一种基于生长分化因子15的风险评分模型,用于预测血液透析患者的死亡率。
A Growth Differentiation Factor 15-Based Risk Score Model to Predict Mortality in Hemodialysis Patients.
作者信息
Chang Jia-Feng, Chen Po-Cheng, Hsieh Chih-Yu, Liou Jian-Chiun
机构信息
Division of Nephrology, Department of Internal Medicine, En Chu Kong Hospital, New Taipei City 237, Taiwan.
Department of Nursing, Yuanpei University of Medical Technology, Hsinchu 300, Taiwan.
出版信息
Diagnostics (Basel). 2021 Feb 11;11(2):286. doi: 10.3390/diagnostics11020286.
BACKGROUND
The risk of cardiovascular (CV) and fatal events remains extremely high in patients with maintenance hemodialysis (MHD), and the growth differentiation factor 15 (GDF15) has emerged as a valid risk stratification biomarker. We aimed to develop a GDF15-based risk score as a death prediction model for MHD patients.
METHODS
Age, biomarker levels, and clinical parameters were evaluated at study entry. One hundred and seventy patients with complete information were finally included for data analysis. We performed the Cox regression analysis of various prognostic factors for mortality. Then, age, GDF15, and robust clinical predictors were included as a risk score model to assess the predictive accuracy for all-cause and CV death in the receiver operating characteristic (ROC) curve analysis.
RESULTS
Age, GDF15, and albumin were significantly associated with higher all-cause and CV mortality risk that were combined as a risk score model. The highest tertile of GDF-15 (>1707.1 pg/mL) was associated with all-cause mortality (adjusted hazard ratios (aHRs): 3.06 (95% confidence interval (CI): 1.20-7.82), < 0.05) and CV mortality (aHRs: 3.11 (95% CI: 1.02-9.50), < 0.05). The ROC analysis of GDF-15 tertiles for all-cause and CV mortality showed 0.68 (95% CI = 0.59 to 0.77) and 0.68 (95% CI = 0.58 to 0.79), respectively. By contrast, the GDF15-based prediction model for all-cause and CV mortality showed 0.75 (95% CI: 0.67-0.82) and 0.72 (95% CI: 0.63-0.81), respectively.
CONCLUSION
Age, GDF15, and hypoalbuminemia predict all-cause and CV death in MHD patients, yet a combination scoring system provides more robust predictive powers. An elevated GDF15-based risk score warns clinicians to determine an appropriate intervention in advance. In light of this, the GDF15-based death prediction model could be developed in the artificial intelligence-based precision medicine.
背景
维持性血液透析(MHD)患者发生心血管(CV)事件和致命事件的风险仍然极高,生长分化因子15(GDF15)已成为一种有效的风险分层生物标志物。我们旨在开发一种基于GDF15的风险评分,作为MHD患者的死亡预测模型。
方法
在研究开始时评估年龄、生物标志物水平和临床参数。最终纳入170例信息完整的患者进行数据分析。我们对各种死亡预后因素进行了Cox回归分析。然后,将年龄、GDF15和可靠的临床预测因素纳入风险评分模型,在受试者工作特征(ROC)曲线分析中评估全因死亡和CV死亡的预测准确性。
结果
年龄、GDF15和白蛋白与全因和CV死亡风险较高显著相关,这些因素被合并为一个风险评分模型。GDF-15最高三分位数(>1707.1 pg/mL)与全因死亡率(调整后危险比(aHRs):3.06(95%置信区间(CI):1.20-7.82),<0.05)和CV死亡率(aHRs:3.11(95%CI:1.02-9.50),<0.05)相关。GDF-15三分位数对全因和CV死亡率的ROC分析分别显示为0.68(95%CI = 0.59至0.77)和0.68(95%CI = 0.58至0.79)。相比之下,基于GDF15的全因和CV死亡率预测模型分别显示为0.75(95%CI:0.67-0.82)和0.72(95%CI:0.63-0.81)。
结论
年龄、GDF15和低白蛋白血症可预测MHD患者的全因和CV死亡,但联合评分系统具有更强的预测能力。基于GDF15的风险评分升高提醒临床医生提前确定适当的干预措施。有鉴于此,基于GDF15的死亡预测模型可在基于人工智能的精准医学中开发。