The Uric Acid to Albumin Ratio Predicts All-cause and Cardiovascular Mortality Among U.S. Adults Results from the National Health and Nutrition Examination Survey in 2003-2018.

IF 3.2 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
International Journal of Medical Sciences Pub Date : 2025-04-22 eCollection Date: 2025-01-01 DOI:10.7150/ijms.106664
Guangyu Wang, Guangyu Li, Pengfei Wang, Minhua Zang, Jun Pu
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引用次数: 0

Abstract

Background: The association between the uric acid to albumin ratio (UAR) and mortality in the general population remains poorly understood. This study aimed to investigate the associations of UAR with all-cause and cardiovascular mortality among American adults. Methods: The study population comprised 19190 U.S. adults from the National Health and Nutrition Examination Survey (NHANES) conducted between 2003 and 2018. Mortality outcomes were ascertained through linkage to National Death Index (NDI) records, with follow-up extending to December 31, 2019. Multivariate Cox proportional hazards regression models with restricted cubic splines and trend analyses were utilized to assess the association between UAR and both all-cause and cardiovascular mortality. Subgroup analyses were conducted to assess whether the association between UAR and mortality varied across different demographic and clinical groups. Results: During a median follow-up period of 98 months, 2296 all-cause deaths were recorded, including 597 deaths related to cardiovascular disease (CVD). After multivariable adjustment, no linear trends were observed between UAR and either all-cause or CVD mortality. Kaplan-Meier curves revealed a significant increase in both all-cause and CVD mortality with associated with higher UAR levels (p for log-rank test < 0.001 for both). Restricted cubic spline models indicated a J-shaped nonlinear association between UAR and both all-cause and CVD mortality, with inflection points at UAR levels of 1.40 for all-cause mortality and 1.88 for CVD mortality. Specifically, UAR values exceeding these inflection points were positively associated with mortality (HR 2.11, 95% CI = 1.74-2.55 for all-cause mortality; HR 5.21, 95% CI = 3.06-8.87 for CVD mortality). Conversely, UAR values below the inflection points were inversely associated with all-cause mortality (HR 0.68, 95% CI = 0.50-0.93) but not significantly associated with CVD mortality (HR 1.07, 95% CI = 0.73-1.58). This association remained consistent across subgroup analyses stratified by sex, age, race, diabetes, hypertension, BMI, and smoking status, with no significant interactions between these characteristics and UAR (p for interaction > 0.05). Conclusion: This study identified a significant association between the UAR and both all-cause and CVD mortality in the general population. A J-shaped nonlinear association was observed, with inflection points at UAR levels of 1.40 for all-cause mortality and 1.88 for CVD mortality.

根据2003-2018年美国国家健康与营养调查结果,尿酸与白蛋白比率预测美国成年人的全因死亡率和心血管死亡率。
背景:在普通人群中,尿酸与白蛋白比(UAR)与死亡率之间的关系仍然知之甚少。本研究旨在调查UAR与美国成年人全因死亡率和心血管死亡率的关系。方法:研究人群包括19190名美国成年人,他们来自2003年至2018年进行的国家健康与营养检查调查(NHANES)。通过与国家死亡指数(NDI)记录的联系确定死亡率结果,随访时间延长至2019年12月31日。采用限制三次样条和趋势分析的多变量Cox比例风险回归模型来评估UAR与全因死亡率和心血管死亡率之间的关系。进行亚组分析以评估UAR与死亡率之间的关联在不同的人口统计学和临床组中是否有所不同。结果:在98个月的中位随访期间,记录了2296例全因死亡,其中597例死亡与心血管疾病(CVD)有关。在多变量调整后,UAR与全因或心血管疾病死亡率之间没有观察到线性趋势。Kaplan-Meier曲线显示全因死亡率和CVD死亡率的显著增加与较高的UAR水平相关(log-rank检验的p均< 0.001)。受限三次样条模型显示,UAR与全因死亡率和心血管疾病死亡率之间呈j型非线性关联,UAR水平下的全因死亡率和心血管疾病死亡率的转折点分别为1.40和1.88。具体来说,超过这些拐点的UAR值与死亡率呈正相关(全因死亡率比为2.11,95% CI = 1.74-2.55;心血管疾病死亡率HR 5.21, 95% CI = 3.06-8.87)。相反,低于拐点的UAR值与全因死亡率呈负相关(HR 0.68, 95% CI = 0.50-0.93),但与CVD死亡率无显著相关(HR 1.07, 95% CI = 0.73-1.58)。这种关联在按性别、年龄、种族、糖尿病、高血压、BMI和吸烟状况分层的亚组分析中保持一致,这些特征与UAR之间没有显著的相互作用(相互作用p < 0.05)。结论:本研究确定了UAR与普通人群全因死亡率和心血管疾病死亡率之间的显著关联。观察到j形非线性关联,在UAR水平上,全因死亡率的拐点为1.40,心血管疾病死亡率的拐点为1.88。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Medical Sciences
International Journal of Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
7.20
自引率
0.00%
发文量
185
审稿时长
2.7 months
期刊介绍: Original research papers, reviews, and short research communications in any medical related area can be submitted to the Journal on the understanding that the work has not been published previously in whole or part and is not under consideration for publication elsewhere. Manuscripts in basic science and clinical medicine are both considered. There is no restriction on the length of research papers and reviews, although authors are encouraged to be concise. Short research communication is limited to be under 2500 words.
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