Querfeld U
University Children's Hospital, Köln, Germany.
Br J Clin Pract Suppl. 1996 Aug;85:54-5.
Growth hormone (GH) can modulate the metabolism of lipoproteins by affecting both their secretion and uptake by the liver and their catabolism by lipolytic enzymes in plasma. Clinical studies in adults indicate that patients with GH deficiency have atherogenic lipoprotein profiles that are ameliorated by GH administration. However, in children with GH deficiency or chronic renal insufficiency (CRI), just modest changes in total plasma lipids and lipoprotein profiles have been observed. In contrast, GH administration results in a significant increase in lipoprotein(a) (Lp(a)) levels that does not seem to be mediated by IGF-I but rather by the direct effect of GH on the hepatic secretion of Lp(a). In patients with CRF, Lp(a) is frequently elevated and GH administration may lead to a further increase in plasma levels necessitating monitoring of this highly atherogenic particle during rhGH treatment.
生长激素(GH)可通过影响肝脏对脂蛋白的分泌与摄取以及血浆中脂解酶对脂蛋白的分解代谢来调节脂蛋白代谢。针对成年人的临床研究表明,生长激素缺乏症患者具有致动脉粥样硬化的脂蛋白谱,给予生长激素后该谱型会得到改善。然而,在生长激素缺乏症或慢性肾功能不全(CRI)的儿童中,仅观察到血浆总脂质和脂蛋白谱有适度变化。相比之下,给予生长激素会导致脂蛋白(a)[Lp(a)]水平显著升高,这似乎并非由胰岛素样生长因子-I(IGF-I)介导,而是由生长激素对肝脏分泌Lp(a)的直接作用所致。在慢性肾衰竭(CRF)患者中,Lp(a)常常升高,给予生长激素可能会导致血浆水平进一步升高,因此在重组人生长激素(rhGH)治疗期间需要监测这种高度致动脉粥样硬化的颗粒。