Evidence map›Paper›PMID 41108393›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Aberrant type 2 dopamine and mu-opioid receptor availability in autism spectrum disorder.

Tuomo Noppari, Jouni Tuisku, Lasse Lukkarinen, Pekka Tani, Nina Lindberg, Emma Saure, Hannu Lauerma, Jari Tiihonen, Jussi Hirvonen, Semi Helin and 3 more

Abstract read
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Subcortical dopamine DEuropean journal of nuclear medicine and molecular imaging · 2026
    Article
  2. 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

13 authors.

Tuomo NoppariTurku PET Centre, University of Turku, Turku, Finland. tuomo.noppari@hus.fi.ORCID 0009-0002-1757-082X
Jouni TuiskuTurku PET Centre, University of Turku, Turku, Finland.
Lasse LukkarinenTurku PET Centre, University of Turku, Turku, Finland.
Pekka TaniDepartment of Psychiatry, Helsinki University Hospital, Helsinki, Finland.
Nina LindbergDepartment of Forensic Psychiatry, Helsinki University Hospital, Helsinki, Finland.
Emma SaureClinicum, Department of Public Health, University of Helsinki, Helsinki, Finland.
Hannu LauermaPsychiatric Hospital for Prisoners, Health Care Services for Prisoners, Turku, Finland.
Jari TiihonenDepartment of Clinical Neuroscience, Karolinska Institute and Center for Psychiatry Research, Stockholm, Sweden.
Jussi HirvonenDepartment of Radiology, Turku University Hospital, Turku, Finland.
Semi HelinRadiopharmaceutical Chemistry Laboratory, Turku PET Centre, University of Turku, Turku, Finland.
Johan RajanderAcceletor Laboratory, Turku PET Centre, Åbo Akademi University, Turku, Finland.
Juha SalmiUnit of Psychology, Faculty of Education and Psychology, University of Oulu, Oulu, Finland.
Lauri NummenmaaTurku PET Centre, University of Turku, Turku, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOpioid and dopamine receptor systems are implicated in the pathoetiology of autism, but in vivo human brain imaging evidence for their role remains elusive.

methodsHere, we investigated regional type 2 dopamine and mu-opioid receptor (D2R and MOR, respectively) availabilities and regional interactions between the two neuromodulatory systems associated with autism spectrum disorder (ASD). In vivo positron emission tomography (PET) with radioligands [11 C]raclopride (D2R) and [11 C]carfentanil (MOR) was carried out in 16 adult males with high functioning ASD and 24 age and sex matched controls. A whole brain voxel-wise analysis was tested with Student´s t-test and regional group differences in D2R and MOR receptor availabilities as total and separate were tested with linear mixed models also examining the associations between regional receptor availabilities with correlations.

resultsThere were no group differences in whole-brain voxel-wise analysis of D2R, but ROI analysis revealed a lower overall mean availability in striatum of the ASD compared to controls. Post hoc regional analysis revealed reduced D2R availability in nucleus accumbens and globus pallidus of the ASD group. The whole-brain voxel-wise analysis of MOR revealed cuneal/precuneal up-regulation in the ASD group, but there was no overall group difference in the ROI analysis for MOR. MOR down-regulation was observed in the hippocampi of the ASD group in a post hoc analysis. Regional correlations between D2R and MOR availabilities were weaker in the ASD group versus control group in the amygdala and nucleus accumbens.

conclusionsThese alterations may translate to disrupted modulation of social motivation and reward in ASD.

Indexed as

Autism Spectrum DisorderReceptors, Dopamine D2Receptors, Opioid, muAdultBrainCase-Control StudiesFentanylHumansMalePositron-Emission TomographyRacloprideYoung AdultcarfentanilFentanylRacloprideReceptors, Dopamine D2Receptors, Opioid, muAutismD2RDopamineMOROpioidPositron emission tomography

Identifiers

PMID41108393
PMCPMC12860854

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Registered trials

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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.