disorder I. Journal of Psychopharmacology. 2008;. pmid:18308812
- View Article
- PubMed/NCBI
- Google Scholar
48. Iwabuchi SJ, Krishnadas R, Li C, Auer DP, Radua J, Palaniyappan L. Localized connectivity in depression: a meta-analysis of resting state functional imaging studies. Neuroscience and Biobehavioral Reviews. 2015;51:77–86. pmid:25597656
- View Article
- PubMed/NCBI
- Google Scholar
49. O’Reilly JX, Beckmann CF, Tomassini V, Ramnani N, Johansen-Berg H. Distinct and overlapping functional zones in the cerebellum defined by resting state functional connectivity. Cerebral Cortex. 2010;20(4):953–965. pmid:19684249
- View Article
- PubMed/NCBI
- Google Scholar
50. Moulton EA, Elman I, Pendse G, Schmahmann J, Becerra L, Borsook D. Aversion-related circuitry in the cerebellum: responses to noxious heat and unpleasant images. Journal of Neuroscience. 2011;31(10):3795–3804. pmid:21389234
- View Article
- PubMed/NCBI
- Google Scholar
51. Liu L, Zeng LL, Li Y, Ma Q, Li B, Shen H, et al. Altered cerebellar functional connectivity with intrinsic connectivity networks in adults with major depressive disorder. PLoS ONE. 2012;7(6):e39516. pmid:22724025
- View Article
- PubMed/NCBI
- Google Scholar

[ref1] 1. Shimizu Y, Yoshimoto J, Toki S, Takamura M, Yoshimura S, Okamoto Y, et al. Toward probabilistic diagnosis and understanding of depression based on functional MRI data analysis with logistic group LASSO. PLoS ONE. 2015;10(5):e0123524. pmid:25932629
View Article
PubMed/NCBI
Google Scholar

[2] View Article

[3] PubMed/NCBI

[4] Google Scholar

[ref2] 2. Wold H, et al. Soft modeling by latent variables: the nonlinear iterative partial least squares approach. Perspectives in Probability and Statistics, papers in honour of MS Bartlett. 1975; p. 520–540.
View Article
Google Scholar

[6] View Article

[7] Google Scholar

[ref3] 3. McIntosh A, Bookstein F, Haxby JV, Grady C. Spatial pattern analysis of functional brain images using partial least squares. NeuroImage. 1996;3(3):143–157. pmid:9345485
View Article
PubMed/NCBI
Google Scholar

[9] View Article

[10] PubMed/NCBI

[11] Google Scholar

[ref4] 4. McIntosh AR, Lobaugh NJ. Partial least squares analysis of neuroimaging data: applications and advances. NeuroImage. 2004;23:S250–S263. pmid:15501095
View Article
PubMed/NCBI
Google Scholar

[13] View Article

[14] PubMed/NCBI

[15] Google Scholar

[ref5] 5. Chen K, Reiman EM, Huan Z, Caselli RJ, Bandy D, Ayutyanont N, et al. Linking functional and structural brain images with multivariate network analyses: a novel application of the partial least square method. NeuroImage. 2009;47(2):602–610. pmid:19393744
View Article
PubMed/NCBI
Google Scholar

[17] View Article

[18] PubMed/NCBI

[19] Google Scholar

[ref6] 6. Ziegler G, Dahnke R, Winkler AD, Gaser C. Partial least squares correlation of multivariate cognitive abilities and local brain structure in children and adolescents. NeuroImage. 2013;82:284–294. pmid:23727321
View Article
PubMed/NCBI
Google Scholar

[21] View Article

[22] PubMed/NCBI

[23] Google Scholar

[ref7] 7. Giessing C, Fink GR, Rösler F, Thiel CM. fMRI data predict individual differences of behavioral effects of nicotine: a partial least square analysis. Journal of Cognitive Neuroscience. 2007;19(4):658–670. pmid:17381256
View Article
PubMed/NCBI
Google Scholar

[25] View Article

[26] PubMed/NCBI

[27] Google Scholar

[ref8] 8. Yahata N, Morimoto J, Hashimoto R, Lisi G, Shibata K, Kawakubo Y, et al. A small number of abnormal brain connections predicts adult autism spectrum disorder. Nature Communications. 2016;7. pmid:27075704
View Article
PubMed/NCBI
Google Scholar

