Cardiovascular and metabolic effects of 48-h glucagon-like peptide-1 infusion in compensated chronic patients with heart failure

Research output: Contribution to journalJournal articleResearchpeer-review

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Cardiovascular and metabolic effects of 48-h glucagon-like peptide-1 infusion in compensated chronic patients with heart failure. / Halbirk, Mads; Nørrelund, Helene; Møller, Niels; Holst, Jens Juul; Schmitz, Ole; Nielsen, Bent Roni Ranghøj; Nielsen-Kudsk, Jens Erik; Nielsen, Søren Steen; Nielsen, Torsten Toftegaard; Eiskjaer, Hans; Bøtker, Hans Erik; Wiggers, Henrik.

In: American Journal of Physiology: Heart and Circulatory Physiology, Vol. 298, No. 3, 01.03.2010, p. H1096-H1102.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Halbirk, M, Nørrelund, H, Møller, N, Holst, JJ, Schmitz, O, Nielsen, BRR, Nielsen-Kudsk, JE, Nielsen, SS, Nielsen, TT, Eiskjaer, H, Bøtker, HE & Wiggers, H 2010, 'Cardiovascular and metabolic effects of 48-h glucagon-like peptide-1 infusion in compensated chronic patients with heart failure', American Journal of Physiology: Heart and Circulatory Physiology, vol. 298, no. 3, pp. H1096-H1102. https://doi.org/10.1152/ajpheart.00930.2009

APA

Halbirk, M., Nørrelund, H., Møller, N., Holst, J. J., Schmitz, O., Nielsen, B. R. R., Nielsen-Kudsk, J. E., Nielsen, S. S., Nielsen, T. T., Eiskjaer, H., Bøtker, H. E., & Wiggers, H. (2010). Cardiovascular and metabolic effects of 48-h glucagon-like peptide-1 infusion in compensated chronic patients with heart failure. American Journal of Physiology: Heart and Circulatory Physiology, 298(3), H1096-H1102. https://doi.org/10.1152/ajpheart.00930.2009

Vancouver

Halbirk M, Nørrelund H, Møller N, Holst JJ, Schmitz O, Nielsen BRR et al. Cardiovascular and metabolic effects of 48-h glucagon-like peptide-1 infusion in compensated chronic patients with heart failure. American Journal of Physiology: Heart and Circulatory Physiology. 2010 Mar 1;298(3):H1096-H1102. https://doi.org/10.1152/ajpheart.00930.2009

Author

Halbirk, Mads ; Nørrelund, Helene ; Møller, Niels ; Holst, Jens Juul ; Schmitz, Ole ; Nielsen, Bent Roni Ranghøj ; Nielsen-Kudsk, Jens Erik ; Nielsen, Søren Steen ; Nielsen, Torsten Toftegaard ; Eiskjaer, Hans ; Bøtker, Hans Erik ; Wiggers, Henrik. / Cardiovascular and metabolic effects of 48-h glucagon-like peptide-1 infusion in compensated chronic patients with heart failure. In: American Journal of Physiology: Heart and Circulatory Physiology. 2010 ; Vol. 298, No. 3. pp. H1096-H1102.

