收稿日期: 2025-01-20
网络出版日期: 2025-04-23
基金资助
河南省科技攻关项目(2023ZY3008)
The correlation between the levels of APC, TXB2, and sB7⁃H3 in peripheral blood of elderly patients with pneumonia and the severity and prognosis of the disease
Received date: 2025-01-20
Online published: 2025-04-23
目的 探讨老年肺炎外周血活化蛋白C(APC)、血栓素B2(TXB2)、可溶性B7-H3(sB7-H3)水平与病情程度和预后的相关性。 方法 选取老年肺炎患者100例作为研究组,另选取同期健康志愿者100例作为对照组。比较两组外周血APC、TXB2、sB7-H3水平。研究组根据英国胸科协会改良肺炎评分(CURB-65评分)判定病情程度,分为低危患者、中危患者和高危患者。比较不同病情程度患者外周血APC、TXB2、sB7-H3水平。Pearson相关性分析外周血APC、TXB2、sB7-H3水平与病情程度的相关性。对研究组随访30 d,根据预后分为预后良好亚组与预后不良亚组,比较研究组不同预后患者临床资料、外周血APC、TXB2、sB7-H3水平。偏相关性分析外周血APC、TXB2、sB7-H3水平与预后的相关性。受试者工作特征(ROC)曲线分析预测价值。 结果 研究组外周血APC水平低于对照组,TXB2、sB7-H3水平高于对照组(P < 0.05);研究组根据CURB-65评分判定病情程度,其中轻度患者33例,中度患者39例,重度患者28例。重度患者外周血APC水平低于中度患者、轻度患者,中度患者低于轻度患者,重度患者TXB2、sB7-H3水平高于中度患者、轻度患者,中度患者高于轻度患者(P < 0.05);Pearson相关性分析,外周血APC与CURB-65评分呈负相关,TXB2、sB7-H3与CURB-65评分呈正相关(P < 0.05);研究组随访30 d,预后不良亚组外周血APC水平低于预后良好亚组,TXB2、sB7-H3水平高于预后良好亚组(P < 0.05);偏相关性分析,外周血APC、TXB2、sB7-H3与预后显著相关(P < 0.05);ROC曲线分析,外周血APC、TXB2、sB7-H3预测老年肺炎患者预后的AUC为0.752、0.738、0.761,敏感度为66.67%、76.19%、66.67%,特异度为78.48%、67.09%、78.48%;三者联合预测老年肺炎患者预后的AUC为0.918,敏感度为85.71%,特异度为87.34%,较各指标单独预测价值显著提升(Z = 2.207、2.666、2.109,P = 0.027、0.008、0.035)。 结论 老年肺炎外周血APC、TXB2、sB7-H3与病情程度和预后显著相关,联合检测时能较为可靠地预测预后情况。
郑富霞 , 苗丽君 , 黄凤祥 , 黄仕夫 , 高增艳 , 张瑞霞 , 孟泳 . 老年肺炎外周血活化蛋白C、血栓素B2、可溶性B7-H3水平与病情程度和预后的相关性[J]. 实用医学杂志, 2025 , 41(7) : 1056 -1061 . DOI: 10.3969/j.issn.1006-5725.2025.07.019
Objective To investigate the correlation between the levels of activated protein C (APC), thromboxane B2 (TXB2), and soluble B7?H3 (sB7?H3) in the peripheral blood of elderly patients with pneumonia and the severity as well as prognosis of the disease. Methods One hundred elderly pneumonia patients admitted to our hospital from March 2022 to June 2024 were enrolled as the study group, and 100 healthy volunteers during the same period were selected as the control group. The levels of APC, TXB2, and sB7?H3 in peripheral blood were compared between the two groups. Study group patients were further categorized into low?risk, medium?risk, and high?risk subgroups based on the CURB?65 score (Confusion, Uremia, Respiratory rate, Blood pressure, Age ≥ 65 years). The levels of APC, TXB2, and sB7?H3 in peripheral blood were compared among patients with varying disease severities. Pearson correlation analysis was performed to evaluate the correlation between the levels of APC, TXB2, and sB7?H3 in peripheral blood and disease severity. The study group was followed up for 30 days and subsequently divided into good prognosis and poor prognosis subgroups according to their clinical outcomes. Clinical data and peripheral blood levels of APC, TXB2, and sB7?H3 were compared between patients with different prognoses. Partial correlation analysis was conducted to assess the relationship between peripheral blood levels of APC, TXB2, and sB7?H3 and prognosis. Finally, the predictive value of these biomarkers was evaluated using the Receiver Operating Characteristic (ROC) curve. Results The level of APC in the peripheral blood of the study group was significantly lower than that of the control group, whereas the levels of TXB2 and sB7?H3 were significantly higher (P <0.05). The severity of the disease in the study group was assessed using the CURB?65 score, which categorized patients into 33 mild cases, 39 moderate cases, and 