Pub Date : 2026-01-28DOI: 10.1016/j.pscychresns.2026.112157
Min-Han Huang , Yi-Chun Yeh , Cheng-Fang Yen , Chiao-Li Khale Ke , Cian-Ruei Jian , Chien-Wen Lin , I-Mei Lin
Patients with major depressive disorder (MDD) exhibit abnormal hypercoherence within the fronto-limbic circuit (FLC), involving core brain regions such as the ventrolateral, ventromedial, dorsolateral, dorsomedial prefrontal cortex (vlPFC, vmPFC, dlPFC, dmPFC), and the amygdala (AMY). This study examined the effects of standardized weighted low-resolution electromagnetic tomography Z-score neurofeedback (swLZNFB) on LFC coherence and emotional symptoms. Sixty-one MDD patients were assigned to either the swLZNFB or control groups. All participants completed the Beck Depression Inventory II (BDI-II), the Beck Anxiety Inventory (BAI), and a five-minute eyes-closed resting-state electroencephalography (EEG) assessment both at pre-test and post-test. EEG coherence values were processed and converted into Z-scores across five frequency bands (delta to high beta), using the NeuroGuide normalization database. Compared to the control group, the swLZNFB group exhibited significantly reduced theta and beta Z-coherence values between vlPFC-AMY and dmPFC-AMY at post-test. Within-group comparisons revealed significantly decreased in beta Z-coherence between vlPFC-AMY from pre-test to post-test. Moreover, the swLZNFB group demonstrated significant decreases in depression and anxiety symptoms, whereas the control group showed improvement in depression only. These findings suggest that swLZNFB effectively modulates FCL hyperconnectivity and alleviates emotional symptoms in MDD, supporting its potential as a non-pharmaceutical intervention targeting dysfunction emotion regulation networks.
{"title":"Effects of swLORETA Z-score neurofeedback in Z-coherence of the fronto-limbic circuit in patients with major depressive disorder","authors":"Min-Han Huang , Yi-Chun Yeh , Cheng-Fang Yen , Chiao-Li Khale Ke , Cian-Ruei Jian , Chien-Wen Lin , I-Mei Lin","doi":"10.1016/j.pscychresns.2026.112157","DOIUrl":"10.1016/j.pscychresns.2026.112157","url":null,"abstract":"<div><div>Patients with major depressive disorder (MDD) exhibit abnormal hypercoherence within the fronto-limbic circuit (FLC), involving core brain regions such as the ventrolateral, ventromedial, dorsolateral, dorsomedial prefrontal cortex (vlPFC, vmPFC, dlPFC, dmPFC), and the amygdala (AMY). This study examined the effects of standardized weighted low-resolution electromagnetic tomography Z-score neurofeedback (swLZNFB) on LFC coherence and emotional symptoms. Sixty-one MDD patients were assigned to either the swLZNFB or control groups. All participants completed the Beck Depression Inventory II (BDI-II), the Beck Anxiety Inventory (BAI), and a five-minute eyes-closed resting-state electroencephalography (EEG) assessment both at pre-test and post-test. EEG coherence values were processed and converted into Z-scores across five frequency bands (delta to high beta), using the NeuroGuide normalization database. Compared to the control group, the swLZNFB group exhibited significantly reduced theta and beta Z-coherence values between vlPFC-AMY and dmPFC-AMY at post-test. Within-group comparisons revealed significantly decreased in beta Z-coherence between vlPFC-AMY from pre-test to post-test. Moreover, the swLZNFB group demonstrated significant decreases in depression and anxiety symptoms, whereas the control group showed improvement in depression only. These findings suggest that swLZNFB effectively modulates FCL hyperconnectivity and alleviates emotional symptoms in MDD, supporting its potential as a non-pharmaceutical intervention targeting dysfunction emotion regulation networks.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112157"},"PeriodicalIF":2.1,"publicationDate":"2026-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146078745","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-24DOI: 10.1016/j.pscychresns.2026.112152
Jeehye Seo, Cagri Yuksel, Katelyn I Oliver, Carolina Daffre, Huijin Song, Natasha B Lasko, Emma R S McCoy, Mohammed R Milad, Byoung-Kyong Min, Edward F Pace-Schott
Deficient extinction learning and memory are hypothesized mechanisms for pathological anxiety that are associated with sleep disturbance. fMRI neural activations to threat conditioning, extinction learning, and extinction recall were measured. Activations were compared, in persons with Generalized Anxiety Disorder (GAD), between those with moderate to severe Insomnia Disorder (ID) and those with absent or sub-threshold ID. Relationships of activations with measures of sleep quality and physiology were examined. Between-group comparisons and whole-sample correlation with sleep parameters were examined in relation to large-scale brain networks using a liberal cluster-determining threshold. Localized activations were then identified using family-wise error correction. Activations to the reinforced stimulus (CS+) that increased from the beginning to end ("across") threat conditioning were more extensive within the GAD+ID group. Increased activations to the CS+ across extinction learning were greater within the GAD-ID than the GAD+ID group, and delayed 24 h in the latter. Greater sleep efficiency was associated with decreased activations across threat conditioning, but with increased activations across extinction learning. Better sleep quality promoted greater engagement of neural substrates of extinction learning. The GAD+ID group failed to engage brain areas supporting extinction learning immediately following threat conditioning, but did so when stimuli were again presented following a delay.
