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代谢状况与房室传导阻滞风险:体力活动的作用

Metabolic Status and Atrioventricular Block Risk: The Role of Physical Activity.

作者信息

Chung Ho-Gi, Yang Pil-Sung, Jang Eunsun, Joung Daeun, Kim Daehoon, Yu Hee Tae, Kim Tae-Hoon, Uhm Jae-Sun, Sung Jung-Hoon, Pak Hui-Nam, Lee Moon-Hyoung, Joung Boyoung

机构信息

Division of Cardiology, Department of Internal Medicine, Severance Cardiovascular Hospital, Yonsei University College of Medicine, 03722 Seoul, Republic of Korea.

Department of Cardiology, CHA Bundang Medical Center, CHA University, 13488 Seongnam, Republic of Korea.

出版信息

Rev Cardiovasc Med. 2025 May 20;26(5):37291. doi: 10.31083/RCM37291. eCollection 2025 May.

Abstract

BACKGROUND

The relationship between metabolic status as a possible risk factor and predictor of response to moderate-to-vigorous physical activity (MVPA) in atrioventricular block (AVB) remains unclear.

METHODS

A total of 82,365 UK Biobank participants without a history of AVB or pacemaker implantation, and who were involved in accelerometer work-up, were chosen for the study population. Metabolic status was classified into two categories, healthy and unhealthy, using modified criteria for metabolic syndrome from the International Diabetes Federation. We used the multivariable Cox proportional model to assess the associations between metabolic status and primary outcome (composite of second-degree AVB or third-degree AVB) or secondary outcomes (each component in the primary outcome and AVB-related pacemaker implantation). The relationship between MVPA min/week and the primary outcome in each metabolic status category was assessed using restricted cubic splines.

RESULTS

Of the 82,365 participants, the mean age was 62.3 years, and 44.1% were men. In total, 299 primary outcome events occurred during the 6.1-year follow-up. Compared to metabolically healthy participants, metabolically unhealthy participants had a 58% higher risk of the primary outcome (hazard ratio (HR): 1.58, 95% confidence interval (CI): 1.25-2.00; < 0.001). This pattern was consistent for second-degree AVB (HR: 1.59, 95% CI: 1.12-2.27; = 0.010), third-degree AVB (HR: 1.50, 95% CI: 1.12-2.03; = 0.008), and AVB-related pacemaker implantation (HR: 2.25, 95% CI: 1.44-3.52; < 0.001). Increased MVPA provided statistically significant protection against the primary outcome only in metabolically unhealthy participants, with a threshold of 830 min/week.

CONCLUSIONS

Generally, in the middle-aged population, metabolically unhealthy participants had a statistically significantly higher risk of second- or third-degree AVB and AVB-related pacemaker implantation than metabolically healthy participants. However, MVPA reduced the risk of second- or third-degree AVB in the metabolically unhealthy participants, though the effect was attenuated with excessive MVPA. From this perspective, identifying and encouraging exercise in metabolically unhealthy individuals is essential. Due to its observational nature, future research should verify the preventive effects of increased MVPA on conduction block in populations with metabolic abnormalities through randomized controlled trials. Moreover, the biological mechanisms and safety of the protective effects of excessive MVPA require further verification.

摘要

背景

代谢状态作为一种可能的风险因素与房室传导阻滞(AVB)患者对中等到剧烈身体活动(MVPA)反应的预测指标之间的关系尚不清楚。

方法

共有82365名英国生物银行参与者被选入研究人群,他们没有AVB病史或起搏器植入史,且参与了加速度计检测。使用国际糖尿病联盟修改后的代谢综合征标准将代谢状态分为健康和不健康两类。我们使用多变量Cox比例模型评估代谢状态与主要结局(二度AVB或三度AVB的复合结局)或次要结局(主要结局的每个组成部分以及与AVB相关的起搏器植入)之间的关联。使用受限立方样条评估每个代谢状态类别中每周MVPA分钟数与主要结局之间的关系。

结果

在82365名参与者中,平均年龄为62.3岁,男性占44.1%。在6.1年的随访期间,共发生299例主要结局事件。与代谢健康的参与者相比,代谢不健康的参与者发生主要结局的风险高58%(风险比(HR):1.58,95%置信区间(CI):1.25 - 2.00;P < 0.001)。这种模式在二度AVB(HR:1.59,95%CI:1.12 - 2.27;P = 0.010)、三度AVB(HR:1.50,95%CI:1.12 - 2.03;P = 0.008)以及与AVB相关的起搏器植入(HR:2.25,95%CI:1.44 - 3.52;P < 0.001)中均一致。仅在代谢不健康的参与者中,增加MVPA对主要结局具有统计学上显著的保护作用,阈值为每周830分钟。

结论

总体而言,在中年人群中,代谢不健康的参与者发生二度或三度AVB以及与AVB相关的起搏器植入的风险在统计学上显著高于代谢健康的参与者。然而,MVPA降低了代谢不健康参与者发生二度或三度AVB的风险,尽管过度的MVPA会减弱这种效果。从这个角度来看,识别并鼓励代谢不健康个体进行运动至关重要。由于其观察性本质,未来研究应通过随机对照试验验证增加MVPA对代谢异常人群传导阻滞的预防作用。此外,过度MVPA保护作用的生物学机制和安全性需要进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2fb/12135636/f035ec05765c/2153-8174-26-5-37291-g1.jpg

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