Evidence map›Paper›PMID 34238350›Full record

ArticleMolecular autism2021

Autism-associated biomarkers: test-retest reliability and relationship to quantitative social trait variation in rhesus monkeys.

Ozge Oztan, Catherine F Talbot, Emanuela Argilli, Alyssa C Maness, Sierra M Simmons, Noreen Mohsin, Laura A Del Rosso, Joseph P Garner, Elliott H Sherr, John P Capitanio and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular autism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Nebulized vasopressin penetrates CSF and improves social cognition without inducing aggression in a rhesus monkey model of autism.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Tales from the life and lab of a female social neuroscientist.Comprehensive psychoneuroendocrinology · 2023
    Review
  6. Article
  7. Article
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  9. 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

11 authors at 4 institutions in 1 country.

Ozge OztanDepartment of Psychiatry and Behavioral Sciences, Stanford University, 1201 Welch Rd., MSLS P-104, Stanford, CA, 94305, USA.
Catherine F TalbotCalifornia National Primate Research Center, 1 Shields Ave., Davis, CA, 95616, USA.
Emanuela ArgilliDepartment of Neurology, University of California, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
Alyssa C ManessCalifornia National Primate Research Center, 1 Shields Ave., Davis, CA, 95616, USA.
Sierra M SimmonsCalifornia National Primate Research Center, 1 Shields Ave., Davis, CA, 95616, USA.
Noreen MohsinDepartment of Psychiatry and Behavioral Sciences, Stanford University, 1201 Welch Rd., MSLS P-104, Stanford, CA, 94305, USA.
Laura A Del RossoCalifornia National Primate Research Center, 1 Shields Ave., Davis, CA, 95616, USA.
Joseph P GarnerDepartment of Psychiatry and Behavioral Sciences, Stanford University, 1201 Welch Rd., MSLS P-104, Stanford, CA, 94305, USA.
Elliott H SherrDepartment of Neurology, University of California, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
John P CapitanioCalifornia National Primate Research Center, 1 Shields Ave., Davis, CA, 95616, USA.
Karen J ParkerDepartment of Psychiatry and Behavioral Sciences, Stanford University, 1201 Welch Rd., MSLS P-104, Stanford, CA, 94305, USA. kjparker@stanford.edu.ORCID 0000-0002-6836-6338
Stanford University · USUniversity of California, San Francisco · USStanford Medicine · USUniversity of California, Davis · US

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
De novo copy number variation and gene discovery in human brain malformationsR01NS058721 · NINDS · UNIVERSITY OF CHICAGO · PI ARGILLI, EMANUELA · 2008 to 2025
$10.9M
A monkey model of naturally occurring social impairmentsR01HD087048 · NICHD · STANFORD UNIVERSITY · PI PARKER, KAREN J. · 2016 to 2020
$3.1M
NICHD NIH HHS R01 HD087048NIH HHS P51 OD011107NINDS NIH HHS R01 NS058721
6 · The paper itself

Abstract

backgroundRhesus monkeys (Macaca mulatta) exhibit pronounced individual differences in social traits as measured by the macaque Social Responsiveness Scale-Revised. The macaque Social Responsiveness Scale was previously adapted from the Social Responsiveness Scale, an instrument designed to assess social and autistic trait variation in humans. To better understand potential biological underpinnings of this behavioral variation, we evaluated the trait-like consistency of several biological measures previously implicated in autism (e.g., arginine vasopressin, oxytocin, and their receptors, as well as ERK1/2, PTEN, and AKT(1-3) from the RAS-MAPK and PI3K-AKT pathways). We also tested which biological measures predicted macaque Social Responsiveness Scale-Revised scores.

methodsCerebrospinal fluid and blood samples were collected from N = 76 male monkeys, which, as a sample, showed a continuous distribution on the macaque Social Responsiveness Scale-Revised. In a subset of these subjects (n = 43), samples were collected thrice over a 10-month period. The following statistical tests were used: "Case 2A" intra-class correlation coefficients of consistency, principal component analysis, and general linear modeling.

resultsAll biological measures (except AKT) showed significant test-retest reliability within individuals across time points. We next performed principal component analysis on data from monkeys with complete biological measurement sets at the first time point (n = 57), to explore potential correlations between the reliable biological measures and their relationship to macaque Social Responsiveness Scale-Revised score; a three-component solution was found. Follow-up analyses revealed that cerebrospinal fluid arginine vasopressin concentration, but no other biological measure, robustly predicted individual differences in macaque Social Responsiveness Scale-Revised scores, such that monkeys with the lowest cerebrospinal fluid arginine vasopressin concentration exhibited the greatest social impairment. Finally, we confirmed that this result held in the larger study sample (in which cerebrospinal fluid arginine vasopressin values were available from n = 75 of the subjects).

conclusionsThese findings indicate that cerebrospinal fluid arginine vasopressin concentration is a stable trait-like measure and that it is linked to quantitative social trait variation in male rhesus monkeys.

Indexed as

Autistic DisorderAnimalsBiomarkersHumansMacaca mulattaMalePhosphatidylinositol 3-KinasesReproducibility of ResultsSocial BehaviorSociological FactorsBiomarkersPhosphatidylinositol 3-KinasesArginine vasopressinAutism spectrum disorderBiomarkerCerebrospinal fluidKinase signaling pathwayOxytocinRhesus macaqueSocial responsiveness scaleSocial trait variation

Identifiers

PMID34238350
PMCPMC8268173
OpenAlexW3179578407

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.