{"title":"Local and network neural activations and their associations with sleep parameters during threat conditioning and extinction in persons with generalized anxiety disorder with and without insomnia disorder.","authors":"Jeehye Seo, Cagri Yuksel, Katelyn I Oliver, Carolina Daffre, Huijin Song, Natasha B Lasko, Emma R S McCoy, Mohammed R Milad, Byoung-Kyong Min, Edward F Pace-Schott","doi":"10.1016/j.pscychresns.2026.112152","DOIUrl":"10.1016/j.pscychresns.2026.112152","url":null,"abstract":"<p><p>Deficient extinction learning and memory are hypothesized mechanisms for pathological anxiety that are associated with sleep disturbance. fMRI neural activations to threat conditioning, extinction learning, and extinction recall were measured. Activations were compared, in persons with Generalized Anxiety Disorder (GAD), between those with moderate to severe Insomnia Disorder (ID) and those with absent or sub-threshold ID. Relationships of activations with measures of sleep quality and physiology were examined. Between-group comparisons and whole-sample correlation with sleep parameters were examined in relation to large-scale brain networks using a liberal cluster-determining threshold. Localized activations were then identified using family-wise error correction. Activations to the reinforced stimulus (CS+) that increased from the beginning to end (\"across\") threat conditioning were more extensive within the GAD+ID group. Increased activations to the CS+ across extinction learning were greater within the GAD-ID than the GAD+ID group, and delayed 24 h in the latter. Greater sleep efficiency was associated with decreased activations across threat conditioning, but with increased activations across extinction learning. Better sleep quality promoted greater engagement of neural substrates of extinction learning. The GAD+ID group failed to engage brain areas supporting extinction learning immediately following threat conditioning, but did so when stimuli were again presented following a delay.</p>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"358 ","pages":"112152"},"PeriodicalIF":2.1,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146126248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
As pathophysiological mechanisms of schizophrenia remain unclear, the development of reliable biomarkers for the disease is highly anticipated. Electroencephalogram with transcranial magnetic stimulation (TMS-EEG) is a developing technique for assessing mental condition. Phase-locking factors (PLFs) are a parameter of phase synchronization, which can assess the brain connectivity of specific areas. Both visual processing impairments and aberrant brain connectivity are implicated in the pathophysiology of schizophrenia. Here, we compared motor area PLFs using visual area-targeted TMS-EEG between three groups: 15 patients with schizophrenia (SZ), 15 patients with major depressive disorder (MD), and 15 healthy controls (HC). The PLF of the SZ group showed a significant decrease in the theta band compared to the HC group without confounding effects from TMS click noises or antipsychotic medication. The reduction of PLF in the theta band between the visual and motor area could reflect visual processing impairments in schizophrenia. Further experiments with larger sample size and appropriate cognitive tasks are required to confirm our conclusion.
