Jensen P B, Hansen T B, Frystyk J, Ladefoged S D, Pedersen F B, Christiansen J S
Department of Nephrology, Odense University Hospital, Denmark.
Clin Nephrol. 1999 Aug;52(2):103-9.
Growth deficiency and malnutrition in uremic children are often caused by malfunction of the growth hormone (GH)/insulin-like growth factor I (IGF-I) axis and can be corrected by treatment with GH. The purpose of this study was to evaluate the levels of GH, IGF-I and II and their binding proteins compared to changes in body composition in adult, enfeebled, uremic patients in chronic hemodialysis (HD), treated for 6 months with recombinant human growth hormone (rhGH).
31 patients were included in a controlled, randomized, double-blinded study using either 4 IU/m2/day of rhGH or placebo injected subcutaneously every evening for 6 months.
Fasting levels of GH were normal at start and increased significantly from 2.2 to 13.5 microg/l (p = 0.01) within the first 4 months of rhGH treatment. Before treatment IGF-I was at the upper limit of normal range (130 to 220 microg/l) in both groups, and it increased significantly from 213 to 348 microg/l (p = 0.01) during rhGH treatment. IGF-II was above the normal range in both groups, and remained unchanged throughout. IGFBP-1 decreased in the rhGH-treated group from 53.1 to 24.7 microg/l (p = 0.004), while IGFBP-3 increased from 5620 to 7100 microg/l (p = 0.004). The molar ratio of IGF-I/IGFBP-3 increased significantly from 14 to 25% (p = 0.01), while the ratio decreased in the placebo group (p = 0.01). During the treatment with rhGH the patients increased their lean body mass (= muscle mass) by a median of 3.18 kg (range 0.82 to 5.12 kg) (p = 0.0001) while their fat mass decreased by a median of 3.33 kg (range 0.18 to 5.82 kg) (p = 0.004). Total body mass (= weight) remained stable. No significant changes were observed in the placebo group.
The baseline GH and IGF-I concentrations were normal in malnourished HD patients. When treated with rhGH in a dosage as used in growth-retarded uremic children, IGF-I increased to the levels seen in acromegalic persons. IGF-I increased more than IGFBP-3 whereby its biological activity obviously improved. This was reflected in an increased muscle mass and a decreased fat mass. The rhGH treatment was well tolerated.
尿毒症患儿生长发育迟缓及营养不良常由生长激素(GH)/胰岛素样生长因子I(IGF-I)轴功能异常所致,可通过GH治疗得到纠正。本研究旨在评估成年、体弱、慢性血液透析(HD)的尿毒症患者在接受重组人生长激素(rhGH)治疗6个月后,GH、IGF-I和II及其结合蛋白水平与身体成分变化的关系。
31例患者纳入一项对照、随机、双盲研究,每晚皮下注射4IU/m²/天的rhGH或安慰剂,持续6个月。
rhGH治疗前空腹GH水平正常,治疗前4个月内从2.2μg/L显著升至13.5μg/L(p = 0.01)。治疗前两组IGF-I均处于正常范围上限(130至220μg/L),rhGH治疗期间从213μg/L显著升至348μg/L(p = 0.01)。两组IGF-II均高于正常范围,且全程无变化。rhGH治疗组IGFBP-1从53.1μg/L降至24.7μg/L(p = 0.004),而IGFBP-3从5620μg/L升至7100μg/L(p = 0.004)。IGF-I/IGFBP-3摩尔比从14%显著升至25%(p = 0.01),而安慰剂组该比值下降(p = 0.01)。rhGH治疗期间患者瘦体重(即肌肉量)中位数增加3.18kg(范围0.82至5.12kg)(p = 0.0001),而脂肪量中位数减少3.33kg(范围0.18至5.82kg)(p = 0.004)。总体重保持稳定。安慰剂组未观察到显著变化。
营养不良的HD患者基线GH和IGF-I浓度正常。以生长发育迟缓的尿毒症患儿所用剂量进行rhGH治疗时,IGF-I升至肢端肥大症患者的水平。IGF-I升高幅度大于IGFBP-3,其生物活性明显改善。这表现为肌肉量增加和脂肪量减少。rhGH治疗耐受性良好。