Previous research has indicated that schizophrenia is heterogeneous in clinical symptoms and time course, suggesting the possibility of identifying subtypes differing in cause and/or pathological mechanism. Reference Tsuang, Lyons and Faraone1 The identification of subtypes could facilitate investigation of cause and mechanism, including the use of genetic and neuroscience approaches. 2–Reference Li, Wang, Zhang, Rolls, Yang and Palaniyappan5 Many approaches consider that there are positive symptoms (including hallucinations and delusions), negative symptoms (including low mood, motivation, and emotion), and cognitive symptoms, including poor attention. Reference Liddle6–Reference Owen, Sawa and Mortensen8 It has been suggested that at least in chronic cases, the positive symptoms split into two subgroups: reality distortion and disorganisation. Reference Liddle7,Reference Bilder, Mukherjee, Rieder and Pandurangi9 Many studies that have included a wider range of symptoms have found evidence for five clusters of symptoms, namely, reality distortion, disorganisation, negative symptoms, depression and excitation (reviewed by Peralta & Cuesta). Reference Peralta and Cuesta10
In order to better understand and treat individuals with schizophrenia, the aims of the present investigation were to understand differences between individuals with schizophrenia; whether there are discrete subtypes of schizophrenia; how first-episode patients (FEP) may differ from multiple episode patients (MEP) and how medication influences the symptoms. Two approaches to delineating the heterogeneity of schizophrenia were taken. One approach was an examination of the pattern of correlation between symptoms to identify underlying symptom communities (or dimensions), presumed to reflect specific pathological processes. Another approach was an examination of the correlations between patients, to identify communities of patients (subtypes) each characterised by a symptom profile reflecting a particular combination of symptom dimensions. In the main text, we employ the standard and well-established hierarchical clustering method using k-means. Reference Strauss, Bartko and Carpenter11 In the supplement, we present qualitatively similar results obtained using a powerful community detection algorithm based on the concept of modularity described by Newman & Girvan, Reference Newman and Girvan12 which was also useful in providing an estimate of the optimum number of communities.
Participants and clinical assessment
Two samples comprising a total of 2567 patients with schizophrenia were diagnosed according to DSM-IV criteria. 13 The first sample included 687 FEP and drug-naive patients with schizophrenia. The second study sample included 1880 multi-episode patients (MEP) with schizophrenia with average duration of illness 7.97 years. The patients were recruited from in-patients from four research centres (the Sixth Hospital of Peking University, the Second Xiangya Hospital of Central South University, Beijing Anding Hospital and Beijing HuiLongGuan Hospital) with institutional approval of the investigation and informed consent of the patients.
The symptoms were assessed by trained researchers with the 30-item Positive and Negative Syndrome Scale for schizophrenia (PANSS). Reference Kay, Fiszbein and Opler14 For reference, in PANSS, positive symptoms P1–P7 are Items 1–7, the negative symptoms N1–N7 are Items 8–14 and the general symptoms G1–G16 are Items 15–30. In the figures, unless otherwise stated, the symptoms are presented in this order, 1–30, with the symptoms listed in the legend to Fig. 1a. The PANSS was measured first in each of these patients when they were not receiving drug treatment. Then the patients were provided with one out of the seven randomly assigned drugs (risperidone, quetiapine, perphenazine, olanzapine, haloperidol, aripiprazole and ziprasidone) for a 6-week treatment period, and then the PANSS scores were measured again. This design with the same patients assessed before and after medication allowed measurement of the PANSS when untreated, and also enabled the effects of the medication to be assessed using exactly the same patients. Further details of the patient populations and the medication used are provided in the Data supplement.
The data consisted for the MEP group of 1880 patient×30 symptom matrix, and for the FEP group of a 687 patient×30 symptom matrix, for the unmedicated pre-treatment state. Corresponding matrices were available for the post-treatment state, providing the symptoms in the same patients after 6 weeks of treatment. The methods included calculating the symptom correlation matrix and the population correlation matrix. We also examined whether there were discrete populations of patients using the k-means clustering method (performed on the population correlation matrix), and then analysed the symptoms in the sub-populations that were detected. We also investigated the distributions of symptoms across the patient sub-populations.
