Evidence map›Paper›PMID 28018753›Full record

ReviewCurrent physical medicine and rehabilitation reports2016

Genetic determinants of swallowing impairment, recovery and responsiveness to treatment.

Alicja Raginis-Zborowska, Neil Pendleton, Shaheen Hamdy

Registry-linked trialOpen access · hybridAbstract readReview
In one paragraph

Review in Current physical medicine and rehabilitation reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04009408 (Interventional Study of Expiratory Muscle Strength Training as a Treatment in Neuromuscular Disorders), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.4field-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.

NCT04009408 naunknown statusnot on this mapstarted 2022, after this paper: background citation

Interventional Study of Expiratory Muscle Strength Training as a Treatment in Neuromuscular Disorders

TypeinterventionalSponsorUniversity of CalgaryRan2022 to 2022Enrolled20ConditionsOculopharyngeal Muscular Dystrophy, Muscular Dystrophies, Myopathy, HereditaryArmsExpiratory muscle strength therapy (EMST150, Aspire LLC)
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Editorial: Dysphagia, Dementia and Frailty.The journal of nutrition, health & aging · 2018
    Article
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

3 authors at 1 institution in 1 country.

Alicja Raginis-ZborowskaCentre for Gastrointestinal Sciences, Institute of Inflammation and Repair Faculty of Medical and Human Sciences, The University of Manchester, Manchester, UK.
Neil PendletonInstitute of Brain, Behaviour and Mental Health, The University of Manchester, Manchester, UK.
Shaheen HamdyCentre for Gastrointestinal Sciences, Institute of Inflammation and Repair Faculty of Medical and Human Sciences, The University of Manchester, Manchester, UK.
University of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewHere we review the latest literature and evidence in the field of genetics and determinants of swallowing and its treatments-specifically, this is a very recent concept in the field of oropharyngeal dysphagia, with only now an emerging research interest in the relationship between our genetic makeup and the effect this has on swallowing function and dysfunction. As such our review will look at preclinical, clinical and hypothesis generating research covering all aspects of the genetics of swallowing, giving new importance to the genotype-phenotype influences pertaining to dysphagia and its recovery. RECENT

findingsThere appear to be a number of candidate gene systems that interact with swallowing or its neurophysiology, which include brain-derived neurotrophic factor, apolipoprotein E and catechol- SUMMARY: There is currently limited research in the field of genetic factors that influence (human) swallowing and oropharyngeal dysphagia, but this is an emerging science and one which, in the future, may herald a new era in precision medicine and better targeting of therapies for dysphagia based on an individual's genetic makeup.

Indexed as

DysphagiaGenesPolymorphismSwallowing

Identifiers

PMID28018753
PMCPMC5148785
OpenAlexW2525472123

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.