Pramlintide: A human amylin analogue reduced postprandial plasma glucose, insulin, and C-peptide concentrations in patients with type 2 diabetes

被引:0
作者
Thompson, RG
Gottlieb, A
Organ, K
Koda, J
Kisicki, J
Kolterman, OG
机构
[1] Amylin Pharmaceuticals, Inc., San Diego, CA
[2] Harris Laboratories, Inc., Lincoln, NE
[3] Amylin Pharmaceutical, Inc., San Diego, CA 92121
关键词
type; 2; diabetes; glucose; C-peptide; amylin; pramlintide;
D O I
10.1002/(SICI)1096-9136(199707)14:7<547::AID-DIA390>3.0.CO;2-U
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In order to determine the influence of a 5 h infusion of pramlintide compared to placebo on postprandial glucose, lactate, insulin, and C-peptide concentrations in patients with Type 2 diabetes, a single-blind, randomized, cross-over study was conducted in 24 patients; 12 treated with exogenous insulin and 12 managed with diet and/or oral hypoglycaemic agents. One hour after initiation of infusion, patients consumed a Sustacal(R) test meal. The protocol was repeated on the following day with each patient receiving the alternate study medication. Pramlintide infusion in the insulin-treated patients resulted in statistically significant reductions in mean glucose, insulin, C-peptide, and lactate concentrations during the 4-h period after the Sustacal(R) test meal. Pramlintide infusion also resulted in significant reductions of mean insulin, C-peptide, and lactate concentrations, but not glucose concentrations, in the patients treated with diet and/or oral hypoglycaemic agents. Within this latter group, reduction in postprandial glucose concentrations in individual patients correlated with glycated haemoglobin values. These results suggest that administration of pramlintide may improve glycaemic control in patients with Type 2 diabetes treated with insulin or poorly controlled on diet and/or oral hypoglycaemic agents. (C) 1997 by John Wiley & Sons, Ltd.
引用
收藏
页码:547 / 555
页数:9
相关论文
共 26 条
  • [1] BROWN K, 1994, DIABETES, V43, pA172
  • [2] FINEMAN MS, 1994, DIABETOLOGIA, V37, pA52
  • [3] Fleiss JL, 1986, The Design and Analysis of Clinical Experiments, P263
  • [4] BASAL AND STIMULATED PLASMA-LEVELS OF PANCREATIC AMYLIN INDICATE ITS CO-SECRETION WITH INSULIN IN HUMANS
    HARTTER, E
    SVOBODA, T
    LUDVIK, B
    SCHULLER, M
    LELL, B
    KUENBURG, E
    BRUNNBAUER, M
    WOLOSZCZUK, W
    PRAGER, R
    [J]. DIABETOLOGIA, 1991, 34 (01) : 52 - 54
  • [5] DISORDERED GASTRIC MOTOR FUNCTION IN DIABETES-MELLITUS
    HOROWITZ, M
    FRASER, R
    [J]. DIABETOLOGIA, 1994, 37 (06) : 543 - 551
  • [6] RELATIONSHIP BETWEEN ORAL GLUCOSE-TOLERANCE AND GASTRIC-EMPTYING IN NORMAL HEALTHY-SUBJECTS
    HOROWITZ, M
    EDELBROEK, MAL
    WISHART, JM
    STRAATHOF, JW
    [J]. DIABETOLOGIA, 1993, 36 (09) : 857 - 862
  • [7] AMYLIN CONCENTRATIONS AND GLUCOSE CONTROL
    KODA, JE
    FINEMAN, M
    RINK, TJ
    DAILEY, GE
    MUCHMORE, DB
    LINARELLI, LG
    [J]. LANCET, 1992, 339 (8802) : 1179 - 1180
  • [8] REDUCTION OF POSTPRANDIAL HYPERGLYCEMIA IN SUBJECTS WITH IDDM BY INTRAVENOUS-INFUSION OF AC137, A HUMAN AMYLIN ANALOG
    KOLTERMAN, OG
    GOTTLIEB, A
    MOYSES, C
    COLBURN, W
    [J]. DIABETES CARE, 1995, 18 (08) : 1179 - 1182
  • [9] Effect of 14 days' subcutaneous administration of the human amylin analogue, pramlintide (AC137), on an intravenous insulin challenge and response to a standard liquid meal in patients with IDDM
    Kolterman, OG
    Schwartz, S
    Corder, C
    Levy, B
    Klaff, L
    Peterson, J
    Gottlieb, A
    [J]. DIABETOLOGIA, 1996, 39 (04) : 492 - 499
  • [10] PHYSIOLOGICAL-ROLE FOR CHOLECYSTOKININ IN REDUCING POSTPRANDIAL HYPERGLYCEMIA IN HUMANS
    LIDDLE, RA
    RUSHAKOFF, RJ
    MORITA, ET
    BECCARIA, L
    CARTER, JD
    GOLDFINE, ID
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (06) : 1675 - 1681