Evidence map›Paper›PMID 25634836›Full record

ArticleJournal of the American College of Cardiology2015

Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1.

Alberto Porta, Giulia Girardengo, Vlasta Bari, Alfred L George, Paul A Brink, Althea Goosen, Lia Crotti, Peter J Schwartz

Open access · greenAbstract read
In one paragraph

Article in Journal of the American College of Cardiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Sleep, Neural Circulatory Control, and Cardiovascular Disease: A Mechanistic Review.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
  3. Article
  4. Article
  5. Holter study of heart rate variability in children and adolescents with long QT syndrome.Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc · 2024
    Article
  6. Article
  7. Radiofrequency catheter ablation in congenital long QT syndrome: an anatomical approach to a supposedly primary electrical disease.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 · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Ventricular repolarization instability quantified by instantaneous frequency of ECG ST intervals.Technology and health care : official journal of the European Society for Engineering and Medicine · 2021
    Article
  15. Heart Rate Influence on the QT Variability Risk Factors.Diagnostics (Basel, Switzerland) · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 3 countries.

Alberto PortaDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy; IRCCS Galeazzi Orthopedic Institute, Milan, Italy. Electronic address: alberto.porta@unimi.it.
Giulia GirardengoCenter for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Vlasta BariDepartment of Cardiothoracic, Vascular Anesthesia and Intensive Care, IRCCS Policlinico San Donato, Milan, Italy.
Alfred L GeorgeDepartment of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, Illinois; Departments of Medicine and Pharmacology, Vanderbilt University, Nashville, Tennessee.
Paul A BrinkDepartment of Internal Medicine, University of Stellenbosch, Stellenbosch, South Africa.
Althea GoosenDepartment of Internal Medicine, University of Stellenbosch, Stellenbosch, South Africa.
Lia CrottiCenter for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, IRCCS Istituto Auxologico Italiano, Milan, Italy; Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Peter J SchwartzCenter for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, IRCCS Istituto Auxologico Italiano, Milan, Italy.
IRCCS Istituto Auxologico Italiano · ITStellenbosch University · ZAIRCCS Policlinico San Donato · ITNorthwestern University · USUniversity of Milan · ITUniversity of Pavia · IT

Funding

Genetic Modifiers of Congenital Long QT SyndromeR01HL068880 · NHLBI · VANDERBILT UNIVERSITY · PI GEORGE, ALFRED L. · 2001 to 2011
$4.8M
NHLBI NIH HHS HL068880NHLBI NIH HHS R01 HL068880Telethon GGP09247
6 · The paper itself

Abstract

backgroundA puzzling feature of the long QT syndrome (LQTS) is that family members carrying the same mutation often have divergent symptoms and clinical outcomes.

objectivesThis study tested the hypothesis that vagal and sympathetic control, as assessed by spectral analysis of spontaneous beat-to-beat variability of RR and QT intervals from standard 24-h electrocardiogram Holter recordings, could modulate the severity of LQTS type 1 (LQT1) in 46 members of a South-African LQT1 founder population carrying the clinically severe KCNQ1 A341V mutation.

methodsNonmutation carriers (NMCs) (n = 14) were compared with mutation carriers (MCs) (n = 32), 22 with and 10 without major symptoms. We assessed the effect of circadian rhythm and beta-blocker therapy over traditional time and frequency domain RR and QT variability indexes.

resultsThe asymptomatic MCs differed significantly from the symptomatic MCs and from NMCs in less vagal control of heart rate and more reactive sympathetic modulation of the QT interval, particularly during daytime when arrhythmia risk for patients with LQT1 is greatest.

conclusionsThe present data identified an additional factor contributing to the differential arrhythmic risk among patients with LQT1 carrying the same mutation. A healthy autonomic control confers a high risk, whereas patients with higher sympathetic control of the QT interval and reduced vagal control of heart rate are at lower risk. This differential "autonomic make-up," likely under genetic control, will allow refinement of risk stratification within families with LQTS, leading to more targeted management.

Indexed as

Adrenergic beta-AntagonistsAdultCase-Control StudiesCircadian RhythmElectrocardiographyHumansKCNQ1 Potassium ChannelRomano-Ward SyndromeSympathetic Nervous SystemVagus NerveAdrenergic beta-AntagonistsKCNQ1 Potassium Channelautonomic nervous systembeta-blocker therapycardiovascular controlheart rate variabilityQT variability

Identifiers

PMID25634836
PMCPMC4312415
OpenAlexW1976103187

What OpenQuestion 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 OpenQuestion graph.