Evidence map›Paper›PMID 33375447›Full record

ReviewInternational journal of molecular sciences2020

Neurological Disorders and Risk of Arrhythmia.

Joyce Bernardi, Kelly A Aromolaran, Ademuyiwa S Aromolaran

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  7. P2X7 receptor inhibition prevents atrial fibrillation in rodent models of depression.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2024
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  13. Analysis ofGenes · 2022
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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

3 authors at 1 institution in 1 country.

Joyce BernardiBiomedical Research and Translational Medicine, Masonic Medical Research Institute, 2150 Bleecker St., Utica, NY 13501, USA.
Kelly A AromolaranBiomedical Research and Translational Medicine, Masonic Medical Research Institute, 2150 Bleecker St., Utica, NY 13501, USA.
Ademuyiwa S AromolaranBiomedical Research and Translational Medicine, Masonic Medical Research Institute, 2150 Bleecker St., Utica, NY 13501, USA.ORCID 0000-0003-3745-9213
Masonic Medical Research Laboratory · US

Funding

Mechanisms of Lipotoxic ArrhythmiasR01HL147044 · NHLBI · UNIVERSITY OF UTAH · PI AROMOLARAN, ADEMUYIWA · 2019 to 2022
$1.5M
National Institute of Health R01HL147044NHLBI NIH HHS R01 HL147044
6 · The paper itself

Abstract

Neurological disorders including depression, anxiety, post-traumatic stress disorder (PTSD), schizophrenia, autism and epilepsy are associated with an increased incidence of cardiovascular disorders and susceptibility to heart failure. The underlying molecular mechanisms that link neurological disorders and adverse cardiac function are poorly understood. Further, a lack of progress is likely due to a paucity of studies that investigate the relationship between neurological disorders and cardiac electrical activity in health and disease. Therefore, there is an important need to understand the spatiotemporal behavior of neurocardiac mechanisms. This can be advanced through the identification and validation of neurological and cardiac signaling pathways that may be adversely regulated. In this review we highlight how dysfunction of the hypothalamic-pituitary-adrenal (HPA) axis, autonomic nervous system (ANS) activity and inflammation, predispose to psychiatric disorders and cardiac dysfunction. Moreover, antipsychotic and antidepressant medications increase the risk for adverse cardiac events, mostly through the block of the human ether-a-go-go-related gene (hERG), which plays a critical role in cardiac repolarization. Therefore, understanding how neurological disorders lead to adverse cardiac ion channel remodeling is likely to have significant implications for the development of effective therapeutic interventions and helps improve the rational development of targeted therapeutics with significant clinical implications.

Indexed as

Antipsychotic AgentsArrhythmias, CardiacCardiovascular DiseasesEther-A-Go-Go Potassium ChannelsHumansIon ChannelsMental DisordersRisk FactorsAntipsychotic AgentsEther-A-Go-Go Potassium ChannelsIon Channelsantipsychotic drugscardiovascular diseaseion channelsmental illness

Identifiers

PMID33375447
PMCPMC7795827
OpenAlexW3115372919

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.