Construction of a 28-Day Mortality Risk Prediction Model in Patients with Acute Left Heart Failure Complicated by Respiratory Failure Based on Serum HIF-1α and CysC
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摘要:
目的 探究急性左心衰(acute left heart failure,AHF)并发呼吸衰竭(respiratory failure,RF)患者血清缺氧诱导因子-1α(hypoxia-inducible factor-1alpha,HIF-1α)、胱抑素C(Cystatin C,CysC)水平预测28 d死亡风险的价值。 方法 回顾性分析2022年1月—2024年12月收治的217例AHF伴RF患者的临床资料,根据患者出院28 d生存情况分组,其中死亡组(n = 62)与存活组(n = 155)。比较两组患者一般资料及血清HIF-1α、CysC水平,分析AHF伴RF患者28 d死亡风险影响因素及血清HIF-1α、CysC水平与28 d死亡风险的关系,采用受试者工作特征(receiver operating characteristic,ROC)曲线评价AHF伴RF患者HIF-1α、CysC对28 d死亡风险的预测价值,并基于联合预测模型的进行风险分层与临床验证。 结果 死亡组急性生理学与慢性健康状况评分Ⅱ(acute physiology and chronic health evaluation Ⅱ,APACHEⅡ)评分(16.59±3.05 vs 13.72±2.47,t = 7.214,P < 0.001)、序贯性脏器衰竭评价评分(sequential organ failure assessment,SOFA)评分(12.61±2.24 vs 11.89±2.15,t = 2.202,P = 0.029)、N端B型脑钠肽前体(n-terminal pro-b-type natriuretic peptide,NT-proBNP)(507.41±82.44 vs 329.49±70.55 pg/mL,t = 15.975,P < 0.001)、HIF-1α(30.14±4.58 vs 21.37±3.82 ng/L,t = 14.410,P < 0.001)、CysC(1.72±0.35 vs 1.30±0.28 mg/L,t = 9.270,P < 0.001)均高于存活组;Logistic回归显示HIF-1α(OR = 1.315,95%CI:1.129~1.532)、CysC(OR = 1.260,95%CI:1.105~1.437)均为AHF伴RF患者28 d死亡风险独立影响因素(P < 0.05);限制性立方样条(restricted cubic spline,RCS)模型分析显示,调整其他变量后,血清HIF-1α、CysC水平仍与AHF伴RF患者28 d死亡风险呈线性正相关(P < 0.05),随血清HIF-1α、CysC升高,AHF伴RF患者的死亡风险逐渐增加;ROC曲线显示,APACHE II评分、SOFA评分、NT-proBNP、HIF-1α、CysC预测AHF伴RF患者28 d死亡风险的曲线下面积(area under curve,AUC)分别为0.737(95%CI:0.673~0.794)、0.711(0.646~0.771)、0.768(0.706~0.822)、0.748(0.684~0.804)、0.753(0.690~0.809),各指标单独预测AUC比较差异无统计学意义(P > 0.05);交互作用分析RERI = 1.09、AP = 0.253、SI = 2.727,HIF-1α与CysC两者同时升高时,对28 d死亡风险存在正向相加交互作用,即联合效应大于各自单独效应之和;血清HIF-1α、CysC联合预测AHF伴RF患者28 d死亡风险的AUC为0.878,明显大于APACHE II评分、SOFA评分、NT-proBNP、HIF-1α、CysC单独预测的AUC(P < 0.05);绘制校准曲线显示,预测风险与实际观察风险在整个风险范围内具有良好的一致性(Hosmer-Lemeshow检验,χ2 = 2.224,P = 0.086);通过Bootstrap法( 1000 次重抽样)进行内部验证,校正后模型的AUC为0.877(95%CI:0.828~0.927),且校准曲线显示预测风险与实际风险一致性良好。DCA表明在0.2~0.8阈值概率范围内,使用该模型具有临床净获益,且时间验证集显示,模型具有较高的稳健性和较高的预测效能。基于联合预测模型将患者分为低、中、高风险组,三组28 d实际死亡率分别为4.17%、27.40%、54.17%(P < 0.05)。结论 AHF伴RF患者血清HIF-1α、CysC水平与28 d死亡风险密切相关,基于二者构建的联合预测模型具有良好的区分能力。 Abstract:Objective To explore the predictive value of serum hypoxia-inducible factor-1alpha (HIF-1α) and Cystatin C (CysC) levels for 28-day mortality risk in patients with acute left heart failure (AHF) complicated with respiratory failure (RF). Methods A retrospective analysis was conducted on clinical data from 217 AHF patients with concurrent RF admitted between January 2022 and December 2024. Patients were stratified based on 28-day survival status post-discharge into a mortality group (n = 62) and a survival group (n = 155). General demographic data and serum HIF-1α and CysC levels were compared between the two groups. The influencing factors for 28-day mortality risk in AHF patients with RF and the relationship between serum HIF-1α, CysC levels and 28-day mortality risk were analyzed. Receiver operating characteristic (ROC) curves were used to evaluate the predictive value of HIF-1α and CysC for 28-day mortality risk in AHF with RF patients. Risk