Wang Zhengjin, Chen Zhangxin, Zhuang Hanxu
Zhangzhou Health Vocational College, Zhangzhou, Fujian Province, China.
Department of Spine Surgery, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China.
Front Nutr. 2025 May 9;12:1528732. doi: 10.3389/fnut.2025.1528732. eCollection 2025.
Urinary albumin-to-creatinine ratio (UACR) is an established biomarker for assessing kidney damage, but recent studies suggest it may also reflect broader health risks. This study aimed to investigate the association between UACR and all-cause and cardiovascular disease (CVD)-cause mortality in patients with metabolic dysfunction-associated steatotic liver disease (MASLD).
In this prospective cohort study, we included sample of 3,412 MASLD enrolled in the National Health and Nutrition Examination Survey 2001-2018. The study population was divided into three different risk categories based on urinary UACR: low level (<4.67 mg/g), intermediate level (4.67-7.67 mg/g), and high level (7.68-30 mg/g). Cox proportional hazards models were used to estimate the hazard ratios (HR) for the association between UACR level and both all-cause and CVD-cause mortality. Restricted cubic spline (RCS) curve analysis was employed to assess the non-linear association between UACR and mortality. Kaplan-Meier (KM) survival curves were used to evaluate survival rates across UACR groups.
The study found that higher UACR levels, even within the normal range, were independently associated with increased risks of both all-cause and CVD-cause mortality. Each 1 mg/g increase in UACR was associated with a 4% higher risk of all-cause mortality (HR 1.04, 95% CI 1.03-1.05) and a 5% higher risk of cardiovascular mortality (HR 1.05, 95% CI 1.02-1.08). Compared with the low UACR group, high UACR both showed an increased all-cause mortality risk [HR, 2.69 (95% CI, 2.07-3.50)] and CVD-cause mortality risk [HR, 2.97 (95% CI, 1.76-4.99)]. RCS curve analysis revealed a non-linear positive correlation between UACR and both all-cause and CVD-cause mortality, identifying UACR thresholds of 7.467 mg/g for all-cause mortality and 7.195 mg/g for CVD-cause mortality. The KM survival curves confirmed that participants with lower UACR levels had higher survival rates.
Elevated UACR levels within the normal range, are associated with increased all-cause and cardiovascular mortality in patients with MASLD. UACR may serve as a useful early biomarker for identifying individuals at higher risk of mortality, supporting more proactive clinical interventions to manage MASLD-related risks.
尿白蛋白与肌酐比值(UACR)是评估肾脏损伤的既定生物标志物,但最近的研究表明它也可能反映更广泛的健康风险。本研究旨在调查代谢功能障碍相关脂肪性肝病(MASLD)患者中UACR与全因死亡率和心血管疾病(CVD)所致死亡率之间的关联。
在这项前瞻性队列研究中,我们纳入了2001 - 2018年国家健康与营养检查调查中登记的3412例MASLD样本。根据尿UACR将研究人群分为三个不同的风险类别:低水平(<4.67 mg/g)、中等水平(4.67 - 7.67 mg/g)和高水平(7.68 - 30 mg/g)。使用Cox比例风险模型估计UACR水平与全因死亡率和CVD所致死亡率之间关联的风险比(HR)。采用受限立方样条(RCS)曲线分析评估UACR与死亡率之间的非线性关联。使用Kaplan - Meier(KM)生存曲线评估各UACR组的生存率。
研究发现,即使在正常范围内,较高的UACR水平也与全因死亡率和CVD所致死亡率的风险增加独立相关。UACR每增加1 mg/g,全因死亡率风险增加4%(HR 1.04,95% CI 1.03 - 1.05),心血管死亡率风险增加5%(HR 1.05,95% CI 1.02 - 1.08)。与低UACR组相比,高UACR组全因死亡率风险[HR,2.69(95% CI,2.07 - 3.50)]和CVD所致死亡率风险[HR,2.97(95% CI,1.76 - 4.99)]均增加。RCS曲线分析显示UACR与全因死亡率和CVD所致死亡率之间存在非线性正相关,确定全因死亡率的UACR阈值为7.467 mg/g,CVD所致死亡率的UACR阈值为7.195 mg/g。KM生存曲线证实UACR水平较低的参与者生存率较高。
正常范围内UACR水平升高与MASLD患者的全因死亡率和心血管死亡率增加相关。UACR可作为识别死亡风险较高个体的有用早期生物标志物,支持更积极的临床干预以管理与MASLD相关的风险。