Self-reported walking pace, polygenic risk scores and risk of coronary artery disease in UK biobank.

Self-reported walking pace, polygenic risk scores and risk of coronary artery disease in UK biobank.
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英国生物样本库中自我报告的步行速度、多基因风险评分和冠状动脉疾病风险。

DOI:
10.1016/j.numecd.2022.08.021
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发表时间:
2022
期刊:
NMCD
影响因子:
--
通讯作者:
Zaccardi F
Zaccardi F
中科院分区:
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文献类型:
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作者:
Zaccardi F

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多基因风险评分(PGS)和自我报告的步行速度都被证明可以预测心血管疾病;方法和结果我们估计了冠状动脉疾病(CAD)的10年绝对风险,调整了传统的风险因素,以及2006年3月至2021年2月期间英国生物库研究参与者9个PGS的C指数和自我报告的步行速度。在380,693例患者(54.8%女性)中,在中位数(第5,第95百分位数)11.9(8.3,13.4)年内,女性发生2,603例(1.2%)CAD事件,男性发生8,259例(4.8%)CAD事件。步行速度和遗传风险与CAD密切相关。高遗传风险(PGS前20%)的慢走者CAD的绝对10年风险最高:女性为2.72%(95%CI:2.30-3.13);男性为9.60%(8.62-10.57)。慢速和快速步行者之间的风险差异在较高[女性1.26%(0.81-1.71);男性3.63%(2.58-4.67)]比较低[分别为0.76%(0.59-0.93)和2.37%(1.96-2.78)]遗传风险更大。具有高遗传风险的快走者与具有中低遗传风险的慢走者(PGS的底部80%)相比具有相同(女性)或更高(男性)的风险。当添加到包含传统风险因素的模型中时,这两个因素分别提高了风险区分度;将它们结合起来导致最大的区分度:C指数为0.801(0.793-0.808); 0.732(0.728-0.737)。结论自我报告的高遗传风险慢走者患冠心病的风险最大,确定潜在的重要人群进行干预。PGS和步行速度都有助于风险歧视。
Background and aimsBoth polygenic risk scores (PGS) and self-reported walking pace have been shown to predict cardiovascular disease; whether combining both factors produces greater risk differentiation is, however, unknown.Methods and resultsWe estimated the 10-year absolute risk of coronary artery disease (CAD), adjusted for traditional risk factors, and the C-index across nine PGS and self-reported walking pace in UK Biobank study participants between Mar/2006–Feb/2021. In 380,693 individuals (54.8% women), over a median (5th, 95th percentile) of 11.9 (8.3, 13.4) years, 2,603 (1.2%) CAD events occurred in women and 8,259 (4.8%) in men. Both walking pace and genetic risk were strongly associated with CAD. The absolute 10-year risk of CAD was highest in slow walkers at high genetic risk (top 20% of PGS): 2.72% (95% CI: 2.30–3.13) in women; 9.60% (8.62–10.57) in men. The risk difference between slow and brisk walkers was greater at higher [1.26% (0.81–1.71) in women; 3.63% (2.58–4.67) in men] than lower [0.76% (0.59–0.93) and 2.37% (1.96–2.78), respectively] genetic risk. Brisk walkers at high genetic risk had equivalent (women) or higher (men) risk than slow walkers at moderate-to-low genetic risk (bottom 80% of PGS). When added to a model containing traditional risk factors, both factors separately improved risk discrimination; combining them resulted in the greatest discrimination: C-index of 0.801 (0.793–0.808) in women; 0.732 (0.728–0.737) in men.ConclusionSelf-reported slow walkers at high genetic risk had the greatest risk of CAD, identifying a potentially important population for intervention. Both PGS and walking pace contributed to risk discrimination.
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DOI: 10.1177/2047487319885041
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