{"title":"Assessment of phase-locking factor with visual area-targeted transcranial magnetic stimulation-electroencephalography shows reduced connectivity in schizophrenia: A preliminary study","authors":"Masayuki Ide , Akihiro Tadamura , Takehiro Miyazaki , Yoshiki Inoue , Aya Sekine , Takumi Takahashi , Masashi Tamura , Asaki Matsuzaki , Kiyotaka Nemoto , Hirokazu Tachikawa , Tetsuaki Arai , Masahiro Kawasaki","doi":"10.1016/j.pscychresns.2026.112153","DOIUrl":"10.1016/j.pscychresns.2026.112153","url":null,"abstract":"<div><div>As pathophysiological mechanisms of schizophrenia remain unclear, the development of reliable biomarkers for the disease is highly anticipated. Electroencephalogram with transcranial magnetic stimulation (TMS-EEG) is a developing technique for assessing mental condition. Phase-locking factors (PLFs) are a parameter of phase synchronization, which can assess the brain connectivity of specific areas. Both visual processing impairments and aberrant brain connectivity are implicated in the pathophysiology of schizophrenia. Here, we compared motor area PLFs using visual area-targeted TMS-EEG between three groups: 15 patients with schizophrenia (SZ), 15 patients with major depressive disorder (MD), and 15 healthy controls (HC). The PLF of the SZ group showed a significant decrease in the theta band compared to the HC group without confounding effects from TMS click noises or antipsychotic medication. The reduction of PLF in the theta band between the visual and motor area could reflect visual processing impairments in schizophrenia. Further experiments with larger sample size and appropriate cognitive tasks are required to confirm our conclusion.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112153"},"PeriodicalIF":2.1,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146078747","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.pscychresns.2026.112150
Si Yang , Lijun Wang , Man Zheng , Suhao Peng
Borderline personality disorder traits (BPD traits) represent subclinical characteristics associated with borderline personality disorder (BPD), which are marked by impaired cognitive control of emotion processing. Although the cognitive control deficit of negative emotions is a core feature of BPD, the characteristics and neural basis of this deficit in non-clinical BPD traits individuals remain unclear. The present study employed a novel facial majority function task (fMFT) combined with event-related potential (ERP) recording to explore the cognitive control of negative facial emotion under varying task difficulty in individuals with high BPD traits. We recruited 50 high BPD traits participants and 50 low BPD traits participants for the fMFT. The behavioral results showed that under low and medium task difficulty conditions, there were no significant differences in reaction time and accuracy between the two groups. However, under negative emotion-high task difficulty conditions, the reaction time of the high BPD traits group was significantly longer than that of the low BPD traits group, and the accuracy was significantly lower than that of the low BPD traits group. The ERP results showed that high BPD traits group exhibited reduced frontal N200 amplitudes and increased parietal P300 amplitudes compared to the low BPD traits group. Furthermore, both groups exhibited decreased LPP amplitudes with increasing task difficulty in positive emotion conditions, but this task difficulty effect was not significant in negative emotion conditions in the high BPD traits group. These findings demonstrate that BPD traits leads to selective deficits in cognitive control of emotion processing, and negative emotion leads to their impairment in the processing of conflict monitoring and inhibition with task difficulty increasing.
{"title":"Neural evidence for the influence of cognitive control by facial emotion under varying task difficulty in individuals with borderline personality disorder traits","authors":"Si Yang , Lijun Wang , Man Zheng , Suhao Peng","doi":"10.1016/j.pscychresns.2026.112150","DOIUrl":"10.1016/j.pscychresns.2026.112150","url":null,"abstract":"<div><div>Borderline personality disorder traits (BPD traits) represent subclinical characteristics associated with borderline personality disorder (BPD), which are marked by impaired cognitive control of emotion processing. Although the cognitive control deficit of negative emotions is a core feature of BPD, the characteristics and neural basis of this deficit in non-clinical BPD traits individuals remain unclear. The present study employed a novel facial majority function task (fMFT) combined with event-related potential (ERP) recording to explore the cognitive control of negative facial emotion under varying task difficulty in individuals with high BPD traits. We recruited 50 high BPD traits participants and 50 low BPD traits participants for the fMFT. The behavioral results showed that under low and medium task difficulty conditions, there were no significant differences in reaction time and accuracy between the two groups. However, under negative emotion-high task difficulty conditions, the reaction time of the high BPD traits group was significantly longer than that of the low BPD traits group, and the accuracy was significantly lower than that of the low BPD traits group. The ERP results showed that high BPD traits group exhibited reduced frontal N200 amplitudes and increased parietal P300 amplitudes compared to the low BPD traits group. Furthermore, both groups exhibited decreased LPP amplitudes with increasing task difficulty in positive emotion conditions, but this task difficulty effect was not significant in negative emotion conditions in the high BPD traits group. These findings demonstrate that BPD traits leads to selective deficits in cognitive control of emotion processing, and negative emotion leads to their impairment in the processing of conflict monitoring and inhibition with task difficulty increasing.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112150"},"PeriodicalIF":2.1,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023332","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Exploiting deep learning methods to accelerate the analysis of medical images and the interpretation of pathology results for early diagnosis of Alzheimer's disease (AD) has recently attracted great attention. However, challenges like sub-optimal classifiers and poor image representation hinder their effectiveness. Computer-aided diagnosis (CADx) can improve performance by classifying patterns. Despite the drawbacks of deep networks such as Visual Geometric Group (VGG), including long processing times and performance issues due to data distribution, many CADx systems still rely on VGG classifiers due to their potential for high accuracy when properly trained. To tackle these issues, this paper introduces two novel deep networks, called optimized VGG-16 (OVGG-16) and optimized VGG-19 (OVGG-19), in light of the concepts of transfer learning and dense layers to improve diagnosis performance. The proposed system was developed for the diagnosis of AD employing the OVGG-16 and OVGG-19 networks as classifiers from rs-fMRI images. The results show that the convergence rate of the proposed OVGG-16 and OVGG-19 networks is more rapid than that of the conventional VGG-16 and VGG-19. Moreover, the proposed system, which uses the OVGG-16 network, yielded a high accuracy of 100% and 98.83% for binary and multiclass classification, respectively, which surpasses existing state-of-the-art approaches.
