Evidence map›Paper›PMID 30556326›Full record

ArticleAutism research : official journal of the International Society for Autism Research2019

PAC1R Genotype to Phenotype Correlations in Autism Spectrum Disorder.

Meredith Goodrich, Anna Chelsea Armour, Karuna Panchapakesan, Xiaozhen You, Joseph Devaney, Susan Knoblach, Catherine A W Sullivan, Maria Jesus Herrero, Abha R Gupta, Chandan J Vaidya and 2 more

Abstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2019. 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
0.5field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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

12 authors at 3 institutions in 1 country.

Meredith GoodrichCenter for Neuroscience Research, Children's Research Institute, Children's National Health System, Washington, DC.ORCID 0000-0003-1897-2433
Anna Chelsea ArmourChildren's Center for Autism Spectrum Disorders, Children's National Health System, Rockville, Maryland.
Karuna PanchapakesanCenter for Genetic Medicine, Children's Research Institute, Children's National Health System, Washington, DC.
Xiaozhen YouDepartment of Psychology, Georgetown University, Washington, DC.
Joseph DevaneyCenter for Genetic Medicine, Children's Research Institute, Children's National Health System, Washington, DC.
Susan KnoblachCenter for Genetic Medicine, Children's Research Institute, Children's National Health System, Washington, DC.
Catherine A W SullivanDepartment of Pediatrics and Child Study Center, Yale School of Medicine, New Haven, Connecticut.
Maria Jesus HerreroCenter for Neuroscience Research, Children's Research Institute, Children's National Health System, Washington, DC.
Abha R GuptaDepartment of Pediatrics and Child Study Center, Yale School of Medicine, New Haven, Connecticut.
Chandan J VaidyaDepartment of Psychology, Georgetown University, Washington, DC.
Lauren KenworthyChildren's Center for Autism Spectrum Disorders, Children's National Health System, Rockville, Maryland.
Joshua G CorbinCenter for Neuroscience Research, Children's Research Institute, Children's National Health System, Washington, DC.
Children's National · USGeorgetown University · USYale University · US

Funding

NEUROIMAGING COREP30HD040677 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2001 to 2015
$15.9M
Development of the Basal Telencephalic Limbic SystemR01DA020140 · NIDA · GEORGETOWN UNIVERSITY · PI CORBIN, JOSHUA G · 2006 to 2020
$7.3M
Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI GIOIA, GERARD A. · 2016 to 2020
$5.9M
Neuroimaging of Top-Down Control and Bottom-Up Processes in Childhood ASDR01MH084961 · NIMH · GEORGETOWN UNIVERSITY · PI VAIDYA, CHANDAN J · 2009 to 2013
$2.1M
Development of an Executive Function-Based Intervention for Autism Spectrum DisorR34MH083053 · NIMH · CHILDREN'S RESEARCH INSTITUTE · PI ANTHONY, LAURA GUTERMUTH, KENWORTHY, LAUREN · 2010 to 2012
$769k
NICHD NIH HHS P30 HD040677NICHD NIH HHS U54 HD090257NIDA NIH HHS R01 DA020140NIMH NIH HHS R01 MH084961NIMH NIH HHS R34 MH083053
6 · The paper itself

Abstract

Amygdala dysfunction has been implicated in numerous neurodevelopmental disorders, including autism spectrum disorder (ASD). Previous studies in mice and humans, respectively, have linked Pac1r/PAC1R function to social behavior and PTSD-susceptibility. Based on this connection to social and emotional processing and the central role played by the amygdala in ASD, we examined a putative role for PAC1R in social deficits in ASD and determined the pattern of gene expression in the developing mouse and human amygdala. We reveal that Pac1r/PAC1R is expressed in both mouse and human amygdala from mid-neurogenesis through early postnatal stages, critical time points when altered brain trajectories are hypothesized to unfold in ASD. We further find that parents of autistic children carrying a previously identified PTSD-risk genotype (CC) report greater reciprocal social deficits compared to those carrying the non-risk GC genotype. Additionally, by exploring resting-state functional connectivity differences in a subsample of the larger behavioral sample, we find higher functional connectivity between the amygdala and right middle temporal gyrus in individuals with the CC risk genotype. Thus, using multimodal approaches, our data reveal that the amygdala-expressed PAC1R gene may be linked to severity of ASD social phenotype and possible alterations in brain connectivity, therefore potentially acting as a modifier of amygdala-related phenotypes. Autism Res 2019, 12: 200-211 © 2018 International Society for Autism Research, Wiley Periodicals, Inc. LAY SUMMARY: In this multimodal study across mouse and human, we examined expression patterns of Pac1r/PAC1R, a gene implicated in social behavior, and further explored whether a previously identified human PTSD-linked mutation in PAC1R can predict brain connectivity and social deficits in ASD. We find that PAC1R is highly expressed in the both the mouse and human amygdala. Furthermore, our human data suggest that PAC1R genotype is linked to severity of social deficits and functional amygdala connectivity in ASD.

Indexed as

GenotypePhenotypeAdolescentAnimalsAutism Spectrum DisorderBrainBrain MappingChildDisease Models, AnimalFemaleHumansMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLReceptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type IADCYAP1R1 protein, humanReceptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type Iamygdalaautismgenetic modifierneuroimagingPAC1R

Identifiers

PMID30556326
PMCPMC6665682
OpenAlexW2904351210

What OpenQuestion holds

Textmetadata
LicenceTDM
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.