瑞士代谢性酸中毒的肾移植受者中应用碳酸氢钠:一项多中心、随机、单盲、安慰剂对照、3 期临床试验。

Sodium bicarbonate for kidney transplant recipients with metabolic acidosis in Switzerland: a multicentre, randomised, single-blind, placebo-controlled, phase 3 trial.

机构信息

Division of Nephrology, University Hospital, Zurich, Switzerland.

Division of Nephrology, University Hospital, Zurich, Switzerland.

出版信息

Lancet. 2023 Feb 18;401(10376):557-567. doi: 10.1016/S0140-6736(22)02606-X. Epub 2023 Jan 25.

Abstract

BACKGROUND

Metabolic acidosis is common in kidney transplant recipients and is associated with declining graft function. Sodium bicarbonate treatment effectively corrects metabolic acidosis, but no prospective studies have examined its effect on graft function. Therefore, we aimed to test whether sodium bicarbonate treatment would preserve graft function and slow the progression of estimated glomerular filtration rate (GFR) decline in kidney transplant recipients.

METHODS

The Preserve-Transplant Study was a multicentre, randomised, single-blind, placebo-controlled, phase 3 trial at three University Hospitals in Switzerland (Zurich, Bern, and Geneva), which recruited adult (aged ≥18 years) male and female long-term kidney transplant recipients if they had undergone transplantation more than 1 year ago. Key inclusion criteria were an estimated GFR between 15 mL/min per 1·73 m and 89 mL/min per 1·73 m, stable allograft function in the last 6 months before study inclusion (<15% change in serum creatinine), and a serum bicarbonate of 22 mmol/L or less. We randomly assigned patients (1:1) to either oral sodium bicarbonate 1·5-4·5 g per day or matching placebo using web-based data management software. Randomisation was stratified by study centre and gender using a permuted block design to guarantee balanced allocation. We did multi-block randomisation with variable block sizes of two and four. Treatment duration was 2 years. Acid-resistant soft gelatine capsules of 500 mg sodium bicarbonate or matching 500 mg placebo capsules were given at an initial dose of 500 mg (if bodyweight was <70 kg) or 1000 mg (if bodyweight was ≥70 kg) three times daily. The primary endpoint was the estimated GFR slope over the 24-month treatment phase. The primary efficacy analyses were applied to a modified intention-to-treat population that comprised all randomly assigned participants who had a baseline visit. The safety population comprised all participants who received at least one dose of study drug. The trial is registered with ClinicalTrials.gov, NCT03102996.

FINDINGS

Between June 12, 2017, and July 10, 2019, 1114 kidney transplant recipients with metabolic acidosis were assessed for trial eligibility. 872 patients were excluded and 242 were randomly assigned to the study groups (122 [50%] to the placebo group and 120 [50%] to the sodium bicarbonate group). After secondary exclusion of two patients, 240 patients were included in the intention-to-treat analysis. The calculated yearly estimated GFR slopes over the 2-year treatment period were a median -0·722 mL/min per 1·73 m (IQR -4·081 to 1·440) and mean -1·862 mL/min per 1·73 m (SD 6·344) per year in the placebo group versus median -1·413 mL/min per 1·73 m (IQR -4·503 to 1·139) and mean -1·830 mL/min per 1·73 m (SD 6·233) per year in the sodium bicarbonate group (Wilcoxon rank sum test p=0·51; Welch t-test p=0·97). The mean difference was 0·032 mL/min per 1·73 m per year (95% CI -1·644 to 1·707). There were no significant differences in estimated GFR slopes in a subgroup analysis and a sensitivity analysis confirmed the primary analysis. Although the estimated GFR slope did not show a significant difference between the treatment groups, treatment with sodium bicarbonate effectively corrected metabolic acidosis by increasing serum bicarbonate from 21·3 mmol/L (SD 2·6) to 23·0 mmol/L (2·7) and blood pH from 7·37 (SD 0·06) to 7·39 (0·04) over the 2-year treatment period. Adverse events and serious adverse events were similar in both groups. Three study participants died. In the placebo group, one (1%) patient died from acute respiratory distress syndrome due to SARS-CoV-2 and one (1%) from cardiac arrest after severe dehydration following diarrhoea with hypotension, acute kidney injury, and metabolic acidosis. In the sodium bicarbonate group, one (1%) patient had sudden cardiac death.

