Four weeks of near-normalisation of blood glucose improves the insulin response to glucagon-like peptide-1 and glucose-dependent insulinotropic polypeptide in patients with type 2 diabetes

被引:342
作者
Hojberg, P. V. [1 ,2 ]
Vilsboll, T. [2 ]
Rabol, R. [1 ]
Knop, F. K. [2 ]
Bache, M. [1 ,2 ]
Krarup, T. [2 ]
Holst, J. J. [3 ]
Madsbad, S. [1 ]
机构
[1] Hvidovre Univ Hosp, Dept Endocrinol, DK-2650 Hvidovre, Denmark
[2] Gentofte Univ Hosp, Dept Internal Med F, Hellerup, Denmark
[3] Univ Copenhagen, Panum Inst, DK-2200 Copenhagen, Denmark
关键词
Beta-cell responsiveness; Glucose-dependent insulinotropic polypeptide; Glugagon like peptide-1; Incretin hormones; Insulin treatment; Type 2 diabetes mellitus; GASTRIC-INHIBITORY POLYPEPTIDE; BETA-CELL FUNCTION; INCRETIN HORMONES; HEALTHY-SUBJECTS; DEFECTIVE AMPLIFICATION; 1ST-DEGREE RELATIVES; ELIMINATION RATES; MATURITY-ONSET; ORAL GLUCOSE; SECRETION;
D O I
10.1007/s00125-008-1195-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The incretin effect is attenuated in patients with type 2 diabetes mellitus, partly as a result of impaired beta cell responsiveness to glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1). The aim of the present study was to investigate whether 4 weeks of near-normalisation of the blood glucose level could improve insulin responses to GIP and GLP-1 in patients with type 2 diabetes. Eight obese patients with type 2 diabetes with poor glycaemic control (HbA(1c) 8.6 +/- 1.3%), were investigated before and after 4 weeks of near-normalisation of blood glucose (mean blood glucose 7.4 +/- 1.2 mmol/l) using insulin treatment. Before and after insulin treatment the participants underwent three hyperglycaemic clamps (15 mmol/l) with infusion of GLP-1, GIP or saline. Insulin responses were evaluated as the incremental area under the plasma C-peptide curve. Before and after near-normalisation of blood glucose, the C-peptide responses did not differ during the early phase of insulin secretion (0-10 min). The late phase C-peptide response (10-120 min) increased during GIP infusion from 33.0 +/- 8.5 to 103.9 +/- 24.2 (nmol/l) x (110 min)(-1) (p < 0.05) and during GLP-1 infusion from 48.7 +/- 11.8 to 126.6 +/- 32.5 (nmol/l) x (110 min)(-1) (p < 0.05), whereas during saline infusion the late-phase response did not differ before vs after near-normalisation of blood glucose (40.2 +/- 11.2 vs 46.5 +/- 12.7 [nmol/l] x [110 min](-1)). Near-normalisation of blood glucose for 4 weeks improves beta cell responsiveness to both GLP-1 and GIP by a factor of three to four. No effect was found on beta cell responsiveness to glucose alone. ClinicalTrials.gov ID no.: NCT 00612950 Funding: This study was supported by The Novo Nordisk Foundation, The Medical Science Research Foundation for Copenhagen.
引用
收藏
页码:199 / 207
页数:9
相关论文
共 47 条
  • [1] Twelve- and 52-week efficacy of the dipeptidyl peptidase IV inhibitor LAF237 in metformin-treated patients with type 2 diabetes
    Ahrén, B
    Gomis, R
    Standl, E
    Mills, D
    Schweizer, A
    [J]. DIABETES CARE, 2004, 27 (12) : 2874 - 2880
  • [2] SUPPRESSION OF BASAL, BUT NOT OF GLUCOSE-STIMULATED INSULIN-SECRETION BY HUMAN INSULIN IN HEALTHY AND OBESE HYPERINSULINEMIC SUBJECTS
    BRATUSCHMARRAIN, PR
    WALDHAUSL, WK
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1985, 34 (02): : 188 - 193
  • [3] β-cell deficit and increased β-cell apoptosis in humans with type 2 diabetes
    Butler, AE
    Janson, J
    Bonner-Weir, S
    Ritzel, R
    Rizza, RA
    Butler, PC
    [J]. DIABETES, 2003, 52 (01) : 102 - 110
  • [4] GUT HORMONES AND DIABETES-MELLITUS
    CREUTZFELDT, W
    NAUCK, M
    [J]. DIABETES-METABOLISM REVIEWS, 1992, 8 (02): : 149 - 177
  • [5] DEGRADATION OF GLUCAGON-LIKE PEPTIDE-1 BY HUMAN PLASMA IN-VITRO YIELDS AN N-TERMINALLY TRUNCATED PEPTIDE THAT IS A MAJOR ENDOGENOUS METABOLITE IN-VIVO
    DEACON, CF
    JOHNSEN, AH
    HOLST, JJ
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (03) : 952 - 957
  • [6] Nutrient, neural and endocrine control of glucagonlike peptide secretion
    Dubé, PE
    Brubaker, PL
    [J]. HORMONE AND METABOLIC RESEARCH, 2004, 36 (11-12) : 755 - 760
  • [7] Exenatide augments first- and second-phase insulin secretion in response to intravenous glucose in subjects with type 2 diabetes
    Fehse, F
    Trautmann, M
    Holst, JJ
    Halseth, AE
    Nanayakkara, N
    Nielsen, LL
    Fineman, MS
    Kim, DD
    Nauck, MA
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (11) : 5991 - 5997
  • [8] THE EFFECT OF INSULIN-TREATMENT ON INSULIN-SECRETION AND INSULIN ACTION IN TYPE-II DIABETES-MELLITUS
    GARVEY, WT
    OLEFSKY, JM
    GRIFFIN, J
    HAMMAN, RF
    KOLTERMAN, OG
    [J]. DIABETES, 1985, 34 (03) : 222 - 234
  • [9] ANTIDIABETOGENIC EFFECT OF GLUCAGON-LIKE PEPTIDE-1 (7-36)AMIDE IN NORMAL SUBJECTS AND PATIENTS WITH DIABETES-MELLITUS
    GUTNIAK, M
    ORSKOV, C
    HOLST, JJ
    AHREN, B
    EFENDIC, S
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (20) : 1316 - 1322
  • [10] IMPROVEMENT OF INSULIN-SECRETION BUT NOT INSULIN RESISTANCE AFTER SHORT-TERM CONTROL OF PLASMA-GLUCOSE IN OBESE TYPE-II DIABETICS
    HIDAKA, H
    NAGULESPARAN, M
    KLIMES, I
    CLARK, R
    SASAKI, H
    ARONOFF, SL
    VASQUEZ, B
    RUBENSTEIN, AH
    UNGER, RH
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1982, 54 (02) : 217 - 222