28 severe cases. Severe patients exhibited a lower level of APC in peripheral blood compared to moderate and mild patients. Additionally, the levels of TXB2 and sB7?H3 in moderate patients were higher than those in mild patients, while severe patients demonstrated even higher levels of TXB2 and sB7?H3 compared to both moderate and mild patients (P < 0.05). Pearson correlation analysis revealed that peripheral blood APC was negatively correlated with the CURB?65 score, whereas TXB2 and sB7?H3 were positively correlated with the CURB?65 score (P < 0.05). During a 30?day follow?up period, the research team identified 79 patients with good prognoses and 21 patients with poor prognoses. Significant differences were observed in diabetes prevalence, disease severity, and APACHEⅡ scores between the poor prognosis subgroup and the good prognosis subgroup (P < 0.05). The levels of APC in peripheral blood were significantly lower in the poor prognosis subgroup compared to the good prognosis subgroup, whereas the levels of TXB2 and sB7?H3 were significantly higher (P < 0.05). Partial correlation analysis revealed that peripheral blood APC, TXB2, and sB7?H3 were significantly associated with prognosis (P < 0.05). The AUC values for predicting the prognosis of elderly pneumonia patients using peripheral blood APC, TXB2, and sB7?H3 were 0.752, 0.738, and 0.761, respectively, with sensitivities of 66.67%, 76.19%, and 66.67%, and specificities of 78.48%, 67.09%, and 78.48%. When combining these three indicators for prognostic prediction, the AUC increased to 0.918, with a sensitivity of 85.71% and a specificity of 87.34%, demonstrating a significant improvement in predictive accuracy compared to each indicator used alone (Z = 2.207, 2.666, 2.109, P = 0.027, 0.008, 0.035). Conclusion The levels of APC, TXB2, and sB7?H3 in the peripheral blood of elderly patients with pneumonia are significantly associated with the severity and prognosis of the disease. Combined detection of these biomarkers can serve as a reliable predictor of clinical outcomes.
| 1 | LUO A H, LIU Y. The effect of low-molecular-weight heparin combined with amikacin on the coagulation function and bacterial clearance in the treatment of patients with severe senile pneumonia[J]. Pak J Med Sci,2023,39(1):172-176. doi:10.12669/pjms.39.1.6627 |
| 2 | 杨幸乐,夏婷婷,左春磊,等. 微生物学快速现场评价在重症肺炎中的应用价值[J]. 实用医学杂志,2023,39(22):2964-2968. |
| 3 | MUHAMMAD W, ZHAI Z L, WANG S Q,et al. Inflammation-modulating nanoparticles for pneumonia therapy[J]. Wiley Interdiscip Rev Nanomed Nanobiotechnol,2022,14(2):e1763. doi:10.1002/wnan.1763 |
| 4 | CONWAY E M, MACKMAN N, WARREN R Q,et al. Understanding COVID-19-associated coagulopathy[J]. Nat Rev Immunol,2022,22(10):639-649. doi:10.1038/s41577-022-00762-9 |
| 5 | 付君静,李闯,陈胜阳. 老年重症肺炎患者血清4-HNE、APC、sCD163预测预后不良的价值[J]. 海南医学,2024,35(11):1633-1638. |
| 6 | CHEN L C, TSENG H M, KUO M L,et al. Levels of 15-HETE and TXB2 in exhaled breath condensates as markers for diagnosis of childhood asthma and its therapeutic outcome[J]. Pediatr Allergy Immunol,2021,32(8):1673-1680. |
| 7 | GENOVA C, TASSO R, ROSA A,et al. Prognostic Role of Soluble and Extracellular Vesicle-Associated PD-L1, B7-H3 and B7-H4 in Non-Small Cell Lung Cancer Patients Treated with Immune Checkpoint Inhibitors[J]. Cells,2023,12(6):832. doi:10.3390/cells12060832 |
