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Improved cardiovascular risk prediction in patients with end-stage renal disease on hemodialysis using machine learning modeling and circulating microribonucleic acids

机译:利用机器学习建模和循环微核酸改善血液透析末期肾病患者的心血管风险预测

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Rationale: To test whether novel biomarkers, such as microribonucleic acids (miRNAs), and nonstandard predictive models, such as decision tree learning, provide useful information for medical decision-making in patients on hemodialysis (HD). Methods: Samples from patients with end-stage renal disease receiving HD included in the AURORA trial were investigated (n=810). The study included two independent phases: phase I (matched cases and controls, n=410) and phase II (unmatched cases and controls, n=400). The composite endpoint was cardiovascular death, nonfatal myocardial infarction or nonfatal stroke. miRNA quantification was performed using miRNA sequencing and RT-qPCR. The CART algorithm was used to construct regression tree models. A bagging-based procedure was used for validation. Results: In phase I, miRNA sequencing in a subset of samples (n=20) revealed miR-632 as a candidate (fold change=2.9). miR-632 was associated with the endpoint, even after adjusting for confounding factors (HR from 1.43 to 1.53). These findings were not reproduced in phase II. Regression tree models identified eight patient subgroups with specific risk patterns. miR-186-5p and miR-632 entered the tree by redefining two risk groups: patients older than 64 years and with hsCRP0.827 mg/L and diabetic patients younger than 64 years. miRNAs improved the discrimination accuracy at the beginning of the follow-up (24 months) compared to the models without miRNAs (integrated AUC [iAUC]=0.71). Conclusions: The circulating miRNA profile complements conventional risk factors to identify specific cardiovascular risk patterns among patients receiving maintenance HD.? The author(s).
机译:基本原理:测试新型生物标志物,如微生核酸(miRNA)和非标准预测模型,如决策树学习,为血液透析患者(HD)提供了有用的医学决策信息。方法:研究了从Aurora试验中包含的高清末期肾病患者的患者样品(n = 810)。该研究包括两个独立的阶段:I阶段I(匹配的病例和对照,N = 410)和II期(无与伦比的病例和对照,N = 400)。复合终点是心血管死亡,非缺乏心肌梗死或非缺失中风。使用miRNA测序和RT-QPCR进行miRNA定量。 CART算法用于构建回归树模型。基于袋装的过程用于验证。结果:在A阶段I中,在样品子集(n = 20)中的miRNA测序揭示了miR-632作为候选者(折叠变化= 2.9)。 MiR-632与端点相关联,即使在调整混淆因子(1.43到1.53)后也会有关。这些发现在II期未复制。回归树模型确定了具有特定风险模式的八个患者子组。 MiR-186-5P和MIR-632通过重新定义两种风险群体进入树:64岁的患者和HSCRP <0.827 mg / L和糖尿病患者,患者年轻超过64岁。与没有miRNA的模型相比,MiRNA在随访开始时的辨别准确性(24个月)(集成AUC [IAC] = 0.71)。结论:循环miRNA型谱补充常规危险因素,以鉴定接受维护HD的患者的特定心血管风险模式。作者。

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