Evidence map›Paper›PMID 27703276›Full record

ArticleScientific reports2016

BDNF Val

Vincent Taschereau-Dumouchel, Sébastien Hétu, Pierre-Emmanuel Michon, Etienne Vachon-Presseau, Elsa Massicotte, Louis De Beaumont, Shirley Fecteau, Judes Poirier, Catherine Mercier, Yvon C Chagnon and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 16 citations in OpenAlex.

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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

11 authors at 7 institutions in 2 countries.

Vincent Taschereau-DumouchelÉcole de psychologie, Université Laval, Québec, G1V 0A6, Canada.
Sébastien HétuHuman Neuroimaging laboratory, Virginia Tech Carilion Research Institute, Roanoke, VA, 24016, USA.
Pierre-Emmanuel MichonCentre interdisciplinaire de recherche en réadaptation et intégration sociale (CIRRIS), Québec, G1M 2S8, Canada.
Etienne Vachon-PresseauDepartment of physiology, Northwestern University, Chicago, 60611, I1. USA.
Elsa MassicotteÉcole de psychologie, Université Laval, Québec, G1V 0A6, Canada.
Louis De BeaumontDepartement de psychologie, Université du Québec à Trois-Rivières, Trois-Rivières, Québec, G9A 5H7, Canada.
Shirley FecteauCentre interdisciplinaire de recherche en réadaptation et intégration sociale (CIRRIS), Québec, G1M 2S8, Canada.
Judes PoirierDepartment of psychiatry and medicine, McGill University, Montréal, Québec, H3A 1A1, Canada.
Catherine MercierCentre interdisciplinaire de recherche en réadaptation et intégration sociale (CIRRIS), Québec, G1M 2S8, Canada.
Yvon C ChagnonCentre de recherche de l'institut universitaire en santé mentale de Québec (CRIUSMQ), Québec, G1J 2G3, Canada.
Philip L JacksonÉcole de psychologie, Université Laval, Québec, G1V 0A6, Canada.
Centre for Interdisciplinary Research in Rehabilitation · CAUniversité Laval · CAInstitut Universitaire en Santé Mentale de Québec · CAMcGill University · CANorthwestern University · USUniversité du Québec à Trois-Rivières · CAVirginia Tech · US

Funding

CIHR
6 · The paper itself

Abstract

Motor representations in the human mirror neuron system are tuned to respond to specific observed actions. This ability is widely believed to be influenced by genetic factors, but no study has reported a genetic variant affecting this system so far. One possibility is that genetic variants might interact with visuomotor associative learning to configure the system to respond to novel observed actions. In this perspective, we conducted a candidate gene study on the Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism, a genetic variant linked to motor learning in regions of the mirror neuron system, and tested the effect of this polymorphism on motor facilitation and visuomotor associative learning. In a single-pulse TMS study carried on 16 Met (Val/Met and Met/Met) and 16 Val/Val participants selected from a large pool of healthy volunteers, Met participants showed significantly less muscle-specific corticospinal sensitivity during action observation, as well as reduced visuomotor associative learning, compared to Val homozygotes. These results are the first evidence of a genetic variant tuning sensitivity to action observation and bring to light the importance of considering the intricate relation between genetics and associative learning in order to further understand the origin and function of the human mirror neuron system.

Indexed as

AdultAllelesBrain-Derived Neurotrophic FactorEvoked PotentialsFemaleGenetic VariationGenotypeHomozygoteHumansMaleMirror NeuronsPolymorphism, Single NucleotideYoung AdultBDNF protein, humanBrain-Derived Neurotrophic Factor

Identifiers

PMID27703276
PMCPMC5050503
OpenAlexW2557886759

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.