Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota, United States of America.
Department of Epidemiology, School of Public Health, University of North Carolina, Chapel Hill, North Carolina, United States of America.
PLoS One. 2023 Jan 30;18(1):e0280657. doi: 10.1371/journal.pone.0280657. eCollection 2023.
Most strategies for prevention of venous thromboembolism focus on preventing recurrent events. Yet, primary prevention might be possible through approaches targeting the whole population or high-risk patients. To inform possible prevention strategies, population-based information on the ability of genetic risk scores to identify risk of incident venous thromboembolism is needed.
We used proportional hazards regression to relate two published genetic risk scores (273-variants versus 5-variants) with venous thromboembolism incidence in the Atherosclerosis Risk in Communities Study (ARIC) cohort (n = 11,292), aged 45-64 at baseline, drawn from 4 US communities.
Over a median of 28 years, ARIC identified 788 incident venous thromboembolism events. Incidence rates rose more than two-fold across quartiles of the 273-variant genetic risk score: 1.7, 2.7, 3.4 and 4.0 per 1,000 person-years. For White participants, age, sex, and ancestry-adjusted hazard ratios (95% confidence intervals) across quartiles were strong [1 (reference), 1.30 (0.99,1.70), 1.85 (1.43,2.40), and 2.58 (2.04,3.28)] but weaker for Black participants [1, 1.05 (0.63,1.75), 1.37 (0.84,2.22), and 1.32 (0.80,2.20)]. The 5-variant genetic risk score showed a less steep gradient, with hazard ratios in Whites of 1, 1.17 (0.89,1.54), 1.48 (1.14,1.92), and 2.18 (1.71,2.79). Models including the 273-variant genetic risk score plus lifestyle and clinical factors had a c-statistic of 0.67.
In the general population, middle-aged adults in the highest quartile of either genetic risk score studied have approximately two-fold higher risk of an incident venous thromboembolism compared with the lowest quartile. The genetic risk scores show a weaker association with venous thromboembolism for Black people.
大多数预防静脉血栓栓塞症的策略都集中在预防复发事件上。然而,通过针对整个人群或高危患者的方法,可能可以进行初级预防。为了提供可能的预防策略,需要基于人群的信息来了解遗传风险评分在识别静脉血栓栓塞症事件风险方面的能力。
我们使用比例风险回归来研究两个已发表的遗传风险评分(273 个变异体与 5 个变异体)与动脉粥样硬化风险社区研究(ARIC)队列(n = 11,292)中静脉血栓栓塞症发生率之间的关系,该队列基线年龄为 45-64 岁,来自美国 4 个社区。
在中位 28 年的随访期间,ARIC 确定了 788 例静脉血栓栓塞症事件。273 个变异体遗传风险评分的四分位数的发病率上升了两倍多:每 1000 人年 1.7、2.7、3.4 和 4.0 例。对于白人参与者,年龄、性别和祖先调整后的危险比(95%置信区间)在四分位数之间很强[1(参考),1.30(0.99,1.70),1.85(1.43,2.40)和 2.58(2.04,3.28)],但对于黑人参与者较弱[1,1.05(0.63,1.75),1.37(0.84,2.22)和 1.32(0.80,2.20)]。5 个变异体遗传风险评分显示出较平缓的梯度,白人的危险比为 1、1.17(0.89,1.54)、1.48(1.14,1.92)和 2.18(1.71,2.79)。包含 273 个变异体遗传风险评分加上生活方式和临床因素的模型的 C 统计量为 0.67。
在一般人群中,与最低四分位相比,研究中处于两个遗传风险评分最高四分位的中年成年人发生静脉血栓栓塞症事件的风险大约高两倍。黑人的遗传风险评分与静脉血栓栓塞症的相关性较弱。