stratification and clinical validation were performed based on a combined predictive model. Results The mortality group demonstrated significantly higher Acute Physiology and Chronic Health Evaluation II (APACHE II) scores (16.59±3.05 vs 13.72±2.47, t = 7.214, P < 0.001), Sequential Organ Failure Assessment (SOFA) scores(12.61±2.24 vs 11.89±2.15, t = 2.202, P = 0.029), N-terminal pro-B-type natriuretic peptide (NT-proBNP) (507.41±82.44 vs 329.49±70.55 pg/mL, t = 15.975, P < 0.001), HIF-1α (30.14±4.58 vs 21.37±3.82 ng/L, t = 14.410, P < 0.001) and CysC (1.72±0.35 vs 1.30±0.28 mg/L, t = 9.270, P < 0.001) compared with the survival group. Logistic regression analysis showed that HIF-1α (OR = 1.315, 95%CI: 1.129-1.532) and CysC (OR = 1.260, 95%CI: 1.105-1.437) were independent influencing factors for 28 day mortality risk in AHF with RF patients (P < 0.05). Restricted cubic spline (RCS) model analysis demonstrated that after adjusting for other variables, serum HIF-1α and CysC levels remained linearly and positively correlated with 28 day mortality risk in AHF with RF patients (P < 0.05), with mortality risk progressively increasing as serum HIF-1α and CysC levels elevated. ROC curve analysis revealed that the area under the curve (AUC) for predicting 28-day mortality risk were as follows: APACHE II score 0.737 (95% CI: 0.673–0.794), SOFA score 0.711 (0.646–0.771), NT-proBNP 0.768 (0.706–0.822), HIF-1α 0.748 (0.684–0.804), and CysC 0.753 (0.690–0.809), with no statistically significant differences in AUC between individual indicators (P>0.05). Interaction analysis revealed RERI=1.09, AP=0.253, and SI=2.727, indicating a positive additive interaction between HIF-1α and CysC when both were simultaneously elevated, with the combined effect exceeding the sum of individual effects. The combined predictive AUC for serum HIF-1α and CysC for 28-day mortality risk in AHF with RF patients was 0.878, significantly higher than the individual AUCs for APACHE II score, SOFA score, NT-proBNP, HIF-1α, and CysC (P < 0.05). Calibration curves demonstrated good concordance between predicted and observed risk across the entire risk spectrum(Hosmer-Lemeshow test, χ2=2.224, P = 0.086). Internal validation via Bootstrap resampling ( 1000 iterations) yielded a corrected model AUC of 0.877 (95% CI: 0.828–0.927), with calibration curves demonstrating good agreement between predicted and actual risk. Decision curve analysis (DCA) indicated clinical net benefit within the threshold probability range of 0.2–0.8, and temporal validation demonstrated high model robustness and predictive performance. Patients stratified into low, intermediate, and high-risk groups based on the combined predictive model had actual 28-day mortality rates of 4.17%, 27.40%, and 54.17%, respectively (P<0.05).Conclusion Serum HIF-1α and CysC levels in AHF patients with concurrent RF are closely associated with 28-day mortality risk. A combined predictive model constructed from these two markers demonstrates excellent discriminative ability. -
表 1 两组一般资料及血清HIF-1α、CysC水平比较[n(%)/($ \bar x \pm s $)]
Table 1. Comparison of general data and serum HIF-1α,CysC levels between two groups [n(%)/($ \bar x \pm s $)]
