SOMATOSTATIN ANALOG, OCTREOTIDE, REDUCES INCREASED GLOMERULAR-FILTRATION RATE AND KIDNEY SIZE IN INSULIN-DEPENDENT DIABETES

被引:99
作者
SERRI, O
BEAUREGARD, H
BRAZEAU, P
ABRIBAT, T
LAMBERT, J
HARRIS, A
VACHON, L
机构
[1] UNIV MONTREAL,HOP NOTRE DAME,FAC MED,CTR RECH,DEPT MED,MONTREAL H3C 3J7,QUEBEC,CANADA
[2] UNIV MONTREAL,HOP NOTRE DAME,FAC MED,CTR RECH,DEPT SOCIAL & PREVENT MED,MONTREAL H3C 3J7,QUEBEC,CANADA
[3] SANDOZ CANADA INC,SANDOZ CLIN RES,DORVAL,QUEBEC,CANADA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1991年 / 265卷 / 07期
关键词
D O I
10.1001/jama.265.7.888
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To determine whether treatment with a somatostatin analogue can reduce kidney hyperfiltration and hypertrophy in insulin-dependent diabetes mellitus, we studied 11 patients with insulin-dependent diabetes mellitus and glomerular hyperfiltration. The patients were assigned randomly to receive continuous subcutaneous infusion of either octreotide, 300-mu-g/24 h (five patients) or placebo (six patients) for 12 weeks. At baseline, mean glomerular filtration rate and mean total kidney volume were not significantly different in the two groups. However, after 12 weeks of treatment, the mean glomerular filtration rate was significantly lower in the octreotide group (136 mL/min per 1.73 m2; range, 91 to 158 mL/min per 1.73 m2) than in the placebo group (157 mL/min per 1.73 m2; range, 138 to 184 mL/min per 1.73 m2). Furthermore, the mean total kidney volume was significantly lower after treatment in the octreotide group (379 mL/1.73 m2; range, 307 to 454 mL/1.73 m2) than in the placebo group (389 mL/1.73 m2; range, 347 to 465 mL/1.73 m2). Glycemic control did not change significantly in either group. We conclude that subcutaneous infusion of octreotide for 12 weeks reduces increased glomerular filtration rate and kidney size in patients with insulin-dependent diabetes mellitus despite the fact that glycemic control remains unchanged.
引用
收藏
页码:888 / 892
页数:5
相关论文
共 31 条
[1]  
ANDERSEN AR, 1983, DIABETOLOGIA, V25, P496
[2]  
ANDERSON S, 1986, KIDNEY INT, V29, P314
[3]   RADIOIMMUNOASSAY OF A BASIC SOMATOMEDIN - COMPARISON OF VARIOUS ASSAY TECHNIQUES AND SOMATOMEDIN LEVELS IN VARIOUS SERA [J].
BALA, RM ;
BHAUMICK, B .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1979, 49 (05) :770-777
[4]  
CARLSEN JE, 1980, J NUCL MED, V21, P126
[5]  
CHRISTENSEN S E, 1988, Diabetes Research and Clinical Practice, V5, pS87
[6]   KIDNEY-FUNCTION AND SIZE IN DIABETICS BEFORE AND DURING INITIAL INSULIN-TREATMENT [J].
CHRISTIANSEN, JS ;
GAMMELGAARD, J ;
TRONIER, B ;
SVENDSEN, PA ;
PARVING, HH .
KIDNEY INTERNATIONAL, 1982, 21 (05) :683-688
[7]   ANALYSIS OF COVARIANCE USING THE RANK TRANSFORMATION [J].
CONOVER, WJ ;
IMAN, RL .
BIOMETRICS, 1982, 38 (03) :715-724
[8]   KIDNEY-FUNCTION DURING 12 MONTHS OF STRICT METABOLIC CONTROL IN INSULIN-DEPENDENT DIABETIC-PATIENTS WITH INCIPIENT NEPHROPATHY [J].
FELDTRASMUSSEN, B ;
MATHIESEN, ER ;
HEGEDUS, L ;
DECKERT, T .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (11) :665-670
[9]   SOMATOSTATIN ANALOG ADMINISTRATION PREVENTS INCREASE IN KIDNEY SOMATOMEDIN-C AND INITIAL RENAL GROWTH IN DIABETIC AND UNINEPHRECTOMIZED RATS [J].
FLYVBJERG, A ;
FRYSTYK, J ;
THORLACIUSUSSING, O ;
ORSKOV, H .
DIABETOLOGIA, 1989, 32 (04) :261-265
[10]   ESTIMATION OF SOMATOMEDIN-C LEVELS IN NORMALS AND PATIENTS WITH PITUITARY DISEASE BY RADIOIMMUNOASSAY [J].
FURLANETTO, RW ;
UNDERWOOD, LE ;
VANWYK, JJ ;
DERCOLE, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 1977, 60 (03) :648-657