Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion. / Kaess, Bernhard M.; Andersson, Charlotte; Duncan, Meredith S.; Larson, Martin G.; Aasbjerg, Kristian; Gislason, Gunnar H.; Torp-Pedersen, Christian; Vasan, Ramachandran S.

I: Circulation: Arrhythmia and Electrophysiology, Bind 12, Nr. 7, e007150, 2019.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Kaess, BM, Andersson, C, Duncan, MS, Larson, MG, Aasbjerg, K, Gislason, GH, Torp-Pedersen, C & Vasan, RS 2019, 'Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion', Circulation: Arrhythmia and Electrophysiology, bind 12, nr. 7, e007150. https://doi.org/10.1161/CIRCEP.119.007150

APA

Kaess, B. M., Andersson, C., Duncan, M. S., Larson, M. G., Aasbjerg, K., Gislason, G. H., Torp-Pedersen, C., & Vasan, R. S. (2019). Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion. Circulation: Arrhythmia and Electrophysiology, 12(7), [e007150]. https://doi.org/10.1161/CIRCEP.119.007150

Vancouver

Kaess BM, Andersson C, Duncan MS, Larson MG, Aasbjerg K, Gislason GH o.a. Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion. Circulation: Arrhythmia and Electrophysiology. 2019;12(7). e007150. https://doi.org/10.1161/CIRCEP.119.007150

Author

Kaess, Bernhard M. ; Andersson, Charlotte ; Duncan, Meredith S. ; Larson, Martin G. ; Aasbjerg, Kristian ; Gislason, Gunnar H. ; Torp-Pedersen, Christian ; Vasan, Ramachandran S. / Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion. I: Circulation: Arrhythmia and Electrophysiology. 2019 ; Bind 12, Nr. 7.

Bibtex

@article{441282e7948b4e00ae54bcf46036220e,
title = "Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion",
abstract = "Background: The etiopathogenesis of electrocardiographic bundle branch and atrioventricular blocks is not fully understood. We investigated familial clustering of cardiac conduction defects and pacemaker insertion in the FHS (Framingham Heart Study). Additionally, we assessed familial clustering of pacemaker insertion in the Danish general population. Methods: In FHS, we used multivariable-adjusted logistic regression models to investigate the association of parental atrioventricular block (PR interval, ≥0.2 s), complete bundle branch block (QRS, ≥0.12 s), or pacemaker insertion with the occurrence of cardiac conduction abnormalities in their offspring. The Danish nationwide administrative registries were interrogated to assess the relations of parental pacemaker insertion with offspring pacemaker insertion. Results: In FHS (n=371 cases with first-degree atrioventricular block, complete bundle branch block, or pacemaker insertion, and 1471 age- and sex-matched controls), individuals with at least 1 affected parent with a conduction defect had a 1.65-fold odds (odds ratio, 95% CI, 1.32-2.07) for manifesting an atrioventricular block and a 1.62-fold odds (95% CI, 1.08-2.42) for developing a complete bundle branch block. If at least 1 parent had any electrocardiographic conduction defect or pacemaker insertion, the offspring had a 1.62-fold odds (95% CI, 1.31-2.00) for experiencing any of these conditions. In Denmark (n=2 824 199 individuals; 5397 incident pacemaker implantations), individuals with at least 1 first-degree relative with history of pacemaker insertion had a multivariable-adjusted 1.68-fold (incidence rate ratio, 95% CI, 1.49-1.89) risk of undergoing a pacemaker insertion. If the affected relative was ≤45 years of age, the incidence rate ratio was markedly increased to 51.0 (95% CI, 32.7-79.9). Conclusions: Cardiac conduction blocks and risk for pacemaker insertion cluster within families. A family history of conduction system disturbance or pacemaker insertion should trigger increased awareness of a similar propensity in other family members, especially so when the conduction system disease occurs at a younger age.",
keywords = "atrioventricular block, bundle branch block, humans, odds ratio, parents",
author = "Kaess, {Bernhard M.} and Charlotte Andersson and Duncan, {Meredith S.} and Larson, {Martin G.} and Kristian Aasbjerg and Gislason, {Gunnar H.} and Christian Torp-Pedersen and Vasan, {Ramachandran S.}",
year = "2019",
doi = "10.1161/CIRCEP.119.007150",
language = "English",
volume = "12",
journal = "Circulation: Arrhythmia and Electrophysiology",
issn = "1941-3149",
publisher = "Lippincott Williams & Wilkins",
number = "7",

}

RIS

TY - JOUR

T1 - Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion

AU - Kaess, Bernhard M.

AU - Andersson, Charlotte

AU - Duncan, Meredith S.

AU - Larson, Martin G.