项目 死亡组(n = 62) 存活组(n = 155) t/χ2 P 性别 男 33(53.23) 84(54.19) 0.017 0.897 女 29(46.77) 71(45.81) 年龄(岁) 61.42 ± 6.83 59.57 ± 7.22 1.731 0.085 体重指数(kg/m2) 21.57 ± 2.43 21.33 ± 2.50 0.644 0.520 基础疾病 高血压 13(20.97) 26(16.77) 0.528 0.467 糖尿病 11(17.74) 20(12.90) 0.847 0.357 冠心病 7(11.29) 14(9.03) 0.258 0.611 高脂血症 11(17.74) 22(14.19) 0.432 0.511 心功能分级 Ⅲ级 45(72.58) 130(83.87) 3.617 0.057 Ⅳ级 17(27.42) 25(16.13) 呼吸衰竭类型 Ⅰ型 32(51.61) 85(54.84) 0.185 0.667 Ⅱ型 30(48.39) 70(45.16) 生命体征 心率(次/min) 119.25 ± 10.31 117.12 ± 9.82 1.423 0.156 舒张压(mmHg) 94.32 ± 9.17 92.14 ± 10.25 1.457 0.147 收缩压(mmHg) 142.83 ± 15.06 140.29 ± 12.88 1.249 0.213 呼吸频率(次/min) 36.24 ± 2.83 35.72 ± 2.77 1.242 0.216 动脉血气 pH 7.11 ± 0.52 7.20 ± 0.45 1.272 0.205 PaO2(mmHg) 54.78 ± 2.11 55.12 ± 2.28 1.013 0.312 PaCO2(mmHg) 67.06 ± 11.03 65.29 ± 10.84 1.081 0.281 病情评分(分) APACHE II评分 16.59 ± 3.05 13.72 ± 2.47 7.214 <0.001 SOFA评分 12.61 ± 2.24 11.89 ± 2.15 2.202 0.029 发病至机械通气时间 ≤2 h 35(56.45) 113(72.90) 5.527 0.019 >2 h 27(43.55) 42(27.10) 血清指标 CRP(mg/L) 22.74 ± 5.69 21.41 ± 7.35 1.279 0.202 PCT(ng/mL) 3.84 ± 0.67 3.78 ± 0.62 0.629 0.530 NT-proBNP(pg/mL) 507.41 ± 82.44 329.49 ± 70.55 15.975 <0.001 HIF-1α(ng/L) 30.14 ± 4.58 21.37 ± 3.82 14.410 <0.001 CysC(mg/L) 1.72 ± 0.35 1.30 ± 0.28 9.270 <0.001 LVEF(%) 33.57 ± 3.47 36.86 ± 3.77 5.938 <0.001 表 2 AHF伴RF患者28 d死亡风险的多因素Logistic回归分析
Table 2. Multivariate Logistic regression analysis of 28-day mortality risk in AHF patients with RF
因素 赋值 β S.E. Waldχ2 OR 95%CI P 模型1 常数项 — 1.987 0.107 22.833 — — <0.001* APACHE II评分 原值带入 0.389 0.112 12.083 1.476 1.079~2.019 <0.001* SOFA评分 原值带入 0.414 0.125 10.952 1.512 1.154~1.982 <0.001* 发病至机械通气时间 ≤2 h=1,>2 h=2 1.408 0.362 15.134 4.089 2.749~6.082 <0.001* NT-proBNP 原值带入 0.469 0.121 15.018 1.598 1.254~2.037 <0.001* HIF-1α 原值带入 0.463 0.140 10.931 1.589 1.191~2.119 <0.001* CysC 原值带入 0.452 0.116 15.191 1.572 1.179~2.095 <0.001* 模型2 常数项 — 1.325 0.084 17.241 — — <0.001* HIF-1α 原值带入 0.274 0.102 7.214 1.315 1.129~1.532 <0.001* CysC 原值带入 0.231 0.074 9.762 1.260 1.105~1.437 <0.001* 模型1为校正APACHE II评分、SOFA评分、发病至机械通气时间前,模型2为校正APACHE II评分、SOFA评分、发病至机械通气时间后;—表示无数据;*P < 0.05。 表 3 APACHE II评分、SOFA评分、NT-proBNP、HIF-1α、CysC对AHF伴RF患者28 d死亡风险的预测价值
Table 3. Predictive value of APACHE II score,SOFA score,NT-proBNP,HIF-1α and CysC for 28-day mortality risk in AHF patients with RF
项目 AUC 95%CI 截断值 P 特异度(%) 敏感度(%) 约登指数 APACHE II评分 0.737 0.673~0.794 14.35分 <0.001* 70.32 70.97 0.413 SOFA评分 0.711 0.646~0.771 11.16分 <0.001* 61.29 79.03 0.403 NT-proBNP 0.768 0.706~0.822 510.53 pg/mL <0.001* 82.58 61.29 0.439 HIF-1α 0.748 0.684~0.804 27.51 ng/L <0.001* 70.81 74.19 0.400 CysC 0.753 0.690~0.809 1.48 mg/L <0.001* 71.61 79.03 0.403 HIF-1α+CysC 0.878 0.826~0.918 0.623 <0.001* 76.77 85.48 0.623 *P < 0.05。 表 4 HIF-1α、CysC对AHF伴RF患者28 d死亡风险的交互作用
Table 4. Interactive effect of HIF-1α and CysC on 28-day mortality risk in AHF patients with RF
HIF-1α CysC 28 d结局 OR(95%CI) RERI AP SI 死亡 生存 低水平 低水平 10 43 1 1.09 0.253 2.727 低水平 高水平 16 48 1.43(0.59~3.48) 高水平 低水平 19 46 1.78(0.74~4.27) 高水平 高水平 18 18 4.30(1.66~11.13) -
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