{"title":"Early diagnosis of Alzheimer's disease from functional rs-fMRI images based on deep learning networks and transfer learning approach","authors":"Azizeh Akbari , Mahda Nasrolahzadeh , Javad Haddadnia","doi":"10.1016/j.pscychresns.2026.112151","DOIUrl":"10.1016/j.pscychresns.2026.112151","url":null,"abstract":"<div><div>Exploiting deep learning methods to accelerate the analysis of medical images and the interpretation of pathology results for early diagnosis of Alzheimer's disease (AD) has recently attracted great attention. However, challenges like sub-optimal classifiers and poor image representation hinder their effectiveness. Computer-aided diagnosis (CADx) can improve performance by classifying patterns. Despite the drawbacks of deep networks such as Visual Geometric Group (VGG), including long processing times and performance issues due to data distribution, many CADx systems still rely on VGG classifiers due to their potential for high accuracy when properly trained. To tackle these issues, this paper introduces two novel deep networks, called optimized VGG-16 (OVGG-16) and optimized VGG-19 (OVGG-19), in light of the concepts of transfer learning and dense layers to improve diagnosis performance. The proposed system was developed for the diagnosis of AD employing the OVGG-16 and OVGG-19 networks as classifiers from rs-fMRI images. The results show that the convergence rate of the proposed OVGG-16 and OVGG-19 networks is more rapid than that of the conventional VGG-16 and VGG-19. Moreover, the proposed system, which uses the OVGG-16 network, yielded a high accuracy of 100% and 98.83% for binary and multiclass classification, respectively, which surpasses existing state-of-the-art approaches.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112151"},"PeriodicalIF":2.1,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146078748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.pscychresns.2026.112149
Aosong Chen , Fujian Chen , Chenchen Zhang , Rui Li , Liju Qian , Cong Zhou , Bin Wang , Kun Li
Obsessive-compulsive disorder (OCD) is a chronic psychiatric disorder characterized by persistent intrusive thoughts and repetitive behaviors, significantly impacting patients' quality of life, social functioning, and overall well-being. Recent advances in neuroimaging techniques, particularly the development and application of the Human Brainnetome Atlas (BNA), have provided precise structural and functional subdivisions of the human brain, greatly enhancing the understanding of OCD neuropathology. This review comprehensively summarizes the latest applications of BNA in OCD research, specifically emphasizing detailed analyses of structural and functional connectivity abnormalities within neural circuits, their associations with clinical symptoms, and potential mechanisms underlying these abnormalities. Additionally, the utility of BNA in classifying patient subtypes based on distinct neurobiological profiles and its role in facilitating early diagnostic interventions are discussed. Methodological limitations are also addressed, underscoring the necessity of controlling confounding variables, such as pharmacological treatments and clinical heterogeneity, to strengthen research outcomes. Finally, future research directions are proposed, including the integration of BNA with advanced technologies such as artificial intelligence, multimodal imaging methods, and individualized neuromodulation strategies, to further refine and expand precision medicine approaches in OCD management.
