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Associations of NPAR index with breast cancer incidence and mortality based on the National Health and Nutrition Examination Survey (NHANES) 2001-2018: a cross-sectional study

医学 全国健康与营养检查调查 四分位数 危险系数 乳腺癌 人口学 比例危险模型 内科学 优势比 入射(几何) 横断面研究 置信区间 癌症 人口 环境卫生 病理 社会学 物理 光学
作者
Yongcheng Su,Beibei Xu,Miaomiao Ma,Wenqing Zhang,Zhong Ouyang,Tianhui Hu
出处
期刊:International Journal of Surgery [Elsevier]
被引量:2
标识
DOI:10.1097/js9.0000000000002543
摘要

Background: Breast cancer (BC) remains one of the most prevalent cancers affecting women globally, imposing significant health and economic burdens on both patients and society. This study aims to investigate the relationship between the neutrophil percentage to albumin ratio (NPAR) and BC risk and mortality. Materials and methods: Clinical data from 13,540 participants in the NHANES database were analyzed, including 331 individuals with a documented history of BC. Survival analysis and advanced machine learning (ML) techniques were applied to assess the data. Results: Higher NPAR levels were significantly associated with increased BC risk in the unadjusted model, with quartile comparisons revealing an odds ratio (OR) of 1.51 (95% CI: 0.99–2.29, p = 0.057). After adjustment, the OR increased to 1.70 (95% CI: 1.12–2.57, p < 0.05), indicating the robustness of this association. Elevated NPAR levels were also linked to higher all-cause mortality (ACM). Multivariate Cox regression models showed that a one-unit increase in NPAR was associated with adjusted hazard ratios of 1.09 (95% CI: 1.07–1.12) for overall mortality and 1.17 (95% CI: 1.13–1.22) for cardiovascular disease mortality, both with p -values < 0.001. Restricted cubic splines analysis revealed a linear correlation between NPAR and BC risk ( p for nonlinearity = 0.15), while a nonlinear relationship was observed for ACM ( p for nonlinearity < 0.01). Among nine ML models evaluated, the LightGBM model exhibited the best diagnostic performance, achieving an area under the receiver operating characteristic curve of 0.995, outperforming models such as CATBoost, Naive Bayes, logistic regression, random forest, K-nearest neighbors, support vector machine, decision tree, and XGBoost. After model selection, an online calculator was built for use in the clinic, and the web-service is available at https://fast.statsape.com/tool/detail?id=11. Conclusion: NPAR emerged as a crucial biomarker in BC risk assessment. This study suggests that NPAR may serve as a dual-purpose biomarker for both BC risk evaluation and prognostic assessment, potentially aiding early screening and personalized treatment strategies.
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