Cardiomyopathy in First-Degree Relatives of Patients Presenting With Acute Myocarditis: Prevalence and Prognostic Significance.

IF 7.8 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Circulation: Heart Failure Pub Date : 2024-06-01 Epub Date: 2024-05-30 DOI:10.1161/CIRCHEARTFAILURE.123.011204
Jacinthe Boulet, Neal K Lakdawala, Mia Nielsen Christiansen, Morten Schou, Lars Køber, Finn Gustafsson, Gunnar H Gislason, Christian Torp-Pedersen, Charlotte Andersson
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Abstract

Background: Acute myocarditis has been genetically linked to dilated cardiomyopathy (DCM), but the clinical significance remains uncertain. We investigated the prevalence and long-term prognosis of DCM and heart failure (HF) among unselected patients hospitalized with acute myocarditis and their first-degree relatives compared with an age- and sex-matched cohort.

Methods: This was an observational study utilizing the Danish nationwide registries, where all patients with a first-time myocarditis diagnosis from 1995 to 2018 were identified and matched (on birth year and sex) with 10 controls from the general population.

Results: Totally 3176 patients with acute myocarditis and 31 760 controls were included (median age, 49.8 [Q1-Q3, 32.5-70.2] years; 35.6% female). At baseline, patients with myocarditis had a higher prevalence of DCM (7 [0.2%] versus 8 [0.0%]) and HF (336 [10.6%] versus 695 [2.2%]) than controls; P<0.0001 for both. Patients with myocarditis more often had siblings with DCM (12 [0.4%] versus 17 [0.05%]) or HF (36 [1.1%] versus 89 [0.3%]); P<0.0001, odds ratios 7.09 (3.38-14.85) and 2.92 (1.25-6.80), respectively, whereas parental DCM and HF did not differ among patients with myocarditis and controls. Patients with myocarditis had greater 20-year incidence of DCM, HF, and all-cause mortality (0.5% [0.3%-0.9%], 15% [13%-17%], and 47% [44%-50%]) compared with controls (0.06% [0.03%-0.11%], 6.8% [6.4%-7.3%], and 34% [33%-35%]; P<0.0001). Having a first-degree relative with DCM or HF was associated with increased long-term mortality among the patients with myocarditis (hazard ratio, 1.40 [1.11-1.77]) but not among the controls (hazard ratio, 0.90 [0.81-1.01]; Pdifference=0.0008).

Conclusions: Acute myocarditis aggregates with DCM within families, where it carries a worsened prognosis. A differential association between parents and siblings (with sibling preponderance) could suggest that additional environmental factors are important for myocarditis development even in predisposed individuals.

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急性心肌炎患者一级亲属中的心肌病:发病率和预后意义。
背景:急性心肌炎与扩张型心肌病(DCM)存在遗传关联,但其临床意义仍不确定。我们调查了未经选择的急性心肌炎住院患者及其一级亲属中 DCM 和心力衰竭(HF)的发病率和长期预后,并与年龄和性别匹配的队列进行了比较:这是一项观察性研究,利用丹麦全国范围内的登记资料,对1995年至2018年期间首次诊断为心肌炎的所有患者进行鉴定,并与普通人群中的10名对照者进行配对(出生年份和性别):共纳入了 3176 名急性心肌炎患者和 31 760 名对照者(中位年龄 49.8 [Q1-Q3, 32.5-70.2] 岁;35.6% 为女性)。基线时,心肌炎患者的 DCM(7 [0.2%] 对 8 [0.0%])和 HF(336 [10.6%] 对 695 [2.2%])患病率高于对照组;PPPPdifference=0.0008):结论:急性心肌炎与 DCM 在家族中聚集,会导致预后恶化。父母和兄弟姐妹之间的不同关联(兄弟姐妹占优势)可能表明,即使在易感人群中,其他环境因素对心肌炎的发展也很重要。
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来源期刊
Circulation: Heart Failure
Circulation: Heart Failure 医学-心血管系统
CiteScore
12.90
自引率
3.10%
发文量
271
审稿时长
6-12 weeks
期刊介绍: Circulation: Heart Failure focuses on content related to heart failure, mechanical circulatory support, and heart transplant science and medicine. It considers studies conducted in humans or analyses of human data, as well as preclinical studies with direct clinical correlation or relevance. While primarily a clinical journal, it may publish novel basic and preclinical studies that significantly advance the field of heart failure.
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