Citation: | LIU Yuxin, YAN Yongmin, REN Jianke, TANG Jianlei, XUE Sheliang, ZHUANG Zhifang, CAI Run, ZHOU Yanjuan. Changes of interleukin-34 levels in serum and bronchoalveolar lavage fluid of patients with severe pneumonia and their prognostic value[J]. Journal of Clinical Medicine in Practice, 2024, 28(24): 31-36, 43. DOI: 10.7619/jcmp.20243604 |
To investigate the changes in interleukin-34 (IL-34)levels in serum and bronchoalveolar lavage fluid (BALF) of patients with severe pneumonia and their prognostic value.
A total of 66 patients with severe pneumonia (severe pneumonia group), 35 patients with non-severe pneumonia (non-severe pneumonia group), and 27 healthy adults (control group) were enrolled. The severe pneumonia group was further divided into survival group of 38 patients and non-survival group of 28 patients based on 28-day survival. Clinical data of all subjects were analyzed. Receiver operating characteristic (ROC) curves were plotted to assess the predictive power of serum IL-34 and relative IL-34 gene expression in BALF for 28-day mortality in patients with severe pneumonia, as well as the predictive power of serum IL-34 for severe pneumonia. Kaplan-Meier survival curves were plotted, and the Log-rank test was used to compare cumulative survival rates. Cox regression analysis was conducted to explore risk factors for 28-day mortality in patients with severe pneumonia. Pearson correlation analysis was used to assess the correlation between serum IL-34 levels and relative IL-34 gene expression in BALF of patients with severe pneumonia.
Serum IL-34 levels were higher in the severe pneumonia group than those in the non-severe pneumonia group, and were higher in the non-severe pneumonia group than in the control group (P < 0.05). Serum IL-34 levels and relative IL-34 gene expression in BALF were higher in the non-survival group than in the survival group (P < 0.05). ROC curve analysis showed that the areas under the curve for predicting 28-day mortality in patients with severe pneumonia were 0.908 for serum IL-34 levels and 0.878 for relative IL-34 gene expression in BALF. The optimal cutoff value for serum IL-34 levels in predicting severe pneumonia was 129.9 pg/mL. Multivariate Cox regression analysis showed that increased serum IL-34 levels and increased relative IL-34 gene expression in BALF were independent risk factors for 28-day mortality in patients with severe pneumonia (P < 0.05). The Kaplan-Meier survival analysis results indicate that, with a cutoff value of 129.9 pg/mL, patients with severe pneumonia who had high serum levels of IL-34 exhibited a lower cumulative survival rate compared to those with low IL-34 level(Log-rank P < 0.001).
Serum IL-34 levels are significantly increased in patients with severe pneumonia, and relative IL-34 gene expression in BALF is positively correlated with serum IL-34 levels. Both can be used as indicators for predicting the prognosis of 28-day mortality in patients with severe pneumonia.
[1] |
中华医学会呼吸病学分会. 中国成人社区获得性肺炎诊断和治疗指南(2016年版)[J]. 中华结核和呼吸杂志, 2016, 39(4): 253-279. doi: 10.3760/cma.j.issn.1001-0939.2016.04.005
|
[2] |
中华医学会呼吸病学分会感染学组. 中国成人医院获得性肺炎与呼吸机相关性肺炎诊断和治疗指南(2018年版)[J]. 中华结核和呼吸杂志, 2018, 41(4): 255-280. doi: 10.3760/cma.j.issn.1001-0939.2018.04.006
