Lanes R, Gunczler P, Orta N, Bosquez M, Scovino R, Dominguez L, Esaa S, Weisinger J R
Unidad de Endocrinologia Pediatrica, Hospital de Clinicas Caracas, Venezuela.
Horm Res. 1996;46(6):263-8. doi: 10.1159/000185098.
Thirteen prepubertal children with a mean chronological age of 6.7 +/- 3.4 years and severe chronic renal failure (mean glomerular filtration rate of 20.8 +/- 17.7 ml/min/1.73 m2) were studied. Patients received recombinant human growth hormone (rhGH) at a dose of 1 IU/kg/week given subcutaneously on a daily basis for 12 months. Mean growth rates of our patients increased significantly from a baseline level of 4.3 +/- 2.1 to 9.1 +/- 2.0 cm/year at 12 months of rhGH therapy. Mean height SDS improved from -3.5 +/- 1.0 at initiation of therapy to -2.6 +/- 1.3 at 12 months. Mean serum creatinine and blood urea nitrogen levels remained stable during the study, while mean glomerular filtration rates decreased initially and then stabilized; however, 2 subjects had a significant deterioration of their renal function at 6 and 9 months of rhGH, requiring discontinuing treatment. Before rhGH treatment, total bone mineral content as well as bone mineral density in cortical and trabecular bone were significantly reduced in our patients when compared to healthy controls paired for chronological age and similar to those of a healthy control group paired for bone age and height. Both these parameters increased significantly during rhGH treatment so that at 12 months our patients had values similar to those seen in a healthy control population paired to our patients for chronological age. While trabecular bone mineral density did not change in a group of untreated uremic controls during 12 months of follow-up, the percent of bone mineral density change in trabecular bone in our uremic patients during 12 months of rhGH treatment was very significant (p < 0.001) and larger than that noted in a group of healthy controls paired for bone age and height during 12 months of follow-up. This study demonstrates how rhGH treatment in prepubertal uremic children increases their growth velocity and their bone mineral density significantly, with an improvement in height for age. Careful followup of the renal function of patients in needed as they improve their height and bone mineral status.
对13名青春期前儿童进行了研究,他们的平均实际年龄为6.7±3.4岁,患有严重慢性肾衰竭(平均肾小球滤过率为20.8±17.7毫升/分钟/1.73平方米)。患者接受重组人生长激素(rhGH)治疗,剂量为1国际单位/千克/周,每天皮下注射,持续12个月。rhGH治疗12个月时,我们患者的平均生长速度从基线水平的4.3±2.1显著增加到9.1±2.0厘米/年。平均身高标准差评分从治疗开始时的-3.5±1.0改善到12个月时的-2.6±1.3。在研究期间,平均血清肌酐和血尿素氮水平保持稳定,而平均肾小球滤过率最初下降然后稳定;然而,2名受试者在rhGH治疗6个月和9个月时肾功能显著恶化,需要停止治疗。与按实际年龄配对的健康对照组相比,在rhGH治疗前,我们患者的总骨矿物质含量以及皮质骨和小梁骨的骨矿物质密度显著降低,与按骨龄和身高配对的健康对照组相似。在rhGH治疗期间,这两个参数均显著增加,因此在12个月时,我们患者的值与按实际年龄与我们患者配对的健康对照人群中观察到的值相似。在一组未治疗的尿毒症对照组随访12个月期间,小梁骨矿物质密度没有变化,而我们的尿毒症患者在rhGH治疗12个月期间小梁骨矿物质密度变化百分比非常显著(p<0.001),且大于按骨龄和身高配对的一组健康对照组在随访12个月期间观察到的变化。这项研究表明,青春期前尿毒症儿童接受rhGH治疗可显著提高其生长速度和骨矿物质密度,并改善其年龄别身高。随着患者身高和骨矿物质状况的改善,需要仔细随访其肾功能。