Journal of Psychiatry & Neuroscience最新文献

{"title":"Association of systemic inflammatory markers with white matter hyperintensities and microstructural injury: an analysis of UK Biobank data.","authors":"Yuan Qiao, Lei Zhao, Chaohua Cong, Yuna Li, Shan Tian, Xirui Zhu, Junting Yang, Shanshan Cao, Panlong Li, Jingjing Su","doi":"10.1503/jpn.240039","DOIUrl":"https://doi.org/10.1503/jpn.240039","url":null,"abstract":"<p><strong>Background: </strong>White matter damage is closely associated with cognitive and psychiatric symptoms and is prevalent in cerebral small vessel disease (CSVD); although the pathophysiological mechanisms involved in CSVD remain elusive, inflammation plays a crucial role. We sought to investigate the relationship between systemic inflammation markers and imaging markers of CVSD, namely white matter hyperintensity (WMH) and microstructural injury.</p><p><strong>Methods: </strong>We conducted a study involving both cross-sectional and longitudinal data from the UK Biobank Cohort. We performed multiple linear regression analyses, adjusted for potential confounders, to explore the associations between systemic inflammation markers (e.g., systemic immune-inflammation index [SII], neutrophil-to-lymphocyte ratio [NLR], C-reactive protein [CRP] levels, monocyte count, neutrophil count) and macro- and microstructural white matter injury, as markers of CSVD. We performed Mendelian randomization analysis to investigate the genetically predictive effect of monocytes on WMH, as well as mediation analysis to clarify whether inflammatory markers affected cognitive function via white matter injury.</p><p><strong>Results: </strong>We included 36 411 participants (mean age 54.8 ± 7.5 yr, 51.9% female) from the UK Biobank Cohort. We found that SII was significantly associated with both WMH and microstructural injury markers (fractional anisotropy, mean diffusivity, intracellular volume fraction, and isotropic compartment volume fraction [ISOVF]), and the neutrophil-to-lymphocyte ratio was significantly associated with WMH and some markers of microstructural injury (mean diffusivity and ISOVF). Our analysis revealed that the CRP level was significantly associated with WMH and WMH progression but not with microstructural injury. We also demonstrated that monocyte count was significantly associated with WMH and ISOVF, and that neutrophil count was significantly associated with WMH, mean diffusivity, and ISOVF. In 2-sample Mendelian randomization analyses, we found positive associations between genetic determinants of monocytes and WMH. The mediating role of WMH suggested that a higher SII value and monocyte count could contribute to cognitive impairment through white matter injury.</p><p><strong>Limitations: </strong>Although the study includes both cross-sectional and longitudinal components, the sample size for the longitudinal aspect is limited, and the use of blood biomarkers from a single timepoint is also a limitation of this research.</p><p><strong>Conclusion: </strong>The SII and neutrophil-to-lymphocyte ratio may be early detection markers for white matter damage in patients with CSVD, whereas the CRP level is more closely associated with disease severity and progression. Our findings highlight the clinical relevance of systemic inflammation markers with white matter macro- and microstructural injuries, revealing that systemic inflammation is likely","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"50 1","pages":"E45-E56"},"PeriodicalIF":4.1,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143030253","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Shorter and inflexible intrinsic neural timescales of the self in schizophrenia.","authors":"Frank Djimbouon, Philipp Klar, Georg Northoff","doi":"10.1503/jpn.240093","DOIUrl":"https://doi.org/10.1503/jpn.240093","url":null,"abstract":"<p><strong>Background: </strong>Schizophrenia is hypothesized to involve a disturbance in the temporal dynamics of self-processing, specifically within the interoceptive, exteroceptive, and cognitive layers of the self. This study aimed to investigate the intrinsic neural timescales (INTs) within these self-processing layers among people with schizophrenia.</p><p><strong>Methods: </strong>We conducted a functional magnetic resonance imaging (fMRI) study to investigate INTs, as measured by the autocorrelation window, among people with schizophrenia and healthy controls during both resting-state and task (memory encoding and retrieval) conditions. We obtained data from the UCLA Consortium for Neuropsychiatric Phenomics data set and preprocessed using fMRIPrep.