The data were analysed using the k-means cluster analysis algorithms that are a well-accepted approach standardised for availability within Matlab, using the distance measure based on correlations. This analysis was complemented by a modern community detection method described in the Data supplement, which has the advantage that it can automatically provide an indication of the optimal number of subgroups or communities into which to cluster the data. Reference Le Martelot and Hankin15,Reference Lu, Wan, Rolls, Liddle, Ma and Yan16 The k-means approach was the method used for analysis described in the main text, because it is a well-known and understood method for clustering data, and because one major difference between the populations that was identified with this approach was in the negative symptoms which have a component that has a unimodal continuous distribution, so we did not wish to rely on a community detection method that might have difficulty if it was forced to determine the number of communities into which to divide the population if it contained at least in part a continuous distribution. However, for comparison key results with the community detection method are provided in the Data supplement.
Multi-episode group pre-treatment (MEP_Pre)
Figure 1a shows the MEP_Pre symptom correlation matrix. The negative symptoms (8–14) form a clear cluster. Some correlation between these negative symptoms and P2 (conceptual disorganisation), G11 (poor attention), G13 (disturbance of volition) and G16 (active social avoidance) are also evident in the symptom correlation matrix shown in Fig. 1a. The community detection method indicated that the symptoms belong to four distinguishable communities (Fig. S1). Symptom community four included the majority of the positive symptoms (P1 P4 P5 P6 P7) and general symptoms (G8 G9 G12 G14). Symptom Community 1 included the majority of the negative symptoms (N1 N2 N3 N4 N6) and general symptoms (G7 G13 G16).
As shown in Fig. S2, the community detection algorithm indicated that the sample contained three distinguishable communities of patients. The patient clusters generate by the three-cluster output of the k-mean algorithm had distinct symptom profiles (Fig. 1b). In the MEP_Pre sample, the sub-population labelled PN (positive and high negative symptoms, 694 cases) had high values for the negative symptoms (N1–N7=symptoms 8–14). The sub-population labelled Pn (positive and intermediate negative symptoms, 535 cases) had intermediate values for the negative symptoms. The sub-population labelled P (positive and low negative symptoms, 651 cases) had low values for the negative symptoms, especially N1 and N2. Little else differed between these clusters, except that the PN cluster had a higher value for P2 (conceptual disorganisation) and relatively small values for P1 and P3–P6; whereas the P cluster had relatively high scores on symptoms P1, P3–P7, G8 and G9.
These analyses provided evidence that the scores of the negative symptoms were an important factor that was different between the three populations detected with k-means, and equally by the community detection algorithm (see Data supplement Fig. S3). Furthermore, Fig. 1a shows that there are moderately high correlations between the seven negative symptoms, N1–N7 (Symptoms 8–14). To investigate how the negative symptoms were distributed across the population of MEP patients, the population × symptom data matrix was sorted by the mean value of symptoms N1–N7. The result shown in Fig. 2a indicates that there is a graded distribution of the negative symptoms across the population of 1880 MEP patients, with patients at one end of the distribution having scores close to 1 (the minimum score possible) and at the other end close to 7 (the maximum score possible). (In a control analysis, it was found that this does not apply to the positive symptoms, which are not continuously graded throughout the range between scores of 1 and 7 as are the negative symptoms shown in Fig. 2a.)
Further evidence was then sought of whether the distribution of the mean score for the seven negative symptoms was continuous and unimodal. Figure 2b and c show that the distribution of the mean of the average of the negative symptom scores in the MEP_Pre group has a unimodal distribution, in one dimension, rather than a bimodal or multimodal distribution. Thus the most important way in which the three sub-populations of MEP–Pre patients differed was in the negative symptom scores, which are continuously distributed from 1 to 7.
Multi-episode group post-treatment (MEP_Post)
The MEP_Post symptom correlation matrix showed, similarly to the MEP_Pre condition illustrated in Fig. 1a, that the negative symptoms (8–14) form a clear cluster (Fig. S5). Three sub-population clusters were again found by the community detection algorithm and the three clusters in the MEP_Post dataset that were detected with the k-means algorithm which had 631 patients in the PN cluster, 643 in the Pn cluster and 606 in the P cluster.
Figure 1c shows the average symptom values in the three patient clusters for the MEP_Post group. The group labelled PN (positive and high negative symptoms) had high values for the negative symptoms (N1–N7=symptoms 8–14). The group labelled Pn (positive and intermediate negative symptoms) had intermediate values for the negative symptoms. The group labelled P (positive and low negative symptoms) had low values for the negative symptoms and relatively low values also for the positive symptoms. It is notable that the scores on all or most of the symptoms have been decreased by the medication (Fig. 4d). Just as in the MEP_Pre condition, a continuously graded distribution of the negative symptoms across the population of 1880 MEP_Post patients was found, with patients at one end of the distribution having scores close to 1 (the minimum score possible) and at the other end close to 7 (the maximum score possible).
