Heart Rate Variability Analysis May Identify Individuals With Williams-Beuren Syndrome at Risk of Sudden Death.
Williams-Beuren syndrome
autonomic nervous system
elastin arteriopathy
genetic syndrome
heart rate variability
sudden death
Journal
JACC. Clinical electrophysiology
ISSN: 2405-5018
Titre abrégé: JACC Clin Electrophysiol
Pays: United States
ID NLM: 101656995
Informations de publication
Date de publication:
03 2023
03 2023
Historique:
received:
23
12
2021
revised:
28
09
2022
accepted:
03
10
2022
pmc-release:
01
03
2024
medline:
31
3
2023
pubmed:
9
2
2023
entrez:
8
2
2023
Statut:
ppublish
Résumé
Williams-Beuren syndrome (WBS) (Online Mendelian Inheritance in Man #194050) is a rare genetic multisystem disorder resulting from a chromosomal microdeletion at 7q11.23. The condition is characterized by distinct facies, intellectual disability, and supravalvar aortic stenosis. Those with WBS have an increased risk of sudden death, but mechanisms underlying this phenotype are incompletely understood. The aim of this study was to quantify and compare autonomic activity as reflected by heart rate variability (HRV) measures in a cohort of individuals with WBS (n = 18) and age- and sex-matched control subjects (n = 18). We performed HRV analysis on 24-hour electrocardiography recordings using nonlinear, time and frequency domain analyses on a cohort of subjects with WBS and age- and sex-matched control subjects enrolled in a prospective cross-sectional study designed to characterize WBS disease natural history. WBS subjects demonstrated diminished HRV (reflected by the SD of the NN intervals [P = 0.0001], SD of the average NN interval for 5-minute intervals over 24 hours [P < 0.0001], average of the 5-minute SDs of NN intervals for 24 hours [P = 0.0002], root mean square of successive differences of NN intervals [P = 0.0004], short axis of the Poincaré plot (SD1) [P < 0.0001], and long axis of the Poincaré plot [P < 0.0001]) and indirect markers of parasympathetic activity (reflected by the percent of NN intervals different from previous by 50% or more of local average [P < 0.0007], root mean square of successive differences of NN intervals [P = 0.0004], natural log high-frequency power [P = 0.0038], and SD1 [P < 0.0001]). Additional parameters were also significantly different, including natural log very low-frequency power (decreased; P = 0.0002), natural log low-frequency power (decreased; P = 0.0024), and SD1 divided by the long axis of the Poincaré plot (decreased; P < 0.0001). Individuals with WBS demonstrate significant HRV abnormalities consistent with diminished autonomic reserve. Future studies will be needed to determine the relationship between autonomic dysregulation observed and sudden death risk seen in these patients. (Impact of Elastin Mediated Vascular Stiffness on End Organs; NCT02840448).
Sections du résumé
BACKGROUND
Williams-Beuren syndrome (WBS) (Online Mendelian Inheritance in Man #194050) is a rare genetic multisystem disorder resulting from a chromosomal microdeletion at 7q11.23. The condition is characterized by distinct facies, intellectual disability, and supravalvar aortic stenosis. Those with WBS have an increased risk of sudden death, but mechanisms underlying this phenotype are incompletely understood.
OBJECTIVES
The aim of this study was to quantify and compare autonomic activity as reflected by heart rate variability (HRV) measures in a cohort of individuals with WBS (n = 18) and age- and sex-matched control subjects (n = 18).
METHODS
We performed HRV analysis on 24-hour electrocardiography recordings using nonlinear, time and frequency domain analyses on a cohort of subjects with WBS and age- and sex-matched control subjects enrolled in a prospective cross-sectional study designed to characterize WBS disease natural history.
RESULTS
WBS subjects demonstrated diminished HRV (reflected by the SD of the NN intervals [P = 0.0001], SD of the average NN interval for 5-minute intervals over 24 hours [P < 0.0001], average of the 5-minute SDs of NN intervals for 24 hours [P = 0.0002], root mean square of successive differences of NN intervals [P = 0.0004], short axis of the Poincaré plot (SD1) [P < 0.0001], and long axis of the Poincaré plot [P < 0.0001]) and indirect markers of parasympathetic activity (reflected by the percent of NN intervals different from previous by 50% or more of local average [P < 0.0007], root mean square of successive differences of NN intervals [P = 0.0004], natural log high-frequency power [P = 0.0038], and SD1 [P < 0.0001]). Additional parameters were also significantly different, including natural log very low-frequency power (decreased; P = 0.0002), natural log low-frequency power (decreased; P = 0.0024), and SD1 divided by the long axis of the Poincaré plot (decreased; P < 0.0001).
