Iglesias Pedro, Díez Juan José, Fernández-Reyes Ma José, Bajo Mc Auxiliadore, Aguilera Abelardo, Méndez Javier, Codoceo Rosa, Selgas Rafael
Department of Endocrinology, Hospital General de Segovia, C/Maria Sevilla Diago, 9, 3o dcha, E-28022 Madrid, Spain.
Nephrol Dial Transplant. 2002 Feb;17(2):260-4. doi: 10.1093/ndt/17.2.260.
Hyperleptinaemia is a well-known biochemical feature found in uraemic patients. However, little is known about the hormonal regulation of leptin in chronic renal disease. Recent studies have shown that circulating leptin levels are modified by treatment with recombinant human growth hormone (rhGH), by recombinant insulin-like growth factor I (rhIGF I), or by a combination of rhIGF I plus rhGH in patients with chronic renal failure. We performed a prospective study to assess plasma leptin concentrations in a group of dialysis patients both before and during short-term rhGH therapy.
We studied eight dialysis patients (four haemodialysis (HD) and four on continuous ambulatory peritoneal dialysis (CAPD); three female, five male; mean age 63.9 +/- 3.1 years). All patients were instructed to maintain a stable diet (35 kcal/kg/day and 1 g protein/kg/day ideal body weight) and were treated with rhGH (0.2 IU/kg/day s.c.) for 4 weeks. Blood samples were taken at 0, 2, 4, and 8 weeks for determination of leptin, GH, and IGF I. Serum insulin concentrations were assessed at 0 and 4 weeks.
Mean plasma leptin concentrations were elevated (36.2 +/- 12.8 ng/ml) at study outset and increased progressively throughout the 4 weeks of rhGH therapy (43.7 +/- 13.5 ng/ml (2 weeks, NS) and 70.6 +/- 18.4 ng/ml (4 weeks, P<0.0001)). These values returned to baseline levels (38.0 +/- 12.0 ng/ml, NS) at 1 month after rhGH withdrawal. rhGH therapy was accompanied by the development of direct correlations between leptin and IGF I concentrations at 2 weeks (r=0.86, P<0.01), and with correlations between leptin and IGF I (r=0.84, P<0.01) and between leptin and insulin (r=0.88, P<0.01) after 4 weeks of rhGH administration.
These results confirm the presence of high circulating plasma leptin in dialysis patients and show that these levels are further increased by exogenous rhGH administration. The increase in plasma leptin after rhGH therapy may be related to the rhGH-induced changes in insulin in these patients.
高瘦素血症是尿毒症患者中一种众所周知的生化特征。然而,关于慢性肾病中瘦素的激素调节知之甚少。最近的研究表明,慢性肾衰竭患者接受重组人生长激素(rhGH)、重组胰岛素样生长因子I(rhIGF I)或rhIGF I加rhGH联合治疗后,循环瘦素水平会发生改变。我们进行了一项前瞻性研究,以评估一组透析患者在短期rhGH治疗前后的血浆瘦素浓度。
我们研究了8名透析患者(4名血液透析(HD)患者和4名持续性非卧床腹膜透析(CAPD)患者;3名女性,5名男性;平均年龄63.9±3.1岁)。所有患者均被要求保持稳定饮食(35千卡/千克/天,1克蛋白质/千克/天理想体重),并接受rhGH(0.2国际单位/千克/天皮下注射)治疗4周。在第0、2、4和8周采集血样,测定瘦素、生长激素(GH)和胰岛素样生长因子I(IGF I)。在第0周和第4周评估血清胰岛素浓度。
研究开始时平均血浆瘦素浓度升高(36.2±12.8纳克/毫升),在rhGH治疗的4周内逐渐升高(43.7±13.5纳克/毫升(2周,无统计学意义)和70.6±18.4纳克/毫升(4周,P<0.0001))。rhGH停用1个月后,这些值恢复到基线水平(38.0±12.0纳克/毫升,无统计学意义)。rhGH治疗在2周时伴随着瘦素与IGF I浓度之间直接相关性的出现(r=0.86,P<0.01),在rhGH给药4周后,瘦素与IGF I之间(r=0.84,P<0.01)以及瘦素与胰岛素之间(r=0.88,P<0.01)出现相关性。
这些结果证实透析患者存在高循环血浆瘦素,并表明外源性rhGH给药会使这些水平进一步升高。rhGH治疗后血浆瘦素的升高可能与这些患者中rhGH诱导的胰岛素变化有关。