AU - Aasbjerg, Kristian

AU - Gislason, Gunnar H.

AU - Torp-Pedersen, Christian

AU - Vasan, Ramachandran S.

PY - 2019

Y1 - 2019

N2 - Background: The etiopathogenesis of electrocardiographic bundle branch and atrioventricular blocks is not fully understood. We investigated familial clustering of cardiac conduction defects and pacemaker insertion in the FHS (Framingham Heart Study). Additionally, we assessed familial clustering of pacemaker insertion in the Danish general population. Methods: In FHS, we used multivariable-adjusted logistic regression models to investigate the association of parental atrioventricular block (PR interval, ≥0.2 s), complete bundle branch block (QRS, ≥0.12 s), or pacemaker insertion with the occurrence of cardiac conduction abnormalities in their offspring. The Danish nationwide administrative registries were interrogated to assess the relations of parental pacemaker insertion with offspring pacemaker insertion. Results: In FHS (n=371 cases with first-degree atrioventricular block, complete bundle branch block, or pacemaker insertion, and 1471 age- and sex-matched controls), individuals with at least 1 affected parent with a conduction defect had a 1.65-fold odds (odds ratio, 95% CI, 1.32-2.07) for manifesting an atrioventricular block and a 1.62-fold odds (95% CI, 1.08-2.42) for developing a complete bundle branch block. If at least 1 parent had any electrocardiographic conduction defect or pacemaker insertion, the offspring had a 1.62-fold odds (95% CI, 1.31-2.00) for experiencing any of these conditions. In Denmark (n=2 824 199 individuals; 5397 incident pacemaker implantations), individuals with at least 1 first-degree relative with history of pacemaker insertion had a multivariable-adjusted 1.68-fold (incidence rate ratio, 95% CI, 1.49-1.89) risk of undergoing a pacemaker insertion. If the affected relative was ≤45 years of age, the incidence rate ratio was markedly increased to 51.0 (95% CI, 32.7-79.9). Conclusions: Cardiac conduction blocks and risk for pacemaker insertion cluster within families. A family history of conduction system disturbance or pacemaker insertion should trigger increased awareness of a similar propensity in other family members, especially so when the conduction system disease occurs at a younger age.

AB - Background: The etiopathogenesis of electrocardiographic bundle branch and atrioventricular blocks is not fully understood. We investigated familial clustering of cardiac conduction defects and pacemaker insertion in the FHS (Framingham Heart Study). Additionally, we assessed familial clustering of pacemaker insertion in the Danish general population. Methods: In FHS, we used multivariable-adjusted logistic regression models to investigate the association of parental atrioventricular block (PR interval, ≥0.2 s), complete bundle branch block (QRS, ≥0.12 s), or pacemaker insertion with the occurrence of cardiac conduction abnormalities in their offspring. The Danish nationwide administrative registries were interrogated to assess the relations of parental pacemaker insertion with offspring pacemaker insertion. Results: In FHS (n=371 cases with first-degree atrioventricular block, complete bundle branch block, or pacemaker insertion, and 1471 age- and sex-matched controls), individuals with at least 1 affected parent with a conduction defect had a 1.65-fold odds (odds ratio, 95% CI, 1.32-2.07) for manifesting an atrioventricular block and a 1.62-fold odds (95% CI, 1.08-2.42) for developing a complete bundle branch block. If at least 1 parent had any electrocardiographic conduction defect or pacemaker insertion, the offspring had a 1.62-fold odds (95% CI, 1.31-2.00) for experiencing any of these conditions. In Denmark (n=2 824 199 individuals; 5397 incident pacemaker implantations), individuals with at least 1 first-degree relative with history of pacemaker insertion had a multivariable-adjusted 1.68-fold (incidence rate ratio, 95% CI, 1.49-1.89) risk of undergoing a pacemaker insertion. If the affected relative was ≤45 years of age, the incidence rate ratio was markedly increased to 51.0 (95% CI, 32.7-79.9). Conclusions: Cardiac conduction blocks and risk for pacemaker insertion cluster within families. A family history of conduction system disturbance or pacemaker insertion should trigger increased awareness of a similar propensity in other family members, especially so when the conduction system disease occurs at a younger age.

KW - atrioventricular block

KW - bundle branch block

KW - humans

KW - odds ratio

KW - parents

U2 - 10.1161/CIRCEP.119.007150

DO - 10.1161/CIRCEP.119.007150

M3 - Journal article

C2 - 31216886

AN - SCOPUS:85068493402

VL - 12

JO - Circulation: Arrhythmia and Electrophysiology

JF - Circulation: Arrhythmia and Electrophysiology

SN - 1941-3149

IS - 7

M1 - e007150

ER -

ID: 236324705