Liao Chen-Mao, Kao Yi-Wei, Chang Yi-Ping, Lin Chih-Ming
Department of Applied Statistics and Information Science, Ming Chuan University, Taoyuan 333, Taiwan.
Department of Nephrology, Taoyuan Branch of Taipei Veterans General Hospital, Taoyuan 333, Taiwan.
Biomedicines. 2024 Mar 11;12(3):622. doi: 10.3390/biomedicines12030622.
Chronic kidney disease (CKD) poses significant challenges to public health and healthcare systems, demanding a comprehensive understanding of its progressive nature. Prior methods have often fallen short in capturing the dynamic and individual variability of renal function. This study aims to address this gap by introducing a novel approach for the individualized assessment of CKD progression. A cohort of 1042 patients, comprising 700 with stage 3a and 342 with stage 3b to stage 5 CKD, treated at a veteran general hospital in Taiwan from 2006 to 2019, was included in the study. A comprehensive dataset spanning 12 years, consisting of clinical measurements, was collected and analyzed using joint models to predict the progression to hemodialysis treatment. The study reveals that the estimated glomerular filtration rate (eGFR) can be considered an endogenous factor influenced by innate biochemical markers. Serum creatinine, blood pressure, and urinary protein excretion emerged as valuable factors for predicting CKD progression. The joint model, combining longitudinal and survival analyses, demonstrated predictive versatility across various CKD severities. This innovative approach enhances conventional models by concurrently incorporating both longitudinal and survival analyses and provides a nuanced understanding of the variables influencing renal function in CKD patients. This personalized model enables a more precise assessment of renal failure risk, tailored to each patient's unique clinical profile. The findings contribute to improving the management of CKD patients and provide a foundation for personalized healthcare interventions in the context of renal diseases.
慢性肾脏病(CKD)对公共卫生和医疗保健系统构成了重大挑战,需要对其进展性质有全面的了解。先前的方法在捕捉肾功能的动态和个体变异性方面往往存在不足。本研究旨在通过引入一种用于CKD进展个体化评估的新方法来填补这一空白。该研究纳入了2006年至2019年在台湾一家退伍军人总医院接受治疗的1042名患者队列,其中包括700名3a期患者和342名3b期至5期CKD患者。收集了一个跨越12年的综合数据集,包含临床测量数据,并使用联合模型进行分析,以预测进展到血液透析治疗的情况。研究表明,估计肾小球滤过率(eGFR)可被视为受先天性生化标志物影响的内源性因素。血清肌酐、血压和尿蛋白排泄成为预测CKD进展的重要因素。结合纵向分析和生存分析的联合模型在各种CKD严重程度下均显示出预测的通用性。这种创新方法通过同时纳入纵向分析和生存分析增强了传统模型,并对影响CKD患者肾功能的变量提供了细致入微的理解。这种个性化模型能够根据每位患者独特的临床特征更精确地评估肾衰竭风险。这些发现有助于改善CKD患者的管理,并为肾脏疾病背景下的个性化医疗干预提供基础。