Chang Alex R, Miller Edgar R, Anderson Cheryl A, Juraschek Stephen P, Moser Melissa, White Karen, Henry Bobbie, Krekel Caitlin, Oh Susan, Charleston Jeanne, Appel Lawrence J
Geisinger Health System, Division of Nephrology, Danville, PA.
Welch Center for Prevention, Epidemiology and Clinical Research, Johns Hopkins University, Baltimore, MD; Division of General Internal Medicine, Johns Hopkins University, Baltimore, MD.
Am J Kidney Dis. 2017 Feb;69(2):200-209. doi: 10.1053/j.ajkd.2016.08.029. Epub 2016 Nov 16.
Little is known about the effects of phosphorus additives on patients with kidney disease.
Randomized, double-blind, crossover trial.
SETTING & PARTICIPANTS: 31 adults with early stages of presumed chronic kidney disease (estimated glomerular filtration rate ≥ 45mL/min/1.73m; urine albumin-creatinine ratio sex-specific cutoff points: men ≥ 17mg/g, women ≥ 25mg/g).
Higher versus lower phosphorus intake for 3 weeks. Higher phosphorus intake was achieved by the addition of commercially available diet beverages and breakfast bars to diet.
Change in 24-hour urine albumin excretion and plasma fibroblast growth factor 23 level.
Two 24-hour urine collections and a single fasting blood draw at the end of each period.
Mean baseline values for phosphorus intake, 24-hour urine phosphorus excretion, and estimated glomerular filtration rate were 1,113±549 (SD) mg/d, 688±300mg/d, and 74.6±22.0mL/min/1.73m. Median urine albumin excretion of 82.7 (IQR, 39.6-174.1) mg/d. Although phosphorus intake from study products increased by 993mg/d (P<0.001) during the higher compared to lower phosphorus additive period, background phosphorus intake decreased by 151mg/d (P=0.004). Higher phosphorus additive consumption increased 24-hour urine phosphorus excretion by 505 (95% CI, 381 to 629) mg/d (P<0.001), but did not significantly increase albuminuria (higher vs lower: 14.3%; 95% CI, -2.5% to 34.0%; P=0.1) or fibroblast growth factor 23 level (higher vs lower: 3.4%; 95% CI, -5.9% to 13.6%; P=0.4).
Small sample size, short duration of intervention, changes in background diet during the intervention.
A 3-week consumption of higher phosphorus food additives did not significantly increase albuminuria. Further studies are needed to confirm these results.
关于磷添加剂对肾病患者的影响,人们了解甚少。
随机、双盲、交叉试验。
31名处于慢性肾病早期的成年人(估计肾小球滤过率≥45mL/min/1.73m²;尿白蛋白肌酐比根据性别设定临界值:男性≥17mg/g,女性≥25mg/g)。
3周内分别摄入高磷饮食和低磷饮食。通过在饮食中添加市售的含磷饮料和早餐棒来实现高磷摄入。
24小时尿白蛋白排泄量和血浆成纤维细胞生长因子23水平的变化。
每个阶段结束时收集两次24小时尿液样本,并进行一次空腹采血。
磷摄入量、24小时尿磷排泄量和估计肾小球滤过率的平均基线值分别为1,113±549(标准差)mg/d、688±300mg/d和74.6±22.0mL/min/1.73m²。尿白蛋白排泄量中位数为82.7(四分位间距为39.6 - 174.1)mg/d。与低磷添加剂阶段相比,高磷添加剂阶段研究产品的磷摄入量增加了993mg/d(P<0.001),但背景磷摄入量减少了151mg/d(P = 0.004)。高磷添加剂的摄入使24小时尿磷排泄量增加了505(95%置信区间为381至629)mg/d(P<0.001),但并未显著增加蛋白尿(高磷组与低磷组相比:14.3%;95%置信区间为 - 2.5%至34.0%;P = 0.1)或成纤维细胞生长因子23水平(高磷组与低磷组相比:3.4%;95%置信区间为 - 5.9%至13.6%;P = 0.4)。
样本量小、干预时间短、干预期间背景饮食发生变化。
食用3周高磷食品添加剂并未显著增加蛋白尿。需要进一步研究来证实这些结果。