INTERPRETATION

In adult kidney transplant recipients, correction of metabolic acidosis by treatment with sodium bicarbonate over 2 years did not affect the decline in estimated GFR. Thus, treatment with sodium bicarbonate should not be generally recommended to preserve estimated GFR (a surrogate marker for graft function) in kidney transplant recipients with chronic kidney disease who have metabolic acidosis.

FUNDING

Swiss National Science Foundation.

摘要

背景

代谢性酸中毒在肾移植受者中很常见,与移植物功能下降有关。碳酸氢钠治疗可有效纠正代谢性酸中毒,但尚无前瞻性研究探讨其对移植物功能的影响。因此,我们旨在检验碳酸氢钠治疗是否能保持移植物功能,并减缓估算肾小球滤过率(eGFR)下降的速度。

方法

保肾移植研究(Preserve-Transplant Study)是一项在瑞士苏黎世、伯尔尼和日内瓦的 3 家大学医院进行的多中心、随机、单盲、安慰剂对照、3 期临床试验,纳入成年(年龄≥18 岁)男性和女性长期肾移植受者,如果他们在研究入组前 1 年以上接受了移植。主要纳入标准为 eGFR 在 15 ml/min/1.73m²和 89 ml/min/1.73m²之间,在研究入组前 6 个月内稳定的同种异体移植物功能(血清肌酐变化<15%),以及血清碳酸氢盐<22 mmol/L。我们使用基于网络的数据管理软件,以 1:1 的比例将患者随机分配至口服碳酸氢钠 1.5-4.5 g/d 或匹配安慰剂组。按研究中心和性别进行分层随机化,采用置换块设计以保证均衡分配。我们采用多块随机化,块大小为 2 和 4。治疗持续 2 年。起始剂量为 500 mg(如果体重<70 kg)或 1000 mg(如果体重≥70 kg),每日 3 次,给予 500 mg 耐酸软明胶胶囊或匹配的 500 mg 安慰剂胶囊。主要终点为 24 个月治疗期间的 eGFR 斜率。主要疗效分析应用于包含所有基线就诊的随机分组参与者的改良意向治疗人群。安全性人群包含至少接受一次研究药物治疗的所有参与者。该试验在 ClinicalTrials.gov 注册,NCT03102996。

结果

2017 年 6 月 12 日至 2019 年 7 月 10 日,对 1114 名患有代谢性酸中毒的肾移植受者进行了试验入选评估。872 名患者被排除在外,242 名患者被随机分配至研究组(安慰剂组 122 名[50%],碳酸氢钠组 120 名[50%])。在对 2 名患者进行二次排除后,240 名患者被纳入意向治疗分析。在 2 年治疗期间,计算得到的每年 eGFR 斜率分别为中位数-0.722 ml/min/1.73m(IQR-4.081 至 1.440)和均值-1.862 ml/min/1.73m(SD 6.344)/年的安慰剂组与中位数-1.413 ml/min/1.73m(IQR-4.503 至 1.139)和均值-1.830 ml/min/1.73m(SD 6.233)/年的碳酸氢钠组(Wilcoxon 秩和检验 p=0.51;Welch t 检验 p=0.97)。平均差异为 0.032 ml/min/1.73m/年(95%CI-1.644 至 1.707)。亚组分析中没有观察到 eGFR 斜率的显著差异,敏感性分析也证实了主要分析结果。虽然治疗组间 eGFR 斜率没有显示出显著差异,但碳酸氢钠治疗可有效纠正代谢性酸中毒,使血清碳酸氢盐从 21.3 mmol/L(SD 2.6)升高至 23.0 mmol/L(2.7),血 pH 值从 7.37(SD 0.06)升高至 7.39(0.04),在 2 年治疗期间。两组的不良事件和严重不良事件相似。有 3 名研究参与者死亡。在安慰剂组中,1 名(1%)患者因 SARS-CoV-2 导致的急性呼吸窘迫综合征死亡,1 名(1%)患者因腹泻后严重脱水导致低血压、急性肾损伤和代谢性酸中毒而发生心脏骤停。在碳酸氢钠组中,1 名(1%)患者发生心源性猝死。

解释

在成年肾移植受者中,碳酸氢钠治疗 2 年纠正代谢性酸中毒并未影响 eGFR 的下降。因此,对于患有慢性肾脏病且代谢性酸中毒的肾移植受者,碳酸氢钠治疗不应普遍用于维持估算肾小球滤过率(eGFR)(移植物功能的替代标志物)。

资金

瑞士国家科学基金会。

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