OPG/TRAIL ratio as a predictive biomarker of mortality in patients with type A acute aortic dissection.
OPG/TRAIL ratio as a predictive biomarker of mortality in patients with type A acute aortic dissection.
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OPG/TRAIL 比值作为 A 型急性主动脉夹层患者死亡率的预测生物标志物
DOI:
10.1038/s41467-021-23787-5
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发表时间:
2021-06-07
影响因子:
16.6
通讯作者:
Li Y
中科院分区:
文献类型:
--
作者:
Lu J;Li P;Ma K;Li Y;Yuan H;Zhu J;Duan W;Ou J;Huang Y;Wu L;Pan X;Zhang H;Du J;Li Y
Following hospital discharge, patients with type A acute aortic dissection (TA-AAD) may present an increase in mortality risk. However, little is known about specific biomarkers associated with post-discharge survival, and there is a paucity of prognostic markers associated with TA-AAD. Here, we identify nine candidate proteins specific for patietns with TA-AAD in a cross-sectional dataset by unbiased protein screening and in-depth bioinformatic analyses. In addition, we explore their association with short-term and long-term mortality in a derivation cohort of patients with TA-AAD, including an internal (n = 300) and external (n = 236) dataset. An elevated osteoprotegerin (OPG)/tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) ratio was the strongest predictor of overall, 30-day, post-30-day mortality in both datasets and was confirmed to be a strong predictor of mortality in an independent validation cohort (n = 400). Based on OPG/TRAIL ratio-guided risk stratification, patients at high risk (>33) had a higher 1-year mortality (55.6% vs. 4.3%; 68.2% vs. 2.6%) than patients at low risk (<4) in both cohorts. In Conclusion, we show that an elevated OPG/TRAIL ratio is associated with a significant increase in short-term and long-term mortality in patients with TA-AAD. Despite many therapeutic improvements, mortality risk in patients with type A acute aortic dissection remains high. Here the authors construct a biomarker-guided risk stratification tool to predict death, which could potentially contribute to treatment decision-making and improvement of the prognosis.
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