{"title":"Advances on the application of the Human Brainnetome Atlas in obsessive-compulsive disorder","authors":"Aosong Chen , Fujian Chen , Chenchen Zhang , Rui Li , Liju Qian , Cong Zhou , Bin Wang , Kun Li","doi":"10.1016/j.pscychresns.2026.112149","DOIUrl":"10.1016/j.pscychresns.2026.112149","url":null,"abstract":"<div><div>Obsessive-compulsive disorder (OCD) is a chronic psychiatric disorder characterized by persistent intrusive thoughts and repetitive behaviors, significantly impacting patients' quality of life, social functioning, and overall well-being. Recent advances in neuroimaging techniques, particularly the development and application of the Human Brainnetome Atlas (BNA), have provided precise structural and functional subdivisions of the human brain, greatly enhancing the understanding of OCD neuropathology. This review comprehensively summarizes the latest applications of BNA in OCD research, specifically emphasizing detailed analyses of structural and functional connectivity abnormalities within neural circuits, their associations with clinical symptoms, and potential mechanisms underlying these abnormalities. Additionally, the utility of BNA in classifying patient subtypes based on distinct neurobiological profiles and its role in facilitating early diagnostic interventions are discussed. Methodological limitations are also addressed, underscoring the necessity of controlling confounding variables, such as pharmacological treatments and clinical heterogeneity, to strengthen research outcomes. Finally, future research directions are proposed, including the integration of BNA with advanced technologies such as artificial intelligence, multimodal imaging methods, and individualized neuromodulation strategies, to further refine and expand precision medicine approaches in OCD management.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112149"},"PeriodicalIF":2.1,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146078750","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-17DOI: 10.1016/j.pscychresns.2026.112147
Tommaso Toffanin , Giulia Ida Perini , Halima Follador , Filippo Zonta , Giovanni Ferri , Giorgio Pigato , Mario Angelo Pagano , Nadia Scupola , Claudia Pinato , Davide Calosci , Maria Ferrara , Angela Muscettola , Giovanni Antonio De Bellis , Chiara Montemitro , Luigi Zerbinati , Maria Giulia Nanni , Rosangela Caruso , Andrea Escelsior , Alessandra Baratto , Nicola Martino , Martino Belvederi Murri
Background and Hypothesis
Hippocampal volume reduction is a consistent finding in schizophrenia (SCZ) and bipolar disorder type I (BP-I), yet the role of genetic factors remains unclear. We investigated the influence of DISC1 (rs821616), AKT1 (rs1130233), COMT (rs4680), and GSK-3ꞵ(rs334558) polymorphisms on hippocampal morphology.
Study Design
Seventy-one participants (25 SCZ, 22 BP-I, 24 healthy controls, HC) underwent 1.5T MRI and genotyping. Bayesian multilevel models estimated associations between corrected hippocampal volume, diagnosis, hemisphere, and genetic variants.
Study Results
Both SCZ and BP-I showed significantly smaller hippocampal volumes compared with HC (Average Marginal Effects: SCZ vs HC = −1.38; BP-I vs HC = −1.46; probability of direction [PD] = 100%). Rightward asymmetry was preserved across groups. The COMT AA genotype was associated with lower hippocampal volume (AME = −0.67; PD = 99%), while DISC1 AT carriers showed moderate reductions (AME = −0.37; PD = 96%). GSK-3ꞵ contributed to variability but not mean volume, and AKT1 showed no clear effects.
Conclusions
Hippocampal atrophy is a shared marker of SCZ and BP-I, with preserved lateralization. COMT and DISC1 variations appear to modulate hippocampal volume, supporting their role in psychosis vulnerability.
背景和假设海马体积减少是精神分裂症(SCZ)和双相情感障碍I型(BP-I)的一致发现,但遗传因素的作用尚不清楚。我们研究了DISC1 (rs821616)、AKT1 (rs1130233)、COMT (rs4680)和GSK-3ꞵ(rs334558)多态性对海马形态的影响。71名参与者(25名SCZ, 22名BP-I, 24名健康对照,HC)进行1.5T MRI和基因分型。贝叶斯多层模型估计校正海马体积、诊断、半球和遗传变异之间的关联。研究结果SCZ和BP-I的海马体积均明显小于HC(平均边际效应:SCZ vs HC = - 1.38; BP-I vs HC = - 1.46;方向概率[PD] = 100%)。各组间均保持向右不对称。COMT AA基因型与海马体积降低相关(AME = - 0.67, PD = 99%),而DISC1 AT携带者表现出中度减少(AME = - 0.37, PD = 96%)。GSK-3ꞵ对变异有影响,但对平均体积没有影响,AKT1没有明显影响。结论海马萎缩是SCZ和BP-I的共同标志,并保留了侧位。COMT和DISC1的变异似乎可以调节海马体积,支持它们在精神病易感性中的作用。
