Your browser doesn't support javascript.
loading
Distinctive alterations in the mesocorticolimbic circuits in various psychiatric disorders.
Nakamura, Yuko; Ishida, Takuya; Tanaka, Saori C; Mitsuyama, Yuki; Yokoyama, Satoshi; Shinzato, Hotaka; Itai, Eri; Okada, Go; Kobayashi, Yuko; Kawashima, Takahiko; Miyata, Jun; Yoshihara, Yujiro; Takahashi, Hidehiko; Aoki, Ryuta; Nakamura, Motoaki; Ota, Haruhisa; Itahashi, Takashi; Morita, Susumu; Kawakami, Shintaro; Abe, Osamu; Okada, Naohiro; Kunimatsu, Akira; Yamashita, Ayumu; Yamashita, Okito; Imamizu, Hiroshi; Morimoto, Jun; Okamoto, Yasumasa; Murai, Toshiya; Hashimoto, Ryu-Ichiro; Kasai, Kiyoto; Kawato, Mitsuo; Koike, Shinsuke.
Affiliation
  • Nakamura Y; Center for Evolutionary Cognitive Sciences, Graduate School of Art and Sciences, University of Tokyo, Tokyo, Japan.
  • Ishida T; University of Tokyo Institute for Diversity & Adaptation of Human Mind (UTIDAHM), Tokyo, Japan.
  • Tanaka SC; Center for Evolutionary Cognitive Sciences, Graduate School of Art and Sciences, University of Tokyo, Tokyo, Japan.
  • Mitsuyama Y; Department of Neuropsychiatry, Graduate School of Wakayama Medical University, Wakayama, Japan.
  • Yokoyama S; Brain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
  • Shinzato H; Information Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, Nara, Japan.
  • Itai E; Department of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.
  • Okada G; Department of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.
  • Kobayashi Y; Department of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.
  • Kawashima T; Department of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.
  • Miyata J; Department of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.
  • Yoshihara Y; Department of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Takahashi H; Department of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Aoki R; Department of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Nakamura M; Department of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Ota H; Department of Psychiatry and Behavioral Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Itahashi T; Medical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
  • Morita S; Medical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
  • Kawakami S; Medical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
  • Abe O; Medical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
  • Okada N; Department of Neuropsychiatry, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
  • Kunimatsu A; Department of Neuropsychiatry, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
  • Yamashita A; Department of Radiology, Graduate School of Medicine, the University of Tokyo, Tokyo, Japan.
  • Yamashita O; The International Research Center for Neurointelligence (WPI-IRCN), Institutes for Advanced Study (UTIAS), University of Tokyo, Tokyo, Japan.
  • Imamizu H; Department of Radiology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
  • Morimoto J; Brain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
  • Okamoto Y; Department of Psychiatry, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Murai T; Brain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
  • Hashimoto RI; Center for Advanced Intelligence Project, RIKEN, Tokyo, Japan.
  • Kasai K; Brain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
  • Kawato M; Department of Psychology, Graduate School of Humanities and Sociology, the University of Tokyo, Tokyo, Japan.
  • Koike S; Brain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
Psychiatry Clin Neurosci ; 77(6): 345-354, 2023 Jun.
Article in En | MEDLINE | ID: mdl-36905180
AIM: Increasing evidence suggests that psychiatric disorders are linked to alterations in the mesocorticolimbic dopamine-related circuits. However, the common and disease-specific alterations remain to be examined in schizophrenia (SCZ), major depressive disorder (MDD), and autism spectrum disorder (ASD). Thus, this study aimed to examine common and disease-specific features related to mesocorticolimbic circuits. METHODS: This study included 555 participants from four institutes with five scanners: 140 individuals with SCZ (45.0% female), 127 individuals with MDD (44.9%), 119 individuals with ASD (15.1%), and 169 healthy controls (HC) (34.9%). All participants underwent resting-state functional magnetic resonance imaging. A parametric empirical Bayes approach was adopted to compare estimated effective connectivity among groups. Intrinsic effective connectivity focusing on the mesocorticolimbic dopamine-related circuits including the ventral tegmental area (VTA), shell and core parts of the nucleus accumbens (NAc), and medial prefrontal cortex (mPFC) were examined using a dynamic causal modeling analysis across these psychiatric disorders. RESULTS: The excitatory shell-to-core connectivity was greater in all patients than in the HC group. The inhibitory shell-to-VTA and shell-to-mPFC connectivities were greater in the ASD group than in the HC, MDD, and SCZ groups. Furthermore, the VTA-to-core and VTA-to-shell connectivities were excitatory in the ASD group, while those connections were inhibitory in the HC, MDD, and SCZ groups. CONCLUSION: Impaired signaling in the mesocorticolimbic dopamine-related circuits could be an underlying neuropathogenesis of various psychiatric disorders. These findings will improve the understanding of unique neural alternations of each disorder and will facilitate identification of effective therapeutic targets.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Depressive Disorder, Major / Autism Spectrum Disorder / Mental Disorders Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Psychiatry Clin Neurosci Journal subject: NEUROLOGIA / PSIQUIATRIA Year: 2023 Document type: Article Affiliation country: Japan Country of publication: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Depressive Disorder, Major / Autism Spectrum Disorder / Mental Disorders Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Psychiatry Clin Neurosci Journal subject: NEUROLOGIA / PSIQUIATRIA Year: 2023 Document type: Article Affiliation country: Japan Country of publication: Australia