Evidence map›Paper›PMID 39864795›Full record

ReviewJournal of molecular and cellular cardiology2025

Circadian influences on sudden cardiac death and cardiac electrophysiology.

Brian P Delisle, Abhilash Prabhat, Don E Burgess, Isabel G Stumpf, John J McCarthy, Spencer B Procopio, Xiping Zhang, Karyn A Esser, Elizabeth A Schroder

Abstract readReview
In one paragraph

Review in Journal of molecular and cellular cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Twenty-Four Hour Rhythms in Cardiovascular Physiology.Acta physiologica (Oxford, England) · 2025
    Review
  6. Effect ofInternational journal of molecular sciences · 2025
    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

9 authors.

Brian P DelisleDepartment of Physiology, University of Kentucky, Lexington, KY, USA. Electronic address: brian.delisle@uky.edu.
Abhilash PrabhatDepartment of Physiology, University of Kentucky, Lexington, KY, USA.
Don E BurgessDepartment of Physiology, University of Kentucky, Lexington, KY, USA.
Isabel G StumpfDepartment of Physiology, University of Kentucky, Lexington, KY, USA.
John J McCarthyDepartment of Physiology, University of Kentucky, Lexington, KY, USA.
Spencer B ProcopioUniversity of Florida, Gainesville, FL, USA.
Xiping ZhangUniversity of Florida, Gainesville, FL, USA.
Karyn A EsserUniversity of Florida, Gainesville, FL, USA.
Elizabeth A SchroderDepartment of Physiology, University of Kentucky, Lexington, KY, USA; Department of Internal Medicine, University of Kentucky, Lexington, KY, USA. Electronic address: eschr0@uky.edu.

Funding

Circadian clock regulation of myocardial ion channel expression and functionR01HL153042 · NHLBI · UNIVERSITY OF FLORIDA · PI DELISLE, BRIAN P, ESSER, KARYN A · 2020 to 2023
$2.6M
Transcriptional Regulation of KCNH2R01HL141343 · NHLBI · UNIVERSITY OF KENTUCKY · PI DELISLE, BRIAN P · 2019 to 2022
$2.3M
Circadian Regulation of Cardiac ElectrophysiologyR01HL172813 · NHLBI · UNIVERSITY OF KENTUCKY · PI Brian P Delisle, ELIZABETH A SCHRODER STUMPF · 2024 to 2026
$2.0M
NHLBI NIH HHS R01 HL141343NHLBI NIH HHS R01 HL153042NHLBI NIH HHS R01 HL172813
6 · The paper itself

Abstract

Cardiologists have analyzed daily patterns in the incidence of sudden cardiac death to identify environmental, behavioral, and physiological factors that trigger fatal arrhythmias. Recent studies have indicated an overall increase in sudden cardiac arrest during daytime hours when the frequency of arrhythmogenic triggers is highest. The risk of fatal arrhythmias arises from the interaction between these triggers such as elevated sympathetic signaling, catecholamine levels, heart rate, afterload, and platelet aggregation and the susceptibility of the heart (myocardial substrate) to them. A healthy myocardial substrate has structural and functional properties that protect against arrhythmias. However, individuals with cardiovascular disease often exhibit structural and electrophysiological alterations in the myocardial substrate that predispose them to sustained lethal arrhythmias. This review focuses on how day-night and circadian rhythms, both extrinsic and intrinsic, influence the protective properties of the myocardial substrate. Specifically, it explores recent advances in the temporal regulation of ion channel gene transcription, drawing on data from comprehensive bioinformatics resources (CircaDB, CircaAge, and CircaMET) and recent RNA sequencing studies. We also examine potential mechanisms underlying the temporal regulation of mRNA expression and the challenges in linking rhythmic mRNA expression to corresponding changes in protein levels. As chronobiological research in cardiology progresses, we anticipate the development of novel therapeutic strategies to enhance the protective properties of the myocardial substrate to reduce the risk of fatal arrhythmias and sudden cardiac arrest.

Indexed as

Arrhythmias, CardiacCircadian RhythmDeath, Sudden, CardiacElectrophysiological PhenomenaAnimalsHumansIon ChannelsIon ChannelsArrhythmiasCircadian clockIon channelsMyocardial substrateSudden cardiac deathTriggers

Identifiers

PMID39864795
PMCPMC12042790

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.