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定义在尸体供肾移植临床试验中 12 个月估算肾小球滤过率的最小临床有意义差异。

Defining a minimal clinically meaningful difference in 12-month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation.

机构信息

Angion Biomedica, San Francisco, California, USA.

Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio, USA.

出版信息

Clin Transplant. 2021 Jul;35(7):e14326. doi: 10.1111/ctr.14326. Epub 2021 May 5.

DOI:10.1111/ctr.14326
PMID:33896052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8365649/
Abstract

BACKGROUND

A Minimal Clinically Meaningful Difference (MCMD) has not been defined for Estimated glomerular filtration rate (eGFR). Our goal was to define the MCMD for eGFR anchored to kidney graft failure.

METHODS

A systematic review of studies with 12-month eGFR and subsequent renal graft failure was conducted. For observational studies, we calculated hazard ratio (HR) differences between adjacent eGFR intervals weighted by population distribution. Interventional trials yielded therapeutically induced changes in eGFR and failure risk. OPTN data analysis divided 12-month eGFR into bands for Cox regressions comparing adjacent eGFR bands with a death-censored graft survival outcome.

RESULTS

Observational studies indicated that lower eGFR was associated with increased death-censored graft failure risk; each 5 ml/min/1.73 m 12-month eGFR band associated with a weighted incremental HR = 1.12 to 1.23. Clinical trial data found a 5 ml/min/1.73 m difference was associated with incremental HR = 1.16 to 1.35. OPTN analyses showed weighted mean HRs across 10, 7, and 5 ml/min/1.73 m bands of 1.47, 1.30, and 1.19.

CONCLUSIONS

A 5 ml/min/1.73 m difference in 12-month eGFR was consistently associated with ~20% increase in death-censored graft failure risk. The magnitude of effect has been interpreted as clinically meaningful in other disease states and should be considered the MCMD in renal transplantation clinical trials.

摘要

背景

尚未定义肾小球滤过率 (eGFR) 的最小临床有意义差异 (MCMD)。我们的目标是定义以肾脏移植物衰竭为基础的 eGFR 的 MCMD。

方法

对具有 12 个月 eGFR 和随后的肾脏移植物衰竭的研究进行了系统回顾。对于观察性研究,我们根据人群分布计算了相邻 eGFR 间隔之间的风险比 (HR) 差异。干预性试验导致 eGFR 发生治疗性变化和失败风险。OPTN 数据分析将 12 个月 eGFR 分为 Cox 回归的 bands,将相邻的 eGFR bands 与以死亡为终点的移植物生存结果进行比较。

结果

观察性研究表明,较低的 eGFR 与增加的以死亡为终点的移植物失败风险相关;每 5 ml/min/1.73 m 的 12 个月 eGFR band 与加权增量 HR 相关 = 1.12 至 1.23。临床试验数据发现,5 ml/min/1.73 m 的差异与增量 HR 相关 = 1.16 至 1.35。OPTN 分析显示,在 10、7 和 5 ml/min/1.73 m bands 中加权平均 HR 分别为 1.47、1.30 和 1.19。

结论

12 个月 eGFR 差异 5 ml/min/1.73 m 与以死亡为终点的移植物失败风险增加约 20%一致相关。该效应的大小在其他疾病状态中被解释为具有临床意义,应被视为肾脏移植临床试验中的 MCMD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/d93ff55bbb25/CTR-35-e14326-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/22a969ada2ca/CTR-35-e14326-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/c5799308b697/CTR-35-e14326-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/fc89216cc8df/CTR-35-e14326-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/d93ff55bbb25/CTR-35-e14326-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/22a969ada2ca/CTR-35-e14326-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/c5799308b697/CTR-35-e14326-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/fc89216cc8df/CTR-35-e14326-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/8365649/d93ff55bbb25/CTR-35-e14326-g004.jpg

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