|
[3] |
WANG Y M, SZRETTER K J, VERMI W, et al. IL-34 is a tissue-restricted ligand of CSF1R required for the development of Langerhans cells and microglia[J]. Nat Immunol, 2012, 13(8): 753-760. doi: 10.1038/ni.2360
|
[4] |
BAGHDADI M, ENDO H, TAKANO A, et al. High co-expression of IL-34 and M-CSF correlates with tumor progression and poor survival in lung cancers[J]. Sci Rep, 2018, 8(1): 418. doi: 10.1038/s41598-017-18796-8
|
[5] |
KUZUMI A, YOSHIZAKI A, TOYAMA S, et al. Serum interleukin-34 levels in patients with systemic sclerosis: clinical association with interstitial lung disease[J]. J Dermatol, 2018, 45(10): 1216-1220. doi: 10.1111/1346-8138.14538
|
[6] |
林玉霞, 陈名智. ROX指数、淋巴细胞指标、血糖对重症肺炎经鼻高流量氧疗后再次气管插管的预测效能及意义[J]. 实用临床医药杂志, 2024, 28(6): 30-36. doi: 10.7619/jcmp.20233382
|
[7] |
康林, 祝莹, 高芸, 等. 血清降钙素、脑钠肽、心肌肌钙蛋白Ⅰ与老年肺炎病情严重程度的关系[J]. 实用临床医药杂志, 2023, 27(17): 93-96. doi: 10.7619/jcmp.20231133
|
[8] |
TORRES A, CHALMERS J D, DELA CRUZ C S, et al. Challenges in severe community-acquired pneumonia: a point-of-view review[J]. Intensive Care Med, 2019, 45(2): 159-171. doi: 10.1007/s00134-019-05519-y
|
[9] |
周曙俊, 周军, 王大明. 单核细胞人白细胞抗原DR监测在重症肺炎患者预后评估中的价值[J]. 江苏大学学报: 医学版, 2013, 23(1): 30-33.
|
[10] |
LIN H S, LEE E, HESTIR K, et al. Discovery of a cytokine and its receptor by functional screening of the extracellular proteome[J]. Science, 2008, 320(5877): 807-811. doi: 10.1126/science.1154370
|
[11] |
FREUCHET A, SALAMA A, REMY S, et al. IL-34 and CSF-1, deciphering similarities and differences at steady state and in diseases[J]. J Leukoc Biol, 2021, 110(4): 771-796. doi: 10.1002/JLB.3RU1120-773R
|
[12] |
XU B L, LIN X, GONG Y, et al. Interleukin-34: an important modifier in the pathogenesis of influenza pneumonia[J]. Crit Care, 2021, 25(1): 274. doi: 10.1186/s13054-021-03708-0
|
[13] |
YU G Z, BING Y T, ZHU S Y, et al. Activation of the interleukin-34 inflammatory pathway in response to influenza A virus infection[J]. Am J Med Sci, 2015, 349(2): 145-150. doi: 10.1097/MAJ.0000000000000373
|
[14] |
肖慧, 徐维国, 范小兵, 等. 血清IL-34、SP-D、CXCL17在甲型流感病毒性肺炎患者中表达及临床意义[J]. 中华肺部疾病杂志(电子版), 2023, 16(3): 349-351. doi: 10.3877/cma.j.issn.1674-6902.2023.03.010
|
[15] |
肖朗, 胡清亮, 冯秀莉, 等. 肺结核合并肺部细菌感染S100A9与IL-34和IFN-γ水平及其诊断价值[J]. 中华医院感染学杂志, 2023, 33(4): 494-497.
|
[16] |
KHAN F, OWENS M B, RESTREPO M, et al. Tools for outcome prediction in patients with community acquired pneumonia[J]. Expert Rev Clin Pharmacol, 2017, 10(2): 201-211. doi: 10.1080/17512433.2017.1268051
|
[17] |
CHRIST-CRAIN M, SCHUETZ P, MVLLER B. Biomarkers in the management of pneumonia[J]. Expert Rev Respir Med, 2008, 2(5): 565-572. doi: 10.1586/17476348.2.5.565
|
[18] |
NIEDERMAN M S, TORRES A. Severe community-acquired pneumonia[J]. Eur Respir Rev, 2022, 31(166): 220123. doi: 10.1183/16000617.0123-2022
|
[19] |
MARTI C, GARIN N, GROSGURIN O, et al. Prediction of severe community-acquired pneumonia: a systematic review and meta-analysis[J]. Crit Care, 2012, 16(4): R141. doi: 10.1186/cc11447
|
[20] |
LANKS C W, MUSANI A I, HSIA D W. Community-acquired pneumonia and hospital-acquired pneumonia[J]. Med Clin North Am, 2019, 103(3): 487-501. doi: 10.1016/j.mcna.2018.12.008
|