{"title":"Impact of genetic variants on hippocampal volume among individuals with schizophrenia and bipolar disorders","authors":"Tommaso Toffanin , Giulia Ida Perini , Halima Follador , Filippo Zonta , Giovanni Ferri , Giorgio Pigato , Mario Angelo Pagano , Nadia Scupola , Claudia Pinato , Davide Calosci , Maria Ferrara , Angela Muscettola , Giovanni Antonio De Bellis , Chiara Montemitro , Luigi Zerbinati , Maria Giulia Nanni , Rosangela Caruso , Andrea Escelsior , Alessandra Baratto , Nicola Martino , Martino Belvederi Murri","doi":"10.1016/j.pscychresns.2026.112147","DOIUrl":"10.1016/j.pscychresns.2026.112147","url":null,"abstract":"<div><h3>Background and Hypothesis</h3><div>Hippocampal volume reduction is a consistent finding in schizophrenia (SCZ) and bipolar disorder type I (BP-I), yet the role of genetic factors remains unclear. We investigated the influence of DISC1 (rs821616), AKT1 (rs1130233), COMT (rs4680), and GSK-3ꞵ(rs334558) polymorphisms on hippocampal morphology.</div></div><div><h3>Study Design</h3><div>Seventy-one participants (25 SCZ, 22 BP-I, 24 healthy controls, HC) underwent 1.5T MRI and genotyping. Bayesian multilevel models estimated associations between corrected hippocampal volume, diagnosis, hemisphere, and genetic variants.</div></div><div><h3>Study Results</h3><div>Both SCZ and BP-I showed significantly smaller hippocampal volumes compared with HC (Average Marginal Effects: SCZ vs HC = −1.38; BP-I vs HC = −1.46; probability of direction [PD] = 100%). Rightward asymmetry was preserved across groups. The COMT AA genotype was associated with lower hippocampal volume (AME = −0.67; PD = 99%), while DISC1 AT carriers showed moderate reductions (AME = −0.37; PD = 96%). GSK-3ꞵ contributed to variability but not mean volume, and AKT1 showed no clear effects.</div></div><div><h3>Conclusions</h3><div>Hippocampal atrophy is a shared marker of SCZ and BP-I, with preserved lateralization. COMT and DISC1 variations appear to modulate hippocampal volume, supporting their role in psychosis vulnerability.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112147"},"PeriodicalIF":2.1,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Neuromelanin-sensitive MRI (NM-MRI) has demonstrated potential as a proxy measure of dopamine functioning in the brain. Altered NM-MRI has been associated with substance use disorders, yet remains unexplored in problematic social media use (PSMU). The current study aims to determine whether higher PSMU is linked to lower NM-MRI signal intensity in the substantia nigra and ventral tegmental area (SN-VTA).
Methods
Seventy-two young adults (18–35 years of age) completed the Bergen Social Media Addiction Scale to measure PSMU and underwent an NM-MRI scan. Half of the participants had a first degree relative (FDR) with a psychotic disorder. Within the SN-VTA, the average contrast-to-noise ratio was calculated on NM-MRI images. Linear regressions included NM-MRI signal intensity and PSMU scores, with age, sex, and FDR status as covariates.
Results
Higher levels of PSMU were not significantly associated with average NM-MRI signal intensity in the whole SN-VTA (p = 0.65). Voxelwise analysis revealed ninety-nine voxels with higher NM-signal intensity (pcorrected > 0.05). No significant main effect or interactions were observed for any covariates.
Conclusions
As the first application of NM-MRI to examine dopaminergic markers in relation to PSMU, these results highlight the importance of further studying brain correlates of PSMU beyond dopaminergic neuroadaptation.
神经黑色素敏感MRI (NM-MRI)已被证明有潜力作为大脑中多巴胺功能的替代测量。改变的核磁共振成像与物质使用障碍有关,但在有问题的社交媒体使用(PSMU)中仍未被探索。本研究旨在确定高PSMU是否与黑质和腹侧被盖区(SN-VTA)的低NM-MRI信号强度有关。方法72名18-35岁的年轻人完成了卑尔根社交媒体成瘾量表(Bergen Social Media Addiction Scale)来测量PSMU,并进行了核磁共振成像(nmr)扫描。一半的参与者有一级亲属(FDR)患有精神病。在SN-VTA内,计算NM-MRI图像的平均噪比。线性回归包括NM-MRI信号强度和PSMU评分,协变量为年龄、性别和FDR状态。结果高PSMU水平与整个SN-VTA的平均NM-MRI信号强度无显著相关性(p = 0.65)。体素分析显示,99个体素具有较高的纳米信号强度(预校正>; 0.05)。未观察到任何协变量的显著主效应或相互作用。结论这是NM-MRI首次应用于检测与PSMU相关的多巴胺能标志物,这些结果强调了进一步研究PSMU的脑相关因素的重要性,而不是多巴胺能神经适应。