[29] View Article

[30] PubMed/NCBI

[31] Google Scholar

[ref9] 9. Craddock RC, Holtzheimer PE, Hu XP, Mayberg HS. Disease state prediction from resting state functional connectivity. Magnetic Resonance in Medicine. 2009;62(6):1619–1628. pmid:19859933
View Article
PubMed/NCBI
Google Scholar

[33] View Article

[34] PubMed/NCBI

[35] Google Scholar

[ref10] 10. Greicius MD, Flores BH, Menon V, Glover GH, Solvason HB, Kenna H, et al. Resting-state functional connectivity in major depression: abnormally increased contributions from subgenual cingulate cortex and thalamus. Biological Psychiatry. 2007;62(5):429–437. pmid:17210143
View Article
PubMed/NCBI
Google Scholar

[37] View Article

[38] PubMed/NCBI

[39] Google Scholar

[ref11] 11. Veer IM, Beckmann CF, Van Tol MJ, Ferrarini L, Milles J, Veltman DJ, et al. Whole brain resting-state analysis reveals decreased functional connectivity in major depression. Frontiers in Systems Neuroscience. 2010;4. pmid:20941370
View Article
PubMed/NCBI
Google Scholar

[41] View Article

[42] PubMed/NCBI

[43] Google Scholar

[ref12] 12. Zhang J, Wang J, Wu Q, Kuang W, Huang X, He Y, et al. Disrupted brain connectivity networks in drug-naive, first-episode major depressive disorder. Biological Psychiatry. 2011;70(4):334–342. pmid:21791259
View Article
PubMed/NCBI
Google Scholar

[45] View Article

[46] PubMed/NCBI

[47] Google Scholar

[ref13] 13. Zeng LL, Shen H, Liu L, Wang L, Li B, Fang P, et al. Identifying major depression using whole-brain functional connectivity: a multivariate pattern analysis. Brain. 2012;135(5):1498–1507. pmid:22418737
View Article
PubMed/NCBI
Google Scholar

[49] View Article

[50] PubMed/NCBI

[51] Google Scholar

[ref14] 14. Zhang X, Yaseen ZS, Galynker II, Hirsch J, Winston A. Can depression be diagnosed by response to mother’s face? A personalized attachment-based paradigm for diagnostic fMRI. PLoS ONE. 2011;6(12):e27253. pmid:22180777
View Article
PubMed/NCBI
Google Scholar

[53] View Article

[54] PubMed/NCBI

[55] Google Scholar

[ref15] 15. Beck AT, Steer RA, Ball R, Ranieri WF. Comparison of Beck Depression Inventories-IA and-II in psychiatric outpatients. Journal of Personality Assessment. 1996;67(3):588–597. pmid:8991972
View Article
PubMed/NCBI
Google Scholar

[57] View Article

[58] PubMed/NCBI

[59] Google Scholar

[ref16] 16. Hasler G, Northoff G. Discovering imaging endophenotypes for major depression. Molecular Psychiatry. 2011;16(6):604–619. pmid:21602829
View Article
PubMed/NCBI
Google Scholar

[61] View Article

[62] PubMed/NCBI

[63] Google Scholar

[ref17] 17. Snaith R, Hamilton M, Morley S, Humayan A, Hargreaves D, Trigwell P. A scale for the assessment of hedonic tone the Snaith-Hamilton Pleasure Scale. The British Journal of Psychiatry. 1995;167(1):99–103. pmid:7551619
View Article
PubMed/NCBI
Google Scholar

[65] View Article

[66] PubMed/NCBI

[67] Google Scholar

[ref18] 18. Watson D, Clark LA, Tellegen A. Development and validation of brief measures of positive and negative affect: the PANAS scales. Journal of Personality and Social Psychology. 1988;54(6):1063. pmid:3397865
View Article
PubMed/NCBI
Google Scholar

[69] View Article

[70] PubMed/NCBI

[71] Google Scholar

[ref19] 19. Katona CL, Watkin V. Depression in old age. Reviews in Clinical Gerontology. 1995;5(04):427–441.
View Article
Google Scholar

[73] View Article

[74] Google Scholar

[ref20] 20. Yoshida K, Shimizu Y, Yoshimoto J, Toki S, Okada G, Takamura M, et al. Resting state functional connectivity explains individual scores of multiple clinical measures for major depression. In: Bioinformatics and Biomedicine (BIBM), 2015 IEEE International Conference on. IEEE; 2015. p. 1078–1083.