Bibtex

@article{f1882fe31c424b46b5636c7cdeaeba49,
title = "Cardiovascular and metabolic effects of 48-h glucagon-like peptide-1 infusion in compensated chronic patients with heart failure",
abstract = "The incretin hormone glucagon-like peptide-1 (GLP-1) and its analogs are currently emerging as antidiabetic medications. GLP-1 improves left ventricular ejection fraction (LVEF) in dogs with heart failure (HF) and in patients with acute myocardial infarction. We studied metabolic and cardiovascular effects of 48-h GLP-1 infusions in patients with congestive HF. In a randomized, double-blind crossover design, 20 patients without diabetes and with HF with ischemic heart disease, EF of 30 +/- 2%, New York Heart Association II and III (n = 14 and 6) received 48-h GLP-1 (0.7 pmol.kg(-1).min(-1)) and placebo infusion. At 0 and 48 h, LVEF, diastolic function, tissue Doppler regional myocardial function, exercise testing, noninvasive cardiac output, and brain natriuretic peptide (BNP) were measured. Blood pressure, heart rate, and metabolic parameters were recorded. Fifteen patients completed the protocol. GLP-1 increased insulin (90 +/- 17 pmol/l vs. 69 +/- 12 pmol/l; P = 0.025) and lowered glucose levels (5.2 +/- 0.1 mmol/l vs. 5.6 +/- 0.1 mmol/l; P <0.01). Heart rate (67 +/- 2 beats/min vs. 65 +/- 2 beats/min; P = 0.016) and diastolic blood pressure (71 +/- 2 mmHg vs. 68 +/- 2 mmHg; P = 0.008) increased during GLP-1 treatment. Cardiac index (1.5 +/- 0.1 l.min(-1).m(-2) vs. 1.7 +/- 0.2 l.min(-1).m(-2); P = 0.54) and LVEF (30 +/- 2% vs. 30 +/- 2%; P = 0.93), tissue Doppler indexes, body weight, and BNP remained unchanged. Hypoglycemic events related to GLP-1 treatment were observed in eight patients. GLP-1 infusion increased circulating insulin levels and reduced plasma glucose concentration but had no major cardiovascular effects in patients without diabetes but with compensated HF. The impact of minor increases in heart rate and diastolic blood pressure during GLP-1 infusion requires further studies. Hypoglycemia was frequent and calls for caution in patients without diabetes but with HF.",
keywords = "Adult, Aged, Blood Glucose, Blood Pressure, Cardiac Output, Chronic Disease, Cross-Over Studies, Dose-Response Relationship, Drug, Double-Blind Method, Exercise Tolerance, Female, Glucagon-Like Peptide 1, Heart Failure, Heart Rate, Humans, Hypoglycemic Agents, Infusions, Intravenous, Insulin, Male, Middle Aged, Treatment Outcome",
author = "Mads Halbirk and Helene N{\o}rrelund and Niels M{\o}ller and Holst, {Jens Juul} and Ole Schmitz and Nielsen, {Bent Roni Rangh{\o}j} and Nielsen-Kudsk, {Jens Erik} and Nielsen, {S{\o}ren Steen} and Nielsen, {Torsten Toftegaard} and Hans Eiskjaer and B{\o}tker, {Hans Erik} and Henrik Wiggers",
year = "2010",
month = mar,
day = "1",
doi = "10.1152/ajpheart.00930.2009",
language = "English",
volume = "298",
pages = "H1096--H1102",
journal = "American Journal of Physiology: Heart and Circulatory Physiology",
issn = "0363-6135",
publisher = "American Physiological Society",
number = "3",

}

RIS

TY - JOUR

T1 - Cardiovascular and metabolic effects of 48-h glucagon-like peptide-1 infusion in compensated chronic patients with heart failure

