Tochihara Yuka, Whiting Malcolm J, Barbara Jeffrey A, Mangoni Arduino A
Department of Clinical Pharmacology, Flinders University and Flinders Medical Centre, Adelaide, Australia.
Br J Clin Pharmacol. 2008 Nov;66(5):717-22. doi: 10.1111/j.1365-2125.2008.03262.x. Epub 2008 Jul 11.
Haemodialysis (HD) is associated with the acute loss through the dialysis membrane of biochemical factors either enhancing [folic acid (F)] or impairing [asymmetric dimethylarginine (ADMA)] arterial function. Changes in these opposing factors might explain the absence of significant modifications in arterial function during HD. We speculated that intra-HD, instead of pre-HD, F administration would provide beneficial effects on arterial wave reflections and endothelial function by preventing HD-induced F loss.
Arterial wave reflections [augmentation index (AIx), pulse-wave analysis], endothelium-dependent vasodilation (salbutamol-mediated changes in AIx) and plasma concentrations of F and ADMA were measured pre-HD and end-HD in 10 patients (age 67.7 +/- 10.3 years). Each subject received F 5 mg either pre-HD or intra-HD in two separate studies 2-4 weeks apart, in an open-label randomized cross-over trial.
Pre-HD F administration did not prevent significant reductions in F during HD (end-HD vs. pre-HD, -865 +/- 465 nmol l(-1), P < 0.001), but no significant changes in AIx (+1.4 +/- 5.7%) or salbutamol-mediated AIx modifications (+0.4 +/- 5.5%) were observed. By contrast, intra-HD F administration was associated with significant increases in F (+298 +/- 283 nmol l(-1), P = 0.010) and a significant reduction of AIx (-4.7 +/- 7.2%, P = 0.013), but no effects on salbutamol-mediated AIx changes (+1.5 +/- 4.4%). There was a trend towards greater HD-induced reductions in plasma ADMA concentrations with intra-HD F administration (P = 0.066).
Intra-HD F administration reduces arterial wave reflections but not endothelial function during HD. Given the prognostic significance of arterial wave reflections in HD patients, the timing of F administration is important in the design of interventional trials in this cohort.
血液透析(HD)与生化因子通过透析膜的急性丢失有关,这些生化因子要么增强[叶酸(F)],要么损害[不对称二甲基精氨酸(ADMA)]动脉功能。这些相反因子的变化可能解释了HD期间动脉功能没有显著改变的原因。我们推测,在HD过程中而非HD前给予F,通过防止HD诱导的F丢失,可能会对动脉波反射和内皮功能产生有益影响。
在10例患者(年龄67.7±10.3岁)中,于HD前和HD结束时测量动脉波反射[增强指数(AIx),脉搏波分析]、内皮依赖性血管舒张(沙丁胺醇介导的AIx变化)以及F和ADMA的血浆浓度。在两项间隔2 - 4周的单独研究中,以开放标签随机交叉试验的方式,让每位受试者在HD前或HD期间接受5mg F。
HD前给予F并不能防止HD期间F的显著降低(HD结束时与HD前相比,-865±465nmol l⁻¹,P < 0.001),但未观察到AIx有显著变化(+1.4±5.7%)或沙丁胺醇介导的AIx变化有显著改变(+0.4±5.5%)。相比之下,HD期间给予F与F显著增加(+298±283nmol l⁻¹,P = 0.010)以及AIx显著降低(-4.7±7.2%,P = 0.013)相关,但对沙丁胺醇介导的AIx变化无影响(+1.5±4.4%)。HD期间给予F有使血浆ADMA浓度降低幅度更大的趋势(P = 0.066)。
HD期间给予F可减少动脉波反射,但对HD期间的内皮功能无影响。鉴于动脉波反射对HD患者的预后意义,在该队列的干预试验设计中,F的给药时机很重要。