Impaired endothelial function and insulin action in first-degree relatives of patients with type 2 diabetes mellitus

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Impaired endothelial function and insulin action in first-degree relatives of patients with type 2 diabetes mellitus. / Sonne, Mette P; Højbjerre, Lise; Alibegovic, Amra A; Vaag, Allan; Stallknecht, Bente; Dela, Flemming.

I: Metabolism - Clinical and Experimental, Bind 58, Nr. 1, 2009, s. 93-101.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Sonne, MP, Højbjerre, L, Alibegovic, AA, Vaag, A, Stallknecht, B & Dela, F 2009, 'Impaired endothelial function and insulin action in first-degree relatives of patients with type 2 diabetes mellitus', Metabolism - Clinical and Experimental, bind 58, nr. 1, s. 93-101. https://doi.org/10.1016/j.metabol.2008.08.011

APA

Sonne, M. P., Højbjerre, L., Alibegovic, A. A., Vaag, A., Stallknecht, B., & Dela, F. (2009). Impaired endothelial function and insulin action in first-degree relatives of patients with type 2 diabetes mellitus. Metabolism - Clinical and Experimental, 58(1), 93-101. https://doi.org/10.1016/j.metabol.2008.08.011

Vancouver

Sonne MP, Højbjerre L, Alibegovic AA, Vaag A, Stallknecht B, Dela F. Impaired endothelial function and insulin action in first-degree relatives of patients with type 2 diabetes mellitus. Metabolism - Clinical and Experimental. 2009;58(1):93-101. https://doi.org/10.1016/j.metabol.2008.08.011

Author

Sonne, Mette P ; Højbjerre, Lise ; Alibegovic, Amra A ; Vaag, Allan ; Stallknecht, Bente ; Dela, Flemming. / Impaired endothelial function and insulin action in first-degree relatives of patients with type 2 diabetes mellitus. I: Metabolism - Clinical and Experimental. 2009 ; Bind 58, Nr. 1. s. 93-101.

Bibtex

@article{483bc5505f2c11dea8de000ea68e967b,
title = "Impaired endothelial function and insulin action in first-degree relatives of patients with type 2 diabetes mellitus",
abstract = "First-degree relatives (FDR) of patients with type 2 diabetes mellitus are at increased risk of developing type 2 diabetes mellitus. We studied if endothelial dysfunction of the resistance vessels is present and may coexist with metabolic insulin resistance in FDR. Male FDR (n = 13; 26 +/- 1 years; body mass index, 25 +/- 1 kg m(2) [mean +/- SEM]) and matched control subjects (CON) (n = 22; 25 +/- 1 years; body mass index, 24 +/- 1 kg m(2)) were studied by hyperinsulinemic (40 mU min(-1)m(-2)) isoglycemic clamp combined with brachial arterial and deep venous catheterization of the forearm. Forearm blood flow (FBF) was measured by venous occlusion plethysmography upon stimulation with systemic hyperinsulinemia (291 +/- 11 pmol/L, pooled data from both groups) and upon intraarterial infusion of adenosine (ADN) and acetylcholine (ACH) +/- hyperinsulinemia. Forearm blood flow response to ADN and ACH was less in FDR vs CON (P < .05); systemic hyperinsulinemia added to the FBF effect of ADN in CON (P < .05) but not in FDR. In addition, FDR demonstrated impaired FBF to hyperinsulinemia (2.1 +/- 0.2 vs 4.0 +/- 0.6 mL 100 mL(-1) min(-1)) in FDR and CON, respectively (P < .05). Both M-value (5.0 +/- 0.7 vs 7.0 +/- 0.5 mg min(-1) kg(-1)) and forearm glucose clearance (0.6 +/- 0.1 vs 1.4 +/- 0.4 mL 100 mL(-1)min(-1)) were diminished in FDR compared with CON (all P < .05). FDR demonstrated endothelial dysfunction of the resistance vessels in addition to impaired insulin-stimulated increase in bulk flow. Moreover, FDR demonstrated whole-body insulin resistance as well as decreased basal and insulin-stimulated forearm glucose uptake. It remains to be established whether FDR also demonstrate impaired insulin-stimulated microvascular function.",
author = "Sonne, {Mette P} and Lise H{\o}jbjerre and Alibegovic, {Amra A} and Allan Vaag and Bente Stallknecht and Flemming Dela",
note = "Keywords: Acetylcholine; Adenosine; Adult; Blood Gas Analysis; Blood Glucose; C-Peptide; C-Reactive Protein; Cholesterol; Diabetes Mellitus, Type 2; Endothelium, Vascular; Family; Glucose Clamp Technique; Homocysteine; Humans; Insulin; Insulin Resistance; Male; Plethysmography; Potassium; Statistics, Nonparametric; Vascular Resistance; Vasodilator Agents",
year = "2009",
doi = "10.1016/j.metabol.2008.08.011",
language = "English",
volume = "58",
pages = "93--101",
journal = "Metabolism",
issn = "0026-0495",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Impaired endothelial function and insulin action in first-degree relatives of patients with type 2 diabetes mellitus