</p><p><strong>Results: </strong>We included 45 people with schizophrenia and 65 healthy controls. Compared with controls, participants with schizophrenia exhibited significantly shorter INTs across all 3 self-processing layers during rest (<i>p</i> < 0.05). In addition, those with schizophrenia showed less INT shortening during task states, leading to reduced rest-task differences in INT across all self-processing layers (<i>p</i> < 0.05). We observed similar patterns of shortened INTs in primary sensory and motor regions.</p><p><strong>Limitations: </strong>We included people with schizophrenia taking medication, which may influence INTs; our study was also limited by the relatively slow temporal resolution of the fMRI data and the higher variability of the autocorrelation function in the schizophrenia group, compared with the control group.</p><p><strong>Conclusion: </strong>Our findings suggest that schizophrenia is characterized by a global temporal disturbance of the self, manifesting as shorter and inflexible INTs across self-processing and sensorimotor regions. These results support the hypothesis that schizophrenia involves a fundamental disruption in the temporal integration of neural signals, contributing to the core self-disturbance observed in the disorder.</p>","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"50 1","pages":"E57-E66"},"PeriodicalIF":4.1,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143030254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Polygenic risk for depression and resting-state functional connectivity of subgenual anterior cingulate cortex in young adults.","authors":"Yu Chen, Huey-Ting Li, Xingguang Luo, Guangfei Li, Jaime S Ide, Chiang-Shan R Li","doi":"10.1503/jpn.240087","DOIUrl":"10.1503/jpn.240087","url":null,"abstract":"<p><strong>Background: </strong>Genetic variants may confer risk for depression by modulating brain structure and function; evidence has underscored the key role of the subgenual anterior cingulate cortex (sgACC) in depression. We sought to examine how the resting-state functional connectivity (rsFC) of the sgACC was associated with polygenic risk for depression in a subclinical population.</p><p><strong>Methods: </strong>Following published protocols, we computed seed-based whole-brain sgACC rsFC and calculated polygenic risk scores (PRS) using data from healthy young adults from the Human Connectome Project. We performed whole-brain regression against PRS and severity of depression symptoms in a single model for all participants and by sex, controlling for age, sex, race or ethnicity, alcohol use severity, and household income. We evaluated the results at a corrected threshold.</p><p><strong>Results: </strong>We included data for 717 healthy young adults. We found lower rsFC between the sgACC and the default mode network and frontal regions in association with PRS and lower sgACC-cerebellar rsFC in association with depression severity. We also noted differences by sex in the connectivity correlates of PRS and depression severity. In an additional set of analyses, we observed a significant correlation between PRS and somatic complaints, as well as altered sgACC-somatosensory cortical connectivity in association with the severity of somatic complaints.</p><p><strong>Limitations: </strong>The current findings should be considered specific to subclinical depression and may not generalize to patients with depressive disorders.</p><p><strong>Conclusion: </strong>Our findings highlight the pivotal role of distinct sgACC-based networks in the genetic predisposition for depression and the manifestation of depression among young adults with subclinical depression. Distinguishing the risk from severity markers of depression may have implications in developing early and effective treatments for people at risk for depression.</p>","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"50 1","pages":"E31-E44"},"PeriodicalIF":4.1,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11737878/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142985254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Functional connectivity gradients and neurotransmitter maps among patients with mild cognitive impairment and depression symptoms.","authors":"Xiaozheng Liu, Xiaojun Chen, Jinming Cheng, Fuquan Wei, Hongtao Hou, Jiapeng Li, Kun Liu, Zhongwei Guo, Zhihan Yan, Aiqin Wu","doi":"10.1503/jpn.240111","DOIUrl":"10.1503/jpn.240111","url":null,"abstract":"<p><strong>Background: </strong>Both depressive symptoms and neurotransmitter changes affect the characteristics of functional brain networks in clinical patients. We sought to explore how brain functional grading is organized among patients with mild cognitive impairment and depressive symptoms (D-MCI) and whether changes in brain organization are related to neurotransmitter distribution.