Evidence map›Paper›PMID 32569795›Full record

ArticleNeurobiology of disease2020

Regional rates of brain protein synthesis are unaltered in dexmedetomidine sedated young men with fragile X syndrome: A L-[1-

Kathleen C Schmidt, Inna Loutaev, Zenaide Quezado, Carrie Sheeler, Carolyn Beebe Smith

Open access · goldAbstract read
In one paragraph

Article in Neurobiology of disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Decreased rates of cerebral protein synthesis in conscious young adults with fragile X syndrome demonstrated by L-[1-Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
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  8. Review
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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

5 authors at 2 institutions in 1 country.

Kathleen C SchmidtSection on Neuroadaptation and Protein Metabolism, National Institute of Mental Health, 10 Center Drive, Room 2D54, Bethesda, MD 20892-1298, United States of America.
Inna LoutaevSection on Neuroadaptation and Protein Metabolism, National Institute of Mental Health, 10 Center Drive, Room 2D54, Bethesda, MD 20892-1298, United States of America.
Zenaide QuezadoDepartment of Perioperative Medicine, Clinical Center, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892-1512, United States of America.
Carrie SheelerSection on Neuroadaptation and Protein Metabolism, National Institute of Mental Health, 10 Center Drive, Room 2D54, Bethesda, MD 20892-1298, United States of America.
Carolyn Beebe SmithSection on Neuroadaptation and Protein Metabolism, National Institute of Mental Health, 10 Center Drive, Room 2D54, Bethesda, MD 20892-1298, United States of America. Electronic address: beebe@mail.nih.gov.
National Institute of Mental Health · USNational Institutes of Health Clinical Center · US

Funding

Studies On Protein Synthesis And Long-Term Adaptive Responses in the CNSZIAMH000889 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI BEEBE SMITH, CAROLYN · 2009 to 2021
$18.6M
Studies On Protein Synthesis And Long-Term Adaptive Responses in the CNSZ01MH000889 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI SMITH, CAROLYN B. · 1985 to 2008
$3.7M
Predoctoral Training of NeuroscientistsT32NS105604 · NINDS · UNIVERSITY OF MINNESOTA · PI A DAVID REDISH · 2018 to 2026
$3.5M
Mathematical and Statistical Analysis Techniques for in Vivo Imaging StudiesZIAMH002935 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI BEEBE SMITH, CAROLYN · 2012 to 2019
$1.4M
Neurobiology of pain and behavior changes associated with rare diseases and developmental disabilitiesZIACL090052 · CLC · CLINICAL CENTER · PI QUEZADO, ZENAIDE · 2017 to 2025
$0k
Development of novel strategies for the treatment of pain in childrenZIACL090054 · CLC · CLINICAL CENTER · PI QUEZADO, ZENAIDE · 2017 to 2025
$0k
Intramural NIH HHS Z01 MH000889Intramural NIH HHS ZIA MH000889Intramural NIH HHS ZIA MH002935NINDS NIH HHS T32 NS105604
6 · The paper itself

Abstract

Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. Fragile X mental retardation protein (FMRP), a putative translation suppressor, is absent or significantly reduced in FXS. One prevailing hypothesis is that rates of protein synthesis are increased by the absence of this regulatory protein. In accord with this hypothesis, we have previously reported increased rates of cerebral protein synthesis (rCPS) in the Fmr1 knockout mouse model of FXS and others have reported similar effects in hippocampal slices. To address the hypothesis in human subjects, we applied the L[1-

Indexed as

AdolescentBrainCarbon RadioisotopesDexmedetomidineFragile X SyndromeHumansHypnotics and SedativesLeucineMalePositron-Emission TomographyProtein BiosynthesisYoung AdultCarbon-11Carbon RadioisotopesDexmedetomidineHypnotics and SedativesLeucineDexmedetomidineFragile X syndromeLeucinePositron emission tomographyProtein synthesisSedationTranslation

Identifiers

PMID32569795
PMCPMC7425798
OpenAlexW3035794098

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.