PM461. Inflammation in schizophrenia: Imaging genetics
نویسندگان
چکیده
s | 67 PM459 Brain Network Characteristics of Individuals at Clinical High Risk for Psychosis in between Normality and Psychosis: A Combined Structural and Functional Imaging Study Soo-Hee Choi, Jun Soo Kwon Seoul National University, Republic of Korea Abstract Objective: In an effort to improve early recognition and intervention in patients with schizophrenia (SZ), individuals at clinical high risk for psychosis (CHR) have been the focus of clinical attention. To distinguish the prodrome of psychosis from transient disturbance of mental state in youth, the authors classified broad spectrum of CHR state into two subgroups according to neurobiological characteristics using the structural and functional network constructs. Method: Structural diffusion tensor imaging and resting-state functional magnetic resonance imaging were scanned in 61healthy controls (HC), 57 individuals at CHR and 29 patients with SZ. The main outcome was a likelihood ratio using measures of structural and functional network efficiencies, coupling strength of the structural and functional networks, disease-specific data analysis using the both network constructs to obtain the most probable classification of CHR into HC or SZ. Results: Likelihood ratios revealed that 33 individuals at CHR were likely close to HC (CHR-HC) and the rest of 24 CHRs were close to SZ (CHR-SZ). CHR subgroups were comparable to each other in demographic characteristics and clinical symptoms. However, verbal functions of CHRCON were akin to CON and those of CHRSZ were akin to SZ. Additionally, CHR-SZ had lower verbal intelligence than CHR-HC. Conclusions: Our findings provide novel neurobiological evidence that heterogeneous CHR population can be divided into subgroups, one of which is more likely to be prone to psychosis. Using a combination of structural and functional data, we could detect vulnerable population and provide an active intervention in early phase of CHR state.Objective: In an effort to improve early recognition and intervention in patients with schizophrenia (SZ), individuals at clinical high risk for psychosis (CHR) have been the focus of clinical attention. To distinguish the prodrome of psychosis from transient disturbance of mental state in youth, the authors classified broad spectrum of CHR state into two subgroups according to neurobiological characteristics using the structural and functional network constructs. Method: Structural diffusion tensor imaging and resting-state functional magnetic resonance imaging were scanned in 61healthy controls (HC), 57 individuals at CHR and 29 patients with SZ. The main outcome was a likelihood ratio using measures of structural and functional network efficiencies, coupling strength of the structural and functional networks, disease-specific data analysis using the both network constructs to obtain the most probable classification of CHR into HC or SZ. Results: Likelihood ratios revealed that 33 individuals at CHR were likely close to HC (CHR-HC) and the rest of 24 CHRs were close to SZ (CHR-SZ). CHR subgroups were comparable to each other in demographic characteristics and clinical symptoms. However, verbal functions of CHRCON were akin to CON and those of CHRSZ were akin to SZ. Additionally, CHR-SZ had lower verbal intelligence than CHR-HC. Conclusions: Our findings provide novel neurobiological evidence that heterogeneous CHR population can be divided into subgroups, one of which is more likely to be prone to psychosis. Using a combination of structural and functional data, we could detect vulnerable population and provide an active intervention in early phase of CHR state. PM460 Association between increased resting-state functional connectivity and reduced symptoms of schizotypal personality disorder: neural evidence for compensatory brain responses Ji-Won Hur1,2, Kang Ik Kevin Cho1, Wi Hoon Jung3, Tae Young Lee4, Sung Nyun Kim5, Jun Soo Kwon1,5* 1 Department of Brain and Cognitive Sciences, College of Natural Sciences, Seoul National University, Seoul, Republic of Korea 2 Department of Psychology, College of Social Sciences, Chung-Ang University, Seoul, Republic of Korea 3 Department of Psychology, University of Pennsylvania, Pennsylvania, United States 4 Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea 5 Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea Abstract Objective: Schizotypal personality disorder (SPD) shares genetic susceptibilities and clinical features with schizophrenia. Despite growing interest for resting functional connectivity networks of schizophrenia, little is known to date about resting–connectivity networks of, and their contributions to the SPD. The current study aimed to examine the resting-state default mode network (DMN) functional connectivity in individuals with SPD. Method: Twenty-five individuals with SPD and 38 normal controls underwent resting-state functional magnetic resonance imaging. We compared group differences for resing-state connectivity and then explored the links between altered connectivity and clinical symptoms in SPD subjects. Results: As a result, both ROI-to-ROI and seed based analysis revealed that during resting state, the SPD group demonstrated increased connectivity from the left middle frontal gyrus to the posterior cingulate cortex compared to the normal controls. In addition, connectivity between the left parahippocampal gyrus and left middle frontal gyrus (ROIs analysis), as well as between the bilateral anterior cingulate cortex and posterior cingulate cortex (whole brain analysis), were also identified. In particular, enhanced middle frontal connectivity was negatively correlated with ideas of references and unusual perceptual experiences of SPD subjects. Conclusions: The current study suggests the first neural evidence of an enhanced functional network with middle frontal regions across the resting–state network in SPD, compared to that of controls. Furthermore, these alterations may possibly take role in compensating for their clinical symptoms including thought disorder and perceptual aberrations in SPD. Our imaging evidence may provide insight on the neurocompensatory responses observed in schizophrenia spectrums.
منابع مشابه
Association study between schizophrenia and the DISC1 gene polymorphism
Abstract Background: The disrupted-in-schizophrenia 1 (DISC1) gene, on the chromosome position 1q42, was initially identified at the breakpoint of a balanced translocation, t(1,11)(q42.1q14.3), which segregated with major mental disorders in a large Scottish family. Methods: Our samples included 200 unrelated patients diagnosed with Schizophrenia on the basis of DSM-IV criteria an...
متن کاملCombined effect of polymorphic sites in the DTNBP1 and GRIN1 genes on schizophrenia
Abstract Background: Schizophrenia is a severe mental disorder and numerous genes and loci are beleived to be involved in this disease. Recent studies have reported a strong genetic association between DTNBP1 (dystrobrevin-binding protein 1) gene variants and schizophrenia. Methods: In this research, we used a case-control study to establish the possible association between the P1635 ...
متن کاملAssociation study of single nucleotide polymorphism rs165599 of COMT gene, with schizophrenia and bipolar mood disorder in the south-west of Iran
Linkage studies and epidemiological findings indicate that some possible genes in schizophrenia (SCZ) and bipolar mood disorder (BPD) are common. Numerous evidences for linkage of two diseases on chromosome 22 have been found. These findings suggest that one or more genes in the 22q11.21 region may be involved in the development of both disorders. In the present case-control study, association ...
متن کاملAdditive effect of MTHFR and GRIN1 genetic polymorphisms on the risk of schizophrenia
Schizophrenia is a complex disorder with polygenic inheritance. The MTHFR gene (OMIM: 607093) plays an important role in the folate metabolism. It has been suggested that C677T (rs1801133) and A1298C (rs1801131) genetic polymorphisms in the MTHFR gene lead to the decreased activity of the methylenetetrahydrofolate reductase enzyme which may have significant effect on developing schizophrenia. W...
متن کاملStudy of the association between DRD2 Gene Ser311Cys and GSTM1 Gene polymorphism in Schizophrenia
Introduction: Schizophrenia is a mental disorder affecting 1% of the world's population. Two of genes have been recognized to be involved in development of this disease: DRD2 and GSTM1. Methods: This case-control study included 100 patients suffering from schizophrenia who referred to Yazd Neuropsychiatry Hospital. Also, 100 healthy patients without schizophrenia were selected as the control g...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 19 شماره
صفحات -
تاریخ انتشار 2016