</p><p><strong>Methods: </strong>Using 3 T magnetic resonance imaging (MRI) we acquired functional MRI (fMRI) data from patients with D-MCI, patients with mild cognitive impairment without depression (nD-MCI), and healthy controls. We used resting-state fMRI and diffusion embedding to examine the pattern of functional connectivity gradients. We used analysis of covariance and post hoc <i>t</i> tests to compare the difference in functional connectivity gradients among the 3 groups. We examined the correlation between variations in functional connectivity gradients and neurotransmitter maps using the JuSpace toolbox.</p><p><strong>Results: </strong>We included 105 participants, including 31 patients with D-MCI, 40 patients with nD-MCI, and 34 healthy controls. Compared with healthy controls, both the nD-MCI and D-MCI groups showed abnormalities in the principal unimodal-transmodal gradient pattern. Compared with controls, the D-MCI group showed an increased secondary gradient in the default mode network. Differences in the functional connectivity gradients between the D-MCI and nD-MCI groups were significantly correlated with the distribution of 5-hydroxytryptamine receptor subtype 1A.</p><p><strong>Limitations: </strong>The small sample size affects the generalizability of the results, and the neurotransmitter template is based on healthy participants, not patients.</p><p><strong>Conclusion: </strong>Our results suggest that depressive symptoms cause abnormalities in the hierarchical segregation of functional brain organization among patients with MCI. Such abnormal changes may be related to the distribution of neurotransmitters.</p>","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"50 1","pages":"E11-E20"},"PeriodicalIF":4.1,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11684923/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142928582","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Correlation between polygenic risk scores of depression and cortical morphology networks.","authors":"Qian Gong, Wei Wang, Zhaowen Nie, Simeng Ma, Enqi Zhou, Zipeng Deng, Xin-Hui Xie, Honggang Lyu, Mian-Mian Chen, Lijun Kang, Zhongchun Liu","doi":"10.1503/jpn.240140","DOIUrl":"10.1503/jpn.240140","url":null,"abstract":"<p><strong>Background: </strong>Cortical morphometry is an intermediate phenotype that is closely related to the genetics and onset of major depressive disorder (MDD), and cortical morphometric networks are considered more relevant to disease mechanisms than brain regions. We sought to investigate changes in cortical morphometric networks in MDD and their relationship with genetic risk in healthy controls.</p><p><strong>Methods: </strong>We recruited healthy controls and patients with MDD of Han Chinese descent. Participants underwent DNA extraction and magnetic resonance imaging, including <i>T</i> ₁-weighted and diffusion tensor imaging. We calculated polygenic risk scores (PRS) based on previous summary statistics from a genome-wide association study of the Chinese Han population. We used a novel method based on Kullback-Leibler divergence to construct the morphometric inverse divergence (MIND) network, and we included the classic morphometric similarity network (MSN) as a complementary approach. Considering the relationship between cortical and white matter networks, we also constructed a streamlined density network. We conducted group comparison and PRS correlation analyses at both the regional and network level.</p><p><strong>Results: </strong>We included 130 healthy controls and 195 patients with MDD. The results indicated enhanced connectivity in the MIND network among patients with MDD and people with high genetic risk, particularly in the somatomotor (SMN) and default mode networks (DMN). We did not observe significant findings in the MSN. The white matter network showed disruption among people with high genetic risk, also primarily in the SMN and DMN. The MIND network outperformed the MSN network in distinguishing MDD status.</p><p><strong>Limitations: </strong>Our study was cross-sectional and could not explore the causal relationships between cortical morphological changes, white matter connectivity, and disease states. Some patients had received antidepressant treatment, which may have influenced brain morphology and white matter network structure.</p><p><strong>Conclusion: </strong>The genetic mechanisms of depression may be related to white matter disintegration, which could also be associated with decoupling of the SMN and DMN. These findings provide new insights into the genetic mechanisms and potential biomarkers of MDD.