Hokken-Koelega A C, Stijnen T, de Jong R C, Donckerwolcke R A, Groothoff J W, Wolff E D, Blum W F, de Muinck Keizer-Schrama S M, Drop S L
Department of Pediatrics, Sophia Children's Hospital, Rotterdam, The Netherlands.
Kidney Int Suppl. 1996 Jan;53:S128-34.
Sustained growth retardation in spite of a successful renal transplantation (RTx) is a serious problem for many pediatric allograft recipients. Biosynthetic growth hormone (GH) was given to 11 prepubertal children with severe growth retardation after RTx in a placebo-controlled double-blind study, assessing its effect on height velocity (HV), bone maturation, renal function, plasma IGF-I and IGF-II, serum IGF-binding proteins (IGFBP), and lipid and carbohydrate metabolism. Six months of GH (4 IU/m2/day s.c.) was either preceded or followed by six months of placebo. The patients underwent a full examination every three months. All children completed the study. Mean HV improved significantly with GH therapy (P < 0.0001), but there was also some improvement with placebo (P = 0.06). The GH-induced HV increment exceeded that of placebo by 2.9 cm/six months. Bone maturation was not accelerated. Acute renal graft rejection did not occur in any of the patients. 125I-thalamate and 131I-hippuran tests showed that mean glomerular filtration rate (GFR) and effective renal plasma flow (ERPF) did not change significantly during GH therapy. GH caused a significant increase in IGF-I (P < 0.0001), which was far greater than the insignificant increase in serum IGFBP-3 levels (P = 0.16). Mean serum levels of total cholesterol, low density lipoprotein, apolipoprotein-A1 and -B, which are elevated at the start of the study compared with that of controls, did not change significantly during GH therapy. GH induced a significant increase in mean integrated plasma insulin levels during oral glucose tolerance test, without changing plasma glucose levels. Serum fructosamine and parathyroid hormone levels remained constant. Impressive HV increment can be achieved with GH therapy in children with growth retardation after RTx, without significant changes in renal function. Bone maturation appears unaffected, suggesting an improve final height.
尽管肾移植(RTx)成功,但持续生长发育迟缓仍是许多小儿同种异体移植受者面临的严重问题。在一项安慰剂对照双盲研究中,对11名青春期前肾移植后严重生长发育迟缓的儿童给予生物合成生长激素(GH),评估其对身高增长速度(HV)、骨成熟、肾功能、血浆胰岛素样生长因子-I(IGF-I)和胰岛素样生长因子-II(IGF-II)、血清胰岛素样生长因子结合蛋白(IGFBP)以及脂质和碳水化合物代谢的影响。6个月的GH治疗(4 IU/m²/天,皮下注射)之前或之后是6个月的安慰剂治疗。患者每三个月接受一次全面检查。所有儿童均完成了研究。GH治疗使平均HV显著改善(P < 0.0001),但安慰剂治疗也有一定改善(P = 0.06)。GH诱导的HV增量比安慰剂组每6个月高出2.9厘米。骨成熟未加速。所有患者均未发生急性肾移植排斥反应。125I-碘肽酸盐和131I-马尿酸试验表明,GH治疗期间平均肾小球滤过率(GFR)和有效肾血浆流量(ERPF)无显著变化。GH导致IGF-I显著增加(P < 0.0001),远大于血清IGFBP-3水平的微小增加(P = 0.16)。与对照组相比,研究开始时升高的总胆固醇、低密度脂蛋白、载脂蛋白-A1和-B的平均血清水平在GH治疗期间无显著变化。GH在口服葡萄糖耐量试验期间使平均血浆胰岛素综合水平显著增加,而血浆葡萄糖水平未改变。血清果糖胺和甲状旁腺激素水平保持不变。RTx后生长发育迟缓的儿童接受GH治疗可实现显著的HV增量,且肾功能无显著变化。骨成熟似乎未受影响,提示最终身高可能改善。