{"title":"Testing dopaminergic markers of problematic social media use using neuromelanin-sensitive MRI","authors":"Holly Shannon , Matteo Montgomery , Clifford Cassidy , Marianne Lemieux , Jasmin A. Yee , Lisa-Sarah Brunier , Kim G.C. Hellemans , Synthia Guimond","doi":"10.1016/j.pscychresns.2026.112144","DOIUrl":"10.1016/j.pscychresns.2026.112144","url":null,"abstract":"<div><h3>Background</h3><div>Neuromelanin-sensitive MRI (NM-MRI) has demonstrated potential as a proxy measure of dopamine functioning in the brain. Altered NM-MRI has been associated with substance use disorders, yet remains unexplored in problematic social media use (PSMU). The current study aims to determine whether higher PSMU is linked to lower NM-MRI signal intensity in the substantia nigra and ventral tegmental area (SN-VTA).</div></div><div><h3>Methods</h3><div>Seventy-two young adults (18–35 years of age) completed the Bergen Social Media Addiction Scale to measure PSMU and underwent an NM-MRI scan. Half of the participants had a first degree relative (FDR) with a psychotic disorder. Within the SN-VTA, the average contrast-to-noise ratio was calculated on NM-MRI images. Linear regressions included NM-MRI signal intensity and PSMU scores, with age, sex, and FDR status as covariates.</div></div><div><h3>Results</h3><div>Higher levels of PSMU were not significantly associated with average NM-MRI signal intensity in the whole SN-VTA (<em>p</em> = 0.65). Voxelwise analysis revealed ninety-nine voxels with higher NM-signal intensity (p<sub>corrected</sub> > 0.05). No significant main effect or interactions were observed for any covariates.</div></div><div><h3>Conclusions</h3><div>As the first application of NM-MRI to examine dopaminergic markers in relation to PSMU, these results highlight the importance of further studying brain correlates of PSMU beyond dopaminergic neuroadaptation.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112144"},"PeriodicalIF":2.1,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023392","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-16DOI: 10.1016/j.pscychresns.2026.112145
Antonio Maria D’Onofrio , Daniela Di Giuda , Eleonora Maggio , Daniele Antonio Pizzuto , Fabrizio Cocciolillo , Federica Cavallo , Rosaria Calia , Alessio Simonetti , Delfina Janiri , Alexia Koukopoulos , Mauro Pettorruso , Giovanni Martinotti , Gabriele Sani , Giovanni Camardese
Background and aim
Seasonal changes, particularly increased daylight exposure, are known to influence dopamine transporter (DAT) availability, potentially affecting mood disorders such as major depressive disorder (MDD). This study aimed to evaluate seasonal variations in the striatum using ¹²³I-FP-CIT SPECT in patients with MDD, and examine associations with specific psychopathological symptoms.
Methods
In this retrospective study, DAT SPECT scans from 85 patients with MDD were analyzed according to the season of imaging—fall-winter (FW) or spring-summer (SS). Psychometric assessments included the Hamilton Depression Rating Scale (HAMD), Hamilton Anxiety Rating Scale (HAMA), Snaith-Hamilton Pleasure Scale (SHAPS), and Depression Retardation Rating Scale (DRRS).
Results
No overall differences in DAT availability were observed between FW and SS. However, anhedonia levels were higher in FW (p = 0.050). Patients with severe depression (HAMD ≥ 25) showed lower DAT availability in the left putamen, especially during SS (p = 0.014). Patients with marked psychomotor retardation (DRRS ≥ 18) exhibited reduced DAT availability in the left putamen (p = 0.002), with further reductions across all striatal regions during SS. Patients with suicidal ideation showed decreased DAT in the right (p = 0.029) and left putamen (p = 0.015). A negative correlation was found between DRRS scores and left putamen DAT availability (p = 0.034).
Conclusion
Reduced DAT availability is associated with key depressive symptoms, notably psychomotor retardation and suicidal ideation. Seasonal effects, especially in the SS period, may exacerbate dopaminergic dysregulation. These findings support integrating seasonal and neurobiological factors in the assessment and management of severe MDD.
