Yaqoob Khadija, Naderi Hafiz, Thomson Ross J, Aksentijevic Dunja, Jensen Magnus T, Munroe Patricia B, Petersen Steffen E, Aung Nay, Yaqoob Muhammed Magdi
Watford General Hospital, West Hertfordshire Teaching Hospitals NHS Trust, Watford, UK.
William Harvey Research Institute, NIHR Barts Biomedical Research Centre, Queen Mary University of London, London, UK.
Heart. 2025 May 12;111(11):506-512. doi: 10.1136/heartjnl-2024-324988.
The impact of early-stage chronic kidney disease (CKD) on cardiovascular outcomes, particularly when albuminuria is present, remains unclear. This study examined the associations between early CKD (stages 1 and 2) with and without albuminuria and the incidence of major adverse cardiovascular events (MACEs), heart failure (HF) and all-cause mortality.
A cohort of 456 015 participants from the UK Biobank was categorised by CKD stage using serum creatinine to calculate estimated glomerular filtration rate (eGFR) and urinary albumin-creatinine ratio (≥3 mg/mmol) to define albuminuria. Multivariable Cox proportional hazard models were applied to evaluate the associations between CKD stages and cardiovascular outcomes. Additionally, left ventricular mass (LVM), an intermediate cardiovascular risk marker, was assessed in a subset of participants using cardiovascular MRI.
Compared with normal kidney function, the risk of adverse outcomes increased progressively with advancing CKD stages, except for stage 2 CKD without albuminuria. Stage 2 CKD with albuminuria was associated with higher risks of MACE (HR 1.32, 95% CI 1.25 to 1.38), HF (HR 1.79, 95% CI 1.67 to 1.92) and all-cause mortality (HR 1.51, 95% CI 1.44 to 1.58), comparable to stage 3A CKD without albuminuria. The presence of albuminuria significantly interacted with the relationships between CKD stages and outcomes. No significant differences in indexed LVM were observed between early-stage CKD with albuminuria and normal renal function.
In early-stage CKD, albuminuria is independently associated with increased risks of MACE, HF and mortality. These findings support the use of albuminuria over eGFR decline alone for cardiovascular risk stratification in early CKD.
早期慢性肾脏病(CKD)对心血管结局的影响,尤其是在存在蛋白尿的情况下,仍不明确。本研究探讨了伴或不伴蛋白尿的早期CKD(1期和2期)与主要不良心血管事件(MACE)、心力衰竭(HF)及全因死亡率之间的关联。
来自英国生物银行的456015名参与者队列,根据CKD分期进行分类,使用血清肌酐计算估计肾小球滤过率(eGFR),并采用尿白蛋白肌酐比值(≥3mg/mmol)定义蛋白尿。应用多变量Cox比例风险模型评估CKD分期与心血管结局之间的关联。此外,在一部分参与者中使用心血管磁共振成像评估左心室质量(LVM),这是一种心血管中间风险标志物。
与肾功能正常者相比,不良结局风险随CKD分期进展而逐渐增加,但2期无蛋白尿的CKD除外。2期有蛋白尿的CKD与MACE(风险比[HR]1.32,95%置信区间[CI]1.25至1.38)、HF(HR 1.79,95%CI 1.67至1.92)及全因死亡率(HR 1.51,95%CI 1.44至1.58)风险较高相关,与3A期无蛋白尿的CKD相当。蛋白尿与CKD分期和结局之间的关系存在显著交互作用。有蛋白尿的早期CKD与肾功能正常者之间,指数化LVM未观察到显著差异。
在早期CKD中,蛋白尿独立与MACE、HF及死亡风险增加相关。这些发现支持在早期CKD的心血管风险分层中,使用蛋白尿而非仅依靠eGFR下降情况。