泛免疫炎症值 (PIV) 与维持性血液透析患者全因死亡率和心血管死亡率的关系:倾向得分匹配回顾性研究

IF 1.8 4区 医学 Q3 UROLOGY & NEPHROLOGY
Chunmin Li, Qian Wen, Geli Zhu, Yanxia Zhang, Yuan Wang, Dan Luo, Jun Wu
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引用次数: 0

摘要

目的 泛免疫炎症值(PIV)是一种新型炎症指标。然而,它在维持性血液透析(MHD)中的作用仍不明确。我们的目标是探索 PIV 对 MHD 患者心血管和全因死亡率的预测价值。方法在这项回顾性队列研究中,纳入了 2017 年 11 月至 2022 年 12 月期间接受 MHD 的 507 名患者。PIV值的计算方法如下:中性粒细胞计数×单核细胞计数×血小板计数/淋巴细胞计数。根据 PIV 的中位数将患者分为两组。倾向评分匹配(PSM)用于调整组间基线信息的不平衡。采用 Kaplan-Meier 曲线、Cox 回归、Fine-Gray 竞争风险模型和受限立方样条曲线 (RCS) 分析 PIV 与死亡率之间的关系。卡普兰-梅耶曲线显示,PIV水平较高的MHD患者全因死亡的预后较差(P = 0.019)。在多变量考克斯比例风险回归中,PIV水平与全因死亡相关(HR = 1.76;95% CI 1.14,2.72;P = 0.011)。Fine-Gray模型显示,PIV值较高组的心血管死亡累积发生率更高(p = 0.035)。在Fine-Gray竞争风险模型中,PIV水平与心血管死亡有关(HR = 2.06; 95% CI 1.25, 3.42; p = 0.005)。RCS 显示 PIV 与死亡风险之间存在非线性关系(p < 0.05)。结论 在 MHD 患者中,PIV 是心血管相关死亡率和全因死亡率的独立危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of the panimmune-inflammatory value (PIV) with all-cause and cardiovascular mortality in maintenance hemodialysis patients: a propensity score matching retrospective study

Association of the panimmune-inflammatory value (PIV) with all-cause and cardiovascular mortality in maintenance hemodialysis patients: a propensity score matching retrospective study

Purpose

The panimmune-inflammatory value (PIV) is a novel inflammatory indicator. However, its role in maintenance hemodialysis (MHD) remains unclear. Our goal was to explore the predictive value of PIV for cardiovascular and all-cause mortality in MHD patients.

Methods

In this retrospective cohort study, 507 patients receiving MHD between November 2017 and December 2022 were enrolled. The PIV value was calculated as follows: neutrophil count × monocyte count × platelet count/lymphocyte count. Patients were divided into two groups on the basis of the median PIV. Propensity score matching (PSM) was used to adjust for imbalances in baseline information between groups. Kaplan‒Meier curves, Cox regression, the Fine‒Gray competing risk model, and restricted cubic spline (RCS) curves were used to analyze the relationship between PIV and mortality.

Results

By the end of follow-up, 126 deaths had occurred, 91 of which were due to cardiovascular disease. The Kaplan‒Meier curves demonstrated that MHD patients with higher PIV levels had a poorer prognosis for all-cause death (p = 0.019). PIV levels were linked to all-cause death in multivariate Cox proportional risk regression (HR = 1.76; 95% CI 1.14, 2.72; p = 0.011). The Fine‒Gray model revealed a greater cumulative incidence of cardiovascular death in the higher PIV group (p = 0.035). PIV levels were linked to cardiovascular mortality in the Fine‒Gray competing risk model (HR = 2.06; 95% CI 1.25, 3.42; p = 0.005). The RCS revealed a nonlinear relationship between PIV and mortality risk (p < 0.05). Using 63 years of age as the threshold, we observed a multiplicative interaction effect between age and PIV for all-cause mortality (p = 0.006).

Conclusion

In MHD patients, PIV is an independent hazard factor for cardiovascular-related mortality and all-cause mortality.

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来源期刊
International Urology and Nephrology
International Urology and Nephrology 医学-泌尿学与肾脏学
CiteScore
3.40
自引率
5.00%
发文量
329
审稿时长
1.7 months
期刊介绍: International Urology and Nephrology publishes original papers on a broad range of topics in urology, nephrology and andrology. The journal integrates papers originating from clinical practice.
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