Evidence map›Paper›PMID 27743527›Full record

ArticleJournal of psychiatric research2017

Initial analysis of peripheral lymphocytic extracellular signal related kinase activation in autism.

Craig A Erickson, Balmiki Ray, Logan K Wink, Baindu L Bayon, Ernest V Pedapati, Rebecca Shaffer, Tori L Schaefer, Debomoy K Lahiri

Open access · greenAbstract read
In one paragraph

Article in Journal of psychiatric research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
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  7. Maternal IL-17A in autism.Experimental neurology · 2018
    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

8 authors at 2 institutions in 1 country.

Craig A EricksonCincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address: Craig.erickson@cchmc.org.
Balmiki RayDepartment of Psychiatry, Indiana University School of Medicine, Neuroscience Research Center, 320 West 15th Street, NB 200C, Indianapolis, IN 46202, USA. Electronic address: rayb@iupui.edu.
Logan K WinkCincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address: Logan.wink@cchmc.org.
Baindu L BayonDepartment of Psychiatry, Indiana University School of Medicine, Neuroscience Research Center, 320 West 15th Street, NB 200C, Indianapolis, IN 46202, USA. Electronic address: bbayon@umail.iu.edu.
Ernest V PedapatiCincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address: Ernest.Pedapati@cchmc.org.
Rebecca ShafferCincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address: Rebecca.Shaffer@cchmc.org.
Tori L SchaeferCincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address: Tori.Schaefer@cchmc.org.
Debomoy K LahiriDepartment of Psychiatry, Indiana University School of Medicine, Neuroscience Research Center, 320 West 15th Street, NB 200C, Indianapolis, IN 46202, USA. Electronic address: dlahiri@iupui.edu.
Cincinnati Children's Hospital Medical Center · USIndiana University School of Medicine

Funding

Research Education ComponentP30AG010133 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SAYKIN, ANDREW J · 1991 to 2020
$37.3M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Neurobiological Role of MicroRNA in Alzheimer'sR01AG051086 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI LAHIRI, DEBOMOY K · 2015 to 2019
$1.9M
Anomalous Sensorimotor Physiology in Fragile X SyndromeK23MH112936 · NIMH · CINCINNATI CHILDRENS HOSP MED CTR · PI PEDAPATI, ERNEST VIJAY · 2017 to 2021
$916k
Exploring FOXO Signaling in Promoting Neurodegeneration in ADR21AG047447 · NIA · PURDUE UNIVERSITY · PI SHAH, KAVITA · 2014 to 2015
$435k
NCATS NIH HHS UL1 TR001108NIA NIH HHS P30 AG010133NIA NIH HHS R01 AG051086NIA NIH HHS R21 AG047447NIMH NIH HHS K23 MH112936
6 · The paper itself

Abstract

backgroundDysregulation of extracellular signal-related kinase (ERK) activity has been potentially implicated in the pathophysiology of autistic disorder (autism). ERK is part of a central intracellular signaling cascade responsible for a myriad of cellular functions. ERK is expressed in peripheral blood lymphocytes, and measurement of activated (phosphorylated) lymphocytic ERK is commonly executed in many areas of medicine. We sought to conduct the first study of ERK activation in humans with autism by utilizing a lymphocytic ERK activation assay. We hypothesized that ERK activation would be enhanced in peripheral blood lymphocytes from persons with autism compared to those of neurotypical control subjects.

methodWe conducted an initial study of peripheral lymphocyte ERK activation in 45 subjects with autism and 26 age- and gender-matched control subjects (total n = 71). ERK activation was measured using a lymphocyte counting method (primary outcome expressed as lymphocytes staining positive for cytosolic phosphorylated ERK divided by total cells counted) and additional Western blot analysis of whole cell phosphorylated ERK adjusted for total ERK present in the lymphocyte lysate sample.

resultsCytosolic/nuclear localization of pERK activated cells were increased by almost two-fold in the autism subject group compared to matched neurotypical control subjects (cell count ratio of 0.064 ± 0.044 versus 0.034 ± 0.031; p = 0.002). Elevated phosphorylated ERK levels in whole cell lysates also showed increased activated ERK in the autism group compared to controls (n = 54 total) in Western blot analysis.

conclusionsThe results of this first in human ERK activation study are consistent with enhanced peripheral lymphocytic ERK activation in autism, as well as suggesting that cellular compartmentalization of activated ERK may be altered in this disorder. Future work will be required to explore the impact of concomitant medication use and other subject characteristics such as level of cognitive functioning on ERK activation.

trial registrationNot applicable.

Indexed as

AdolescentAdultAutistic DisorderBiomarkersBlotting, WesternCell CountChildChild, PreschoolCytosolExtracellular Signal-Regulated MAP KinasesFemaleHumansImmunohistochemistryLymphocytesMaleMiddle AgedBiomarkersExtracellular Signal-Regulated MAP KinasesPsychotropic DrugsAutistic disorderBiomarkerExtracellular signal related kinaseLymphocytesNeurodevelopmental disorder

Identifiers

PMID27743527
PMCPMC5903443
OpenAlexW2520784721

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.