Evidence map›Paper›PMID 32024554›Full record

ArticleMolecular autism2020

Serotonergic innervation of the amygdala is increased in autism spectrum disorder and decreased in Williams syndrome.

C H Lew, K M Groeniger, K L Hanson, D Cuevas, D M Z Greiner, B Hrvoj-Mihic, U Bellugi, C M Schumann, K Semendeferi

Open access · goldAbstract read
In one paragraph

Article in Molecular autism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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  8. Increasing Central Serotonin with 5-hydroxytryptophan Disrupts the Inhibition of Social Gaze in Nonhuman Primates.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
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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

9 authors at 3 institutions in 1 country.

C H LewDepartment of Anthropology, University of California, San Diego, USA.
K M GroenigerDepartment of Anthropology, University of California, San Diego, USA.
K L HansonDepartment of Anthropology, University of California, San Diego, USA.
D CuevasDepartment of Biological Sciences, University of California, San Diego, USA.
D M Z GreinerDepartment of Biological Sciences, University of California, San Diego, USA.
B Hrvoj-MihicDepartment of Anthropology, University of California, San Diego, USA.
U BellugiSalk Institute for Biological Sciences, San Diego, USA.
C M SchumannDepartment of Psychiatry and Behavioral Sciences, University of California, Davis School of Medicine, the MIND Institute, Sacramento, USA.
K SemendeferiDepartment of Anthropology, University of California, San Diego, USA. ksemende@ucsd.edu.ORCID 0000-0002-9867-9554
University of California San Diego · USSalk Institute for Biological Studies · USUniversity of California, Davis · US

Funding

TRAINING PROGRAM IN COGNITIVE NEUROSCIENCET32MH020002 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SEJNOWSKI, TERRENCE J · 1999 to 2020
$6.1M
Typical and Pathological Cellular Development of the Human AmygdalaR01MH097236 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SCHUMANN, CYNTHIA · 2011 to 2022
$3.9M
A human neurodevelopmental model for Williams syndromeR56MH109587 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MUOTRI, ALYSSON R., SEMENDEFERI, KATERINA · 2016 to 2016
$376k
Dissecting the Social Brain: Amygdala Changes in Williams SyndromeR03MH103697 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SEMENDEFERI, KATERINA · 2014 to 2015
$155k
NIH HHS 5R03MH103697NIH HHS P01 NICHD033113NIH HHS R56MH109587NIMH NIH HHS R01 MH097236NIMH NIH HHS R03 MH103697NIMH NIH HHS R56 MH109587NIMH NIH HHS T32 MH020002
6 · The paper itself

Abstract

backgroundWilliams syndrome (WS) and autism spectrum disorder (ASD) are neurodevelopmental disorders that demonstrate overlapping genetic associations, dichotomous sociobehavioral phenotypes, and dichotomous pathological differences in neuronal distribution in key social brain areas, including the prefrontal cortex and the amygdala. The serotonergic system is critical to many processes underlying neurodevelopment and is additionally an important neuromodulator associated with behavioral variation. The amygdala is heavily innervated by serotonergic projections, suggesting that the serotonergic system is a significant mediator of neuronal activity. Disruptions to the serotonergic system, and atypical structure and function of the amygdala, are implicated in both WS and ASD.

methodsWe quantified the serotonergic axon density in the four major subdivisions of the amygdala in the postmortem brains of individuals diagnosed with ASD and WS and neurotypical (NT) brains.

resultsWe found opposing directions of change in serotonergic innervation in the two disorders, with ASD displaying an increase in serotonergic axons compared to NT and WS displaying a decrease. Significant differences (p < 0.05) were observed between WS and ASD data sets across multiple amygdala nuclei. LIMITATIONS: This study is limited by the availability of human postmortem tissue. Small sample size is an unavoidable limitation of most postmortem human brain research and particularly postmortem research in rare disorders.

conclusionsDifferential alterations to serotonergic innervation of the amygdala may contribute to differences in sociobehavioral phenotype in WS and ASD. These findings will inform future work identifying targets for future therapeutics in these and other disorders characterized by atypical social behavior.

Indexed as

SerotoninAdolescentAdultAgedAmygdalaAutism Spectrum DisorderAxonsFemaleHumansInfantMaleMiddle AgedWilliams SyndromeYoung AdultSerotonin

Identifiers

PMID32024554
PMCPMC7003328
OpenAlexW3008741569

What OpenQuestion holds

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LicenceCC BY
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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.