Laine J, Krogerus L, Sarna S, Jalanko H, Rönnholm K, Holmberg C
Children's Hospital and Transplantation Laboratory, University of Helsinki, Finland.
Transplantation. 1996 Mar 27;61(6):898-903. doi: 10.1097/00007890-199603270-00010.
Our objective was to investigate the effects of recombinant human growth hormone (rhGH) treatment on long-term renal allograft function and histopathology. RhGH is a potent therapy for poor growth after renal transplantation. However, rhGH has proinflammatory properties and may induce acute rejection or accelerate chronic rejection. Nine prepubertal rhGH-treated renal transplanted children and nine pair-matched controls were studied 18 (before the start of rhGH) and 36 months after transplantation (mean duration of rhGH-treatment 14 months). 51Cr-EDTA- and PAH-clearances were performed. A protocol renal biopsy was done at 36 months. Growth showed significant improvement during rhGH (P<0.01). One graft loss occurred in both groups. One acute rejection was seen in the control group. There was no difference in the rate pf change in 51Cr-EDTA-or PAH-clearance between the two groups. Histopathological findings were mostly mild. One new onset chronic rejection developed in both groups. Proximal tubular atrophy was more extensive in the rhGH-treated patients (P<0.05), but there was no uniform trend toward more severe findings. RhGH improved growth, and no significant differences were seen in allograft function or histopathology; however, larger trials controlled for pretreatment renal function and immunosuppression are needed.
我们的目的是研究重组人生长激素(rhGH)治疗对长期肾移植功能和组织病理学的影响。rhGH是治疗肾移植后生长发育不良的有效疗法。然而,rhGH具有促炎特性,可能会诱发急性排斥反应或加速慢性排斥反应。我们对9名青春期前接受rhGH治疗的肾移植儿童及其9名配对对照进行了研究,分别在移植后18个月(rhGH治疗开始前)和36个月(rhGH平均治疗时长14个月)进行。检测了51Cr-EDTA和PAH清除率。在36个月时进行了方案规定的肾活检。rhGH治疗期间生长情况有显著改善(P<0.01)。两组均有1例移植物丢失。对照组出现1例急性排斥反应。两组间51Cr-EDTA或PAH清除率的变化率无差异。组织病理学结果大多为轻度。两组均有1例新发慢性排斥反应。rhGH治疗的患者近端肾小管萎缩更广泛(P<0.05),但在更严重的结果方面没有统一的趋势。rhGH改善了生长情况,在移植肾功能或组织病理学方面未发现显著差异;然而,需要开展更大规模的试验,对预处理肾功能和免疫抑制进行控制。