</p>","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"50 1","pages":"E21-E30"},"PeriodicalIF":4.1,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11684925/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142928573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Network pharmacology and molecular docking to explore mechanisms of clozapine-induced cardiac arrest.","authors":"Ximing Chen, Chuanjun Zhuo, Lei Yang, Qiuyu Zhang, Li Chao","doi":"10.1503/jpn.240065","DOIUrl":"10.1503/jpn.240065","url":null,"abstract":"<p><strong>Background: </strong>Clozapine is superior to all other antipsychotics in treating schizophrenia in terms of its curative efficacy; however, this drug is prescribed only as a last resort in the treatment of schizophrenia, given its potential to induce cardiac arrest. The mechanism of clozapine-induced cardiac arrest remains unclear, so we aimed to elucidate the potential mechanisms of clozapine-induced cardiac arrest using network pharmacology and molecular docking.</p><p><strong>Methods: </strong>We identified and analyzed the overlap between potential cardiac arrest-related target genes and clozapine target genes. We conducted Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. We then constructed a protein-protein interaction (PPI) network and screened the core targets. We used molecular docking to evaluate the binding energy between clozapine and core targets.</p><p><strong>Results: </strong>We identified a total of 2405 target genes related to cardiac arrest and 107 target genes for clozapine. Among these, we found 41 overlapping target genes. The main enriched GO biological processes included the upregulation of the mitogen-activated protein kinase (MAPK) cascade and the adenylate cyclase-activating adrenergic receptor signalling pathway. The KEGG enrichment analysis showed that the neuroactive ligand-receptor interaction and the forkhead box O (FoxO) signalling pathway seemed to be the key signalling pathways involved in clozapine-induced cardiac arrest. The 7 core targets identified in the established PPI network were G-protein-coupled receptor kinase 2, 5-hydroxytryptamine 2A receptor, dopamine D2 receptor, glycogen synthase kinase 3β, cyclin-dependent kinase 2, CREB-binding protein, and signal transducer and activator of transcription 3. The molecular docking results indicated a high affinity between clozapine and all of these core targets.</p><p><strong>Limitations: </strong>The relatively small scope of the predictive and modelling methods, which predominantly comprised network pharmacology and molecular docking strategies, is a limitation of this study.</p><p><strong>Conclusion: </strong>Network pharmacology and molecular docking approaches unveiled target genes for clozapine and potential mechanisms by which it may cause cardiac arrest, including the MAPK cascade, neuroactive ligand-receptor interactions, and the FoxO signalling pathway.</p>","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"50 1","pages":"E1-E10"},"PeriodicalIF":4.1,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11684924/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142928589","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Neuroscience education for people living with addiction.","authors":"Stephanie L Borgland","doi":"10.1503/jpn.240153","DOIUrl":"10.1503/jpn.240153","url":null,"abstract":"","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"49 6","pages":"E440-E443"},"PeriodicalIF":4.1,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11665812/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142847441","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Effective connectivity of default mode network subsystems and automatic smoking behaviour among males.","authors":"Mengzhe Zhang, Jinghan Dang, Jieping Sun, Qiuying Tao, Xiaoyu Niu, Weijian Wang, Shaoqiang Han, Jingliang Cheng, Yong Zhang","doi":"10.1503/jpn.240058","DOIUrl":"10.1503/jpn.240058","url":null,"abstract":"<p><strong>Background: </strong>The default mode network (DMN) is not a single system, but rather is composed of smaller and distinct functional subsystems that interact with each other. The functional relevance of these subsystems in tobacco use disorder (TUD) and the neurobiological features associated with smoking motivation are still unclear; thus, we sought to assess causal or direct connectivity alterations within 3 subsystems of the DMN among people with TUD.</p><p><strong>Methods: </strong>We recruited male smokers and nonsmokers. We conducted resting-state functional magnetic resonance imaging (rs-fMRI) and collected ratings on smoking-related clinical scales. We applied dynamic causal modelling (DCM) to rs-fMRI to characterize changes of effective connectivity in TUD from 3 DMN subsystems, including the midline core network (i.e., the posterior cingulate cortex and the anterior medial prefrontal cortex [PCC-aMPFC] core DMN), the medial temporal subsystem (MTL-DMN), and the dorsal medial prefrontal cortex subsystem (dMPFC-DMN). We used leave-one-out cross-validation to investigate whether the neural response could predict smoking reasons, evaluated using the Russell Reason for Smoking Questionnaire).