Insulin resistance and hyperinsulinemia are already present in patients with incipient renal disease

被引:294
作者
Fliser, D
Pacini, G
Engelleiter, R
Kautzky-Willer, A
Prager, R
Franek, E
Ritz, E
机构
[1] Univ Heidelberg, Dept Internal Med, Div Nephrol, D-69115 Heidelberg, Germany
[2] CNR, LADSEB, Inst Syst Sci & Biomed Engn, Padua, Italy
[3] Univ Vienna, Dept Med 3, Div Endocrinol & Metab, Vienna, Austria
关键词
ADPKD; insulin resistance; glucose metabolism; IgA glomerulonephritis; renal disease; uremia;
D O I
10.1046/j.1523-1755.1998.00898.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
In uremic patients resistance to the action of insulin has been documented, but it is not known at what stage of renal disease it appears. We therefore examined 29 patients with IgA glomerulonephritis (IgAGN) and 21 patients with adult polycystic kidney disease (ADPKD) in different stages of renal failure, and ill addition, healthy age-matched subjects. Insulin sensitivity and other variables of glucose metabolism were assessed using a frequent sampling intravenous glucose tolerance test (minimal-model technique). Glomerular filtration rate (GFR) was assessed in renal patients using the inulin-clearance technique. Mean insulin sensitivity index (SI), that is, insulin sensitivity, was significantly lower (P < 0.001) in all patients combined than in matched healthy subjects (N = 16; 14 males, mean age 42 +/- 3 years; mean SI 8.6 +/- 0.8 min(-1) mu U/ml). The mean SI was not significantly different in patients with renal disease of immune (IgAGN) or non-immune (ADPKD) origin, and it was not correlated with GFR (r = 0.01, P < 0.52), intact PTH (r = 0.23, P < 0.11) or calcitriol concentration (r = -0.03, P < 0.82). Consequently, the mean SI was similar in renal patients with GFR within the normal range (N = 19; 17 males, mean age 41 +/- 2 years: mean GFR 119 +/- 5 ml/min/1.73 m(2); mean SI 5.1 +/- 0.7 min(-1) mu U/ml), in patients with mild to moderate renal failure (N = 16, 15 males, 46 +/- 3 years: 67 +/- 4 ml/min/1.73 m(2); 5.1 +/- 0.7 min(-1) mu U/ml) and in patients with advanced renal failure (N = 15; 13 males. 46 +/- 3 years. 25 +/- 2 ml/min/1.73 m(2); 4.7 +/- 0.6 min(-1) mu U/ml). Mean fasted plasma insulin concentration, the area under the curve for plasma insulin concentration (AUC) and total insulin delivery (TID) during the glucose tolerance test were significantly higher in patients than in healthy subjects, reflecting hyperinsulinemia in renal patients. Further, fasted plasma insulin concentration (r= -0.32, P < 0.009): AUC (r = -0.62. P < 0.0001) and TID (r = -0.34. P < 0.001) in patients were significantly correlated with insulin sensitivity (SI). Thr present data document that insulin resistance and concomitant hyperinsulinemia are present early in the course of renal disease: that is, even in patients with GFR within the normal range, irrespective of the type of renal disease. This observation may have potential implications with respect to the high cardiovascular morbidity and mortality in patients with renal disease.
引用
收藏
页码:1343 / 1347
页数:5
相关论文
共 36 条
[1]  
ALVESTRAND A, 1989, CLIN NEPHROL, V31, P175
[2]   ASSESSMENT OF INSULIN SENSITIVITY INVIVO [J].
BERGMAN, RN ;
FINEGOOD, DT ;
ADER, M .
ENDOCRINE REVIEWS, 1985, 6 (01) :45-86
[3]   TOWARD PHYSIOLOGICAL UNDERSTANDING OF GLUCOSE-TOLERANCE - MINIMAL-MODEL APPROACH [J].
BERGMAN, RN .
DIABETES, 1989, 38 (12) :1512-1527
[4]   PHYSIOLOGIC EVALUATION OF FACTORS CONTROLLING GLUCOSE-TOLERANCE IN MAN - MEASUREMENT OF INSULIN SENSITIVITY AND BETA-CELL GLUCOSE SENSITIVITY FROM THE RESPONSE TO INTRAVENOUS GLUCOSE [J].
BERGMAN, RN ;
PHILLIPS, LS ;
COBELLI, C .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (06) :1456-1467
[5]   EFFECTS OF RENAL-FAILURE ON SKELETAL-MUSCLE [J].
CLYNE, N ;
ESBJORNSSON, M ;
JANSSON, E ;
JOGESTRAND, T ;
LINS, LE ;
PEHRSSON, SK .
NEPHRON, 1993, 63 (04) :395-399
[6]   INSULIN RESISTANCE IN UREMIA [J].
DEFRONZO, RA ;
ALVESTRAND, A ;
SMITH, D ;
HENDLER, R ;
HENDLER, E ;
WAHREN, J .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 67 (02) :563-568
[7]  
DEFRONZO RA, 1983, KIDNEY INT S16, V24, pS102
[8]   ON THE MECHANISM OF IMPAIRED INSULIN-SECRETION IN CHRONIC-RENAL-FAILURE [J].
FADDA, GZ ;
HAJJAR, SM ;
PERNA, AF ;
ZHOU, XJ ;
LIPSON, LG ;
MASSRY, SG .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (01) :255-261
[9]  
FLISER D, 1993, J AM SOC NEPHROL, V3, P1371
[10]   Subacute infusion of physiological doses of parathyroid hormone raises blood pressure in humans [J].
Fliser, D ;
Franek, E ;
Fode, P ;
Stefanski, A ;
Schmitt, CP ;
Lyons, M ;
Ritz, E .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1997, 12 (05) :933-938