Evidence map›Paper›PMID 29203579›Full record

ArticleJournal of the American Heart Association2017

Heads and Tails of Natriuretic Peptides: Neuroprotective Role of Brain Natriuretic Peptide.

Héctor Fernández-Susavila, Manuel Rodríguez-Yáñez, Antonio Dopico-López, Susana Arias, María Santamaría, Paulo Ávila-Gómez, Juan M Doval-García, Tomás Sobrino, Ramón Iglesias-Rey, José Castillo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Article
  3. 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

11 authors at 1 institution in 1 country.

Héctor Fernández-SusavilaClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
Manuel Rodríguez-YáñezClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
Antonio Dopico-LópezClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
Susana AriasClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
María SantamaríaClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
Paulo Ávila-GómezClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
Juan M Doval-GarcíaClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
Tomás SobrinoClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
Ramón Iglesias-ReyClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain.
José CastilloClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain jose.castillo.sanchez@sergas.es francisco.campos.perez@sergas.es.
Francisco CamposClinical Neurosciences Research Laboratory, Department of Neurology, Hospital Clínico Universitario, Health Research Institute of Santiago de Compostela (IDIS) Universidade de Santiago de Compostela, Spain jose.castillo.sanchez@sergas.es francisco.campos.perez@sergas.es.
Universidade de Santiago de Compostela · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBesides the relevant role of brain-type natriuretic peptide (BNP) as biomarker of cardioembolic strokes, new experimental evidences suggest that this peptide may mediate neuroprotective effects. In this study, we have evaluated for the first time the clinical association between BNP (by means of proBNP) and good outcome in ischemic stroke patients, and analyzed the effect of blood BNP increase in an ischemic animal model. METHODS AND

resultsA retrospective study with 2 different cohorts (262 patients in cohort I and 610 in cohort II) from the same prospective stroke registry was performed. proBNP concentration was analyzed within the first 12 hours from stroke onset. The primary predictor variable was functional outcome evaluated by modified Rankin Scale at 3 months. For the experimental study, BNP pretreatment was tested in an ischemic animal model subjected to a transient occlusion of the cerebral artery, and the infarct volume and sensorimotor deficit were evaluated for 14 days. Cardioembolic strokes presented a positive correlation between proBNP concentration and modified Rankin Scale at 3 months; however, noncardioembolic strokes presented a negative correlation. In the logistic regression analysis, noncardioembolic strokes with concentrations of proBNP ≥340 pg/mL were associated with a good outcome. In line with these clinical findings, the experimental study revealed that those BNP pretreated animals presented a reduction on infarct volumes at 24 hours and functional recovery at days 7 and 14 compared with the control groups.

conclusionsThese clinical and experimental evidences support the potential role of BNP as a protective factor against cerebral ischemia.

Indexed as

AnimalsBiomarkersBrain IschemiaChi-Square DistributionDisability EvaluationDisease Models, AnimalInfarction, Middle Cerebral ArteryLogistic ModelsMaleMotor ActivityNatriuretic Peptide, BrainNeuroprotective AgentsOdds RatioPrognosisProtective FactorsRats, Sprague-DawleyBiomarkersNatriuretic Peptide, BrainNeuroprotective Agentsbrain natriuretic peptidecardioembolic strokeneuroprotectionnoncardioembolic stroke

Identifiers

PMID29203579
PMCPMC5779043
OpenAlexW2774219952

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.