Reinhard Mark, Frystyk Jan, Jespersen Bente, Bjerre Mette, Christiansen Jens S, Flyvbjerg Allan, Ivarsen Per
BMC Nephrol. 2013 Apr 4;14:80. doi: 10.1186/1471-2369-14-80.
A marked reduction in serum levels of bioactive insulin-like growth factor-I (IGF-I) has been observed in fasting hemodialysis (HD) patients during a 4-h HD session. The aim of the present study was to investigate the beneficial effect of hyperinsulinemia during HD on bioactive IGF-I and inflammatory biomarkers.
In a randomized cross-over study, 11 non-diabetic HD patients received a standardised HD session with either: 1) no treatment, 2) glucose infusion (10% glucose, 2.5 mL/kg/h), or 3) glucose-insulin infusion (10% glucose added 30 IU NovoRapid® per litre, 2.5 mL/kg/h). Each experiment consisted of three periods: pre-HD (-120 to 0 min), HD (0 to 240 min), and post-HD (240 to 360 min). A meal was served at baseline (-120 min); infusions were administered from baseline to 240 min. The primary outcome was change in bioactive IGF-I during the experiment. Secondary outcomes were changes in high-sensitivity C-reactive protein, interleukin-1β, interleukin-6, and tumor necrosis factor α. Comparisons were performed using mixed-model analysis of variance for repeated measures.
From baseline to the end of study, no significant differences were observed in the changes in either serum bioactive IGF-I or total IGF-I between study days. Overall, serum bioactive IGF-I levels rose above baseline at 120 to 300 min with a maximum increase of 20% at 120 min (95% confidence interval (CI), 9 to 31%; p < 0.001), whereas total IGF-I levels rose above baseline at 180 to 300 min with a maximum increase of 5% at 240 min (95% CI, 2 to 9%; p = 0.004). A significant difference was observed in the changes in serum IGF-binding protein-1 (IGFBP-1) between study days (p = 0.008), but differences were only significant in the post-HD period. From baseline to the end of HD, no significant difference was observed in the changes in serum IGFBP-1 levels between study days, and in this time period overall serum IGFBP-1 levels were below baseline at all time points with a maximum decrease of 51% at 180 min (95% CI, 45 to 57%; p < 0.001). None of the investigated inflammatory biomarkers showed any differences in the changes over time between study days.
Postprandial insulin secretion stimulated the IGF-system during HD with no further effect of adding glucose or glucose-insulin infusion. Hyperinsulinemia during HD had no effect on biomarkers of inflammation.
ClinicalTrials.gov registry: NCT01209403.
在空腹血液透析(HD)患者进行4小时血液透析期间,观察到生物活性胰岛素样生长因子-I(IGF-I)血清水平显著降低。本研究的目的是探讨血液透析期间高胰岛素血症对生物活性IGF-I和炎症生物标志物的有益作用。
在一项随机交叉研究中,11名非糖尿病HD患者接受标准化血液透析治疗,治疗方式分别为:1)不治疗;2)葡萄糖输注(10%葡萄糖,2.5 mL/kg/h);或3)葡萄糖-胰岛素输注(每升10%葡萄糖中加入30 IU诺和锐®,2.5 mL/kg/h)。每个实验包括三个阶段:透析前(-120至0分钟)、透析期间(0至240分钟)和透析后(240至360分钟)。在基线(-120分钟)时提供一顿餐;输注从基线持续至240分钟。主要结局是实验期间生物活性IGF-I的变化。次要结局是高敏C反应蛋白、白细胞介素-1β、白细胞介素-6和肿瘤坏死因子α的变化。使用重复测量的混合模型方差分析进行比较。
从基线到研究结束,各研究日之间血清生物活性IGF-I或总IGF-I的变化均无显著差异。总体而言,血清生物活性IGF-I水平在120至300分钟时高于基线水平,在120分钟时最大增幅为20%(95%置信区间(CI),9%至31%;p<0.001),而总IGF-I水平在180至300分钟时高于基线水平,在240分钟时最大增幅为5%(95%CI,2%至9%;p=0.004)。各研究日之间血清IGF结合蛋白-1(IGFBP-1)的变化存在显著差异(p=0.008),但差异仅在透析后阶段显著。从基线到透析结束,各研究日之间血清IGFBP-1水平的变化无显著差异,在此时间段内,总体血清IGFBP-1水平在所有时间点均低于基线水平,在180分钟时最大降幅为51%(95%CI,45%至57%;p<0.001)。所研究的炎症生物标志物在各研究日之间随时间的变化均无差异。
餐后胰岛素分泌在血液透析期间刺激了IGF系统,添加葡萄糖或葡萄糖-胰岛素输注没有进一步影响。血液透析期间的高胰岛素血症对炎症生物标志物没有影响。
ClinicalTrials.gov注册编号:NCT01209403。