治疗期间HDL胆固醇可预测左心室肥厚高血压患者房颤的发生。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2020-10-01 Epub Date: 2020-06-25 DOI:10.1080/08037051.2020.1782171
Peter M Okin, Darcy A Hille, Kristian Wachtell, Sverre E Kjeldsen, Stevo Julius, Richard B Devereux
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引用次数: 3

摘要

目的:高血压患者心房颤动(AF)的风险增加。虽然低基线高密度脂蛋白(HDL)胆固醇与房颤的高风险相关,但这在最近的基于人群的研究中尚未得到证实。是否随着时间的推移HDL水平的变化与高血压患者新发房颤的风险有更强的相关性还没有研究。材料和方法:8267例无房颤史的高血压患者,基线心电图窦性心律,随机分配到以氯沙坦或阿替洛尔为基础的治疗组,检查房颤事件与基线和治疗期间HDL水平的关系。基线时的HDL水平和每年的测试根据基线HDL水平分为四分位数。结果:在4.7±1.10年的随访期间,645名患者(7.8%)发生了新的房颤。在单因素Cox分析中,与HDL水平最高的四分位数(>1.78 mmol/l)相比,治疗中HDL水平最低的四分位数(≤1.21 mmol/l)的患者发生新的房颤的风险增加了53%。第二和第三四分位数的患者发生房颤的风险中等增加。最低四分位数的基线HDL并不是新房颤的显著预测因子(危险比(HR)):1.14, 95%置信区间(CI): 0.90-1.43)。在调整多个基线和时变协变量的多变量Cox分析中,治疗期间HDL的最低四分位数仍然与新房颤风险增加近54%相关(HR: 1.54, 95% CI: 1.16-2.05),而基线HDL≤≤1.21 mmol/l不能预测新房颤(HR: 1.01, 95% CI: 0.78-1.31)。结论:治疗时较低的HDL与新发房颤的风险密切相关。这些发现表明,在左心室肥厚的高血压患者中,HDL的连续评估可以比基线HDL更好地估计房颤的风险。未来的研究可能会调查增加HDL的治疗是否可以降低发生af的风险。临床试验注册:http://clinicaltrials.gov/ct/show/NCT00338260?order=1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
On-treatment HDL cholesterol predicts incident atrial fibrillation in hypertensive patients with left ventricular hypertrophy.

Purpose: Hypertensive patients are at increased risk of atrial fibrillation (AF). Although low baseline high density lipoprotein (HDL) cholesterol has been associated with a higher risk of AF, this has not been verified in recent population-based studies. Whether changing levels of HDL over time are more strongly related to the risk of new AF in hypertensive patients has not been examined.Material and methods: Incident AF was examined in relation to baseline and on-treatment HDL levels in 8267 hypertensive patients with no history of AF, in sinus rhythm on their baseline electrocardiogram, randomly assigned to losartan- or atenolol-based treatment. HDL levels at baseline and each year of testing were categorised into quartiles according to baseline HDL levels.Results: During 4.7 ± 1.10 years of follow-up, 645 patients (7.8%) developed new AF. In univariate Cox analyses, compared with the highest quartile of HDL levels (>1.78 mmol/l), patients with on-treatment HDL in the lowest quartile (≤ 1.21 mmol/l) had a 53% greater risk of new AF. Patients with on-treatment HDL in the second and third quartiles had intermediate increased risks of AF. Baseline HDL in the lowest quartile was not a significant predictor of new AF (hazard ratio (HR): 1.14, 95% confidence interval (CI): 0.90-1.43). In multivariable Cox analyses adjusting for multiple baseline and time-varying covariates, the lowest quartile of on-treatment HDL remained associated with a nearly 54% increased risk of new AF (HR: 1.54, 95% CI: 1.16-2.05) whereas a baseline HDL≤ ⩽1.21 mmol/l was not predictive of new AF (HR: 1.01, 95% CI: 0.78-1.31).Conclusion: Lower on-treatment HDL is strongly associated with risk of new AF. These findings suggest that serial assessment of HDL can estimate AF risk better than baseline HDL in hypertensive patients with left ventricular hypertrophy. Future studies may investigate whether therapies that increase HDL can lower risk of developing AF.Clinical Trials Registration: http://clinicaltrials.gov/ct/show/NCT00338260?order=1.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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