Evidence map›Paper›PMID 36905180›Full record

ArticlePsychiatry and clinical neurosciences2023

Distinctive alterations in the mesocorticolimbic circuits in various psychiatric disorders.

Yuko Nakamura, Takuya Ishida, Saori C Tanaka, Yuki Mitsuyama, Satoshi Yokoyama, Hotaka Shinzato, Eri Itai, Go Okada, Yuko Kobayashi, Takahiko Kawashima and 22 more

Open access · hybridAbstract read
In one paragraph

Article in Psychiatry and clinical neurosciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Hallmarks of primary headache: part 3 - cluster headache.The journal of headache and pain · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors at 12 institutions in 2 countries.

Yuko NakamuraCenter for Evolutionary Cognitive Sciences, Graduate School of Art and Sciences, University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7696-8152
Takuya IshidaCenter for Evolutionary Cognitive Sciences, Graduate School of Art and Sciences, University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7152-910X
Saori C TanakaBrain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
Yuki MitsuyamaDepartment of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.
Satoshi YokoyamaDepartment of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-1309-1103
Hotaka ShinzatoDepartment of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-0354-1801
Eri ItaiDepartment of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.
Go OkadaDepartment of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-5451-8513
Yuko KobayashiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takahiko KawashimaDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Jun MiyataDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-1803-1975
Yujiro YoshiharaDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hidehiko TakahashiDepartment of Psychiatry and Behavioral Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Ryuta AokiMedical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
Motoaki NakamuraMedical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
Haruhisa OtaMedical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
Takashi ItahashiMedical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
Susumu MoritaDepartment of Neuropsychiatry, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Shintaro KawakamiDepartment of Neuropsychiatry, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Osamu AbeDepartment of Radiology, Graduate School of Medicine, the University of Tokyo, Tokyo, Japan.
Naohiro OkadaThe International Research Center for Neurointelligence (WPI-IRCN), Institutes for Advanced Study (UTIAS), University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-8338-2758
Akira KunimatsuDepartment of Radiology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Ayumu YamashitaBrain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
Okito YamashitaBrain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
Hiroshi ImamizuBrain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
Jun MorimotoBrain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
Yasumasa OkamotoDepartment of Psychiatry and Neurosciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0001-8813-7551
Toshiya MuraiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Ryu-Ichiro HashimotoMedical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
Kiyoto KasaiCenter for Evolutionary Cognitive Sciences, Graduate School of Art and Sciences, University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4443-4535
Mitsuo KawatoBrain Information Communication Research Laboratory Group, Advanced Telecommunications Research Institutes International (ATR), Kyoto, Japan.
Shinsuke KoikeCenter for Evolutionary Cognitive Sciences, Graduate School of Art and Sciences, University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3375-236X
Hiroshima University · JPKyoto University · JPShowa University · JPMusashino Art University · JPAdvanced Telecommunications Research Institute International · JPThe University of Tokyo · JPBoston University · USMita Hospital · JPRIKEN Center for Advanced Intelligence Project · JPTokyo Medical and Dental University · JPTokyo University of the Arts · JPUniversity of Tokyo Hospital · JP

Funding

AMED JP18dm0307001AMED JP18dm0307004AMED JP18dm0307008AMED JP19dm0207069AMED JP21uk1024002JSPS KAKENHI JP20H03596JSPS KAKENHI JP20H05064JSPS KAKENHI JP20KK0193JSPS KAKENHI JP21H02851JSPS KAKENHI JP21H05171JSPS KAKENHI JP21H05174JSPS KAKENHI JP21H05324JST Moonshot R&D JPMJMS2021Naito FoundationTakeda Science FoundationUniversity of Tokyo
6 · The paper itself

Abstract

aimIncreasing 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.

methodsThis 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.

resultsThe 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.

conclusionImpaired 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.

Indexed as

Autism Spectrum DisorderMajor Depressive DisorderMental DisordersBayes TheoremDopamineFemaleHumansMagnetic Resonance ImagingMaleNeural PathwaysPrefrontal CortexDopamineautism spectrum disorderdynamic causal modelingmajor depressive disordermesocorticolimbic circuitsschizophrenia

Identifiers

PMID36905180
PMCPMC11488596
OpenAlexW4323921241

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.