CONCLUSIONS
Individuals with WBS demonstrate significant HRV abnormalities consistent with diminished autonomic reserve. Future studies will be needed to determine the relationship between autonomic dysregulation observed and sudden death risk seen in these patients. (Impact of Elastin Mediated Vascular Stiffness on End Organs; NCT02840448).
Identifiants
pubmed: 36752464
pii: S2405-500X(22)00860-X
doi: 10.1016/j.jacep.2022.10.010
pmc: PMC10065881
mid: NIHMS1841832
pii:
doi:
Banques de données
ClinicalTrials.gov
['NCT02840448']
Types de publication
Journal Article
Research Support, N.I.H., Intramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
359-370Subventions
Organisme : Intramural NIH HHS
ID : ZIA HL006210
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA HL006212
Pays : United States
Informations de copyright
Published by Elsevier Inc.
Déclaration de conflit d'intérêts
Funding Support and Author Disclosures Funding for this work was provided by National Heart, Lung, and Blood Institute Division of Intramural Research intramural research programs grants ZIA HL 006210 and ZIA HL 006212. The authors have reported that they have no relationships relevant to the contents of this paper to disclose.
Références
J Transl Med. 2020 Jan 6;18(1):4
pubmed: 31906988
Am J Physiol. 1996 Jul;271(1 Pt 2):H244-52
pubmed: 8760181
Ciba Found Symp. 1983;100:37-55
pubmed: 6557898
J Cardiovasc Electrophysiol. 2005 Jan;16(1):13-20
pubmed: 15673380
Circ Arrhythm Electrophysiol. 2016 Feb;9(2):e001359
pubmed: 26810594
J Thorac Cardiovasc Surg. 2015 Jun;149(6):1516-22.e1
pubmed: 25791950
Hum Mol Genet. 1997 Jul;6(7):1021-8
pubmed: 9215670
Eur Heart J. 1980 Dec;1(6):445-52
pubmed: 6791925
J Med Eng Technol. 2001 Nov-Dec;25(6):240-8
pubmed: 11780765
Am Heart J. 2004 Feb;147(2):309-16
pubmed: 14760330
J Am Coll Cardiol. 2001 Apr;37(5):1395-402
pubmed: 11300452
IEEE Eng Med Biol Mag. 2007 Nov-Dec;26(6):14-8
pubmed: 18189081
Clin Physiol. 2001 May;21(3):365-76
pubmed: 11380537
Am Heart J. 1992 Mar;123(3):704-10
pubmed: 1539521
Circulation. 1997 Aug 5;96(3):842-8
pubmed: 9264491
J Pediatr. 1996 Dec;129(6):926-31
pubmed: 8969740
Science. 1981 Jul 10;213(4504):220-2
pubmed: 6166045
Circ Res. 2014 Mar 14;114(6):1004-21
pubmed: 24625726
Prog Cardiovasc Dis. 2013 Sep-Oct;56(2):153-9
pubmed: 24215747
Neuropediatrics. 1999 Jun;30(3):146-8
pubmed: 10480210
Europace. 2015 Sep;17(9):1341-53
pubmed: 26177817
J Cardiovasc Electrophysiol. 2003 May;14(5):467-73
pubmed: 12776861
Nat Genet. 1993 Sep;5(1):11-6
pubmed: 7693128
Circulation. 1996 Mar 1;93(5):1043-65
pubmed: 8598068
J Clin Monit. 1991 Oct;7(4):335-45
pubmed: 1744678
Eur Heart J. 2000 Mar;21(6):475-82
pubmed: 10681488
Am Heart J. 1995 May;129(5):975-81
pubmed: 7732987
J Am Coll Cardiol. 1994 Mar 1;23(3):565-9
pubmed: 8113535
Circulation. 1961 Dec;24:1311-8
pubmed: 14007182
Am J Med Genet A. 2004 Jun 15;127A(3):234-7
pubmed: 15150772
Am J Physiol. 1990 Mar;258(3 Pt 2):H713-21
pubmed: 2316686
Am J Physiol Regul Integr Comp Physiol. 2002 Sep;283(3):R789-97
pubmed: 12185014
J Clin Invest. 2005 Sep;115(9):2305-15
pubmed: 16138184
Am J Cardiol. 1988 Feb 1;61(4):208-15
pubmed: 3341195