Division of Nephrology, Department of Medicine.
Division of Pediatric Nephrology, Department of Pediatrics, and.
Clin J Am Soc Nephrol. 2018 May 7;13(5):693-701. doi: 10.2215/CJN.10360917. Epub 2018 Mar 30.
Traditional approaches to modeling risk of CKD progression do not provide estimates of the time it takes for disease progression to occur, which could be useful in guiding therapeutic interactions between patients and providers. Our objective was to estimate median time spent in each of CKD stages 3a-5 and how the time differs according to risk factors associated with progression of disease.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: We included 3682 participants of the Chronic Renal Insufficiency Cohort in mixed models to estimate person-specific trajectories of function, and used these trajectories to estimate time spent in each CKD stage.
During 9.5 years of median follow-up, participants spent longer in earlier rather than later CKD stages, ranging from a median of 7.9 years (interquartile range, 2.3 to >12 years) in stage 3a to 0.8 years (interquartile range, 0.3-1.6) in stage 5. Known risk factors for CKD progression were also associated with larger differences in time until progression to the next CKD stage in earlier versus later stages of disease. For example, compared with systolic BP <140 mm Hg, systolic BP ≥140 mm Hg was associated with 6.1 years shorter time (95% confidence interval [95% CI], 4.5 to 7.5) spent in stage 3a, 3.3 years shorter time (95% CI, 2.7 to 4.0) in stage 3b, but only 2.4 months shorter time (95% CI, 0.8 to 3.6) in stage 5. Compared with those with proteinuria <1 g/g, proteinuria ≥1 g/g was associated with 8 years shorter time spent (95% CI, 6.8 to 9.6) in stage 3a, 5.6 years shorter time (95% CI, 5.0 to 6.4) in stage 3b, but only 6 months shorter time (95% CI, 3.8 to 8) in stage 5.
There are marked variations in the time spent in the different stages of CKD, according to risk factors and stage of disease.
传统的慢性肾脏病(CKD)进展风险模型并不能提供疾病进展所需时间的估计,而这在指导患者与医生之间的治疗互动方面可能很有用。我们的目的是估计 CKD 3a-5 期患者分别花费在各期的中位时间,以及根据与疾病进展相关的风险因素,时间差异如何。
设计、设置、参与者和测量:我们纳入了慢性肾功能不全队列研究中的 3682 名参与者,使用混合模型来估计每个患者的功能特定轨迹,并使用这些轨迹来估计他们在每个 CKD 期的时间。
在中位随访 9.5 年期间,参与者在早期而非晚期 CKD 期花费的时间更长,从 3a 期的中位 7.9 年(四分位距,2.3 至>12 年)到 5 期的 0.8 年(四分位距,0.3-1.6 年)。CKD 进展的已知风险因素也与疾病早期和晚期阶段进展到下一个 CKD 期的时间差异较大相关。例如,与收缩压<140mmHg 相比,收缩压≥140mmHg 与 3a 期的时间缩短 6.1 年(95%置信区间[95%CI],4.5 至 7.5)、3b 期的时间缩短 3.3 年(95%CI,2.7 至 4.0),但在 5 期的时间仅缩短 2.4 个月(95%CI,0.8 至 3.6)。与蛋白尿<1g/g 相比,蛋白尿≥1g/g 与 3a 期的时间缩短 8 年(95%CI,6.8 至 9.6)、3b 期的时间缩短 5.6 年(95%CI,5.0 至 6.4)有关,但在 5 期的时间仅缩短 6 个月(95%CI,3.8 至 8.0)。
根据风险因素和疾病阶段,CKD 不同阶段的时间存在明显差异。