Department of Cardiology, Changzhou No.2 people's Hospital, Affiliated to Nanjing Medical University, Changzhou, China.
PLoS One. 2018 May 23;13(5):e0197609. doi: 10.1371/journal.pone.0197609. eCollection 2018.
To investigate the association between growth differentiation factor-15 (GDF-15) and contrast-induced nephropathy (CIN) in patients with acute myocardial infarction (AMI) undergoing percutaneous coronary intervention (PCI).
A total of 311 patients with AMI were studied retrospectively. All patients were divided into two groups according to the occurrence of CIN after PCI. Baseline clinical data were compared between two groups. Multivariate logistic regression analysis was used to identify the risk factors for CIN. Cox regression analysis was used to identify the association between GDF-15, CIN and short-term outcome.
There were 80 patients in CIN group (average age was 71.60 ± 13.00 years; 67.5% male) and 231 patients in non-CIN group (average age was 63.80 ± 11.70 years; 71.9%male). The concentration of GDF-15 in CIN group was higher than that of non-CIN group (1232 ± 366.6 ng/L vs. 939.20 ± 309.6 ng/L, P <0.001). According to GDF-15 quartiles, patients were divided into four groups. Multivariate logistic model indicated that the highest quartile(Q4) was significantly associated with an increased risk of CIN compared with lower level of GDF-15 (Q1, Q2 and Q3) (OR : 3.572, 1.803-7.078, P < 0.001). Of 243 patients who could calculate the ACEF risk score, area under the curve (AUC) of GDF-15 was 0.793, 95%CI: 0.729-0.856, P < 0.001, while AUC of ACEF was 0.708, 95%CI: 0.630-0.786, P < 0.001. Using 10% and 30% as arbitrary thresholds to define patients at low, intermediate, and high risk, GDF-15 achieved a net reclassification improvement (NRI) of 0.32 (95%CI: 0.123-0.518, P = 0.001) compared with the ACEF risk score. Cox regression model showed that high concentration of GDF-15 (Q4) was significantly associated with an increased risk of all-cause mortality and major adverse clinical events (MACE) (HR: 8.434, 95%CI: 2.650-26.837, P <0.001; HR: 3.562, 95%CI: 1.658-7.652, P = 0.001) compared with low level of GDF-15 (Q1, Q2 and Q3). CIN was an independent predictor of all-cause mortality and MACE in AMI patients (HR: 3.535, 95%CI: 1.135-11.005, P = 0.029; HR: 5.154, 95%CI: 2.228-11.925, P <0.001).
GDF-15 levels increased in CIN group in AMI patients underwent PCI. GDF-15 was an independent risk factor for CIN in AMI patients underwent PCI. GDF-15 level and CIN are independent risk factors for all-cause mortality and MACE in short-term follow-ups.
探讨生长分化因子 15(GDF-15)与急性心肌梗死(AMI)经皮冠状动脉介入治疗(PCI)后对比剂诱导肾病(CIN)的关系。
回顾性研究 311 例 AMI 患者。所有患者均根据 PCI 后 CIN 的发生情况分为两组。比较两组间的基线临床资料。采用多因素 logistic 回归分析识别 CIN 的危险因素。采用 Cox 回归分析识别 GDF-15、CIN 与短期预后的关系。
CIN 组 80 例(平均年龄 71.60±13.00 岁;67.5%为男性),非 CIN 组 231 例(平均年龄 63.80±11.70 岁;71.9%为男性)。CIN 组 GDF-15 浓度高于非 CIN 组(1232±366.6ng/L 比 939.20±309.6ng/L,P<0.001)。根据 GDF-15 四分位数,将患者分为四组。多因素 logistic 模型表明,与较低水平的 GDF-15(Q1、Q2 和 Q3)相比,最高四分位数(Q4)与 CIN 的发生风险显著增加(OR:3.572,1.803-7.078,P<0.001)。在 243 例可计算 ACEF 风险评分的患者中,GDF-15 的曲线下面积(AUC)为 0.793,95%CI:0.729-0.856,P<0.001,而 ACEF 的 AUC 为 0.708,95%CI:0.630-0.786,P<0.001。以 10%和 30%为任意阈值,将患者定义为低危、中危和高危,GDF-15 的净重新分类改善(NRI)为 0.32(95%CI:0.123-0.518,P=0.001),优于 ACEF 风险评分。Cox 回归模型显示,GDF-15 浓度高(Q4)与全因死亡率和主要不良临床事件(MACE)风险增加显著相关(HR:8.434,95%CI:2.650-26.837,P<0.001;HR:3.562,95%CI:1.658-7.652,P=0.001),与 GDF-15 水平较低(Q1、Q2 和 Q3)相比。CIN 是 AMI 患者全因死亡率和 MACE 的独立预测因子(HR:3.535,95%CI:1.135-11.005,P=0.029;HR:5.154,95%CI:2.228-11.925,P<0.001)。
AMI 患者 PCI 后 CIN 组 GDF-15 水平升高。GDF-15 是 AMI 患者 PCI 后 CIN 的独立危险因素。GDF-15 水平和 CIN 是短期随访全因死亡率和 MACE 的独立危险因素。