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非糖尿病慢性肾脏病患者的白蛋白尿严重程度与心血管和肾脏结局:来自 CRIC 研究的结果。

Cardiovascular and Kidney Outcomes of Non-Diabetic CKD by Albuminuria Severity: Findings From the CRIC Study.

机构信息

Renal-Electrolyte and Hypertension Division, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Am J Kidney Dis. 2024 Dec;84(6):742-750.e1. doi: 10.1053/j.ajkd.2024.05.008. Epub 2024 Jul 19.

DOI:10.1053/j.ajkd.2024.05.008
PMID:39032679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11585431/
Abstract

RATIONALE & OBJECTIVE: The clinical trajectory of normoalbuminuric chronic kidney disease (CKD), particularly in the absence of diabetes, has not yet been well-studied. This study evaluated the association of kidney and cardiovascular outcomes with levels of albuminuria in a cohort of patients with nondiabetic CKD.

STUDY DESIGN

Prospective cohort study.

SETTING & PARTICIPANTS: 1,463 adults with nondiabetic CKD without known glomerulonephritis and diagnosed with hypertensive nephrosclerosis or unknown cause of CKD participating in the Chronic Renal Insufficiency Cohort (CRIC) Study.

EXPOSURE

Albuminuria stage at study entry.

OUTCOME

Primary outcome: Composite kidney (halving of estimated glomerular filtration rate [eGFR], kidney transplantation, or dialysis), Secondary outcomes: (1) eGFR slope, (2) composite cardiovascular disease events (hospitalization for heart failure, myocardial infarction, stroke, or all-cause death), (3) all-cause death.

ANALYTICAL APPROACH

Linear mixed effects and Cox proportional hazards regression analyses.

RESULTS

Lower levels of albuminuria were associated with female sex and older age. For the primary outcome, compared with normoalbuminuria, those with moderate and severe albuminuria had higher rates of kidney outcomes (adjusted hazard ratio [AHR], 3.3 [95% CI, 2.4-4.6], and AHR, 8.6 [95% CI, 6.0-12.0], respectively) and cardiovascular outcomes (AHR, 1.5 [95% CI, 1.2-1.9], and AHR, 1.5 [95% CI, 1.1-2.0], respectively). Those with normoalbuminuria (<30μg/mg; n=863) had a slower decline in eGFR (-0.46mL/min/1.73m per year) compared with those with moderate (30-300μg/mg, n=372; 1.41mL/min/1.73m per year) or severe albuminuria (>300μg/mg, n=274; 2.63mL/min/1.73m per year). In adjusted analyses, kidney outcomes occurred, on average, sooner among those with moderate (8.6 years) and severe (7.3 years) albuminuria compared with those with normoalbuminuria (9.3 years) whereas the average times to cardiovascular outcomes were similar across albuminuria groups (8.2, 8.1, and 8.6 years, respectively).

LIMITATIONS

Self-report of CKD etiology without confirmatory kidney biopsies; residual confounding.

CONCLUSIONS

Participants with normoalbuminuric nondiabetic CKD experienced substantially slower CKD progression but only modestly lower cardiovascular risk than those with high levels of albuminuria. These findings inform the design of future studies investigating interventions among individuals with lower levels of albuminuria.

PLAIN-LANGUAGE SUMMARY: Diabetes and hypertension are the leading causes of chronic kidney disease (CKD). Urine albumin levels are associated with cardiovascular and kidney disease outcomes among individuals with CKD. However, previous studies of long-term clinical outcomes in CKD largely included patients with diabetes. As well, few studies have evaluated long-term outcomes across different levels of urine albumin among people without diabetes. In this study, we found individuals with nondiabetic CKD and low urine albumin had much slower decline of kidney function but only a modestly lower risk of a cardiovascular events compared with those with high levels of urine albumin. Individuals with low urine albumin were much more likely to have a cardiovascular event than progression of their kidney disease. These findings inform the design of future studies investigating treatments among individuals with lower levels of albuminuria.

摘要

背景与目的

在没有糖尿病的情况下,正常白蛋白尿慢性肾脏病(CKD)的临床轨迹尚未得到很好的研究。本研究评估了非糖尿病性 CKD 患者队列中白蛋白尿水平与肾脏和心血管结局的相关性。

研究设计

前瞻性队列研究。

设置与参与者

参加慢性肾功能不全队列(CRIC)研究的 1463 名无已知肾小球肾炎的非糖尿病性 CKD 成年患者,且诊断为高血压性肾硬化症或 CKD 病因不明。

暴露

研究入组时的白蛋白尿阶段。

主要结局

复合肾脏结局(估计肾小球滤过率[eGFR]减半、肾移植或透析);次要结局:(1)eGFR 斜率,(2)复合心血管疾病事件(心力衰竭住院、心肌梗死、卒中和全因死亡),(3)全因死亡。

分析方法

线性混合效应和 Cox 比例风险回归分析。

结果

较低的白蛋白尿水平与女性和年龄较大有关。对于主要结局,与正常白蛋白尿相比,中重度白蛋白尿患者的肾脏结局发生率更高(调整后的危险比[AHR],3.3[95%CI,2.4-4.6]和 AHR,8.6[95%CI,6.0-12.0])和心血管结局(AHR,1.5[95%CI,1.2-1.9]和 AHR,1.5[95%CI,1.1-2.0])。那些白蛋白尿正常(<30μg/mg;n=863)的患者 eGFR 下降速度较慢(每年-0.46mL/min/1.73m),而那些白蛋白尿中度(30-300μg/mg,n=372;1.41mL/min/1.73m 每年)或重度(>300μg/mg,n=274;2.63mL/min/1.73m 每年)的患者下降速度较快。在调整分析中,与白蛋白尿正常的患者(9.3 年)相比,白蛋白尿中度(8.6 年)和重度(7.3 年)患者的肾脏结局发生时间更早,而白蛋白尿组之间发生心血管结局的平均时间相似(分别为 8.2、8.1 和 8.6 年)。

局限性

CKD 病因的自我报告而没有进行确认性肾活检;存在残余混杂因素。

结论

患有正常白蛋白尿的非糖尿病性 CKD 的患者经历了显著较慢的 CKD 进展,但与高白蛋白尿患者相比,其心血管风险仅略低。这些发现为未来研究提供了信息,这些研究旨在探讨在低白蛋白尿水平的个体中进行干预的效果。

简单来说

糖尿病和高血压是慢性肾脏病(CKD)的主要原因。尿液白蛋白水平与 CKD 患者的心血管和肾脏疾病结局有关。然而,之前关于 CKD 长期临床结局的研究大多包括患有糖尿病的患者。此外,很少有研究评估了无糖尿病患者不同水平白蛋白尿的长期结局。在这项研究中,我们发现与高水平白蛋白尿相比,患有非糖尿病性 CKD 和低水平白蛋白尿的患者的肾功能下降速度要慢得多,但心血管事件的风险仅略低。与肾脏疾病进展相比,患有低水平白蛋白尿的患者更有可能发生心血管事件。这些发现为未来研究提供了信息,这些研究旨在评估在低水平白蛋白尿的患者中进行治疗的效果。