[ref21] 21. Lecrubier Y, Sheehan DV, Weiller E, Amorim P, Bonora I, Harnett Sheehan K, et al. The Mini International Neuropsychiatric Interview (MINI). A short diagnostic structured interview: reliability and validity according to the CIDI. European Psychiatry. 1997;12(5):224–231.
View Article
Google Scholar

[77] View Article

[78] Google Scholar

[ref22] 22. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR). American Psychiatric Association; 2000.

[ref23] 23. Ehring T, Tuschen-Caffier B, Schnülle J, Fischer S, Gross JJ. Emotion regulation and vulnerability to depression: spontaneous versus instructed use of emotion suppression and reappraisal. Emotion. 2010;10(4):563. pmid:20677873
View Article
PubMed/NCBI
Google Scholar

[81] View Article

[82] PubMed/NCBI

[83] Google Scholar

[ref24] 24. Van Dijk KR, Sabuncu MR, Buckner RL. The influence of head motion on intrinsic functional connectivity MRI. NeuroImage. 2012;59(1):431–438. pmid:21810475
View Article
PubMed/NCBI
Google Scholar

[85] View Article

[86] PubMed/NCBI

[87] Google Scholar

[ref25] 25. Zeng LL, Wang D, Fox MD, Sabuncu M, Hu D, Ge M, et al. Neurobiological basis of head motion in brain imaging. Proceedings of the National Academy of Sciences. 2014;111(16):6058–6062.
View Article
Google Scholar

[89] View Article

[90] Google Scholar

[ref26] 26. Tzourio-Mazoyer N, Landeau B, Papathanassiou D, Crivello F, Etard O, Delcroix N, et al. Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. NeuroImage. 2002;15(1):273–289. pmid:11771995
View Article
PubMed/NCBI
Google Scholar

[92] View Article

[93] PubMed/NCBI

[94] Google Scholar

[ref27] 27. Manne R. Analysis of two partial-least-squares algorithms for multivariate calibration. Chemometrics and Intelligent Laboratory Systems. 1987;2(1):187–197.
View Article
Google Scholar

[96] View Article

[97] Google Scholar

[ref28] 28. Rosipal R, Trejo LJ. Kernel partial least squares regression in reproducing kernel hilbert space. Journal of Machine Learning Research. 2002;2:97–123.
View Article
Google Scholar

[99] View Article

[100] Google Scholar

[ref29] 29. Rännar S, Lindgren F, Geladi P, Wold S. A PLS kernel algorithm for data sets with many variables and fewer objects. Part 1: Theory and algorithm. Journal of Chemometrics. 1994;8(2):111–125.
View Article
Google Scholar

[102] View Article

[103] Google Scholar

[ref30] 30. Bennett K, Embrechts M. An optimization perspective on kernel partial least squares regression. NATO Science Series sub series III Computer and Systems Sciences. 2003;190:227–250.
View Article
Google Scholar

[105] View Article

[106] Google Scholar

[ref31] 31. Schölkopf B, Smola A, Müller KR. Nonlinear component analysis as a kernel eigenvalue problem. Neural Computation. 1998;10(5):1299–1319.
View Article
Google Scholar

[108] View Article

[109] Google Scholar

[ref32] 32. Xia M, Wang J, He Y. BrainNet Viewer: a network visualization tool for human brain connectomics. PLoS ONE. 2013;8(7):e68910. pmid:23861951
View Article
PubMed/NCBI
Google Scholar

[111] View Article

[112] PubMed/NCBI

[113] Google Scholar

[ref33] 33. Price J, Ziolko S, Weissfeld L, Klunk W, Lu X, Hoge J, et al. Quantitative and statistical analyses of PET imaging studies of amyloid deposition in humans. In: Nuclear Science Symposium Conference Record, 2004 IEEE. vol. 5. IEEE; 2004. p. 3161–3164.

