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CX3CL1和D-二聚体水平在COVID-19合并慢性阻塞性肺疾病患者死亡风险分层中的预测作用

Predictive Role of CX3CL1 and D-dimer Levels in Mortality Risk Stratification for COPD Patients With COVID-19.

作者信息

Xue Jing, Liu Meimei, Liu Xin, Gao Na, Hao Wendong

机构信息

Department of Internal Medicine, Jingbian County Hospital of Traditional Chinese Medicine, Yulin, CHN.

Department of Respiratory and Critical Care Medicine, Yulin Hospital, the First Affiliated Hospital of Xi'an Jiaotong University, Yulin, CHN.

出版信息

Cureus. 2025 Jul 25;17(7):e88782. doi: 10.7759/cureus.88782. eCollection 2025 Jul.

Abstract

OBJECTIVE

In this retrospective study conducted at Yulin Hospital, the First Affiliated Hospital of Xi'an Jiaotong University (Yulin, SN, CHN), we aimed to investigate the predictive role of CX3CL1 and D-dimer for mortality in hospitalized chronic obstructive pulmonary disease (COPD) patients with COVID-19.

METHODS

Complete blood counts and inflammatory cytokine levels were collected at admission from hospitalized COPD patients with COVID-19 to explore the relationship between inflammatory parameters and mortality of COPD patients with COVID-19.

RESULTS

Compared to severe COPD with COVID-19 patients, circulating biomarkers of CX3CL1 (453.3 vs. 305.3 pg/mL,p<0.01) and D-dimer (1231.8 ng/mL vs. 680 ng/mL,p<0.01) were significantly elevated in critical illness participants. The C indices of inflammatory biomarkers CX3CL1 and D-dimer were 0.78 and 0.68, respectively. Furthermore, the prolonged illness of COPD patients with COVID-19 was associated with circulating inflammatory biomarkers of CX3CL1 (p=0.021) and D-dimer (p=0.041).

CONCLUSION

Circulating inflammatory biomarkers of CX3CL1 and D-dimer have shown the potential to predict mortality among COPD patients with severe COVID-19. Monitoring CX3CL1 and D-dimer levels could enhance clinical decision-making and risk stratification, potentially guiding more effective treatment strategies to improve patient outcomes.

摘要

目的

在西安交通大学第一附属医院榆林医院(中国陕西省榆林市)进行的这项回顾性研究中,我们旨在探讨CX3CL1和D - 二聚体对住院的新冠肺炎慢性阻塞性肺疾病(COPD)患者死亡率的预测作用。

方法

收集新冠肺炎COPD住院患者入院时的全血细胞计数和炎症细胞因子水平,以探讨炎症参数与新冠肺炎COPD患者死亡率之间的关系。

结果

与新冠肺炎重度COPD患者相比,危重症患者循环生物标志物CX3CL1(453.3 vs. 305.3 pg/mL,p<0.01)和D - 二聚体(1231.8 ng/mL vs. 680 ng/mL,p<0.01)显著升高。炎症生物标志物CX3CL1和D - 二聚体的C指数分别为0.78和0.68。此外,新冠肺炎COPD患者病程延长与循环炎症生物标志物CX3CL1(p = 0.021)和D - 二聚体(p = 0.041)有关。

结论

CX3CL1和D - 二聚体的循环炎症生物标志物已显示出预测重度新冠肺炎COPD患者死亡率的潜力。监测CX3CL1和D - 二聚体水平可加强临床决策和风险分层,可能指导更有效的治疗策略以改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf1/12375886/a63dcdc695f0/cureus-0017-00000088782-i01.jpg

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