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净内源性酸排泄与肾移植结局。

Net Endogenous Acid Excretion and Kidney Allograft Outcomes.

机构信息

Department of Internal Medicine, University Medical Centre Groningen, Groningen, The Netherlands.

Department of Laboratory Medicine, University Medical Centre Groningen, Groningen, The Netherlands.

出版信息

Clin J Am Soc Nephrol. 2021 Sep;16(9):1398-1406. doi: 10.2215/CJN.00780121. Epub 2021 Jun 16.

Abstract

BACKGROUND AND OBJECTIVES

High dietary acid load may accelerate a decline in kidney function. We prospectively investigated whether dietary acid load is associated with graft outcomes in kidney transplant recipients, and whether venous bicarbonate mediates this association.

DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: We used data from 642 kidney transplant recipients with a functioning graft ≥1 year after transplantation. Net endogenous acid production was estimated using food frequency questionnaires and, alternatively, 24-hour urinary urea and potassium excretion to estimate net endogenous acid production. We defined the composite kidney end point as a doubling of plasma creatinine or graft failure. Multivariable Cox regression analyses, adjusted for potential confounders, were used to study the associations of dietary acid load with the kidney end point. We evaluated potential mediation effects of venous bicarbonate, urinary bicarbonate excretion, urinary ammonium excretion, titratable acid excretion, and net acid excretion on the association between net endogenous acid production and the kidney end point.

RESULTS

The median net endogenous acid production using food frequency questionnaires and net endogenous acid production using urinary excretion were 40 (interquartile range, 35-45) and 54 (interquartile range, 44-66) mEq/day, respectively. During a median follow-up of 5.3 years (interquartile range, 4.1-6.0), 121 (19%) participants reached the kidney end point. After multivariable adjustment, net endogenous acid production using food frequency questionnaires and net endogenous acid production using urinary excretion (per SD higher) were independently associated with higher risk for kidney end point (hazard ratio, 1.33; 95% confidence interval, 1.12 to 1.57, =0.001 and hazard ratio, 1.44; 95% confidence interval, 1.24 to 1.69, <0.001, respectively). Baseline venous bicarbonate mediated 20% of the association between net endogenous acid production using food frequency questionnaires and the kidney end point. Baseline venous bicarbonate, urinary ammonium excretion, and net acid excretion mediated 25%, -14%, and -18%, respectively, of the association between net endogenous acid production using urinary excretion and the kidney end point.

CONCLUSIONS

Higher dietary acid load was associated with a higher risk of doubling of plasma creatinine or graft failure, and this association was partly mediated by venous bicarbonate, urinary ammonium, and net acid excretion.

摘要

背景与目的

高膳食酸负荷可能会加速肾功能下降。我们前瞻性地研究了膳食酸负荷是否与肾移植受者的移植物结局相关,以及静脉碳酸氢盐是否介导这种关联。

设计、设置、参与者和测量:我们使用了 642 名移植后 1 年以上肾功能正常的肾移植受者的数据。使用食物频率问卷估计净内源性酸生成,或者使用 24 小时尿尿素和钾排泄来估计净内源性酸生成。我们将复合肾脏终点定义为血肌酐加倍或移植物衰竭。使用多变量 Cox 回归分析,调整潜在混杂因素,研究膳食酸负荷与肾脏终点的关系。我们评估了静脉碳酸氢盐、尿碳酸氢盐排泄、尿铵排泄、可滴定酸排泄和净酸排泄对净内源性酸生成与肾脏终点之间关联的潜在中介作用。

结果

使用食物频率问卷和尿排泄估计的中位数净内源性酸生成分别为 40(四分位距,35-45)和 54(四分位距,44-66)mEq/天。在中位随访 5.3 年(四分位距,4.1-6.0)期间,121 名(19%)参与者达到肾脏终点。经过多变量调整后,使用食物频率问卷和尿排泄估计的净内源性酸生成(每标准差升高)与肾脏终点风险增加独立相关(风险比,1.33;95%置信区间,1.12 至 1.57,=0.001 和风险比,1.44;95%置信区间,1.24 至 1.69,<0.001)。基线静脉碳酸氢盐介导了食物频率问卷估计的净内源性酸生成与肾脏终点之间 20%的关联。基线静脉碳酸氢盐、尿铵排泄和净酸排泄分别介导了尿排泄估计的净内源性酸生成与肾脏终点之间 25%、-14%和-18%的关联。

结论

较高的膳食酸负荷与血肌酐加倍或移植物衰竭的风险增加相关,这种关联部分由静脉碳酸氢盐、尿铵和净酸排泄介导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7798/8729579/d23602d380f1/CJN.00780121absf1.jpg

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