| 8 | 中华医学会,中华医学会杂志社,中华医学会全科医学分会,等. 成人社区获得性肺炎基层诊疗指南(2018年)[J]. 中华全科医师杂志,2019,18(2):117-126. |
| 9 | CARLOS P, GOMES R, COELHO J,et al. CURB-65 and Long-Term Mortality of Community-Acquired Pneumonia: A Retrospective Study on Hospitalized Patients[J]. Cureus,2023,15(3):e36052. |
| 10 | SILVA B R D S, SIDARTA-OLIVEIRA D, MORARI J,et al. Protein C Pretreatment Protects Endothelial Cells from SARS-CoV-2-Induced Activation[J]. Viruses,2024,16(7):1049. doi:10.3390/v16071049 |
| 11 | 李汉冬,孙立宇,韩永梅,等. 血清FKN、APC与老年社区获得性肺炎患者病情和预后不良的关系[J]. 现代生物医学进展,2024,24(2):333-337. |
| 12 | OI I, ITO I, TANABE N,et al. Protein C activity as a potential prognostic factor for nursing home-acquired pneumonia[J]. PLoS One,2022,7(10):e0274685. doi:10.1371/journal.pone.0274685 |
| 13 | KHOSHNEGAH Z, SIYADAT P, ROSTAMI M,et al. Protein C and S activities in COVID-19: A systematic review and meta-analysis[J]. J Thromb Thrombolysis,2024,57(6):1018-1030. doi:10.1007/s11239-024-02971-6 |
| 14 | SILVA B R S, JARA C P, SIDARTA-OLIVEIRA D,et al. Downregulation of the Protein C Signaling System Is Associated with COVID-19 Hypercoagulability-A Single-Cell Transcriptomics Analysis[J]. Viruses,2022,14(12):2753. doi:10.3390/v14122753 |
| 15 | FURUKAWA T, AKAIKE K, IYAMA S,et al. Interstitial Lung Disease in Adulthood Associated with Surfactant Protein C Gene Mutation in a Patient with a History of Lipoid Pneumonia in Infancy[J]. Intern Med,2023,62(17):2521-2525. doi:10.2169/internalmedicine.0980-22 |
| 16 | RADE J J, BARTON B A, VASAN R S,et al. Association of Thromboxane Generation With Survival in Aspirin Users and Nonusers[J]. J Am Coll Cardiol,2022,80(3):233-250. doi:10.1016/j.jacc.2022.04.034 |
| 17 | 梁利红. 血清及肺泡灌洗液γ干扰素,血栓素和可溶性B7-H3在难治性肺炎支原体肺炎中的鉴别诊断价值分析[J]. 安徽医药,2020,24(10):2054-2058. |
| 18 | LIU X, CHEN R H, LI B H,et al. Oxidative stress indexes as biomarkers of the severity in COVID-19 patients[J]. Int J Med Sci,2024,21(15):3034-3045. doi:10.7150/ijms.102879 |
| 19 | GARSHICK M S, TAWIL M, BARRETT T J,et al. Activated Platelets Induce Endothelial Cell Inflammatory Response in Psoriasis via COX-1[J]. Arterioscler Thromb Vasc Biol,2020,40(5):1340-1351. doi:10.1161/atvbaha.119.314008 |
| 20 | 吴会芳,张景丽,刘晓娟,等. 支气管镜治疗儿童肺炎支原体肺炎临床观察及黏液栓形成的危险因素[J]. 国际呼吸杂志,2021,41(12):908-913. |
| 21 | 刘庆,卢蓉,赵力芳. 支原体肺炎患儿血栓素B2嗜酸性细胞阳离子蛋白T-IgE水平与支气管镜下气道改变的关系分析[J].山西医药杂志,2021,50(7):1128-1131. |
| 22 | 郭静,刘泮力. 肿瘤坏死因子-α、内皮素-1、免疫球蛋白E和血栓素B2水平与肺炎支原体感染老年哮喘患者病情严重程度的关系[J]. 陕西医学杂志,2022,51(7):863-865,869. |
| 23 | PICARDA E, GALBO P M JR, ZONG H H,et al. The immune checkpoint B7-H3 (CD276) regulates adipocyte progenitor metabolism and obesity development[J]. Sci Adv,2022,8(17):eabm7012. doi:10.1126/sciadv.abm7012 |
| 24 | 臧瑗,刘亚丽,张中. 血浆可溶性B7-H3预测老年肺炎支原体肺炎严重程度的价值[J]. 实用老年医学,2020,34(7):670-673. |
| 25 | WU P, WANG J. Changes and Significance of Serum sB7-H3 and Cytokines in Children with Mycoplasma pneumonae Pneumonia[J]. J Coll Physicians Surg Pak,2020,30(3):268-271. doi:10.29271/jcpsp.2020.03.268 |
| 26 | GU W J, LI G, ZHANG W L,et al. MiR-29b regulates Th2 cell differentiation in asthma by targeting inducible B7-H3 and STAT3[J]. Clin Transl Allergy,2022,12(1):e12114. doi:10.1002/clt2.12114 |
| 27 | FENG Y, LEE J, YANG L P,et al. Engineering CD276/B7-H3-targeted antibody-drug conjugates with enhanced cancer-eradicating capability[J]. Cell Rep,2023,42(12):113503. doi:10.1016/j.celrep.2023.113503 |
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