AU - Halbirk, Mads

AU - Nørrelund, Helene

AU - Møller, Niels

AU - Holst, Jens Juul

AU - Schmitz, Ole

AU - Nielsen, Bent Roni Ranghøj

AU - Nielsen-Kudsk, Jens Erik

AU - Nielsen, Søren Steen

AU - Nielsen, Torsten Toftegaard

AU - Eiskjaer, Hans

AU - Bøtker, Hans Erik

AU - Wiggers, Henrik

PY - 2010/3/1

Y1 - 2010/3/1

N2 - The incretin hormone glucagon-like peptide-1 (GLP-1) and its analogs are currently emerging as antidiabetic medications. GLP-1 improves left ventricular ejection fraction (LVEF) in dogs with heart failure (HF) and in patients with acute myocardial infarction. We studied metabolic and cardiovascular effects of 48-h GLP-1 infusions in patients with congestive HF. In a randomized, double-blind crossover design, 20 patients without diabetes and with HF with ischemic heart disease, EF of 30 +/- 2%, New York Heart Association II and III (n = 14 and 6) received 48-h GLP-1 (0.7 pmol.kg(-1).min(-1)) and placebo infusion. At 0 and 48 h, LVEF, diastolic function, tissue Doppler regional myocardial function, exercise testing, noninvasive cardiac output, and brain natriuretic peptide (BNP) were measured. Blood pressure, heart rate, and metabolic parameters were recorded. Fifteen patients completed the protocol. GLP-1 increased insulin (90 +/- 17 pmol/l vs. 69 +/- 12 pmol/l; P = 0.025) and lowered glucose levels (5.2 +/- 0.1 mmol/l vs. 5.6 +/- 0.1 mmol/l; P <0.01). Heart rate (67 +/- 2 beats/min vs. 65 +/- 2 beats/min; P = 0.016) and diastolic blood pressure (71 +/- 2 mmHg vs. 68 +/- 2 mmHg; P = 0.008) increased during GLP-1 treatment. Cardiac index (1.5 +/- 0.1 l.min(-1).m(-2) vs. 1.7 +/- 0.2 l.min(-1).m(-2); P = 0.54) and LVEF (30 +/- 2% vs. 30 +/- 2%; P = 0.93), tissue Doppler indexes, body weight, and BNP remained unchanged. Hypoglycemic events related to GLP-1 treatment were observed in eight patients. GLP-1 infusion increased circulating insulin levels and reduced plasma glucose concentration but had no major cardiovascular effects in patients without diabetes but with compensated HF. The impact of minor increases in heart rate and diastolic blood pressure during GLP-1 infusion requires further studies. Hypoglycemia was frequent and calls for caution in patients without diabetes but with HF.

AB - The incretin hormone glucagon-like peptide-1 (GLP-1) and its analogs are currently emerging as antidiabetic medications. GLP-1 improves left ventricular ejection fraction (LVEF) in dogs with heart failure (HF) and in patients with acute myocardial infarction. We studied metabolic and cardiovascular effects of 48-h GLP-1 infusions in patients with congestive HF. In a randomized, double-blind crossover design, 20 patients without diabetes and with HF with ischemic heart disease, EF of 30 +/- 2%, New York Heart Association II and III (n = 14 and 6) received 48-h GLP-1 (0.7 pmol.kg(-1).min(-1)) and placebo infusion. At 0 and 48 h, LVEF, diastolic function, tissue Doppler regional myocardial function, exercise testing, noninvasive cardiac output, and brain natriuretic peptide (BNP) were measured. Blood pressure, heart rate, and metabolic parameters were recorded. Fifteen patients completed the protocol. GLP-1 increased insulin (90 +/- 17 pmol/l vs. 69 +/- 12 pmol/l; P = 0.025) and lowered glucose levels (5.2 +/- 0.1 mmol/l vs. 5.6 +/- 0.1 mmol/l; P <0.01). Heart rate (67 +/- 2 beats/min vs. 65 +/- 2 beats/min; P = 0.016) and diastolic blood pressure (71 +/- 2 mmHg vs. 68 +/- 2 mmHg; P = 0.008) increased during GLP-1 treatment. Cardiac index (1.5 +/- 0.1 l.min(-1).m(-2) vs. 1.7 +/- 0.2 l.min(-1).m(-2); P = 0.54) and LVEF (30 +/- 2% vs. 30 +/- 2%; P = 0.93), tissue Doppler indexes, body weight, and BNP remained unchanged. Hypoglycemic events related to GLP-1 treatment were observed in eight patients. GLP-1 infusion increased circulating insulin levels and reduced plasma glucose concentration but had no major cardiovascular effects in patients without diabetes but with compensated HF. The impact of minor increases in heart rate and diastolic blood pressure during GLP-1 infusion requires further studies. Hypoglycemia was frequent and calls for caution in patients without diabetes but with HF.

KW - Adult

KW - Aged

KW - Blood Glucose

KW - Blood Pressure

KW - Cardiac Output

KW - Chronic Disease

KW - Cross-Over Studies

KW - Dose-Response Relationship, Drug

KW - Double-Blind Method

KW - Exercise Tolerance

KW - Female

KW - Glucagon-Like Peptide 1

KW - Heart Failure

KW - Heart Rate

KW - Humans

KW - Hypoglycemic Agents

KW - Infusions, Intravenous

KW - Insulin

KW - Male

KW - Middle Aged

KW - Treatment Outcome

U2 - 10.1152/ajpheart.00930.2009

DO - 10.1152/ajpheart.00930.2009

M3 - Journal article

C2 - 20081109

VL - 298

SP - H1096-H1102

JO - American Journal of Physiology: Heart and Circulatory Physiology

JF - American Journal of Physiology: Heart and Circulatory Physiology

SN - 0363-6135

IS - 3

ER -

ID: 33940315