RENAL-FUNCTION IN LARON SYNDROME PATIENTS TREATED BY INSULIN-LIKE GROWTH-FACTOR-I

被引:21
作者
KLINGER, B [1 ]
LARON, Z [1 ]
机构
[1] CHILDRENS MED CTR ISRAEL,ENDOCRINOL & DIABET RES UNIT,IL-49202 PETAH TIQWA,ISRAEL
关键词
INSULIN-LIKE GROWTH FACTOR-I TREATMENT; LARON SYNDROME; RENAL FUNCTION; GLOMERULAR FILTRATION RATE; TUBULAR REABSORPTION OF PHOSPHORUS;
D O I
10.1007/BF00869089
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Eight children with Laron syndrome (5 males, 3 females) aged 3-14.5 years received daily subcutaneous injections of 150 mu g/kg recombinant insulin-like growth factor-I (IGF-I) for 5 months. The children were examined weekly for the Ist month and then once monthly. At each visit, overnight fasting blood was drawn for serum IGF-I and blood chemistry measurements and a 24-h urine collection was performed for the determination of calcium, phosphorus, creatinine and nitrogen. The main effects related to kidney function were: an initial weight gain with a mild transitory reduction in the urinary volume, an increase in serum electrolyte concentrations and a decrease in urinary electrolyte excretion. The lower than normal mean (+/- SEM) basal creatinine clearance (76.7 +/- 15.8 ml/min per 1.73 m(2)) increased towards the normal range during treatment to 124.9 +/- 13 ml/min per 1.73 m(2), with a mean increment of 73.4 +/- 28% (P < 0.02) from basal values after 2 months of treatment, without changes in the serum creatinine. Initially an increase in blood urea nitrogen was observed together with a reduction in urinary nitrogen excretion. During the IGF-I therapy the urinary calcium excretion increased from 0.7 +/- 0.2 nmol/day to 1.5 +/- 0.3 nmol/day and the tubular reabsorption of phosphate increased from 1.24 +/- 0.06 to more than 1.38 +/- 0.04 nmol/l (P < 0.002), resulting in a significant increase in serum phosphate levels from 1.51 +/- 0.06 to more than 1.63 +/- 0.04 nmol/l (P < 0.005). The present study shows for the first time that long-term IGF-I deficiency in man results in a subnormal glomerular filtration rate and that chronic substitution therapy with IGF-I has marked renotropic effects identical to those ascribed to growth hormone.
引用
收藏
页码:684 / 688
页数:5
相关论文
共 27 条
[1]  
Finkelstein J.W., Kowarski S., Spaulding J.S., Migeon C.J., Effect of various preparations of human growth hormone on aldosterone secretion rates of hypopituitary dwarfs, Am J Med, 38, pp. 517-521, (1965)
[2]  
Gershberg H., Hecht A., Javier Z., Growth hormone and blood calcium homeostasis, J Clin Endocrinol, 27, pp. 1492-1494, (1967)
[3]  
Ho K.Y., Kelly J.J., Role of growth hormone in fluid homeostasis, Horm Res, 36, pp. 44-48, (1991)
[4]  
Christiansen J.S., Jorgensen J.O.L., Beneficial effects of GH replacement therapy in adults, Acta Endocrinol (Copenh), 125, pp. 7-13, (1991)
[5]  
Ogle G.D., Rosenberg A.R., Kainer G., Renal effects of growth hormone. I. Renal function and kidney growth, Pediatr Nephrol, 6, pp. 394-398, (1992)
[6]  
Ogle G.D., Rosenberg A.R., Kainer G., Renal effects of growth hormone. II. Electrolyte homeostasis and body composition, Pediatr Nephrol, 6, pp. 483-489, (1992)
[7]  
Bell N.H., Bartter F.C., Studies f<sup>47</sup>Ca metabolism in acromegaly, J Clin Endocrinol, 27, pp. 178-184, (1967)
[8]  
Laron Z., Pertzelan A., Mannheimer S., Genetic pituitary dwarfism with high serum concentration of growth hormone. A new inborn error of metabolism?, Isr J Med Sci, 2, pp. 152-155, (1966)
[9]  
Laron Z., Kochsiek G.A., Laron type dwarfism (hereditary somatomedin deficiency): a review, Advances in internal medicine and pediatric, pp. 117-150, (1984)
[10]  
Eshet R., Laron Z., Pertzelan A., Dintzman M., Defect of human growth hormone receptors in the liver of two patients with Laren type dwarfism, Isr J Med Sci, 20, pp. 8-11, (1984)