{"title":"“Summertime sadness”: Striatal dopamine binding decreases during warmer seasons in patients with severe depression","authors":"Antonio Maria D’Onofrio , Daniela Di Giuda , Eleonora Maggio , Daniele Antonio Pizzuto , Fabrizio Cocciolillo , Federica Cavallo , Rosaria Calia , Alessio Simonetti , Delfina Janiri , Alexia Koukopoulos , Mauro Pettorruso , Giovanni Martinotti , Gabriele Sani , Giovanni Camardese","doi":"10.1016/j.pscychresns.2026.112145","DOIUrl":"10.1016/j.pscychresns.2026.112145","url":null,"abstract":"<div><h3>Background and aim</h3><div>Seasonal changes, particularly increased daylight exposure, are known to influence dopamine transporter (DAT) availability, potentially affecting mood disorders such as major depressive disorder (MDD). This study aimed to evaluate seasonal variations in the striatum using ¹²³I-FP-CIT SPECT in patients with MDD, and examine associations with specific psychopathological symptoms.</div></div><div><h3>Methods</h3><div>In this retrospective study, DAT SPECT scans from 85 patients with MDD were analyzed according to the season of imaging—fall-winter (FW) or spring-summer (SS). Psychometric assessments included the Hamilton Depression Rating Scale (HAMD), Hamilton Anxiety Rating Scale (HAMA), Snaith-Hamilton Pleasure Scale (SHAPS), and Depression Retardation Rating Scale (DRRS).</div></div><div><h3>Results</h3><div>No overall differences in DAT availability were observed between FW and SS. However, anhedonia levels were higher in FW (p = 0.050). Patients with severe depression (HAMD ≥ 25) showed lower DAT availability in the left putamen, especially during SS (p = 0.014). Patients with marked psychomotor retardation (DRRS ≥ 18) exhibited reduced DAT availability in the left putamen (p = 0.002), with further reductions across all striatal regions during SS. Patients with suicidal ideation showed decreased DAT in the right (p = 0.029) and left putamen (p = 0.015). A negative correlation was found between DRRS scores and left putamen DAT availability (p = 0.034).</div></div><div><h3>Conclusion</h3><div>Reduced DAT availability is associated with key depressive symptoms, notably psychomotor retardation and suicidal ideation. Seasonal effects, especially in the SS period, may exacerbate dopaminergic dysregulation. These findings support integrating seasonal and neurobiological factors in the assessment and management of severe MDD.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112145"},"PeriodicalIF":2.1,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023330","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Formal thought disorder (FTD), a prominent feature of schizophrenia, encompasses disruptions in thought, language, and communication. This study examines cortical thickness (CT) alterations in first-episode psychosis (FEP) patients (N = 24), their siblings (SIB) (N = 21), and healthy controls (CON) (N = 21) to explore potential neural correlates of FTD. Using structural MRI, we analyzed whole-brain CT and its relationship with positive and negative FTD measured by Thought and Language Index. Out-of-sample spatial correlations of gene expression with regional CT were also performed using a transcriptomic dataset. FEP had significant CT reductions in right middle frontal gyrus (MFG) compared with SIB and CON and in superior frontal gyrus (SFG) compared to CON; but SIB did not differ from CON. GLM analyses demonstrated that negative FTD exerted a significant main effect on CT in the MFG and SFG. By contrast, positive FTD showed no significant associations with CT. Neuroimaging-transcriptomic association analysis identified key biological pathways linked to cortical morphology. These findings emphasize the specific association between negative FTD and CT alterations in frontal brain regions, confirming prior reports. Future research should examine larger cohorts and investigate additional FTD subtypes to further elucidate neural correlates and potential familial risks of schizophrenia.
{"title":"Formal thought disorder and familial risk in first-episode psychosis: A study of cortical thickness and neuroimaging-transcriptomic association analysis","authors":"Tuğçe Çabuk , Yuanchao Zhang , Lena Palaniyappan , Didenur Şahin-Çevik , Hanife Avcı , Işık Batuhan Çakmak , Helin Yılmaz Kafalı , Bedirhan Şenol , Kader Karlı Oğuz , Timothea Toulopoulou","doi":"10.1016/j.pscychresns.2026.112148","DOIUrl":"10.1016/j.pscychresns.2026.112148","url":null,"abstract":"<div><div>Formal thought disorder (FTD), a prominent feature of schizophrenia, encompasses disruptions in thought, language, and communication. This study examines cortical thickness (CT) alterations in first-episode psychosis (FEP) patients (<em>N</em> = 24), their siblings (SIB) (<em>N</em> = 21), and healthy controls (CON) (<em>N</em> = 21) to explore potential neural correlates of FTD. Using structural MRI, we analyzed whole-brain CT and its relationship with positive and negative FTD measured by Thought and Language Index. Out-of-sample spatial correlations of gene expression with regional CT were also performed using a transcriptomic dataset. FEP had significant CT reductions in right middle frontal gyrus (MFG) compared with SIB and CON and in superior frontal gyrus (SFG) compared to CON; but SIB did not differ from CON. GLM analyses demonstrated that negative FTD exerted a significant main effect on CT in the MFG and SFG. By contrast, positive FTD showed no significant associations with CT. Neuroimaging-transcriptomic association analysis identified key biological pathways linked to cortical morphology. These findings emphasize the specific association between negative FTD and CT alterations in frontal brain regions, confirming prior reports. Future research should examine larger cohorts and investigate additional FTD subtypes to further elucidate neural correlates and potential familial risks of schizophrenia.</div></div>","PeriodicalId":20776,"journal":{"name":"Psychiatry Research: Neuroimaging","volume":"357 ","pages":"Article 112148"},"PeriodicalIF":2.1,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}