First-episode group pre-treatment (FEP_Pre)
Figure 3a shows the FEP_Pre symptom correlation matrix. The negative symptoms (8–14) form a clear cluster.
The community detection algorithm detected three clusters or sub-populations of patients, and Fig. 3b shows the average symptom values in the three patient clusters for the FEP_Pre group from the k-means analysis. The group labelled PN (positive and high negative symptoms) had high values for the negative symptoms (N1–N7=symptoms 8–14). The group labelled Pn (positive and intermediate negative symptoms) had intermediate values for the negative symptoms. The group labelled P (positive and low negative symptoms) had low values for the negative symptoms. Little else differed between these clusters, except that the PN cluster has a smaller value for P1 (delusions) and P3 (hallucinatory behaviour) (Symptoms 1 and 3) and has higher scores for Symptoms 27–30 (G13–G16). The three clusters contained 228, 233 and 226 patients, respectively. The symptom profiles of the groups detected by the k-means algorithm (Fig. 3b) are very similar to the profiles of the corresponding groups detected by the community detection algorithm (Figs. S9 and S10).
Figure 3a shows that there are moderately high correlations between the seven negative symptoms, N1–N7 (Symptoms 8–14). To investigate how the negative symptoms were distributed across the population of FEP patients, the population × symptom data matrix was sorted by the mean value of Symptoms N1–N7. The result shown in Fig. 4a indicates that there is a graded distribution of the negative symptoms across the population of 687 FEP_Pre patients, with patients at one end of the distribution having scores close to 1 (the minimum score possible) and at the other end close to 7 (the maximum score possible).
Figure 4b and c shows that the distribution of the mean of the average of the negative symptom scores in the FEP_Pre group has a unimodal distribution, in one dimension, rather than a bimodal or multimodal distribution. Thus the most important way in which the three sub-populations of FEP_Pre patients differed was in the negative symptom scores, which are continuously distributed from 1 to 7.
First-episode group post-treatment (FEP_Post)
The FEP_Post symptom correlation matrix showed, similarly to the FEP_Pre condition illustrated in Fig. 3a, that the negative symptoms (8–14) form a clear cluster (Fig. S12). Three sub-population clusters were again found by the community detection algorithm (Fig. S13), and the three clusters in the FEP_Post dataset that were detected with the k-means algorithm had 288 patients in the PN cluster, 221 in the Pn cluster and 178 in the P cluster.
Figure 3c shows the average symptom values in the three patient clusters for the FEP_Post group. The group labelled PN (positive and high negative symptoms) had high values for the negative symptoms (N1–N7=symptoms 8–14). The group labelled Pn (yellow) had high scores for P1–P7 and intermediate values for the negative symptoms. The group labelled P had low values for the negative and positive symptoms. It is notable that the scores on all or most of the symptoms have been decreased by the medication (Fig. 4e). Just as in the FEP_Pre condition, a continuously graded distribution of the negative symptoms across the population of 687 FEP_Post patients was found, with patients at one end of the distribution having scores close to 1 (the minimum score possible) and at the other end close to 7 (the maximum score possible).
Effects of treatment on the PANSS scores
The effects of treatment with antipsychotic drugs on the PANSS symptom scores for the MEP and FEP groups are shown in Fig. 4d and e. Interestingly, the treatment reduced almost all the symptoms (with smaller effects for those close to baseline). The effects on the symptoms were highly similar in the MEP and FEP groups. Moreover, the reductions in the scores of the negative symptoms for the different sub-populations PN, Pn and P produced by the medication were similar (making allowance for the fact that the pre-treatment value was different in the three sub-populations). The treatment consisted of one out of seven randomly assigned drugs (risperidone, quetiapine, perphenazine, olanzapine, haloperidol, aripiprazole and ziprasidone) for a 6-week treatment period. Further details on the effects of the treatments are available from the authors on request and will be provided elsewhere. Reference Lu, Wan, Rolls, Liddle, Ma and Yan16
Comparison of MEP and FEP groups
It is evident from Fig. 4d and e that in the pre-treatment condition, the FEP and MEP groups had almost identical scores, and this is confirmed by the explicit comparison shown in Fig. S19. It is evident from Fig. 4d and e that in the post-treatment condition, the FEP and MEP groups had almost identical scores (though lower than in the pre-treatment groups), and this is confirmed by the explicit comparison shown in Fig. S20.
