CCL26和CCR3水平对阿奇霉素治疗肺炎支原体肺炎患儿预后评估的预测价值

IF 1.7 4区 医学 Q2 PEDIATRICS
Translational pediatrics Pub Date : 2025-08-31 Epub Date: 2025-08-27 DOI:10.21037/tp-2025-296
Lingyan Ma, Shenghua Ge, Dongqing Song
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引用次数: 0

摘要

背景:肺炎支原体肺炎(MPP)是学童中常见的一种社区获得性肺炎(CAP),尽管阿奇霉素治疗,仍有15-25%的病例经常导致持续发烧或并发症。这突出了迫切需要新的生物标志物来识别高危病例。本研究旨在探讨血清C-C基序趋化因子配体26 (CCL26)和C-C趋化因子受体3 (CCR3)水平对接受阿奇霉素治疗的MPP患儿治疗预后的预测价值。方法:收集我院2023年2月至2025年2月收治的205例小儿MPP患者的临床资料。采用酶联免疫吸附法(ELISA)检测血清CCL26、CCR3、白细胞介素-6 (IL-6)、肿瘤坏死因子-α (TNF-α)、d -二聚体(DD)水平,采用被动凝集法检测肺炎支原体(MP)抗体滴度。Pearson相关分析评价CCL26、CCR3与炎症因子(IL-6、TNF-α)的关系。Logistic回归分析确定不良预后的危险因素,用受试者工作特征(ROC)曲线分析评价CCL26和CCR3的预测价值。结果:与健康对照组相比,MPP患者治疗前后血清CCL26、CCR3和炎症因子(TNF-α、IL-6)均升高。结论:阿奇霉素治疗后血清CCL26和CCR3水平降低,与炎症标志物和临床结局显著相关,可作为MPP患者预后不良的可靠预测指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Predictive value of CCL26 and CCR3 levels for prognosis assessment in children with <i>Mycoplasma pneumoniae</i> pneumonia treated with azithromycin.

Predictive value of CCL26 and CCR3 levels for prognosis assessment in children with <i>Mycoplasma pneumoniae</i> pneumonia treated with azithromycin.

Predictive value of CCL26 and CCR3 levels for prognosis assessment in children with <i>Mycoplasma pneumoniae</i> pneumonia treated with azithromycin.

Predictive value of CCL26 and CCR3 levels for prognosis assessment in children with Mycoplasma pneumoniae pneumonia treated with azithromycin.

Background: Mycoplasma pneumoniae pneumonia (MPP), a prevalent form of community-acquired pneumonia (CAP) in schoolchildren, frequently results in persistent fever or complications in 15-25% of cases despite azithromycin treatment. This highlights the urgent need for novel biomarkers to identify high-risk cases. This study aims to investigate the predictive value of serum C-C motif chemokine ligand 26 (CCL26) and C-C chemokine receptor 3 (CCR3) levels for treatment prognosis in children with MPP receiving azithromycin therapy.

Methods: Clinical data of 205 pediatric MPP patients treated in our hospital from February 2023 to February 2025 were collected. Serum levels of CCL26, CCR3, interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), and D-dimer (DD) were measured by enzyme-linked immunosorbent assay (ELISA), while Mycoplasma pneumoniae (MP) antibody titers were determined using passive agglutination. Pearson correlation analysis evaluated relationships between CCL26 and CCR3 and inflammatory cytokines (IL-6, TNF-α). Logistic regression identified risk factors for poor prognosis, with receiver operating characteristic (ROC) curve analysis assessing the predictive value of CCL26 and CCR3.

Results: Compared with healthy controls, MPP patients showed elevated serum CCL26, CCR3 and inflammatory cytokines (TNF-α, IL-6) both pre- and post-treatment (all P<0.05). These markers significantly decreased after therapy (all P<0.05). Pretreatment CCL26 and CCR3 levels positively correlated with inflammatory cytokines (P<0.05). Poor prognosis cases exhibited higher levels of CCL26, CCR3, TNF-α, IL-6, C-reactive protein (CRP), DD, MP antibody titers (≥1:160), fever duration (≥5 d), and peak temperature (≥38.5 °C) (P<0.05). Multivariate analysis identified MP antibody titer ≥1:160, elevated CCL26, CCR3, TNF-α, and IL-6 levels, fever ≥5 days, and temperature ≥38.5 °C as independent risk factors. The area under the curve (AUC) for CCL26 and CCR3 in predicting poor prognosis was 0.709 and 0.751, respectively, increasing to 0.798 when combined.

Conclusions: Serum CCL26 and CCR3 levels decrease following azithromycin treatment and demonstrate significant associations with inflammatory markers and clinical outcomes, serving as reliable predictors for poor prognosis in MPP patients.

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来源期刊
Translational pediatrics
Translational pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
4.50
自引率
5.00%
发文量
108
期刊介绍: Information not localized
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