Evidence map›Paper›PMID 30118755›Full record

ReviewNeurobiology of disease2019

Genetics of stroke recovery: BDNF val66met polymorphism in stroke recovery and its interaction with aging.

Mustafa Balkaya, Sunghee Cho

2 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in Neurobiology of disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 45 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 3 pooled it
2.6field-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.

NCT03866057 unknown statusnot on this map

Post Stroke Intensive Rehabilitation: Predictors of Outcome and Response to Specific Interventions

TypeobservationalSponsorFondazione Don Carlo Gnocchi ETSRan2019 to 2020Enrolled270ConditionsStroke Rehabilitation
NCT03968627 completednot on this map

Development of a National, Evidence Based Protocol for Stroke Rehabilitation in a Multicenter Italian no Profit Institution: Implementation and Results of a Pilot Study

TypeobservationalSponsorFondazione Don Carlo Gnocchi ETSRan2017 to 2018Enrolled443ConditionsStroke, RehabilitationArmsRehabilitative intervention
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 3 syntheses or guidelines pooled it, 70 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

2 authors at 1 institution in 1 country.

Mustafa BalkayaBurke-Cornell Medical Research Institute, 785 Mamaroneck Ave, White Plains, NY 10605, USA; Feil Family Brain and Mind Research Institute, Weill Cornell Medicine at Burke Medical Research Institute, 785 Mamaroneck Ave, White Plains, NY 10605, USA.
Sunghee ChoBurke-Cornell Medical Research Institute, 785 Mamaroneck Ave, White Plains, NY 10605, USA; Feil Family Brain and Mind Research Institute, Weill Cornell Medicine at Burke Medical Research Institute, 785 Mamaroneck Ave, White Plains, NY 10605, USA. Electronic address: suc2002@med.cornell.edu.
Cornell University · US

Funding

Role of CD36 in functional recovery in chronic strokeR01NS095359 · NINDS · WINIFRED MASTERSON BURKE MED RES INST · PI CHO, SUNGHEE · 2015 to 2019
$2.1M
Targeting stroke-induced brain swelling in obese subjects: role of VEGFR01NS103326 · NINDS · WINIFRED MASTERSON BURKE MED RES INST · PI CHO, SUNGHEE · 2018 to 2022
$2.0M
Impact of BDNF SNP on stroke-induced plasticity and motor functionR01NS077897 · NINDS · WINIFRED MASTERSON BURKE MED RES INST · PI CHO, SUNGHEE · 2012 to 2016
$2.0M
NINDS NIH HHS R01 NS077897NINDS NIH HHS R01 NS095359NINDS NIH HHS R01 NS103326
6 · The paper itself

Abstract

Stroke leads to long term sensory, motor and cognitive impairments. Most patients experience some degree of spontaneous recovery which is mostly incomplete and varying greatly among individuals. The variation in recovery outcomes has been attributed to numerous factors including lesion size, corticospinal tract integrity, age, gender and race. It is well accepted that genetics play a crucial role in stroke incidence and accumulating evidence suggests that it is also a significant determinant in recovery. Among the number of genes and variations implicated in stroke recovery the val66met single nucleotide polymorphism (SNP) in the BDNF gene influences post-stroke plasticity in the most significant ways. Val66met is the most well characterized BDNF SNP and is common (40-50 % in Asian and 25-32% in Caucasian populations) in humans. It reduces activity-dependent BDNF release, dampens cortical plasticity and is implicated in numerous diseases. Earlier studies on the effects of val66met on stroke outcome and recovery presented primarily a maladaptive role. Novel findings however indicate a much more intricate interaction between val66met and stroke recovery which appears to be influenced by lesion location, post-stroke stage and age. This review will focus on the role of BDNF and val66met SNP in relation to stroke recovery and try to identify potential pathophysiologic mechanisms involved. The effects of age on val66met associated alterations in plasticity and potential consequences in terms of stroke are also discussed.

Indexed as

AgingBrain-Derived Neurotrophic FactorHumansNeuronal PlasticityPolymorphism, Single NucleotideRecovery of FunctionStrokeBDNF protein, humanBrain-Derived Neurotrophic FactorBDNFRecoveryStrokeval66met

Identifiers

PMID30118755
PMCPMC7653673
OpenAlexW2887501882

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.