Community detection results
The community detection algorithm fast_mo Reference Le Martelot and Hankin15 and its modified form fast_mo_sgn Reference Lu, Wan, Rolls, Liddle, Ma and Yan16 applied to the population correlation matrix produced very similar results as shown in the Data supplement (Figs. S1–S14) to those described in the main text using k-means, with the main difference that the numbers of patients in the different clusters or communities differed somewhat.
Factor analysis and multidimensional scaling on the symptom correlation matrices
To provide further insight into how the different PANSS symptoms are related to each other and how they separate from each other, factor analyses and multidimensional scaling were performed on the symptom correlation matrices, as described in the Data supplement. These confirm that the major source of variation between individuals with schizophrenia is in the negative symptoms.
The results of the analysis on the datasets with 687 FEP with schizophrenia before treatment (FEP_Pre) and after treatment (FEP_Post), and 1880 MEP before treatment (MEP_Pre) and after treatment (MEP_Post), provide evidence that a major difference between patients is the extent of the negative symptoms (Figs 1–4). There is little evidence for very discrete populations, with instead a gradation in the amount of the negative symptoms found across the patient populations (Figs 1–4). Indeed, the distributions for the mean of the negative symptoms N1–N7 are unimodal (Figs 2 and 4), so there is little support for discrete subtypes of schizophrenia, on the basis of PANSS scores. Indeed, when the k-means and the community detection algorithms did separate the patient populations into three groups, these groups were distinguished mainly by the amount of the negative symptoms, as illustrated in Figs 1, 3, S3, S4, S10 and S11. Figures 4d, e and S19 show that the PANSS symptoms are almost identical before treatment in the FEP and MEP groups. Figures 4d, e and S20 show that the PANSS symptoms are almost identical after treatment in the FEP and MEP groups. The results shown in Fig. 4d and e show that medication decreases the scores on essentially all PANSS symptom scores.
Our finding of a continuous unimodal distribution of negative symptoms is consistent with many cross-sectional studies that have described the heterogeneity of schizophrenia in terms of multiple dimensions (reviewed by Peralta & Cuesta Reference Peralta and Cuesta10 ). Our findings indicate that the negative dimension plays a particularly important role in differentiating patients, but do not provide evidence for discrete subtypes of illness. However, our cross-sectional analyses do not address the question of whether or not taking account of persistence of symptoms or treatment response might help identify discrete subtypes. Some previous studies that have taken account of the tendency of symptoms to persist have identified a subtype of illness designated deficit schizophrenia, characterised by persistent primary negative symptoms. Reference Kirkpatrick and Galderisi17,Reference Ahmed, Strauss, Buchanan, Kirkpatrick and Carpenter18 Other studies, reviewed by Gillespie et al, Reference Gillespie, Samanaite, Mill, Egerton and MacCabe19 have concluded that treatment-resistant schizophrenia might be categorically distinct from treatment-responsive schizophrenia.
Evidence from many treatment trials, reviewed by Barry et al, Reference Barry, Gaughan and Hunter20 indicates that negative symptoms tend to be poorly responsive to treatment. However, we found in our very large patient sample that positive and negative symptoms reduced to a similar degree during treatment. An issue that must be considered is the characteristics of the patient sample, including selection criteria. It is illustrative to compare our findings with Tollefson et al Reference Tollefson, Beasley, Tran, Street, Krueger and Tamura21 in a trial of olanzapine compared with haloperidol in a large sample of approximately 2000 patients. (Although the focus of Tollefson et al study was on the differences between responses to the two different antipsychotics, those differences were small and for the purpose of this discussion the differences between the antipsychotics is of limited relevance.) Tollefson et al reported a reduction of six points in PANSS negative symptom scores after 6 weeks of treatment with olanzapine and five points after 6-weeks treatment with haloperidol. We found a reduction in PANSS negative symptom scores of 8.2 points in MEP and 8.3 points in FEP cases. It is possible that the fact that we excluded cases with treatment resistant illness, whereas Tollefson et al did not, contributed to the difference in the magnitude of the reduction produced by antipsychotics. In addition, it is possible that social, cultural or ethnic influences contributed to the greater reduction in negative symptoms in our sample. We discuss this in greater detail in the Data supplement in the ‘Social, cultural and ethnic influences on response to treatment’ section.
