Willemsen Ruben H, Willemsen Sten P, Hokken-Koelega Anita C S
Department of Pediatrics, Division of Endocrinology, Erasmus Medical Center Sophia, GJ Rotterdam, The Netherlands.
J Clin Endocrinol Metab. 2008 Sep;93(9):3449-54. doi: 10.1210/jc.2008-0623. Epub 2008 Jun 17.
GH treatment reduces insulin sensitivity (Si). For small-for-gestational-age (SGA) subjects, who might have an increased risk to develop cardiovascular disease and type 2 diabetes, it is still uncertain how Si, beta-cell function, and body composition change over time after stopping GH treatment.
Our objective was to investigate longitudinal changes in Si, beta-cell function, and body composition after cessation of long-term GH treatment.
We conducted a longitudinal study that included 48 SGA adolescents studied at adult height, while still on GH, and 6 months after GH stop and compared them with 38 appropriate-for-gestational-age (AGA) controls at both time points.
We took paired measurements of Si and beta-cell function, assessed by frequently sampled iv glucose tolerance tests with tolbutamide, and body composition, measured by dual-energy x-ray absorptiometry.
After stopping GH, Si (P = 0.006), glucose effectiveness (Sg; P = 0.009) and beta-cell function (disposition index; P = 0.024) increased, whereas insulin secretion (acute insulin response; not significant) decreased. Fat percentage increased (P < 0.0005), and lean body mass decreased (P < 0.0005), but fat distribution remained unaltered, and body composition remained within the normal range. Compared with AGA controls, Si was lower during GH and became similar after GH stop, acute insulin response was higher at both time points, and glucose effectiveness and disposition index became higher.
The GH-induced lower Si in SGA adolescents increases after stopping long-term GH treatment and becomes similar to that of AGA controls. Discontinuation of GH treatment is, however, also associated with an increase in percent body fat and with a decrease in lean body mass, without changes in fat distribution.
生长激素(GH)治疗会降低胰岛素敏感性(Si)。对于可能有患心血管疾病和2型糖尿病风险增加的小于胎龄儿(SGA)受试者,在停止GH治疗后,Si、β细胞功能和身体组成如何随时间变化仍不确定。
我们的目的是研究长期GH治疗停止后Si、β细胞功能和身体组成的纵向变化。
我们进行了一项纵向研究,纳入了48名SGA青少年,在其成年身高时、仍接受GH治疗时以及停止GH治疗6个月后进行研究,并在这两个时间点将他们与38名适于胎龄儿(AGA)对照进行比较。
我们通过使用甲苯磺丁脲的频繁采样静脉葡萄糖耐量试验对Si和β细胞功能进行配对测量,并通过双能X线吸收法测量身体组成。
停止GH治疗后,Si(P = 0.006)、葡萄糖效能(Sg;P = 0.009)和β细胞功能(处置指数;P = 0.024)增加,而胰岛素分泌(急性胰岛素反应;无显著性差异)减少。脂肪百分比增加(P < 0.0005),瘦体重减少(P < 0.0005),但脂肪分布未改变,身体组成仍在正常范围内。与AGA对照相比,在接受GH治疗期间Si较低,停止GH治疗后变得相似,在两个时间点急性胰岛素反应均较高,葡萄糖效能和处置指数变得更高。
SGA青少年中由GH诱导的较低Si在停止长期GH治疗后增加,并变得与AGA对照相似。然而,停止GH治疗也与体脂百分比增加和瘦体重减少有关,脂肪分布无变化。