Evidence map›Paper›PMID 20814256›Full record

ReviewJournal of developmental and behavioral pediatrics : JDBP2010

Emerging pharmacotherapies for neurodevelopmental disorders.

Daniel Z Wetmore, Craig C Garner

Abstract readReview
In one paragraph

Review in Journal of developmental and behavioral pediatrics : JDBP, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Plexiform neurofibromatosis involving face and oral cavity.Journal of oral and maxillofacial pathology : JOMFP · 2014
    Article
  11. Article
  12. Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  13. Treatment of neurodevelopmental disorders in adulthood.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Review
  14. Astrocyte-derived thrombospondins mediate the development of hippocampal presynaptic plasticity in vitro.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  15. Article
  16. Trisomy 21 and early brain development.Trends in neurosciences · 2012
    Review
  17. Article
  18. Transcript catalogs of human chromosome 21 and orthologous chimpanzee and mouse regions.Mammalian genome : official journal of the International Mammalian Genome Society · 2011
    Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Daniel Z WetmoreDepartment of Psychiatry and Behavioral Sciences, Nancy Pritzker Laboratory, Stanford University, Stanford, CA 94305-5485, USA.
Craig C Garner
Stanford University · US

Funding

The Roles of Presynaptic Plasticity in Circuit Function and BehaviorP01NS053862 · NINDS · STANFORD UNIVERSITY · PI GARNER, CRAIG C · 2006 to 2010
$6.7M
NINDS NIH HHS NS353862NINDS NIH HHS P01 NS053862
6 · The paper itself

Abstract

A growing and interdisciplinary translational neuroscience research effort for neurodevelopmental disorders (NDDs) is investigating the mechanisms of dysfunction and testing effective treatment strategies in animal models and, when possible, in the clinic. NDDs with a genetic basis have received particular attention. Transgenic animals that mimic genetic insults responsible for disease in man have provided insight about mechanisms of dysfunction, and, surprisingly, have shown that cognitive deficits can be addressed in adult animals. This review will present recent translational research based on animal models of genetic NDDs, as well as pharmacotherapeutic strategies under development to address deficits of brain function for Down syndrome, fragile X syndrome, Rett syndrome, neurofibromatosis-1, tuberous sclerosis, and autism. Although these disorders vary in underlying causes and clinical presentation, common pathways and mechanisms for dysfunction have been observed. These include abnormal gene dosage, imbalance among neurotransmitter systems, and deficits in the development, maintenance and plasticity of neuronal circuits. NDDs affect multiple brain systems and behaviors that may be amenable to drug therapies that target distinct deficits. A primary goal of translational research is to replace symptomatic and supportive drug therapies with pharmacotherapies based on a principled understanding of the causes of dysfunction. Based on this principle, several recently developed therapeutic strategies offer clear promise for clinical development in man.

Indexed as

AnimalsAnimals, Genetically ModifiedAutistic DisorderBrainChildCognitionDevelopmental DisabilitiesDisease Models, AnimalDown SyndromeFragile X SyndromeGenetic Predisposition to DiseaseHumansNervous System DiseasesNeurofibromatosis 1Rett SyndromeTuberous Sclerosis

Identifiers

PMID20814256
PMCPMC2967570
OpenAlexW2085242610

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.