It should be noted that we did not attempt to distinguish primary from secondary negative symptoms. Our finding of a significant correlation between the reduction in positive symptoms and the reduction in negative symptoms raises the possibility that a proportion of the negative symptoms reported in our study might be secondary negative symptoms which are expected to decrease during treatment. However, the results of an analysis of covariance presented in the Data supplement show that the reduction in the negative symptoms produced by the medication was in part independent of the reduction in the positive symptoms.
Furthermore, it is noteworthy that we found MEP and FEP cases exhibited similar decreases in symptom severity during 6-weeks treatment. In contrast, other moderately large studies have reported that FEP cases show a greater reduction in symptoms during treatment than MEP cases. Reference Jager, Riedel, Messer, Laux, Pfeiffer and Naber22 In a longitudinal study extending over the first 5 years of illness, Lieberman et al Reference Lieberman, Koreen, Chakos, Sheitman, Woerner and Alvir23 found that treatment response diminished with increasing number of relapses. It is possible that the exclusion of participants with treatment-resistant illness from our MEP sample contributed to our finding of a relatively large reduction of negative symptoms in MEP cases.
Further analyses showed the following
The negative symptoms (N1–N7) are moderately well correlated with each other (Figs 1a and 3a). As demonstrated in the Data supplement, the results of applying the community detection algorithm fast_mo_sgn to the symptoms showed that in the MEP and FEP groups, both Pre- and Post-treatment, four symptom communities were detected (with one minor exception). One community generally included most of the positive symptoms and another community included most of the negative symptoms (Figs S1, S5, S8 and S12). The analysis of symptom communities identified a community of symptoms dominated by anxiety and depression (G6) in both FEP (Fig. S8) and MEP (Fig. S1) groups, both before and after treatment. This is consistent with many studies that have reported a depression syndrome in schizophrenia (see the review by Peralta & Cuesta Reference Peralta and Cuesta10 ). Furthermore, in the MEP_Pre cases, there was a community of symptoms reflecting disorganisation of thought and behaviour, together with cognitive symptoms such as poor attention, resembling the disorganisation syndrome identified in symptomatic cases of chronic schizophrenia by Bilder et al Reference Bilder, Mukherjee, Rieder and Pandurangi9 and Liddle. Reference Liddle7 Further analysis of just the negative symptoms found that they could be separated into three communities (N1, N2 and N4; N3 and N6; and N5 and N7), and that these symptom communities were all similarly reduced by medication (Data supplement).
The results shown in Figs S19 and S20 show that the PANSS symptoms are very similar between FEP and MEP groups without medication; and that the medication produces changes in both groups which make the FEP_Post and MEP_Post groups very similar after medication. These findings have major implications for ‘staging’ hypotheses of schizophrenia. Any ‘staging’ hypothesis would need to carefully factor out the effects of treatment for its results to be interpretable. It may be that very long-term patients with schizophrenia do show symptom differences. Reference Li, Wang, Zhang, Rolls, Yang and Palaniyappan5 But if so, that would be related to the long-term nature of the disease not clearly evident in the MEP and FEP groups described here.
K-means cluster analysis can be used to divide the patients into 2–4 sub-populations (with results for three sub-populations presented), which differ from each other mainly in the extent of the negative symptoms. Community detection analysis (using fast_mo_sgn) Reference Lu, Wan, Rolls, Liddle, Ma and Yan16 (modified from Reference Le Martelot and Hankin15 ) provides a very similar set of three sub-populations of both the MEP and FEP group, though the numbers of patients in each population are not identical. To the extent that the distribution of the negative symptoms is in part continuous, the cluster/community detection may not imply that the sub-populations are very discrete. Instead, a continuous distribution of the negative symptom scores from 1 to 7 across the population, as illustrated in Figs 1–4, needs to be considered. One way to assess patients clinically might be on the mean of the seven negative symptom PANSS scores, and clinicians may wish to consider different treatments with the graded distribution across the population in mind, with for example some findings becoming available from Lu et al (in preparation). Reference Lu, Wan, Rolls, Liddle, Ma and Yan16
The finding that the main difference in the PANSS scores of different patients is in the extent of the negative symptoms is of considerable interest. If a k-means analysis is performed using only the values of the negative symptoms, then three population communities are found which differ in the mean value of the negative symptoms (Figs S4 and S11). This adds to the evidence that the values of the negative symptom scores are an important factor in producing different sub-populations or communities, and moreover that what distinguishes these communities includes a difference in the mean negative symptom scores. Furthermore, the evidence in the Data supplement indicates that the negative symptoms are independent of the positive and general symptoms (i.e. the correlations between these symptoms pre-treatment is close to zero), so that there must be at least two partly independent underlying brain processes that are involved.
