Chavers B M, Doherty L, Nevins T E, Cook M, Sane K
Department of Pediatrics, University of Minnesota Medical Center, Minneapolis 55455, USA.
Pediatr Nephrol. 1995 Apr;9(2):176-81. doi: 10.1007/BF00860737.
Recent evidence suggests that treatment with recombinant human growth hormone (rhGH) after a successful kidney transplant improves the growth rate of children with short stature. We prospectively investigated eight children (6 boys, 2 girls), focusing on acute rejection episodes and changes in serum creatinine levels during rhGH treatment. The children (mean age 11.6 +/- 3.4 years) received rhGH daily (0.04-0.05 mg/kg subcutaneously). Seven patients completed at least 12 months (20 +/- 8 months) of rhGH treatment. Their mean serum creatinine level was 1.3 +/- 0.7 mg/dl 12 months before, and increased to 3.4 +/- 4.2 mg/dl after 12 months of rhGH treatment, but did not achieve statistical significance (P = 0.06). Their mean calculated glomerular filtration rate was 58 +/- 20 ml/min per 1.73 m2 12 months before, and decreased to 38 +/- 21 ml/min per 1.73 m2 after 12 months of rhGH treatment, but did not achieve statistical significance (P = 0.08). Of the seven patients, two developed acute rejection after 5 and 6 rejection-free years; three lost their grafts and returned to dialysis. These preliminary observations describe untoward renal events in children receiving rhGH treatment after a kidney transplant.
近期证据表明,肾移植成功后使用重组人生长激素(rhGH)治疗可提高身材矮小儿童的生长速度。我们前瞻性地研究了8名儿童(6名男孩,2名女孩),重点关注rhGH治疗期间的急性排斥反应发作情况及血清肌酐水平变化。这些儿童(平均年龄11.6±3.4岁)每日接受rhGH治疗(皮下注射0.04 - 0.05mg/kg)。7名患者完成了至少12个月(20±8个月)的rhGH治疗。他们在rhGH治疗前12个月的平均血清肌酐水平为1.3±0.7mg/dl,治疗12个月后升至3.4±4.2mg/dl,但未达到统计学显著性(P = 0.06)。他们在rhGH治疗前12个月的平均计算肾小球滤过率为每1.73m²58±20ml/min,治疗12个月后降至每1.73m²38±21ml/min,但未达到统计学显著性(P = 0.08)。在这7名患者中,2名在经历5年和6年无排斥反应后发生了急性排斥反应;3名患者移植肾失功并重新开始透析。这些初步观察描述了肾移植后接受rhGH治疗儿童的不良肾脏事件。