Yan Chunyu, Zhou Yabin, Wang He, Fu Jiamei, Xu Qian
Department of Cardiology, The First Hospital Affiliated to Heilongjiang University of Traditional Chinese Medicine, Harbin, People's Republic of China.
Department of Cardiology, The Second Hospital Affiliated to Heilongjiang University of Traditional Chinese Medicine, Harbin, People's Republic of China.
PLoS One. 2025 Jun 5;20(6):e0325620. doi: 10.1371/journal.pone.0325620. eCollection 2025.
The aim of this study was mainly to investigate the association between Serum uric acid (SUA) to high-density lipoprotein cholesterol (HDL-C) ratio (UHR) and all-cause mortality in hypertensive patients,and to further investigate the mediating role of neutrophils.
Our cohort study included 4533 hypertensive patients drawn from the 2005-2018 National Health and Nutrition Examination Survey (NHANES) database and combined with the National Death Index (NDI) database to obtain mortality data for subjects. Kaplan-Meier survival curves, multifactorial Cox risk-proportional modeling, restricted cubic spline (RCS)-based smoothed curve fitting, threshold effects analysis, and subgroup analyses were performed to evaluate the associations between UHR and all-cause mortality, and, finally,causal mediating effects were performed to analyze the mediating role of neutrophils.
Over a mean duration of 90.32 months, the follow-up all-cause mortality occurred in 1003 individuals, and the mean age of all subjects included was (61.69 ± 14.28) years, and the Kaplan-Meier survival curves demonstrated that high levels of UHR were notably connected to lower survival. In multivariate Cox regression analysis, high quartile UHR was positively connected to all-cause mortality (HR: 1.36, 95% CI: 1.03,1.80, P = 0.031), and smoothed curve fitting combined with threshold effect analysis showed a nonlinear relationship between UHR and all-cause mortality, with a curve inflection point of 0.14, i.e., when UHR < 0.14, an increase in UHR did not affect the increase in all-cause mortality (HR: 0.84, 95% CI: 0.06, 11.51, P = 0.8968), and when UHR > 0.14, the all-cause mortality increased with the increase in UHR. We further stratify by gender and find that the inflection point for male UHR is 0.13, the suggesting that the association between UHR and all-cause mortality increased with increasing UHR when UHR was < 0.13, HR (95% CI): 0.01 (0.00, 0.22), P < 0.01 and when UHR > 0.13, HR (95% CI): 0.41 (0.04, 1.36), P < 0.01. However there was a significant linear correlation for females (HR: 1.31 95% CI: 0.15, 11.55, P < 0.0001). Analysis of causal mediating effects elucidated that the proportion of neutrophils mediating the association between UHR and all-cause mortality was 18.63%.
There was a significant positive correlation between elevated UHR and all-cause mortality in hypertensive patients, and this association may be mediated with neutrophils.
本研究的主要目的是调查血清尿酸(SUA)与高密度脂蛋白胆固醇(HDL-C)比值(UHR)与高血压患者全因死亡率之间的关联,并进一步研究中性粒细胞的中介作用。
我们的队列研究纳入了从2005 - 2018年国家健康与营养检查调查(NHANES)数据库中选取的4533例高血压患者,并与国家死亡指数(NDI)数据库相结合以获取研究对象的死亡率数据。采用Kaplan-Meier生存曲线、多因素Cox风险比例模型、基于限制性立方样条(RCS)的平滑曲线拟合、阈值效应分析和亚组分析来评估UHR与全因死亡率之间的关联,最后进行因果中介效应分析以分析中性粒细胞的中介作用。
在平均90.32个月的随访期内,1003例个体发生了全因死亡,纳入的所有研究对象的平均年龄为(61.69±14.28)岁,Kaplan-Meier生存曲线表明高水平的UHR与较低的生存率显著相关。在多因素Cox回归分析中,高四分位数的UHR与全因死亡率呈正相关(HR:1.36,95%CI:1.03,1.80,P = 0.031),平滑曲线拟合结合阈值效应分析显示UHR与全因死亡率之间存在非线性关系,曲线拐点为0.14,即当UHR < 0.14时,UHR的升高不影响全因死亡率的增加(HR:0.84,95%CI:0.06,11.51,P = 0.8968),而当UHR > 0.14时,全因死亡率随UHR的增加而增加。我们进一步按性别分层,发现男性UHR的拐点为0.13,这表明当UHR < 0.13时,UHR与全因死亡率之间的关联随UHR的增加而增加,HR(95%CI):0.01(0.00,0.22),P < 0.01,当UHR > 0.13时,HR(95%CI):0.41(0.04,1.36),P < 0.01。然而,女性存在显著的线性相关性(HR:1.31,95%CI:0.15,11.55,P < 0.0001)。因果中介效应分析表明,中性粒细胞介导UHR与全因死亡率之间关联的比例为18.63%。
高血压患者中升高的UHR与全因死亡率之间存在显著正相关,且这种关联可能由中性粒细胞介导。