Fu Yufen, Wang Yuxin, Wang Yujiao, Mou Ting, He Xiang, Wang Junyi, Xiong Anying, Qing Bomiao, Wu Dehong, Li Guoping
Department of Pulmonary and Critical Care Medicine, Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Laboratory of Allergy and Precision Medicine, Chengdu Institute of Respiratory Health, the Third People's Hospital of Chengdu, Affiliated Hospital of Southwest Jiaotong University, Chengdu, 610031, People's Republic of China.
Int J Chron Obstruct Pulmon Dis. 2025 Apr 5;20:987-998. doi: 10.2147/COPD.S510118. eCollection 2025.
To evaluate the diagnostic and predictive value of the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and systemic immune-inflammation index (SII) for frequent exacerbations of chronic obstructive pulmonary disease (AECOPD), and to develop a risk stratification scoring system to optimize clinical management in resource-limited healthcare settings.
This retrospective observational study enrolled 16,849 AECOPD patients, categorized into frequent exacerbators (≥2 exacerbations/year, n=3,488) and non-frequent exacerbators (<2 exacerbations/year, n=13,361). Comparative analyses of clinical characteristics and inflammatory biomarkers (NLR, PLR, SII, CRP, PCT) were conducted. Spearman correlation, receiver operating characteristic (ROC) curve analysis, and binary logistic regression were employed to assess biomarker performance. A risk scoring system was developed using odds ratios (OR) and regression coefficients (β) of NLR and PLR.
The frequent exacerbators group exhibited significantly higher median NLR (6.71 vs 5.10, P < 0.001), mean PLR (239 ± 204 vs 218 ± 195, P < 0.001), and median SII (1,137.48 vs 847.54, P < 0.001). NLR, PLR and SII showed strong positive correlations with CRP and PCT (P < 0.001). ROC analysis identified NLR (specificity = 84.1%) and PLR (sensitivity = 55%) as optimal diagnostic indicators. Regression analysis confirmed NLR and PLR as independent risk factors for frequent exacerbations. The risk stratification system categorized patients into low-risk (<290 points; annual exacerbation rate 17%), intermediate-risk (290-768 points; 19.1%), and high-risk (>768 points; 23.4%) groups.
NLR and PLR serve as cost-effective biomarkers for identifying high-risk frequent exacerbators patients with COPD in primary care settings. The percentile-based scoring system enables management strategies to address clinical needs in resource-constrained healthcare environments.
评估中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)及全身免疫炎症指数(SII)对慢性阻塞性肺疾病频繁急性加重(AECOPD)的诊断及预测价值,并建立风险分层评分系统以优化资源有限的医疗环境中的临床管理。
这项回顾性观察性研究纳入了16849例AECOPD患者,分为频繁急性加重组(≥2次/年,n = 3488)和非频繁急性加重组(<2次/年,n = 13361)。对临床特征和炎症生物标志物(NLR、PLR、SII、CRP、PCT)进行了比较分析。采用Spearman相关性分析、受试者工作特征(ROC)曲线分析和二元逻辑回归评估生物标志物的性能。利用NLR和PLR的比值比(OR)和回归系数(β)建立了风险评分系统。
频繁急性加重组的NLR中位数显著更高(6.71对5.10,P < 0.001),PLR均值更高(239±204对218±195,P < 0.001),SII中位数更高(1137.48对847.54,P < 0.001)。NLR、PLR和SII与CRP和PCT呈强正相关(P < 0.001)。ROC分析确定NLR(特异性 = 84.1%)和PLR(敏感性 = 55%)为最佳诊断指标。回归分析证实NLR和PLR是频繁急性加重的独立危险因素。风险分层系统将患者分为低风险组(<290分;年急性加重率17%)、中风险组(290 - 768分;19.1%)和高风险组(>768分;23.4%)。
NLR和PLR是在基层医疗环境中识别慢性阻塞性肺疾病高风险频繁急性加重患者的经济有效的生物标志物。基于百分位数的评分系统能够制定管理策略以满足资源受限的医疗环境中的临床需求。