</p><p><strong>Results: </strong>We recruited 88 smokers and 54 nonsmokers. Among people with TUD, the parahippocampal cortex (PHC) region showed enhanced self-connection, which was associated with the severity of TUD after nighttime withdrawal. Compared with nonsmokers, people with TUD displayed significant increased effective connectivity within the dMPFC-DMN, and decreased effective connectivity from the dMPFC-DMN to the PCC-aMPFC core DMN. Moreover, decreased effective connectivity from the lateral temporal cortex to the dMPFC could predict the smoking reason related to automatic behaviour.</p><p><strong>Limitations: </strong>Although we found aberrance in causal connections in DMN subsystems among people with TUD, our cross-sectional study could not be used to investigate changes in effective connectivity over time and their relationship with clinical features.</p><p><strong>Conclusion: </strong>This study emphasized the aberrant causal connections of different functional subsystems of the DMN in TUD and revealed the neural correlates of automatic smoking behaviours. These findings suggested DMN subsystem-derived indicators could be a potential biomarker for TUD and could be used to identify the heterogeneity in motivation for smoking behaviour.</p>","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"49 6","pages":"E429-E439"},"PeriodicalIF":4.1,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11665814/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142848331","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The amino acid metabolism pathway of peripheral T lymphocytes and ketamine-induced schizophrenia-like phenotype.","authors":"Peipei Wang, Linzhi Jiang, Junmei Hu, Zihan Jiang, Yu Zhang, Congliang Chen, Yanchen Lin, Mi Su, Xia Wang, Linchuan Liao","doi":"10.1503/jpn-240038","DOIUrl":"10.1503/jpn-240038","url":null,"abstract":"<p><strong>Background: </strong>The intricate interplay between peripheral adaptive immune cells and the central nervous system (CNS) has garnered increasing recognition. Given that alterations in cell quantities often translate into modifications in metabolite profiles and that these metabolic changes can potentially traverse the bloodstream and enter the CNS, thereby modulating the progression of mental illnesses, we sought to explore the metabolic profiles of peripheral immune cells in a ketamine-treated mouse model of schizophrenia.</p><p><strong>Methods: </strong>We used flow cytometry to scrutinize the alterations in peripheral adaptive immune cells in a ketamine-induced schizophrenia mouse model. Subsequently, we implemented an untargeted metabolomic approach with ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) to detect the metabolite profiles of peripheral abnormal lymphocytes and identify differential metabolites present in plasma. We then employed targeted metabolomics using UPLC-MS/MS to quantify the common differential metabolites detected in mouse plasma.</p><p><strong>Results: </strong>Flow cytometry analysis detected a notable increase in the count of peripheral CD3⁺ T cells in a ketamine-induced schizophrenia mouse model. Subsequent untargeted metabolomics analysis revealed that the amino acid metabolism pathway underwent substantial alterations. A detailed quantification of 22 amino acid profiles in the peripheral plasma indicated significant elevation in the levels of glycine, alanine, asparagine, and aspartic acid.</p><p><strong>Limitations: </strong>Our ongoing research has yet to conclusively identify the precise amino acid metabolism pathway that serves as the pivotal factor in the manifestation of the schizophrenia-like phenotype induced by ketamine.</p><p><strong>Conclusion: </strong>The peripheral amino acid metabolism pathway is involved in the ketamine-induced schizophrenia-like phenotype. The metabolic profile of peripheral immune cells could provide accurate biomarkers for the diagnosis and treatment of psychiatric diseases.</p>","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"49 6","pages":"E413-E426"},"PeriodicalIF":4.1,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633891/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142774291","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Canadian College of Neuropsychopharmacology 2024 award winners.","authors":"","doi":"10.1503/jpn-240152","DOIUrl":"https://doi.org/10.1503/jpn-240152","url":null,"abstract":"","PeriodicalId":50073,"journal":{"name":"Journal of Psychiatry & Neuroscience","volume":"49 6","pages":"E427-E428"},"PeriodicalIF":4.1,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142774286","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}