Sun Jinjun, Chen Weiwei, Xu Hongli
Department of Tuberculosis, Affiliated Hospital of Shaoxing University, No. 999 South Zhongxing Road, Shaoxing, 312000, Zhejiang, China.
BMC Pulm Med. 2025 Mar 8;25(1):106. doi: 10.1186/s12890-025-03556-6.
Chronic obstructive pulmonary disease (COPD) is a leading cause of global morbidity and death. The blood urea nitrogen-to-creatinine ratio (BCR) is recognized as a crucial marker to assess renal function and cardiovascular risk. Nevertheless, the effects of BCR on COPD patients suffering comorbid congestive heart failure (CHF) is not clarified. This study aims to elucidate the association between BCR and CHF risk in the COPD population.
Data from COPD patients meeting the eligibility criteria were from the Medical Information Mart for Intensive Care IV (MIMIC-IV) database. The cumulative incidence curve was utilized for examining the link of BCR to CHF. Kaplan-Meier (KM) analysis was carried out for evaluating the relation of BCR to in-hospital mortality(IHM). Multivariable Cox regression assisted in assessing the correlation of BCR with CHF risk. Restricted cubic splines (RCS) were leveraged for unraveling the association of BCR (as a continuous variable) with CHF.
Our study included 2,840 COPD patients in the intensive care unit for the first time, with hospital stays exceeding 24 h. The incidence of CHF was 57.18% among these patients. Cumulative incidence curve analysis demonstrated a notably increased CHF incidence in patients having higher BCR (18.889 < BCR ≤ 92.5) in contrast to those with lower BCR (2.877 ≤ BCR ≤ 18.889) (p < 0.0001). KM survival analysis indicated a markedly elevated IHM risk in patients with higher BCR in comparison to those with lower BCR (p < 0.0001). Multivariable Cox regression and RCS analysis further confirmed that higher BCR was linked to a risen likelihood of CHF [hazard ratio (HR) = 1.28, 95% confidence interval (CI, 1.15-1.44), p < 0.001]. Subgroup analysis revealed a higher risk of CHF [HR = 1.41, 95% CI (1.13-1.76), p = 0.002] in patients with diabetes than those without [HR = 1.24, 95% CI (1.08-1.41), p = 0.002].
Elevated BCR is an independent risk factor for CHF in critically ill COPD individuals and strongly related to a risen risk of CHF. The findings prove BCR as a reliable clinical predictor, facilitating risk stratification and personalized treatment for COPD patients with comorbid CHF.
慢性阻塞性肺疾病(COPD)是全球发病和死亡的主要原因。血尿素氮与肌酐比值(BCR)被认为是评估肾功能和心血管风险的关键指标。然而,BCR对合并充血性心力衰竭(CHF)的COPD患者的影响尚不清楚。本研究旨在阐明COPD人群中BCR与CHF风险之间的关联。
符合纳入标准的COPD患者数据来自重症监护医学信息数据库IV(MIMIC-IV)。累积发病率曲线用于检验BCR与CHF的关联。采用Kaplan-Meier(KM)分析评估BCR与院内死亡率(IHM)的关系。多变量Cox回归用于评估BCR与CHF风险的相关性。利用限制立方样条(RCS)来揭示BCR(作为连续变量)与CHF的关联。
我们的研究首次纳入了2840例入住重症监护病房且住院时间超过24小时的COPD患者。这些患者中CHF的发生率为57.18%。累积发病率曲线分析表明,BCR较高(18.889<BCR≤92.5)的患者与BCR较低(2.877≤BCR≤18.889)的患者相比,CHF发生率显著增加(p<0.0001)。KM生存分析表明,BCR较高的患者与BCR较低的患者相比,IHM风险显著升高(p<0.0001)。多变量Cox回归和RCS分析进一步证实,较高的BCR与CHF风险增加相关[风险比(HR)=1.28,95%置信区间(CI,1.15-1.44),p<0.001]。亚组分析显示,糖尿病患者发生CHF的风险[HR=1.41,95%CI(1.13-1.76),p=0.002]高于非糖尿病患者[HR=1.24,95%CI(1.08-1.41),p=0.002]。
BCR升高是重症COPD患者发生CHF的独立危险因素,且与CHF风险增加密切相关。这些发现证明BCR是一个可靠的临床预测指标,有助于对合并CHF的COPD患者进行风险分层和个性化治疗。