Nephrology Division and.
Divisions of Nephrology and.
Clin J Am Soc Nephrol. 2018 Mar 7;13(3):436-444. doi: 10.2215/CJN.08790817. Epub 2018 Feb 14.
In-center, extended duration nocturnal hemodialysis has been associated with variable clinical benefits, but the effect of extended duration hemodialysis on many established uremic solutes and other components of the metabolome is unknown. We determined the magnitude of change in metabolite profiles for patients on extended duration nocturnal hemodialysis.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: In a 52-week prospective, observational study, we followed 33 patients receiving conventional thrice weekly hemodialysis who converted to nocturnal hemodialysis (7-8 hours per session, three times per week). A separate group of 20 patients who remained on conventional hemodialysis (3-4 hours per session, three times per week) served as a control group. For both groups, we applied liquid chromatography-mass spectrometry-based metabolite profiling on stored plasma samples collected from all participants at baseline and after 1 year. We examined longitudinal changes in 164 metabolites among those who remained on conventional hemodialysis and those who converted to nocturnal hemodialysis using Wilcoxon rank sum tests adjusted for multiple comparisons (false discovery rate <0.05).
On average, the nocturnal group had 9.6 hours more dialysis per week than the conventional group. Among 164 metabolites, none changed significantly from baseline to study end in the conventional group. Twenty-nine metabolites changed in the nocturnal group, 21 of which increased from baseline to study end (including all branched-chain amino acids). Eight metabolites decreased after conversion to nocturnal dialysis, including l-carnitine and acetylcarnitine. By contrast, several established uremic retention solutes, including -cresol sulfate, indoxyl sulfate, and trimethylamine -oxide, did not change with extended dialysis.
Across a wide array of metabolites examined, extended duration hemodialysis was associated with modest changes in the plasma metabolome, with most differences relating to metabolite increases, despite increased dialysis time. Few metabolites showed reduction with more dialysis, and no change in several established uremic toxins was observed.
中心静脉置管、延长夜间血液透析与多种临床益处相关,但目前尚不清楚延长时间的血液透析对许多已确定的尿毒症溶质和代谢组学的其他成分的影响。我们旨在确定延长夜间血液透析患者代谢物谱的变化程度。
设计、设置、参与者和测量:在一项为期 52 周的前瞻性、观察性研究中,我们随访了 33 名接受常规每周三次血液透析的患者,他们转为夜间血液透析(每次 7-8 小时,每周三次)。另一组 20 名继续接受常规血液透析(每次 3-4 小时,每周三次)的患者作为对照组。对于两组患者,我们应用基于液相色谱-质谱的代谢组学方法对所有参与者在基线和 1 年后采集的储存血浆样本进行检测。我们使用经过多次比较调整的威尔科克森秩和检验(错误发现率<0.05),比较了继续接受常规血液透析和转为夜间血液透析的患者的 164 种代谢物的纵向变化。
平均而言,夜间组每周的透析时间比常规组多 9.6 小时。在 164 种代谢物中,常规组在基线到研究结束时没有一种代谢物发生显著变化。夜间组有 29 种代谢物发生变化,其中 21 种代谢物从基线到研究结束时增加(包括所有支链氨基酸)。8 种代谢物在转为夜间透析后减少,包括左旋肉碱和乙酰左旋肉碱。相比之下,几种已确定的尿毒症潴留溶质,包括 - 对甲酚硫酸盐、吲哚硫酸酯和三甲胺 -N-氧化物,并未随着延长透析时间而改变。
在广泛的代谢物中,延长时间的血液透析与血浆代谢组的适度变化相关,尽管透析时间增加,但大多数差异与代谢物的增加有关。随着透析次数的增加,很少有代谢物减少,也没有观察到几种已确定的尿毒症毒素的变化。