[ref34] 34. Menzies L, Achard S, Chamberlain SR, Fineberg N, Chen CH, Del Campo N, et al. Neurocognitive endophenotypes of obsessive-compulsive disorder. Brain. 2007;130(12):3223–3236. https://doi.org/10.1093/brain/awm205 pmid:17855376

[ref35] 35. Nestor PG, O’Donnell BF, McCarley RW, Niznikiewicz M, Barnard J, Shen ZJ, et al. A new statistical method for testing hypotheses of neuropsychological/MRI relationships in schizophrenia: partial least squares analysis. Schizophrenia Research. 2002;53(1):57–66. pmid:11728838
View Article
PubMed/NCBI
Google Scholar

[117] View Article

[118] PubMed/NCBI

[119] Google Scholar

[ref36] 36. Hermundstad AM, Bassett DS, Brown KS, Aminoff EM, Clewett D, Freeman S, et al. Structural foundations of resting-state and task-based functional connectivity in the human brain. Proceedings of the National Academy of Sciences. 2013;110(15):6169–6174.
View Article
Google Scholar

[121] View Article

[122] Google Scholar

[ref37] 37. Zhu X, Wang X, Xiao J, Liao J, Zhong M, Wang W, et al. Evidence of a dissociation pattern in resting-state default mode network connectivity in first-episode, treatment-naive major depression patients. Biological Psychiatry. 2012;71(7):611–617. pmid:22177602
View Article
PubMed/NCBI
Google Scholar

[124] View Article

[125] PubMed/NCBI

[126] Google Scholar

[ref38] 38. Zeng LL, Shen H, Liu L, Hu D. Unsupervised classification of major depression using functional connectivity MRI. Human Brain Mapping. 2014;35(4):1630–1641. pmid:23616377
View Article
PubMed/NCBI
Google Scholar

[128] View Article

[129] PubMed/NCBI

[130] Google Scholar

[ref39] 39. Kaiser RH, Andrews-Hanna JR, Wager TD, Pizzagalli DA. Large-scale network dysfunction in major depressive disorder: a meta-analysis of resting-state functional connectivity. JAMA psychiatry. 2015;72(6):603–611. pmid:25785575
View Article
PubMed/NCBI
Google Scholar

[132] View Article

[133] PubMed/NCBI

[134] Google Scholar

[ref40] 40. Mulders PC, van Eijndhoven PF, Schene AH, Beckmann CF, Tendolkar I. Resting-state functional connectivity in major depressive disorder: A review. Neuroscience and Biobehavioral Reviews. 2015;56:330–344. pmid:26234819
View Article
PubMed/NCBI
Google Scholar

[136] View Article

[137] PubMed/NCBI

[138] Google Scholar

[ref41] 41. Fitzgerald PB, Laird AR, Maller J, Daskalakis ZJ. A meta-analytic study of changes in brain activation in depression. Human Brain Mapping. 2008;29(6):683–695. pmid:17598168
View Article
PubMed/NCBI
Google Scholar

[140] View Article

[141] PubMed/NCBI

[142] Google Scholar

[ref42] 42. Exner C, Lange C, Irle E. Impaired implicit learning and reduced pre-supplementary motor cortex size in early-onset major depression with melancholic features. Journal of Affective Disorders. 2009;119(1-3):156–62. pmid:19345999
View Article
PubMed/NCBI
Google Scholar

[144] View Article

[145] PubMed/NCBI

[146] Google Scholar

[ref43] 43. Phan KL, Wager T, Taylor SF, Liberzon I. Functional neuroanatomy of emotion: a meta-analysis of emotion activation studies in PET and fMRI. NeuroImage. 2002;16(2):331–348. pmid:12030820
View Article
PubMed/NCBI
Google Scholar