AU - Sonne, Mette P

AU - Højbjerre, Lise

AU - Alibegovic, Amra A

AU - Vaag, Allan

AU - Stallknecht, Bente

AU - Dela, Flemming

N1 - Keywords: Acetylcholine; Adenosine; Adult; Blood Gas Analysis; Blood Glucose; C-Peptide; C-Reactive Protein; Cholesterol; Diabetes Mellitus, Type 2; Endothelium, Vascular; Family; Glucose Clamp Technique; Homocysteine; Humans; Insulin; Insulin Resistance; Male; Plethysmography; Potassium; Statistics, Nonparametric; Vascular Resistance; Vasodilator Agents

PY - 2009

Y1 - 2009

N2 - First-degree relatives (FDR) of patients with type 2 diabetes mellitus are at increased risk of developing type 2 diabetes mellitus. We studied if endothelial dysfunction of the resistance vessels is present and may coexist with metabolic insulin resistance in FDR. Male FDR (n = 13; 26 +/- 1 years; body mass index, 25 +/- 1 kg m(2) [mean +/- SEM]) and matched control subjects (CON) (n = 22; 25 +/- 1 years; body mass index, 24 +/- 1 kg m(2)) were studied by hyperinsulinemic (40 mU min(-1)m(-2)) isoglycemic clamp combined with brachial arterial and deep venous catheterization of the forearm. Forearm blood flow (FBF) was measured by venous occlusion plethysmography upon stimulation with systemic hyperinsulinemia (291 +/- 11 pmol/L, pooled data from both groups) and upon intraarterial infusion of adenosine (ADN) and acetylcholine (ACH) +/- hyperinsulinemia. Forearm blood flow response to ADN and ACH was less in FDR vs CON (P < .05); systemic hyperinsulinemia added to the FBF effect of ADN in CON (P < .05) but not in FDR. In addition, FDR demonstrated impaired FBF to hyperinsulinemia (2.1 +/- 0.2 vs 4.0 +/- 0.6 mL 100 mL(-1) min(-1)) in FDR and CON, respectively (P < .05). Both M-value (5.0 +/- 0.7 vs 7.0 +/- 0.5 mg min(-1) kg(-1)) and forearm glucose clearance (0.6 +/- 0.1 vs 1.4 +/- 0.4 mL 100 mL(-1)min(-1)) were diminished in FDR compared with CON (all P < .05). FDR demonstrated endothelial dysfunction of the resistance vessels in addition to impaired insulin-stimulated increase in bulk flow. Moreover, FDR demonstrated whole-body insulin resistance as well as decreased basal and insulin-stimulated forearm glucose uptake. It remains to be established whether FDR also demonstrate impaired insulin-stimulated microvascular function.

AB - First-degree relatives (FDR) of patients with type 2 diabetes mellitus are at increased risk of developing type 2 diabetes mellitus. We studied if endothelial dysfunction of the resistance vessels is present and may coexist with metabolic insulin resistance in FDR. Male FDR (n = 13; 26 +/- 1 years; body mass index, 25 +/- 1 kg m(2) [mean +/- SEM]) and matched control subjects (CON) (n = 22; 25 +/- 1 years; body mass index, 24 +/- 1 kg m(2)) were studied by hyperinsulinemic (40 mU min(-1)m(-2)) isoglycemic clamp combined with brachial arterial and deep venous catheterization of the forearm. Forearm blood flow (FBF) was measured by venous occlusion plethysmography upon stimulation with systemic hyperinsulinemia (291 +/- 11 pmol/L, pooled data from both groups) and upon intraarterial infusion of adenosine (ADN) and acetylcholine (ACH) +/- hyperinsulinemia. