Hostname: page-component-76fb5796d-wq484 Total loading time: 0 Render date: 2024-04-27T15:32:47.469Z Has data issue: false hasContentIssue false
  • English
  • Français

White matter tract alterations in schizophrenia identified by DTI-based probabilistic tractography: a multisite harmonisation study

Published online by Cambridge University Press:  13 February 2024

Young Tak Jo Open the ORCID record for Young Tak Jo [Opens in a new window] ,
Sung Woo Joo Open the ORCID record for Sung Woo Joo [Opens in a new window] ,
Woohyeok Choi ,
Soohyun Joe  and
Jungsun Lee Open the ORCID record for Jungsun Lee [Opens in a new window]
Young Tak Jo
Affiliation:
Department of Psychiatry, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea
Sung Woo Joo
Affiliation:
Department of Psychiatry, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
Woohyeok Choi
Affiliation:
Department of Psychiatry, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
Soohyun Joe
Affiliation:
Brain Laboratory in the Department of Psychiatry, School of Medicine, University of California, San Diego, CA, USA
Jungsun Lee*
Affiliation:
Department of Psychiatry, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
*
Corresponding author: J. Lee; Email: js_lee@amc.seoul.kr
Rights & Permissions [Opens in a new window]

Abstract

Introduction:

It has been suggested that schizophrenia involves dysconnectivity between functional brain regions and also the white matter structural disorganisation. Thus, diffusion tensor imaging (DTI) has widely been used for studying schizophrenia. However, most previous studies have used the region of interest (ROI) based approach. We, therefore, performed the probabilistic tractography method in this study to reveal the alterations of white matter tracts in the schizophrenia brain.

Methods:

A total of four different datasets consisted of 189 patients with schizophrenia and 213 healthy controls were investigated. We performed retrospective harmonisation of raw diffusion MRI data by dMRIharmonisation and used the FMRIB Software Library (FSL) for probabilistic tractography. The connectivities between different ROIs were then compared between patients and controls. Furthermore, we evaluated the relationship between the connection probabilities and the symptoms and cognitive measures in patients with schizophrenia.

Results:

After applying Bonferroni correction for multiple comparisons, 11 different tracts showed significant differences between patients with schizophrenia and healthy controls. Many of these tracts were associated with the basal ganglia or cortico-striatal structures, which aligns with the current literature highlighting striatal dysfunction. Moreover, we found that these tracts demonstrated statistically significant relationships with few cognitive measures related to language, executive function, or processing speed.

Conclusion:

We performed probabilistic tractography using a large, harmonised dataset of diffusion MRI data, which enhanced the statistical power of our study. It is important to note that most of the tracts identified in this study, particularly callosal and cortico-striatal streamlines, have been previously implicated in schizophrenia within the current literature. Further research with harmonised data focusing specifically on these brain regions could be recommended.

Keywords

schizophreniaDTIharmonisationprobabilistic tractographymultisite study
Type
Original Article
Information
Acta Neuropsychiatrica , First View , pp. 1 - 10
Check for updates
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of Scandinavian College of Neuropsychopharmacology

Significant Outcomes:

  • We utilised probabilistic tractography with diffusion MRI data, offering an alternative methodological approach that complements the deterministic tractography’s limitations.

  • By merging datasets from multiple study sites and applying harmonisation methods, we significantly enhanced our statistical power and adjusted for inter-site image variabilities, ensuring more reliable and generalisable results.

  • We revealed significant alterations in various brain white matter tracts in schizophrenia patients and further elucidated their relationship with cognitive measures.

Limitations:

  • Our study did not encompass some demographic variables, such as ethnicity, education attainment, and socioeconomic status, constraining a more comprehensive understanding of factors influencing white matter integrity in schizophrenia.

  • We did not account for certain clinical variables, such as current clinical status, illness duration, or the potential influence of antipsychotic medications, which could affect the observed relationships and results.

Introduction

Schizophrenia is a chronic, debilitating psychiatric disorder characterised by hallucination, delusion, and disorganised behavior. It has been recognised as a severe mental illness that results in a significant global disease burden (Charlson et al., Reference Charlson, Ferrari, Santomauro, Diminic, Stockings, Scott, Mcgrath and Whiteford2018). Therefore, there has been much research focusing on the pathophysiology of schizophrenia, including various imaging studies (Karlsgodt et al., Reference Karlsgodt, Sun and Cannon2010; Jo et al., Reference Jo, Lee, Joo, Kim, Shon, Yoon and Hong2020; Joo et al., Reference Joo, Kim, Jo, Ahn, Choi, Park, Kang and Lee2021a; Reference Joo, Kim, Jo, Yoon, Kim and Lee2021b). As the name schizophrenia refers to, it has been suggested that schizophrenia involves the disintegration of connectivity between functional brain regions (Friston et al., Reference Friston, Brown, Siemerkus and Stephan2016, Schmitt et al., Reference Schmitt, Hasan, Gruber and Falkai2011).

The diffusion tensor imaging (DTI), which allows for in vivo examination of white matter microstructures, has widely been used for studying the brain with schizophrenia (Kubicki et al., Reference Kubicki, McCarley, Westin, Park, Maier, Kikinis, Jolesz and Shenton2007; Lee et al., Reference Lee, Kubicki, Asami, Seidman, Goldstein, Mesholam-Gately, McCarley and Shenton2013). Specifically, tractography, which builds a three-dimensional model from DTI, has been a promising investigation method to visualise nerve tracts within the brain (Yamada et al., Reference Yamada, Sakai, Akazawa, Yuen and Nishimura2009) and explore the connectivity between functional regions. Nevertheless, most studies have used the region of interest (ROI) based approach, which relies on only one of the tractography methods, the deterministic tractography. Deterministic tractography has been widely used in the study of the brain, particularly in patients with schizophrenia, due to its relative simplicity and time-efficient image acquisition procedures.

However, there are limitations to deterministic tractography that may hinder its accuracy and ability to fully characterise the brain’s white matter microstructures. One of the primary limitations of deterministic tractography is its reliance on a single diffusion orientation per voxel. Considering that the voxel size of around 2–3 mm per dimension in diffusion-weighted imaging acquisitions is usually larger than the 1 mm diameter of fibre bundles, using only one diffusion orientation may not adequately capture the complexity of the brain’s white matter tracts. This limitation can lead to false tracts or the tracking process stopping in regions with isotropic tensors (Descoteaux et al., Reference Descoteaux, Deriche, Knösche and Anwander2009). Specifically, some voxels containing crossing, branching, or fanning fibres or bottleneck formations are not adequately represented by deterministic tractography (Jones, Reference Jones2010). Furthermore, deterministic tractrography can follow false tracts or may stop in regions with isotropic tensors.

Probabilistic tractography, on the other hand, differs from deterministic tractography in that it estimates the diffusion parameters’ distribution at each voxel using statistical techniques (Parker & Alexander, Reference Parker and Alexander2003; Reference Parker and Alexander2005). By repeating thousands of statistical samplings, researchers can evaluate the existing probabilities of streamlined brain tracts with diffusion measures (Price et al., Reference Price, Cercignani, Parker, Altmann, Barnes, Barker, Joyce and Ron2008; Shon et al., Reference Shon, Yoon, Kim, Joo, Kim and Lee2018). As a result, probabilistic tractography is generally more sensitive in detecting fibres than deterministic tractography, particularly in regions with low anisotropy (Fillard et al., Reference Fillard, Descoteaux, Goh, Gouttard, Jeurissen, Malcolm, Ramirez-Manzanares, Reisert, Sakaie, Tensaouti, Yo, Mangin and Poupon2011). It can therefore offer a more comprehensive assessment of white matter connectivity by considering uncertainties in the diffusion data and generating a distribution of possible fibre pathways, thus reducing potential for subjective bias and providing a more robust evaluation of white matter alterations in schizophrenia (Behrens et al., Reference Behrens, Berg, Jbabdi, Rushworth and Woolrich2007; Descoteaux et al., Reference Descoteaux, Deriche, Knösche and Anwander2009).

Therefore, we tried to use probabilistic tractography to overcome the limitation of deterministic tractography. In fact, few previous studies have explored the potential value of probabilistic fibre tracking for studying white matter microstructures in schizophrenia (Khalsa et al., Reference Khalsa, Mayhew, Chechlacz, Bagary and Bagshaw2014; Cho et al., Reference Cho, Shenton, Kubicki, Jung, Lee, Yun, Kim and Kwon2016; Schlaier et al., Reference Schlaier, Beer, Faltermeier, Fellner, Steib, Lange, Greenlee, Brawanski and Anthofer2017), with most focusing on disrupted thalamo-cortical connectivity. Furthermore, we utilised data from different study sites, including public data, to overcome sample size limitations. In fact, it has been suggested that a multicentre study including a large number of brain image samples is required (Pearlson, Reference Pearlson2009; Van Horn & Toga, Reference Van Horn and Toga2009). The recent ENIGMA study indeed involved many study participants recruited from different centres (Kelly et al., Reference Kelly, Jahanshad, Zalesky, Kochunov, Agartz, Alloza, Andreassen, Arango, Banaj, Bouix, Bousman, Brouwer, Bruggemann, Bustillo, Cahn, Calhoun, Cannon, Carr, Catts, Chen, Chen, Chen, Chiapponi, Cho, Ciullo, Corvin, Crespo-Facorro, Cropley, De Rossi, Diaz-Caneja, Dickie, Ehrlich, Fan, Faskowitz, Fatouros-Bergman, Flyckt, Ford, Fouche, Fukunaga, Gill, Glahn, Gollub, Goudzwaard, Guo, Gur, Gur, Gurholt, Hashimoto, Hatton, Henskens, Hibar, Hickie, Hong, Horacek, Howells, Hulshoff Pol, Hyde, Isaev, Jablensky, Jansen, Janssen, Jönsson, Jung, Kahn, Kikinis, Liu, Klauser, Knöchel, Kubicki, Lagopoulos, Langen, Lawrie, Lenroot, Lim, Lopez-Jaramillo, Lyall, Magnotta, Mandl, Mathalon, McCarley, McCarthy-Jones, McDonald, McEwen, McIntosh, Melicher, Mesholam-Gately, Michie, Mowry, Mueller, Newell, O’Donnell, Oertel-Knöchel, Oestreich, Paciga, Pantelis, Pasternak, Pearlson, Pellicano, Pereira, Pineda Zapata, Piras, Potkin, Preda, Rasser, Roalf, Roiz, Roos, Rotenberg, Satterthwaite, Savadjiev, Schall, Scott, Seal, Seidman, Shannon Weickert, Whelan, Shenton, Kwon, Spalletta, Spaniel, Sprooten, Stäblein, Stein, Sundram, Tan, Tan, Tang, Temmingh, Westlye, Tønnesen, Tordesillas-Gutierrez, Doan, Vaidya, van Haren, Vargas, Vecchio, Velakoulis, Voineskos, Voyvodic, Wang, Wan, Wei, Weickert, Whalley, White, Whitford, Wojcik, Xiang, Xie, Yamamori, Yang, Yao, Zhang, Zhao, van Erp, Turner, Thompson and Donohoe2018). Our hypothesis is that using probabilistic tractography in combination with a larger, multicentre sample will yield more consistent and informative results regarding the dysconnectivity in the brain of patients with schizophrenia. Moreover, we aim to explore the correlations between alterations in white matter tracts and clinical symptoms, as well as cognitive performance, to better understand the clinical relevance of our findings.

Furthermore, we applied the new method called harmonisation, which has recently been developed to integrate and utilise neuroimaging data from various sites (Mirzaalian et al., Reference Mirzaalian, Ning, Savadjiev, Pasternak, Bouix, Michailovich, Karmacharya, Grant, Marx, Morey, Flashman, George, McAllister, Andaluz, Shutter, Coimbra, Zafonte, Coleman, Kubicki, Westin, Stein, Shenton and Rathi2018; Karayumak et al., Reference Karayumak, Bouix, Ning, James, Crow, Shenton, Kubicki and Rathi2019), to merge many brain images from multiple locations by eliminating scanner-related differences. Although previous studies had calculated and combined z-scores of diffusion measures for joint analysis (Jahanshad et al., Reference Jahanshad, Kochunov, Sprooten, Mandl, Nichols, Almasy, Blangero, Brouwer, Curran, De Zubicaray, Duggirala, Fox, Hong, Landman, Martin, Mcmahon, Medland, Mitchell, Olvera, Peterson, Starr, Sussmann, Toga, Wardlaw, Wright, Hulshoff Pol, Bastin, Mcintosh, Deary, Thompson and Glahn2013; Kochunov et al., Reference Kochunov, Jahanshad, Sprooten, Nichols, Mandl, Almasy, Booth, Brouwer, Curran, de Zubicaray, Dimitrova, Duggirala, Fox, Hong, Landman, Lemaitre, Lopez, Martin, McMahon, Mitchell, Olvera, Peterson, Starr, Sussmann, Toga, Wardlaw, Wright, Wright, Bastin, McIntosh, Boomsma, Kahn, den Braber, de Geus, Deary, Hulshoff Pol, Williamson, Blangero, van ‘t Ent, Thompson and Glahn2014; Kelly et al., Reference Kelly, Jahanshad, Zalesky, Kochunov, Agartz, Alloza, Andreassen, Arango, Banaj, Bouix, Bousman, Brouwer, Bruggemann, Bustillo, Cahn, Calhoun, Cannon, Carr, Catts, Chen, Chen, Chen, Chiapponi, Cho, Ciullo, Corvin, Crespo-Facorro, Cropley, De Rossi, Diaz-Caneja, Dickie, Ehrlich, Fan, Faskowitz, Fatouros-Bergman, Flyckt, Ford, Fouche, Fukunaga, Gill, Glahn, Gollub, Goudzwaard, Guo, Gur, Gur, Gurholt, Hashimoto, Hatton, Henskens, Hibar, Hickie, Hong, Horacek, Howells, Hulshoff Pol, Hyde, Isaev, Jablensky, Jansen, Janssen, Jönsson, Jung, Kahn, Kikinis, Liu, Klauser, Knöchel, Kubicki, Lagopoulos, Langen, Lawrie, Lenroot, Lim, Lopez-Jaramillo, Lyall, Magnotta, Mandl, Mathalon, McCarley, McCarthy-Jones, McDonald, McEwen, McIntosh, Melicher, Mesholam-Gately, Michie, Mowry, Mueller, Newell, O’Donnell, Oertel-Knöchel, Oestreich, Paciga, Pantelis, Pasternak, Pearlson, Pellicano, Pereira, Pineda Zapata, Piras, Potkin, Preda, Rasser, Roalf, Roiz, Roos, Rotenberg, Satterthwaite, Savadjiev, Schall, Scott, Seal, Seidman, Shannon Weickert, Whelan, Shenton, Kwon, Spalletta, Spaniel, Sprooten, Stäblein, Stein, Sundram, Tan, Tan, Tang, Temmingh, Westlye, Tønnesen, Tordesillas-Gutierrez, Doan, Vaidya, van Haren, Vargas, Vecchio, Velakoulis, Voineskos, Voyvodic, Wang, Wan, Wei, Weickert, Whalley, White, Whitford, Wojcik, Xiang, Xie, Yamamori, Yang, Yao, Zhang, Zhao, van Erp, Turner, Thompson and Donohoe2018), they had a few limitations that z-scores might not capture the variance of the entire population and diffusion measures should have Gaussian distribution to use the z-score. By using training subsets from reference and target sites to determine inter-site differences, the harmonisation method can overcome the above mentioned limitations. It has been suggested that harmonisation has the advantage of allowing researchers to remove potential for scanner-related biases, while accounting for differences related to image acquisition parameters such as b value, spatial resolution, or gradient directions. We acknowledge that our sample size may not be as large as some other recent schizophrenia studies. However, we believe that the combination of probabilistic tractography, a larger sample size, and retrospective harmonisation will provide valuable insights into the white matter abnormalities in schizophrenia.

Materials and methods

Study participants

We combined brain images from four different studies: AMC, COBRE, NMorphCH, and UCLA. To achieve a homogeneous patient population, we only included subjects diagnosed with schizophrenia, excluding other schizophrenia spectrum disorders. Each study was approved by the applicable Institutional Review Board (IRB) and performed following the Declaration of Helsinki. The Asan Medical Center IRB approved the current study (IRB Number: 2021-0423).

Asan medical center (AMC)

Study participants were recruited from Asan Medical Center, Seoul, Korea. This dataset was previously approved by the Asan Medical Center Institutional Review Board (2012-0485). Patients were diagnosed with schizophrenia using the DSM-IV-TR, and healthy controls were those without any Axis I psychiatric diagnosis or any first-degree relative diagnosed with any Axis I psychiatric diagnosis. All subjects were between 20 and 40 years old, were right-handed, and did not have any organic disease affecting brain function. All brain images were acquired using a 3T scanner with an 8-channel SENSE head coil (Achieva; Philips Healthcare, Best, The Netherlands). Diffusion-weighted echo-planar imaging was conducted (TR[repetition time]/TE[echo time] = 5,422/70 ms; flip angle = 90°; field of view = 224 × 224 × 135 mm; and voxel size = 2 × 2 × 3 mm) for one baseline (b value = 0 s/mm ^ 2) and 32 gradient directions (b value = 1,000 s/mm ^ 2).

Center for biomedical research excellence (COBRE)

The Center for Biomedical Research Excellence (COBRE) project integrates multiple neuroimaging techniques with psychiatric, neuropsychological, and genetic testing. We obtained publicly available data from SchizConnect (http://schizconnect.org) (Wang et al., Reference Wang, Alpert, Calhoun, Cobia, Keator, King, Kogan, Landis, Tallis, Turner, Potkin, Turner and Ambite2016). Imaging was conducted on a 3T scanner (Trio, Siemens Healthcare, Erlangen, Germany). Diffusion-weighted images were collected by a multiple-channel radiofrequency coil with GRAPPA(X2) (TE = 84 ms; TR = 9000 ms; number of excitations = 1; 72 slices with slice thickness = 2 mm; field of view = 256 × 256 mm; and matrix = 128 × 128) for 30 gradient directions (b = 800 s/mm ^ 2).

Neuromorphometry in schizophrenia by computer algorithm (NMorphCH)

The Neuromorphometry in Schizophrenia by Computer Algorithm (NMorphCH) project is a longitudinal study examining the clinical, cognitive, and neuroimaging data conducted at Northwestern University. We obtained publicly available data from SchizConnect (http://schizconnect.org). Imaging was conducted on a 3T scanner (Trio, Siemens Healthcare, Erlangen, Germany), and diffusion-weighted images were collected (TE = 86 ms; TR = 8000 ms; flip angle = 90°; matrix = 896 × 896; 35 slices with slice thickness = 2 mm) for 30 gradient directions (b = 0 and 800s/mm ^ 2).

UCLA consortium for neuropsychiatric phenomics LA5c study (UCLA)

The UCLA Consortium for Neuropsychiatric Phenomic LA5c study focused on understanding the dimensional structure of memory and cognitive control functions in healthy individuals and psychiatric patients(Gorgolewski et al., Reference Gorgolewski, Durnez and Poldrack2017). We obtained a publicly available dataset from OpenNeuro (https://openneuro.org). All participants were aged between 21 and 50 years old, without significant medical illness. Based on the Structured Clinical Interview for DSM-IV (SCID), patients were diagnosed with DSM-IV-TR. Imaging was conducted on a 3T scanner (Trio, Siemens Healthcare, Erlangen, Germany), and diffusion-weighted images were collected using an echo-planar sequence (TE = 93ms; TR = 9000ms; flip angle = 90°; matrix = 96 × 96; and slice thickness = 2 mm) for 64 directions (b = 1000s/mm ^ 2).

Image processing and harmonisation

We used SliceDiffusionQC (https://github.com/pnlbwh/SlicerDiffusionQC) to eliminate bad gradient volumes for diffusion-weighted brain images. Specifically, each diffusion volume was categorised as good or bad based its distance to a median line, which was estimated from Kullback–Leibler divergence between consecutive diffusion volumes. Next, we conducted pre-processing, including axis alignment, centring, head motion, and eddy current correction through the Psychiatry Neuroimaging Laboratory (PNL) pipeline (https://github.com/pnlbwh/pnlutil).

We also implemented a retrospective harmonisation method to remove inter-site scanner-specific differences in diffusion-weighted brain images. We used the dMRIharmonisation (https://github.com/pnlbwh/dMRIharmonization) with default settings. As the UCLA dataset was designated as the reference dataset for harmonisation, age, sex, and handedness-matched subjects were selected from AMC, COBRE, and NMorphCH. We calculated the differences between the reference and target datasets by generating scale maps from rotation-invariant spherical harmonics feature templates. Then, harmonised data was obtained by applying scale maps to the target dataset. Overall image processing and harmonisation processes for diffusion-weighted brain images were described elsewhere in detail (Joo et al., Reference Joo, Kim, Jo, Ahn, Choi, Park, Kang and Lee2021a).

Probabilistic tractography

We applied the probabilistic tractography method to track white matter streamlines in the brain. Unlike the deterministic tractography, which assigns fixed direction at each voxel, the probabilistic tractography generates the distribution of the diffusion parameters at each voxel using Metropolis-Hastings Markov chain Monte Carlo sampling. We utilised the BEDPOSTX tool from the Diffusion Toolbox in the FMRIB software library (FSL) (Jenkinson et al., Reference Jenkinson, Beckmann, Behrens, Woolrich and Smith2012). After that, we used the PROBTRACKX tool in FSL to generate a set of streamlines from the seed ROI to the target ROI. Five thousand samples were performed for each seed ROI. Then, we could estimate the degree of connectivity, or connection probability, as the number of streamline tracts from one seeding ROI that passed through a given target ROI divided by the total number of generated streamlines. The non-directional connection probability between two ROIs were defined by averaging the two probabilities obtained from tracking from each given ROI. The ROIs were determined according to the Desikan-Killiany atlas, and therefore there were 87 ROIs in each brain (Fischl et al., Reference Fischl, Salat, Busa, Albert, Dieterich, Haselgrove, van der Kouwe, Killiany, Kennedy, Klaveness, Montillo, Makris, Rosen and Dale2002).

Symptoms and cognitive measures

Study participants from each dataset underwent standardised scales for measuring their psychiatric symptoms and cognitive functions. First, the symptom severity of patients was measured by the Positive and Negative Syndrome Scale (PANSS). Since the NMorphCH and UCLA datasets utilised the Scale for the Assessment of Positive Symptoms (SAPS) and Scale for the Assessment of Negative Symptoms (SANS) for assessing the symptom, instead of the PANSS, we converted these scores into PANSS scores using validated conversion equations for later analysis (Van Erp et al., Reference van Erp, Preda, Nguyen, Faziola, Turner, Bustillo, Belger, Lim, McEwen, Voyvodic, Mathalon, Ford and Potkin2014). Second, for cognitive measures, different cognitive measurement tools were used in each dataset. Thus, we only investigated commonly used few cognitive measures across different datasets: the vocabulary and block design subtests of the Wechsler Abbreviated Scale of Intelligence-II (WASI-II) or the Korean Wechsler Adult Intelligence Scale-IV (K-WAIS-IV), Word Fluency Test, and Trails Making Test A (TMT-A) or Color Trails Test part 1. These measures, respectively, represent visuospatial function, semantic language function, and executive function and have generally been suggested to be influenced by schizophrenia.

Statistical analysis

After probabilistic tractography, we compared connection probabilities between patients with schizophrenia and healthy controls. We also compared demographic and clinical variables between patients and healthy controls. Independent t test, Mann–Whitney U test, and Chi-squared test were used to compare connection probabilities with demographic and clinical variables. We applied the Bonferroni correction method to correct multiple comparisons problems. Since it was argued that enhanced sensitivity of probabilistic tractography may counteract selectivity (Thomas et al., Reference Thomas, Ye, Irfanoglu, Modi, Saleem, Leopold and Pierpaoli2014), we tried to strictly control Type I error in testing the primary hypothesis that the connection probabilities estimated by probabilistic tractography were different between patients and healthy controls. In addition, we also evaluated the relationships between connection probabilities and symptoms or cognitive measures in the patient group using linear regression analysis and Bonferroni correction. Because cognitive measures could be affected by the age and sex of the study participants, we adjusted these variables during the regression analysis. All statistical analyses were performed using R (ver. 4.1.3) and Jamovi (ver. 2.3.21) (R Core Team, 2013, The Jamovi Project, 2021). Statistically significant p was set as < 0.05.

Results

Demographics and clinical characteristics

The final study sample consisted of 189 patients with schizophrenia and 213 healthy controls: 48 patients and 23 healthy controls for AMC; 57 patients and 73 healthy controls for COBRE; 40 patients and 32 healthy controls for NMorphCH; and 44 patients and 85 healthy controls for UCLA. The mean age of all patients with schizophrenia was 34.1 [9.93] years, which showed no statistically significant difference to 33.7 [10.1] years of controls (U = 19,660.0, p = 0.687). Of 189 patients and 213 healthy controls, 124 patients (65.6%) and 127 controls (59.6%) were male, and there was no significant difference in sex ratio (χ 2 = 1.530, p = 0.216). The mean total PANSS score was 63.9 [16.9] in the patients’ group. Specifically, the positive scale score was 17.1 [6.29], the negative scale score was 18.1 [6.19], and the general psychopathology scale score was 30.8 [8.05]. There was a significant difference in the age and sex of study participants between four different datasets (χ 2 = 30.7, p < 0.001; χ 2 = 29.1, p < 0.001). They also showed a significant difference in the mean PANSS score. Table 1 shows each dataset’s demographic and clinical characteristics and the final study sample in detail. Table 2 shows comparisons between four different datasets.

Table 1. Demographics and clinical characteristics of study participants

Mean [Standard deviation]; Number (Percentage).

† Mann–Whitney U test.

‡ Chi-squared test.

* Statistically significant p<0.05.

Table 2. Demographics and clinical characteristics of each dataset

SPR, Schizophrenia; CTR, Control; CTT-1, Color Trails Test, part 1; AMC, Asan Medical Center; COBRE, Center for Biomedical Research Excellence; NMorphCH, Neuromorphometry in Schizophrenia by Computer Algorithm; UCLA, UCLA Consortium for Neuropsychiatric Phenomic LA5c study; Mean [Standard deviation]; Number (Percentage); Kruskal–Wallis H test was done between four different datasets.

* Statistically significant p<0.05.

White matter tracts with probabilistic tractography

Since there were 87 ROIs, 3741 streamlines were generated during the tractography methods. We compared the probabilities of these streamlines between patients with schizophrenia and healthy controls. After Bonferroni correction for multiple comparisons, 11 different tracts showed statistically significant differences between patients with schizophrenia and healthy controls. First, tracts between the anterior corpus callosum and left caudate show significant differences (U = 25,995, Adjusted p = 0.002). The tracts between the anterior corpus callosum and both pallidum also showed significant differences (left: U = 25,704, Adjusted p = 0.006; right: U = 25,606, Adjusted p = 0.009). Moreover, the tract between left and right caudate also showed a significant difference (U = 25,861, Adjusted p = 0.003). In addition, the tract from left caudate to right pallidum and the tract from right caudate to left pallidum showed significant differences (U = 25,978, Adjusted p = 0.002; U = 25,734, Adjusted p = 0.005). The tract from right pallidum to both right caudal anterior cingulate and right pars opercularis also showed significant differences (U = 25,329, Adjusted p = 0.029; U = 25,565, Adjusted p = 0.011). Furthermore, the tract between right hippocampus and right superior temporal showed a significant difference (U = 25,252, Adjusted p = 0.039). Lastly, the tract from right paracentral to right postcentral and the tract from right ventral diencephalon to right parahippocampal showed significant differences (U = 25,412, Adjusted p = 0.021; U = 25,697, Adjusted p = 0.006). In all of these tracts, healthy controls exhibited stronger connection probabilities compared to patients with schizophrenia. Table 3 shows the comparisons of white matter tracts between patients with schizophrenia and healthy controls in detail.

Table 3. Comparison of connection probabilities between patients and controls

SPR, Schizophrenia; CTR, Control; Mean [Standard deviation]; Mann–Whitney U test.

* Statistically significant Bonferroni-adjusted p<0.05.

Relationship with symptoms and cognitive measures

We evaluated the relationships between connection probabilities of the 11 white matter tracts and symptoms or cognitive measures in patients with schizophrenia. As a result of linear regression analysis, we found that there was no significant relationship with the PANSS score after Bonferroni correction. Meanwhile, many tracts showed significant correlations for cognitive measures, even after adjusting for age and sex in regression models. For the vocabulary subtests, the tracts from the anterior corpus callosum to left caudate and right pallidum both showed significant correlations with the subtest scores (β = 16.8, Adjusted p = 0.003; β = 24.6, Adjusted p = 0.036). Moreover, the tract from left to right caudate and the tract from right paracentral to right postcentral also showed significant correlations (β = 25.2, Adjusted p = 0.004; β = 41.7, Adjusted p = 0.009).

In addition, nine out of 11 tracts showed significant relationships between the block design subtest scores. Three tracts, the tract between left pallidum and right caudate, the tract between left caudate and right pallidum, and the tract between right pallidum and right pars opercularis, showed much stronger correlations (|β| > 100.0) than others (β = 135.7, p = 0.012; β = 101.5, p = 0.017; β = 116.9, p < 0.001). Furthermore, the tract from left caudate to right caudate and the tract from right pallidum to right pars opercularis also showed significant correlations with the word fluency test score (β = 17.2, Adjusted p = 0.044; β = 66.9, Adjusted p = 0.006). The tract between right paracentral and right postcentral also showed significant correlation (β = 39.6, Adjusted p = 0.020).

Lastly, the Color Trails Test (CTT-1) scores showed a significant relationship with four tracts. The tracts from the anterior corpus callosum to left caudate and right pallidum both showed significant correlations (β = −15.4, Adjusted p = 0.013; β = −25.1, Adjusted p = 0.049). Moreover, the tract from left to right caudate and the tract from right paracentral to right postcentral also showed significant correlations with the CTT-1 scores (β = −20.6, Adjusted p = 0.032; β = −41.8, Adjusted p = 0.024). Table 4 shows the correlations between brain tract connectivity and symptoms or cognitive measures in detail.

Table 4. Correlations of connection probabilities to symptoms and cognitive measures in patients

PANSS, Positive and Negative Syndrome Scale; β, beta coefficient in a regression model controlled for age and sex.

* Statistically significant Bonferroni-adjusted p<0.05.

Discussion

In this study, we performed probabilistic tractography using diffusion MRI data to investigate the alterations of brain white matter tracts in patients with schizophrenia, overcoming the limitations of deterministic tractography methods. Furthermore, we significantly enhanced the statistical power of our findings by merging datasets from multiple study sites to create a large, combined dataset. By utilising the harmonisation method, we were able to adjust for inter-site image variabilities stemming from scanner-related differences, rather than simply merge disparate datasets.

Our results revealed significant differences in multiple brain white matter tracts between patients with schizophrenia and healthy controls. First of all, we observed significant differences in several tracts related to anterior corpus callosum. The corpus callosum, a major commissural pathway between the cerebral hemispheres, has been a highly interesting region in schizophrenia research (Arnone et al., Reference Arnone, Mcintosh, Tan and Ebmeier2008; Patel et al., Reference Patel, Mahon, Wellington, Zhang, Chaplin and Szeszko2011) due to its relationship with the severity of psychotic symptoms. Patients with schizophrenia have previously shown structural (Keshavan et al., Reference Keshavan, Diwadkar, Harenski, Rosenberg, Sweeney and Pettegrew2002; Rao et al., Reference Rao, Venkatasubramanian, Arasappa and Gangadhar2011) and diffusional abnormalities (Whitford et al., Reference Whitford, Kubicki, Schneiderman, O’Donnell, King, Alvarado, Khan, Markant, Nestor, Niznikiewicz, McCarley, Westin and Shenton2010) in the corpus callosum, indicative of impaired inter-hemispheric connectivity. Moreover, tracts associated with the pallidum and caudate displayed significant differences between patients and controls. While findings about anatomical alterations have sometimes been inconsistent, cortico-striatal streamlines have often been reported as altered in patients with schizophrenia. These alterations are associated with hypokinesia (Bracht et al., Reference Bracht, Schnell, Federspiel, Razavi, Horn, Strik, Wiest, Dierks, Mþller and Walther2013), cognitive impairment mediated by an impaired default mode network (Huang et al., Reference Huang, Shu, Chen, Zou, Chen, Wu, Xiao, Liu, Wang, Zhou, Wang and Jiang2018), and both positive and negative symptoms of schizophrenia (McCutcheon et al., Reference McCutcheon, Abi-Dargham and Howes2019). In addition, we identified significant differences in tracts related to other brain regions, such as pars opercularis, hippocampus, and superior temporal areas. Despite occasional inconsistencies in research findings, some studies suggest that these regions exhibit decreased volume or reduced cortical thickness in schizophrenia (Kasai et al., Reference Kasai, Shenton, Salisbury, Hirayasu, Lee, Ciszewski, Yurgelun-Todd, Kikinis, Jolesz and McCarley2003; Harrison, Reference Harrison2004, Knøchel et al., Reference Knöchel, Reuter, Reinke, Stäblein, Marbach, Feddern, Kuhlmann, Alves, Prvulovic, Wenzler, Linden and Oertel-Knöchel2016). In particular, structural alterations in the superior temporal lobe or gyrus, especially progressive volume reduction, are emphasised in the pathophysiology of schizophrenia (Sun et al., Reference Sun, Maller, Guo and Fitzgerald2009; Takahashi et al., Reference Takahashi, Wood, Yung, Soulsby, McGorry, Suzuki, Kawasaki, Phillips, Velakoulis and Pantelis2009).

Among these white matter tracts, we identified significant relationships between various white matter tracts and cognitive measures. First, the language function, as measured by the vocabulary subtest, was associated with the caudate and corpus callosum. Furthermore, the pallidum and pars opercularis showed relationships with word fluency test scores. Previous studies have suggested that these regions play crucial roles in language control and are altered in patients with schizophrenia (Friederici, Reference Friederici2006; Li et al., Reference Li, Black, Xia, Zhan, Bertisch, Branch and DeLisi2015, Trëhout et al., Reference Tréhout, Leroux, Delcroix and Dollfus2017). Notably, the pars opercularis is part of the well-known language-related brain region, Broca’s area. The block design subtest score, which measures visuospatial and executive functions, also showed significant relationships with numerous white matter tracts. It is widely recognised that executive function is impaired in schizophrenia (Orellana and Slachevsky, Reference Orellana and Slachevsky2013). Lastly, the CTT-1 scores showed significant relationships with certain regions. Although the corpus callosum has been implicated in attention and processing speed (Hinkley et al., Reference Hinkley, Marco, Findlay, Honma, Jeremy, Strominger, Bukshpun, Wakahiro, Brown, Paul, Barkovich, Mukherjee, Nagarajan, Sherr and Maurits2012), the relationships between other regions and these cognitive processes remain insufficiently explored. Further research on these relationships are recommended.

On the other hand, we did not identify a significant relationship between psychiatric symptoms, as measured by the PANSS score, and white matter tracts. Given that prior research has reported associations between alterations in white matter tracts and symptoms of schizophrenia, this finding was somewhat unexpected. This discrepancy might be due to the conservative nature of our multiple comparisons correction or to the heterogeneity of our study participants. Furthermore, we did not account for whether participants were in acute or remission phases, potentially leading to a wide variation in symptoms. Another potential confounding factor we did not consider is the use of antipsychotic medications in the correlation analysis between the PANSS score and white matter tracts.

Our study has several limitations. As mentioned above, we did not account for certain demographic and clinical variables, including ethnicity, current clinical status, and illness duration, while conducting statistical analysis. For instance, the open dataset participants were primarily Caucasian, while all participants in the AMC dataset were Asian. Thus, there were ethnic differences within the merged dataset. Nevertheless, we performed retrospective harmonisation to mitigate inter-site differences in brain images, which could also likely attenuate this difference. Moreover, we were unable to examine the potential influence of antipsychotics due to data unavailability. While some studies have recommended considering medication when investigating DTI (Karlsgodt, Reference Karlsgodt2016), several other studies have found no significant relationship between diffusion measures and medication (Kanaan et al., Reference Kanaan, Barker, Brammer, Giampietro, Shergill, Woolley, Picchioni, Toulopoulou and Mcguire2009; Koshiyama et al., Reference Koshiyama, Fukunaga, Okada, Morita, Nemoto, Usui, Yamamori, Yasuda, Fujimoto, Kudo, Azechi, Watanabe, Hashimoto, Narita, Kusumi, Ohi, Shimada, Kataoka, Yamamoto, Ozaki, Okada, Okamoto, Harada, Matsuo, Yamasue, Abe, Hashimoto, Takahashi, Hori, Nakataki, Onitsuka, Holleran, Jahanshad, van Erp, Turner, Donohoe, Thompson, Kasai and Hashimoto2020). Lastly, we did not compare the relationships between connection probabilities and other clinical features such as intellectual ability, education attainment, or socioeconomic status. As some previous studies have suggested associations between these factors and white matter integrity (Penke et al., Reference Penke, Maniega, Bastin, Valdés Hernández, Murray, Royle, Starr, Wardlaw and Deary2012; Noble et al., Reference Noble, Korgaonkar, Grieve and Brickman2013; Shaked et al., Reference Shaked, Leibel, Katzel, Davatzikos, Gullapalli, Seliger, Erus, Evans, Zonderman and Waldstein2019), further research incorporating more detailed demographic information is required.

In conclusion, our study observed significant alterations in white matter tracts within the brains of patients with schizophrenia. Even after applying a conservative multiple comparisons correction method, numerous brain tracts demonstrated significant differences between patients with schizophrenia and healthy controls. Importantly, several of these tracts exhibited significant correlations with cognitive measures, suggesting that these tracts might play a role in the pathophysiology of schizophrenia. Future research is encouraged to examine these brain regions more specifically and to investigate their involvement in the progression of schizophrenia. Longitudinal studies could also provide valuable insights into the dynamic changes in white matter tracts over time and their potential impact on symptom severity and cognitive functioning. Building on these findings, future research can contribute to a deeper understanding of the underlying neural mechanisms of schizophrenia.

Acknowledgments

The public data from this study were obtained from the SchizConnect database (http://schizconnect.org), the COllaborative Informatics and Neuroimaging Suite Data Exchange tool (COINS; http://coins.mrn.org/dx) and the Mind Research Network, the Neuromorphometry by Computer Algorithm Chicago (NMorphCH) dataset (http://nunda.northwestern.edu/nunda/data/projects/NMorphCH), and the OpenfMRI database (https://openfmri.org/dataset/ds000030/). The investigators within these databases contributed to each database and provided data but did not participate in this study.

Data collection and sharing for these public databases was funded by NIMH cooperative agreement 1U01 MH097435, Center of Biomedical Research Excellence (COBRE) grant 5P20RR021938/P20GM103472 from the NIH to Dr Vince Calhoun, NIMH grant R01 MH056584, and NIH Roadmap for Medical Research grants UL1-DE019580, RL1MH083268, RL1MH083269, RL1DA024853, RL1MH083270, RL1LM009833, PL1MH083271, and PL1NS062410.

Financial support

This study was supported by the National Research Foundation of Korea grants (NRF-2012R1A1A1006514 and NRF-2017R1D1A1B03032707).

Competing interests

None.

References

Arnone, D, Mcintosh, AM, Tan, GMY and Ebmeier, KP (2008) Meta-analysis of magnetic resonance imaging studies of the corpus callosum in schizophrenia. Schizophrenia Research 101(1-3), 124–132.CrossRefGoogle ScholarPubMed
Behrens, TE, Berg, HJ, Jbabdi, S, Rushworth, MF and Woolrich, MW (2007) Probabilistic diffusion tractography with multiple fibre orientations: what can we gain? Neuroimage 34(1), 144–155.CrossRefGoogle ScholarPubMed
Bracht, T, Schnell, S, Federspiel, A, Razavi, N, Horn, H, Strik, W, Wiest, R, Dierks, T, Mþller, TJ and Walther, S (2013) Altered cortico-basal ganglia motor pathways reflect reduced volitional motor activity in schizophrenia. Schizophrenia Research 143(2-3), 269–276.CrossRefGoogle ScholarPubMed
Charlson, FJ, Ferrari, AJ, Santomauro, DF, Diminic, S, Stockings, E, Scott, JG, Mcgrath, JJ and Whiteford, HA (2018) Global epidemiology and Burden of schizophrenia: findings from the global Burden of disease study 2016. Schizophrenia Bulletin 44(6), 1195–1203.CrossRefGoogle ScholarPubMed
Cho, KIK, Shenton, ME, Kubicki, M, Jung, WH, Lee, TY, Yun, J-Y, Kim, SN and Kwon, JS (2016) Altered thalamo-cortical white matter connectivity: probabilistic tractography study in clinical-high risk for psychosis and first-episode psychosis. Schizophrenia Bulletin 42(3), 723–731.CrossRefGoogle ScholarPubMed
Descoteaux, M, Deriche, R, Knösche, TR and Anwander, A (2009) Deterministic and probabilistic tractography based on complex fibre orientation distributions. IEEE Transactions on Medical Imaging 28(2), 269–286.CrossRefGoogle ScholarPubMed
Fillard, P, Descoteaux, M, Goh, A, Gouttard, S, Jeurissen, B, Malcolm, J, Ramirez-Manzanares, A, Reisert, M, Sakaie, K, Tensaouti, F, Yo, T, Mangin, JF and Poupon, C (2011) Quantitative evaluation of 10 tractography algorithms on a realistic diffusion MR phantom. Neuroimage 56(1), 220–234.CrossRefGoogle ScholarPubMed
Fischl, B, Salat, DH, Busa, E, Albert, M, Dieterich, M, Haselgrove, C, van der Kouwe, A, Killiany, R, Kennedy, D, Klaveness, S, Montillo, A, Makris, N, Rosen, B and Dale, AM (2002) Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain. Neuron 33(3), 341–355.CrossRefGoogle ScholarPubMed
Friederici, AD (2006) What’s in control of language? Nature Neuroscience 9(8), 991–992.CrossRefGoogle ScholarPubMed
Friston, K, Brown, HR, Siemerkus, J and Stephan, KE (2016) The dysconnection hypothesis, 2016. Schizophrenia Research 176(2-3), 83–94.CrossRefGoogle ScholarPubMed
Gorgolewski, KJ, Durnez, J and Poldrack, RA (2017) Preprocessed consortium for neuropsychiatric phenomics dataset. F1000Research 6, 1262.CrossRefGoogle Scholar
Harrison, PJ (2004) The hippocampus in schizophrenia: a review of the neuropathological evidence and its pathophysiological implications. Psychopharmacology 174(1), 151–162.CrossRefGoogle ScholarPubMed
Hinkley, LBN, Marco, EJ, Findlay, AM, Honma, S, Jeremy, RJ, Strominger, Z, Bukshpun, P, Wakahiro, M, Brown, WS, Paul, LK, Barkovich, AJ, Mukherjee, P, Nagarajan, SS, Sherr, EH and Maurits, NM (2012) The role of corpus callosum development in functional connectivity and cognitive processing. PLOS ONE 7(8), e39804.CrossRefGoogle ScholarPubMed
Huang, H, Shu, C, Chen, J, Zou, J, Chen, C, Wu, S, Xiao, L, Liu, Z, Wang, H, Zhou, Y, Wang, G and Jiang, T (2018) Altered corticostriatal pathway in first-episode paranoid schizophrenia: resting-state functional and causal connectivity analyses. Psychiatry Research: Neuroimaging 272, 38–45.CrossRefGoogle ScholarPubMed
Jahanshad, N, Kochunov, PV, Sprooten, E, Mandl, RC, Nichols, TE, Almasy, L, Blangero, J, Brouwer, RM, Curran, JE, De Zubicaray, GI, Duggirala, R, Fox, PT, Hong, LE, Landman, BA, Martin, NG, Mcmahon, KL, Medland, SE, Mitchell, BD, Olvera, RL, Peterson, CP, Starr, JM, Sussmann, JE, Toga, AW, Wardlaw, JM, Wright, MJ, Hulshoff Pol, HE, Bastin, ME, Mcintosh, AM, Deary, IJ, Thompson, PM and Glahn, DC (2013) Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA-DTI working group. NeuroImage 81, 455–469.CrossRefGoogle ScholarPubMed
Jenkinson, M, Beckmann, CF, Behrens, TE, Woolrich, MW and Smith, SM (2012) FSL. NeuroImage 62(2), 782–790.CrossRefGoogle ScholarPubMed
Jo, YT, Lee, J, Joo, SW, Kim, H, Shon, S-H, Yoon, W and Hong, Y (2020) Additive burden of abnormal diffusivity in the brain with schizophrenia: a diffusion tensor imaging study with public neuroimaging data. Psychiatry Investigation 17(4), 341–349.CrossRefGoogle ScholarPubMed
Jones, DK (2010) Challenges and limitations of quantifying brain connectivity in vivo with diffusion MRI. Imaging in Medicine 2(3), 341–355.CrossRefGoogle Scholar
Joo, SW, Kim, H, Jo, YT, Ahn, S, Choi, YJ, Park, S, Kang, Y and Lee, J (2021a) White matter impairments in patients with schizophrenia: a multisite diffusion MRI study. Progress in Neuro-Psychopharmacology and Biological Psychiatry 111, 110381.CrossRefGoogle ScholarPubMed
Joo, SW, Kim, H, Jo, YT, Yoon, W, Kim, Y and Lee, J (2021b) Shared and distinct white matter abnormalities in schizophrenia and bipolar disorder. Progress in Neuro-Psychopharmacology and Biological Psychiatry 108, 110175.CrossRefGoogle ScholarPubMed
Kanaan, R, Barker, G, Brammer, M, Giampietro, V, Shergill, S, Woolley, J, Picchioni, M, Toulopoulou, T and Mcguire, P (2009) White matter microstructure in schizophrenia: effects of disorder, duration and medication. The British Journal of Psychiatry 194(3), 236–242.CrossRefGoogle ScholarPubMed
Karayumak, SC, Bouix, S, Ning, L, James, A, Crow, T, Shenton, M, Kubicki, M and Rathi, Y (2019) Retrospective harmonization of multi-site diffusion MRI data acquired with different acquisition parameters. Neuroimage 184, 180–200.CrossRefGoogle Scholar
Karlsgodt, KH (2016) Diffusion imaging of white matter in schizophrenia: progress and future directions. Biological psychiatry: Cognitive Neuroscience and Neuroimaging 1(3), 209–217.Google ScholarPubMed
Karlsgodt, KH, Sun, D and Cannon, TD (2010) Structural and functional brain abnormalities in schizophrenia. Current Directions in Psychological Science 19(4), 226–231.CrossRefGoogle ScholarPubMed
Kasai, K, Shenton, ME, Salisbury, DF, Hirayasu, Y, Lee, C-U, Ciszewski, AA, Yurgelun-Todd, D, Kikinis, R, Jolesz, FA and McCarley, RW (2003) Progressive decrease of left superior temporal gyrus gray matter volume in patients with first-episode schizophrenia. American Journal of Psychiatry 160(1), 156–164.CrossRefGoogle ScholarPubMed
Kelly, S, Jahanshad, N, Zalesky, A, Kochunov, P, Agartz, I, Alloza, C, Andreassen, O A, Arango, C, Banaj, N, Bouix, S, Bousman, C A, Brouwer, R M, Bruggemann, J, Bustillo, J, Cahn, W, Calhoun, V, Cannon, D, Carr, V, Catts, S, Chen, J, Chen, J-X, Chen, X, Chiapponi, C, Cho, KK, Ciullo, V, Corvin, A S, Crespo-Facorro, B, Cropley, V, De Rossi, P, Diaz-Caneja, C M, Dickie, E W, Ehrlich, S, Fan, F-M, Faskowitz, J, Fatouros-Bergman, H, Flyckt, L, Ford, J M, Fouche, J-P, Fukunaga, M, Gill, M, Glahn, D C, Gollub, R, Goudzwaard, E D, Guo, H, Gur, R E, Gur, R C, Gurholt, T P, Hashimoto, R, Hatton, S N, Henskens, F A, Hibar, D P, Hickie, I B, Hong, L E, Horacek, J, Howells, F M, Hulshoff Pol, H E, Hyde, C L, Isaev, D, Jablensky, A, Jansen, P R, Janssen, J, Jönsson, E G, Jung, L A, Kahn, R S, Kikinis, Z, Liu, K, Klauser, P, Knöchel, C, Kubicki, M, Lagopoulos, J, Langen, C, Lawrie, S, Lenroot, R K, Lim, K O, Lopez-Jaramillo, C, Lyall, A, Magnotta, V, Mandl, R C W, Mathalon, D H, McCarley, R W, McCarthy-Jones, S, McDonald, C, McEwen, S, McIntosh, A, Melicher, T, Mesholam-Gately, R I, Michie, P T, Mowry, B, Mueller, B A, Newell, D T, O’Donnell, P, Oertel-Knöchel, V, Oestreich, L, Paciga, S A, Pantelis, C, Pasternak, O, Pearlson, G, Pellicano, G R, Pereira, A, Pineda Zapata, J, Piras, F, Potkin, S G, Preda, A, Rasser, P E, Roalf, D R, Roiz, R, Roos, A, Rotenberg, D, Satterthwaite, T D, Savadjiev, P, Schall, U, Scott, R J, Seal, M L, Seidman, L J, Shannon Weickert, C, Whelan, C D, Shenton, M E, Kwon, J S, Spalletta, G, Spaniel, F, Sprooten, E, Stäblein, M, Stein, D J, Sundram, S, Tan, Y, Tan, S, Tang, S, Temmingh, H S, Westlye, L T, Tønnesen, S, Tordesillas-Gutierrez, D, Doan, N T, Vaidya, J, van Haren, N E M, Vargas, C D, Vecchio, D, Velakoulis, D, Voineskos, A, Voyvodic, J Q, Wang, Z, Wan, P, Wei, D, Weickert, T W, Whalley, H, White, T, Whitford, T J, Wojcik, J D, Xiang, H, Xie, Z, Yamamori, H, Yang, F, Yao, N, Zhang, G, Zhao, J, van Erp, T G M, Turner, J, Thompson, P M and Donohoe, G (2018) Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA schizophrenia DTI working group. Molecular psychiatry 23(5), 1261–1269.CrossRefGoogle ScholarPubMed
Keshavan, MS, Diwadkar, VA, Harenski, K, Rosenberg, DR, Sweeney, JA and Pettegrew, JW (2002) Abnormalities of the corpus callosum in first episode, treatment naive schizophrenia. Journal of Neurology, Neurosurgery & Psychiatry 72, 757.CrossRefGoogle ScholarPubMed
Khalsa, S, Mayhew, SD, Chechlacz, M, Bagary, M and Bagshaw, AP (2014) The structural and functional connectivity of the posterior cingulate cortex: comparison between deterministic and probabilistic tractography for the investigation of structure-function relationships. NeuroImage 102, 118–127.CrossRefGoogle ScholarPubMed
Knöchel, C, Reuter, J, Reinke, B, Stäblein, M, Marbach, K, Feddern, R, Kuhlmann, K, Alves, G, Prvulovic, D, Wenzler, S, Linden, DE J and Oertel-Knöchel, V (2016) Cortical thinning in bipolar disorder and schizophrenia. Schizophrenia Research 172(1-3), 78–85.CrossRefGoogle Scholar
Kochunov, P, Jahanshad, N, Sprooten, E, Nichols, TE, Mandl, Ré C, Almasy, L, Booth, T, Brouwer, RM, Curran, JE, de Zubicaray, GI, Dimitrova, R, Duggirala, R, Fox, PT, Hong, L E, Landman, BA, Lemaitre, Hé, Lopez, LM, Martin, NG, McMahon, KL, Mitchell, BD, Olvera, RL, Peterson, CP, Starr, JM, Sussmann, JE, Toga, AW, Wardlaw, JM, Wright, MJ, Wright, SN, Bastin, ME, McIntosh, AM, Boomsma, DI, Kahn, Ré S, den Braber, A, de Geus, EJ C, Deary, IJ, Hulshoff Pol, HE, Williamson, DE, Blangero, J, van ‘t Ent, D, Thompson, PM and Glahn, DC (2014) Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: comparing meta and megaanalytical approaches for data pooling. NeuroImage 95, 136–150.CrossRefGoogle ScholarPubMed
Koshiyama, D, Fukunaga, M, Okada, N, Morita, K, Nemoto, K, Usui, K, Yamamori, H, Yasuda, Y, Fujimoto, M, Kudo, N, Azechi, H, Watanabe, Y, Hashimoto, N, Narita, H, Kusumi, I, Ohi, K, Shimada, T, Kataoka, Y, Yamamoto, M, Ozaki, N, Okada, G, Okamoto, Y, Harada, K, Matsuo, K, Yamasue, H, Abe, O, Hashimoto, R, Takahashi, T, Hori, T, Nakataki, M, Onitsuka, T, Holleran, L, Jahanshad, N, van Erp, TG M, Turner, J, Donohoe, G, Thompson, PM, Kasai, K, Hashimoto, R and COCORO (2020) White matter microstructural alterations across four major psychiatric disorders: mega-analysis study in 2937 individuals. Molecular Psychiatry 25(4), 883–895.CrossRefGoogle ScholarPubMed
Kubicki, M, McCarley, R, Westin, C-F, Park, H-J, Maier, S, Kikinis, R, Jolesz, FA and Shenton, ME (2007) A review of diffusion tensor imaging studies in schizophrenia. Journal of Psychiatric Research 41(1-2), 15–30.CrossRefGoogle ScholarPubMed
Lee, S-H, Kubicki, M, Asami, T, Seidman, LJ, Goldstein, JM, Mesholam-Gately, RI, McCarley, RW and Shenton, ME (2013) Extensive white matter abnormalities in patients with first-episode schizophrenia: a diffusion tensor imaging (DTI) study. Schizophrenia Research 143(2-3), 231–238.CrossRefGoogle ScholarPubMed
Li, X, Black, M, Xia, S, Zhan, C, Bertisch, HC, Branch, CA and DeLisi, LE (2015) Subcortical structure alterations impact language processing in individuals with schizophrenia and those at high genetic risk. Schizophrenia Research 169(1-3), 76–82.CrossRefGoogle ScholarPubMed
McCutcheon, RA, Abi-Dargham, A and Howes, OD (2019) Schizophrenia, dopamine and the striatum: from biology to symptoms. Trends in Neurosciences 42(3), 205–220.CrossRefGoogle ScholarPubMed
Mirzaalian, H, Ning, L, Savadjiev, P, Pasternak, O, Bouix, S, Michailovich, O, Karmacharya, S, Grant, G, Marx, CE, Morey, RA, Flashman, LA, George, MS, McAllister, TW, Andaluz, N, Shutter, L, Coimbra, R, Zafonte, RD, Coleman, MJ, Kubicki, M, Westin, C-F, Stein, MB, Shenton, ME and Rathi, Y (2018) Multi-site harmonization of diffusion MRI data in a registration framework. Brain Imaging and Behavior 12(1), 284–295.CrossRefGoogle Scholar
Noble, KG, Korgaonkar, MS, Grieve, SM and Brickman, AM (2013) Higher education is an age-independent predictor of white matter integrity and cognitive control in late adolescence. Developmental Science 16(5), 653–664.CrossRefGoogle ScholarPubMed
Orellana, G and Slachevsky, A (2013) Executive functioning in schizophrenia. Frontiers in Psychiatry 4.CrossRefGoogle ScholarPubMed
Parker, GJ and Alexander, DC (2005) Probabilistic anatomical connectivity derived from the microscopic persistent angular structure of cerebral tissue. Philosophical Transactions of the Royal Society B: Biological Sciences 360(1457), 893–902.CrossRefGoogle ScholarPubMed
Parker, GJ and Alexander, DC (2003) Probabilistic monte carlo based mapping of cerebral connections utilising whole-brain crossing fibre information. Information Processing in Medical Imaging 18, 684–695.CrossRefGoogle ScholarPubMed
Patel, S, Mahon, K, Wellington, R, Zhang, J, Chaplin, W and Szeszko, PR (2011) A meta-analysis of diffusion tensor imaging studies of the corpus callosum in schizophrenia. Schizophrenia Research 129(2-3), 149–155.CrossRefGoogle ScholarPubMed
Pearlson, G (2009) Multisite collaborations and large databases in psychiatric neuroimaging: advantages, problems, and challenges. Schizophrenia Bulletin 35(1), 1–2.CrossRefGoogle Scholar
Penke, L, Maniega, S Mñoz, Bastin, M E, Valdés Hernández, M C, Murray, C, Royle, N A, Starr, J M, Wardlaw, J M and Deary, I J (2012) Brain white matter tract integrity as a neural foundation for general intelligence. Molecular Psychiatry 17(10), 1026–1030.CrossRefGoogle ScholarPubMed
Price, G, Cercignani, M, Parker, GJM, Altmann, DR, Barnes, TRE, Barker, GJ, Joyce, EM and Ron, MA (2008) White matter tracts in first-episode psychosis: a DTI tractography study of the uncinate fasciculus. NeuroImage 39(3), 949–955.CrossRefGoogle ScholarPubMed
Rao, NP, Venkatasubramanian, G, Arasappa, R and Gangadhar, BN (2011) Relationship between corpus callosum Abnormalities and schneiderian first-rank symptoms in antipsychotic-naïve schizophrenia patients. The Journal of Neuropsychiatry and Clinical Neurosciences 23(2), 155–162.CrossRefGoogle ScholarPubMed
R Core Team (2013) R: A Language and Environment for Statistical Computing.Google Scholar
Schlaier, JR, Beer, AL, Faltermeier, R, Fellner, C, Steib, K, Lange, M, Greenlee, MW, Brawanski, AT and Anthofer, JM (2017) Probabilistic vs. deterministic fiber tracking and the influence of different seed regions to delineate cerebellar-thalamic fibers in deep brain stimulation. European Journal of Neuroscience 45(12), 1623–1633.CrossRefGoogle ScholarPubMed
Schmitt, A., Hasan, A., Gruber, O. and Falkai, P. (2011) Schizophrenia as a disorder of disconnectivity. European Archives of Psychiatry and Clinical Neuroscience 261(Suppl 2), S150–S154.CrossRefGoogle ScholarPubMed
Shaked, D, Leibel, DK, Katzel, LI, Davatzikos, C, Gullapalli, RP, Seliger, SL, Erus, G, Evans, MK, Zonderman, AB and Waldstein, SR (2019) Disparities in diffuse cortical white matter integrity between socioeconomic groups. Frontiers in Human Neuroscience 13, 198.CrossRefGoogle ScholarPubMed
Shon, S-H, Yoon, W, Kim, H, Joo, SW, Kim, Y and Lee, J (2018) Deterioration in global organization of structural brain networks in schizophrenia: a diffusion MRI tractography study. Frontiers in Psychiatry 9.CrossRefGoogle ScholarPubMed
Sun, J, Maller, JJ, Guo, L and Fitzgerald, PB (2009) Superior temporal gyrus volume change in schizophrenia: a review on region of interest volumetric studies. Brain Research Reviews 61(1), 14–32.CrossRefGoogle ScholarPubMed
Takahashi, T, Wood, SJ, Yung, AR, Soulsby, B, McGorry, PD, Suzuki, M, Kawasaki, Y, Phillips, LJ, Velakoulis, D and Pantelis, C (2009) Progressive gray matter reduction of the superior temporal gyrus during transition to psychosis. Archives of General Psychiatry 66(4), 366–376.CrossRefGoogle ScholarPubMed
The Jamovi Project (2021) Jamovi (Version 1.6).Google Scholar
Thomas, C, Ye, FQ, Irfanoglu, MO, Modi, P, Saleem, KS, Leopold, DA and Pierpaoli, C (2014) Anatomical accuracy of brain connections derived from diffusion MRI tractography is inherently limited. Proceedings of the National Academy of Sciences 111(46), 16574–16579.CrossRefGoogle ScholarPubMed
Tréhout, M, Leroux, E, Delcroix, N and Dollfus, S (2017) Relationships between corpus callosum and language lateralization in patients with schizophrenia and bipolar disorders. Bipolar Disorders 19(6), 496–504.CrossRefGoogle ScholarPubMed
van Erp, TGM, Preda, A, Nguyen, D, Faziola, L, Turner, J, Bustillo, J, Belger, A, Lim, KO, McEwen, S, Voyvodic, J, Mathalon, DH, Ford, J, Potkin, SG and FBIRN (2014) Converting positive and negative symptom scores between PANSS and SAPS/SANS. Schizophrenia Research 152(1), 289–294.CrossRefGoogle ScholarPubMed
Van Horn, JD and Toga, AW (2009) Multi-site neuroimaging trials. Current Opinion in Neurology 22(4), 370–378.CrossRefGoogle Scholar
Wang, L, Alpert, KI, Calhoun, VD, Cobia, DJ, Keator, DB, King, MD, Kogan, A, Landis, D, Tallis, M, Turner, MD, Potkin, SG, Turner, JA and Ambite, JL (2016) SchizConnect: mediating neuroimaging databases on schizophrenia and related disorders for large-scale integration. NeuroImage 124, 1155–1167.CrossRefGoogle ScholarPubMed
Whitford, TJ, Kubicki, M, Schneiderman, JS, O’Donnell, LJ, King, R, Alvarado, JL, Khan, U, Markant, D, Nestor, PG, Niznikiewicz, M, McCarley, RW, Westin, C-F and Shenton, ME (2010) Corpus callosum abnormalities and their association with psychotic symptoms in patients with schizophrenia. Biological Psychiatry 68(1), 70–77.CrossRefGoogle ScholarPubMed
Yamada, K, Sakai, K, Akazawa, K, Yuen, S and Nishimura, T (2009) MR tractography: a review of its clinical applications. Magnetic Resonance in Medical Sciences 8(4), 165–174.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Demographics and clinical characteristics of study participants

Figure 1

Table 2. Demographics and clinical characteristics of each dataset

Figure 2

Table 3. Comparison of connection probabilities between patients and controls

Figure 3

Table 4. Correlations of connection probabilities to symptoms and cognitive measures in patients