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首页> 外文期刊>Clinical journal of the American Society of Nephrology: CJASN >Improvement in growth after 1 year of growth hormone therapy in well-nourished infants with growth retardation secondary to chronic renal failure: Results of a multicenter, controlled, randomized, open clinical trial
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Improvement in growth after 1 year of growth hormone therapy in well-nourished infants with growth retardation secondary to chronic renal failure: Results of a multicenter, controlled, randomized, open clinical trial

机译:营养丰富的婴儿患有慢性肾衰竭继发生长迟缓的一年生长激素治疗后的生长改善:一项多中心,对照,随机,开放性临床试验的结果

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摘要

Background and objectives: Our aim was to evaluate the growth-promoting effect of growth hormone (GH) treatment in infants with chronic renal failure (CRF) and persistent growth retardation despite adequate nutritional and metabolic management. Design, setting, participants, & measurements: The study design included randomized, parallel groups in an open, multicenter trial comparing GH (0.33 mg/kg per wk) with nontreatment with GH during 12 months. Sixteen infants who had growth retardation, were aged 12 ± 3 months, had CRF (GFR ≤60 ml/min per 1.73 m2), and had adequate nutritional intake and good metabolic control were recruited from eight pediatric nephrology departments from Spain and Portugal. Main outcome measures were body length, body weight, bone age, biochemical and hormonal analyses, renal function, bone mass, and adverse effects. Results: Length gain in infants who were treated with GH was statistically greater (P 0.05) than that of nontreated children (14.5 versus 9.5 cm/yr; SD score 1.43 versus -0.11). The GH-induced stimulation of growth was associated with no undesirable effects on bone maturation, renal failure progression, or metabolic control. In addition, GH treatment improved forearm bone mass and increased serum concentrations of total and free IGF-I and IGF-binding protein 3 (IGFBP-3), whereas IGF-II, IGFBP-1, IGFBP-2, GH-binding protein, ghrelin, and leptin were not modified. Conclusions: Infants with CRF and growth retardation despite good metabolic and nutritional control benefit from GH treatment without adverse effects during 12 months of therapy.
机译:背景与目的:我们的目的是评估尽管有足够的营养和代谢管理方法,但生长激素(GH)治疗对患有慢性肾衰竭(CRF)和持续性发育迟缓的婴儿的生长促进作用。设计,设置,参与者和测量:该研究设计包括一个开放的多中心试验中的随机平行组,在12个月内比较了GH(每星期0.33 mg / kg)与未进行GH治疗的情况。从西班牙和葡萄牙的八个儿科肾脏病科招募了16名发育迟缓,年龄为12±3个月,CRF(GFR≤60 ml / min每1.73 m2)并具有足够的营养摄入和良好的代谢控制的婴儿。主要结局指标为体长,体重,骨龄,生化和激素分析,肾功能,骨量和不良反应。结果:接受GH治疗的婴儿的身长增加在统计学上比未接受治疗的儿童长(P <0.05)(14.5对9.5 cm / yr; SD评分1.43对-0.11)。 GH诱导的生长刺激与骨成熟,肾衰竭进展或代谢控制没有不良影响。此外,GH治疗可改善前臂骨质量,并增加总和游离IGF-I和IGF结合蛋白3(IGFBP-3)的血清浓度,而IGF-II,IGFBP-1,IGFBP-2,GH结合蛋白ghrelin和leptin未修饰。结论:尽管具有良好的代谢和营养控制,但具有CRF和生长迟缓的婴儿可从GH治疗中受益,在治疗12个月内无不良反应。

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