Familial risk of sinus node dysfunction indicating pacemaker implantation: A nation-wide cohort study.

IF 7.9 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Europace Pub Date : 2024-11-13 DOI:10.1093/europace/euae287
Morten Krogh Christiansen, Erik Thorlund Parner, Jens Brock Johansen, Jens Cosedis Nielsen, Henrik Kjærulf Jensen
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Abstract

Background and aims: We aimed to investigate the risk of sinus node dysfunction (SND) indicating cardiac pacing and mortality in first-degree relatives to patients with a pacemaker implanted on this indication and assess the effect of onset-age on disease risk.

Methods: In this nationwide register-based study we used the Danish civil registration registry to establish family structures and merged data with the Danish National Patient Registry and the Danish Pacemaker and ICD registry containing information on all pacemakers implanted due to SND in Denmark.

Results: We followed 6,027,090 individuals born after 1954 for 180,775,041 personyears between 1982-2022 among whom 2.477 pacemakers were implanted due to SND. The adjusted rate ratio (RR) of pacemaker-treated SND was 2.9 (2.4-3.6) for individuals having any father, mother or sibling with a pacemaker implanted on this indication compared with the general population (derived cumulative incidence at the age of 68 years: 0.79% and 0.27%, respectively). This risk was inversely proportional to implantation-age in the index person (≤60 years: RR=5.5 (3.4-9.0)). Overall, mortality was similar between individuals having a father, mother or sibling with SND and the general population, but higher for relatives to index-persons with an early onset (≤60 years: RR=1.22 (1.05-1.41)).

Conclusions: First-degree relatives to SND patients are at increased risk of SND with risk being inversely associated with implantation-age in the index person. Mortality in first-degree relatives was comparable to the general population, although subgroup findings suggest an increased mortality among individuals with a family history of earlyonset SND.

窦房结功能障碍的家族风险提示起搏器植入:全国范围内的队列研究
背景和目的:我们旨在调查心脏起搏器植入患者一级亲属的窦房结功能障碍(SND)风险和死亡率,并评估发病年龄对疾病风险的影响:在这项基于登记的全国性研究中,我们利用丹麦民事登记处建立了家庭结构,并将数据与丹麦全国患者登记处和丹麦起搏器与 ICD 登记处的数据合并,后者包含丹麦所有因 SND 而植入起搏器的信息:我们对 1954 年后出生的 6,027,090 人进行了跟踪调查,在 1982-2022 年间共跟踪调查了 180,775,041 人年,其中有 2,477 人因 SND 而植入了心脏起搏器。与普通人群相比,父亲、母亲或兄弟姐妹中任何一人因这一适应症而植入心脏起搏器的,其心脏起搏器治疗 SND 的调整率比(RR)为 2.9(2.4-3.6)(68 岁时的累积发病率分别为 0.79% 和 0.27%):分别为 0.79% 和 0.27%)。该风险与指标受试者的植入年龄成反比(≤60 岁:RR=5.5(3.4-9.0))。总体而言,父亲、母亲或兄弟姐妹患有 SND 的患者的死亡率与普通人群相似,但发病较早的指数患者的亲属的死亡率较高(≤60 岁:RR=1.22(1.5-9.0)):RR=1.22 (1.05-1.41)).Conclusions:结论:SND患者的一级亲属罹患SND的风险增加,风险与患者的植入年龄成反比。一级亲属的死亡率与普通人群相当,但亚组研究结果表明,有早发SND家族史的人死亡率更高。
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来源期刊
Europace
Europace 医学-心血管系统
CiteScore
10.30
自引率
8.20%
发文量
851
审稿时长
3-6 weeks
期刊介绍: EP - Europace - European Journal of Pacing, Arrhythmias and Cardiac Electrophysiology of the European Heart Rhythm Association of the European Society of Cardiology. The journal aims to provide an avenue of communication of top quality European and international original scientific work and reviews in the fields of Arrhythmias, Pacing and Cellular Electrophysiology. The Journal offers the reader a collection of contemporary original peer-reviewed papers, invited papers and editorial comments together with book reviews and correspondence.
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