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采用多标志物方法评估炎症对女性心房颤动发生率的影响。

A multimarker approach to assess the influence of inflammation on the incidence of atrial fibrillation in women.

机构信息

Center for Arrhythmia Prevention Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Eur Heart J. 2010 Jul;31(14):1730-6. doi: 10.1093/eurheartj/ehq146. Epub 2010 May 25.

Abstract

AIMS

To assess the joint influence of inflammatory biomarkers on the risk of incident atrial fibrillation (AF) in women.

METHODS AND RESULTS

We performed a prospective cohort study among women participating in the Women's Health Study. All women were free of AF at study entry and provided a baseline blood sample assayed for high-sensitivity C-reactive protein, soluble intercellular adhesion molecule-1, and fibrinogen. To evaluate the joint effect of these three biomarkers, an inflammation score was created that ranged from 0 to 3 and reflected the number of biomarkers in the highest tertile per individual. During a median follow-up of 14.4 years, 747 of 24,734 women (3.0%) experienced a first AF event. Assessed individually, all three biomarkers were associated with incident AF, even after adjustment for traditional risk factors. When combined into an inflammation score, a strong and independent relationship between inflammation and incident AF emerged. Across increasing inflammation score categories, there were 1.66, 2.22, 2.73, and 3.25 AF events per 1000 person-years of follow-up. The corresponding hazard ratios (95% confidence intervals) across inflammation score categories were 1.0, 1.22 (1.00-1.49), 1.32 (1.06-1.65), and 1.59 (1.22-2.06) (P for linear trend 0.0006) after multivariable adjustment.

CONCLUSION

In this large-scale prospective study among women without a history of cardiovascular disease, markers of systemic inflammation were significantly related to AF even after controlling for traditional risk factors.

摘要

目的

评估炎症生物标志物对女性新发心房颤动(AF)风险的联合影响。

方法和结果

我们在参加妇女健康研究的女性中进行了一项前瞻性队列研究。所有女性在研究入组时均无 AF 病史,并提供了基线血液样本,用于检测高敏 C 反应蛋白、可溶性细胞间黏附分子-1 和纤维蛋白原。为了评估这三种生物标志物的联合效应,创建了一个炎症评分,范围为 0 至 3,反映了个体中每个标志物处于最高三分位的数量。在中位数为 14.4 年的随访期间,24734 名女性中有 747 人(3.0%)发生了首次 AF 事件。单独评估时,所有三种生物标志物均与新发 AF 相关,即使在调整了传统危险因素后也是如此。当将它们组合成一个炎症评分时,炎症与新发 AF 之间出现了强烈且独立的关系。在炎症评分不断增加的类别中,每 1000 人年随访分别有 1.66、2.22、2.73 和 3.25 例 AF 事件。炎症评分类别中,风险比(95%置信区间)分别为 1.0、1.22(1.00-1.49)、1.32(1.06-1.65)和 1.59(1.22-2.06)(P 趋势检验值为 0.0006),经多变量调整后。

结论

在这项针对无心血管疾病史的女性的大型前瞻性研究中,系统性炎症标志物与 AF 显著相关,即使在控制了传统危险因素后也是如此。

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