Subtypes of schizophrenia are no longer included in DSM-5, and this large study with unmedicated patients is of interest in that context, for no highly discrete subtypes of patients were detected in this study, but instead there was a continuous distribution of the mean value of the negative symptoms in both the FEP and MEP populations. The subtypes of symptoms illustrated in Figs S1, S5, S8 and S12 do show how a modern community detection algorithm clusters together different symptoms, with one symptom community including, for example, most of the positive symptoms, and a second community including most of the negative symptoms.
The present investigation adds to previous analyses of subtypes of schizophrenia (e.g. Reference Strauss, Bartko and Carpenter11,Reference Carpenter and Stephens24–Reference Strauss, Carpenter and Bartko26 ) by using a very much larger sample of patients (2567) than in any previous investigation; by investigating the symptoms in the same patients in both the unmedicated and medicated states; by comparing the symptoms in FEP and MEP and by including a more powerful machine learning, community detection, approach. This investigation differs from the analysis of a partly overlapping FEP patient population by Lu et al (in preparation) Reference Lu, Wan, Rolls, Liddle, Ma and Yan16 in that we used here the same participants unmedicated and medicated to understand the effects of the medication, which may produce clearer results than comparing two different groups when unmedicated or not; in the use of more classical clustering approaches to define how the symptoms cluster and how the members of the population cluster; and in the emphasis on the continuous unimodal distribution of the negative symptoms which differs between individuals, instead of focusing on communities that are thought to be distinct because they have been categorised separately by a community detection algorithm which looks for distinct communities. Reference Le Martelot and Hankin15
Apart from the large sample size in this study, a strength is that the patients came from several centres, and that similar results were obtained from the different centers. Reference Lu, Wan, Rolls, Liddle, Ma and Yan16 Another strength is assessment of the PANSS when unmedicated and after 6 weeks of medication in the same patients. Several limitations may be mentioned. PANSS data were used to identify the communities in the present investigation and the communities may become further refined when further measures of differences between patients are included. Some PANSS items, such as difficulty in abstract thinking (N5) and poor attention (G11), include what may be different aspects of impoverished and disorganised thinking within single items, and separate assessment might lead to a richer categorisation. Reference Liddle7,Reference Baxter and Liddle27 Further we suggest that the classification of possible subtypes of schizophrenia could be enhanced by also including information from functional neuroimaging and from genetics.
In conclusion, in a very large sample of cases of schizophrenia, we have demonstrated that variation in the negative symptoms is an important aspect of the variation between patients with schizophrenia. The severity of the negative symptoms has a continuous unimodal distribution supporting a dimensional description of the heterogeneity of the illness, at least with respect to the negative symptoms. Furthermore, in this sample from which treatment resistant cases were excluded, the severity of the negative symptoms decreased substantially during 6 weeks of antipsychotic treatment in both FEP and MEP cases.
J.F.F. is a Royal Society Wolfson Research Merit Award holder, partially supported by the NCMIS of the Chinese Academy of Sciences (CAS) and Key Program of National Natural Science Foundation of China (NSFC) grant (No. 91230201). W.H.Y. was supported by grants from the National Key Research and Development Program (2016YFC1307000), National Key Technology R&D Program of China (2015BAI13B01) and National High Technology Research and Development Program of China (2008AA02Z401, 2009AA022702). L.W. is supported by the Strategic Priority Research Program of the CAS (XDB13050000), the NCMIS of the CAS, the LSC of the CAS, the Youth Innovation Promotion Association of the CAS, and NSFC grant (No.11571349). S.X.G. is supported by the NSFC grant (No. 11271121), Program for New Century Excellent Talents in University (NCET-13-0786) grant, and Natural Science Foundation of Hunan Province (2015JJ1010). P.F.L. is supported by MRC grant MR/K020803/1 for an investigation of brain function in schizophrenia. L.P. is supported by the Academic Medical Organization of Southwestern Ontario (AMOSO) and Canadian Institute of Health Research [CIHR Grant No. (377213/ 201610PJT)].
The work of the Chinese Schizophrenia Collaboration Group (contact Prof W Yue, firstname.lastname@example.org) is fully acknowledged. The members and their affiliations are listed in the data supplement.
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