Zhou Qing, Xue Jisu, Hao Lu
Central Laboratory, The People's Hospital of Baoan Shenzhen, No.118 Longjing Second Road, Shenzhen, 518000, China.
Department of Endocrinology, Shenzhen Baoan Shiyan People's Hospital, Shenzhen, China.
BMC Gastroenterol. 2025 Jul 1;25(1):460. doi: 10.1186/s12876-025-04064-x.
BACKGROUND AND AIM: Systemic inflammatory markers derived from immune cell counts have been associated with mortality risk in metabolic dysfunction-associated steatotic liver disease (MASLD). However, the clinical relevance of the pan-immune-inflammation value (PIV), a composite index incorporating neutrophil, platelet, monocyte, and lymphocyte counts, in relation to mortality has not been fully elucidated. This study aimed to evaluate the association between PIV and both all-cause and cardiovascular mortality in individuals with MASLD. METHODS: In this population-based cohort study, 15,471 participants with MASLD were identified from the 1999-2018 National Health and Nutrition Examination Survey (NHANES). Baseline demographic characteristics, including age, sex, and ethnicity, were collected. Multivariate Cox proportional hazards models and restricted cubic spline analyses were employed to examine the associations between PIV and mortality outcomes. RESULTS: In fully adjusted models, log-transformed PIV (LnPIV) was independently associated with higher risks of all-cause (hazard ratio [HR] 1.26; 95% confidence interval [CI], 1.14-1.38) and cardiovascular mortality (HR 1.31; 95% CI, 1.10-1.56). Notably, a U-shaped nonlinear association was observed between PIV and all-cause mortality, while a J-shaped relationship was found for cardiovascular mortality. These associations were more pronounced among individuals with a poverty-income ratio (PIR) < 1, suggesting increased vulnerability in socioeconomically disadvantaged populations. CONCLUSION: PIV may be a biomarker associated with increased mortality risk in individuals with MASLD, particularly among those from lower socioeconomic backgrounds. These findings underscore the association between PIV and mortality risk and highlight the need for further prospective validation to evaluate its potential role in risk stratification.
背景与目的:源自免疫细胞计数的全身炎症标志物与代谢功能障碍相关脂肪性肝病(MASLD)的死亡风险相关。然而,包含中性粒细胞、血小板、单核细胞和淋巴细胞计数的综合指标——全免疫炎症值(PIV)与死亡率的临床相关性尚未完全阐明。本研究旨在评估PIV与MASLD患者全因死亡率和心血管死亡率之间的关联。 方法:在这项基于人群的队列研究中,从1999 - 2018年国家健康与营养检查调查(NHANES)中识别出15471名MASLD参与者。收集了包括年龄、性别和种族在内的基线人口统计学特征。采用多变量Cox比例风险模型和受限立方样条分析来检验PIV与死亡结局之间的关联。 结果:在完全调整模型中,对数转换后的PIV(LnPIV)与全因死亡风险较高独立相关(风险比[HR] 1.26;95%置信区间[CI],1.14 - 同1.38)和心血管死亡率(HR 1.31;95% CI,1.10 - 1.56)。值得注意的是,PIV与全因死亡率之间观察到U型非线性关联,而心血管死亡率则呈现J型关系。这些关联在贫困收入比(PIR)< 1的个体中更为明显,表明社会经济弱势群体的易感性增加。 结论:PIV可能是与MASLD患者死亡风险增加相关的生物标志物,特别是在社会经济背景较低的人群中。这些发现强调了PIV与死亡风险之间的关联,并突出了进一步进行前瞻性验证以评估其在风险分层中潜在作用的必要性。
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