[148] View Article

[149] PubMed/NCBI

[150] Google Scholar

[ref44] 44. Hamilton JP, Etkin A, Furman DJ, Lemus MG, Johnson RF, Gotlib IH. Functional neuroimaging of major depressive disorder: a meta-analysis and new integration of baseline activation and neural response data. American Journal of Psychiatry. 2012;. pmid:22535198
View Article
PubMed/NCBI
Google Scholar

[152] View Article

[153] PubMed/NCBI

[154] Google Scholar

[ref45] 45. Yao Z, Wang L, Lu Q, Liu H, Teng G. Regional homogeneity in depression and its relationship with separate depressive symptom clusters: a resting-state fMRI study. Journal of Affective Disorders. 2009;115(3):430–438. pmid:19007997
View Article
PubMed/NCBI
Google Scholar

[156] View Article

[157] PubMed/NCBI

[158] Google Scholar

[ref46] 46. Liu Z, Xu C, Xu Y, Wang Y, Zhao B, Lv Y, et al. Decreased regional homogeneity in insula and cerebellum: a resting-state fMRI study in patients with major depression and subjects at high risk for major depression. Psychiatry Research: Neuroimaging. 2010;182(3):211–215. pmid:20493670
View Article
PubMed/NCBI
Google Scholar

[160] View Article

[161] PubMed/NCBI

[162] Google Scholar

[ref47] 47. Haldane M, Cunningham G, Androutsos C, Frangou S. Structural brain correlates of response inhibition in Bipolar Disorder I. Journal of Psychopharmacology. 2008;. pmid:18308812
View Article
PubMed/NCBI
Google Scholar

[164] View Article

[165] PubMed/NCBI

[166] Google Scholar

[ref48] 48. Iwabuchi SJ, Krishnadas R, Li C, Auer DP, Radua J, Palaniyappan L. Localized connectivity in depression: a meta-analysis of resting state functional imaging studies. Neuroscience and Biobehavioral Reviews. 2015;51:77–86. pmid:25597656
View Article
PubMed/NCBI
Google Scholar

[168] View Article

[169] PubMed/NCBI

[170] Google Scholar

[ref49] 49. O’Reilly JX, Beckmann CF, Tomassini V, Ramnani N, Johansen-Berg H. Distinct and overlapping functional zones in the cerebellum defined by resting state functional connectivity. Cerebral Cortex. 2010;20(4):953–965. pmid:19684249
View Article
PubMed/NCBI
Google Scholar

[172] View Article

[173] PubMed/NCBI

[174] Google Scholar

[ref50] 50. Moulton EA, Elman I, Pendse G, Schmahmann J, Becerra L, Borsook D. Aversion-related circuitry in the cerebellum: responses to noxious heat and unpleasant images. Journal of Neuroscience. 2011;31(10):3795–3804. pmid:21389234
View Article
PubMed/NCBI
Google Scholar

[176] View Article

[177] PubMed/NCBI

[178] Google Scholar

[ref51] 51. Liu L, Zeng LL, Li Y, Ma Q, Li B, Shen H, et al. Altered cerebellar functional connectivity with intrinsic connectivity networks in adults with major depressive disorder. PLoS ONE. 2012;7(6):e39516. pmid:22724025
View Article
PubMed/NCBI
Google Scholar

[180] View Article

[181] PubMed/NCBI

[182] Google Scholar

Figures

Abstract

Introduction

Data set

Subjects

Clinical measures

Beck Depression Inventory II (BDI-II).

Snaith-Hamilton Pleasure Scale (SHAPS).

Positive and Negative Affect Schedule (PANAS).

Functional connectivity of resting-state fMRI

Methods

Partial Least Squares Regression (PLS)

Kernel Partial Least Squares Regression (KPLS)

Classification

Pre-screening

Nested leave-one-out cross validation

Age

Interpretation

Results

Regression performance

Classification performance

Interpretation

Discussion

Contributing brain regions

Conclusion

Supporting information

S1 Appendix. Partial least squares regression.

S1 Table. Root mean squared errors in output-age.

S2 Table. Root mean squared errors in input-age.

S3 Table. Root mean squared errors in no-age.

S4 Table. Classification performance.

S5 Table. Classification performance without subjects over 60.

S6 Table. Root mean squared errors in extended AAL.

Acknowledgments

Author Contributions

References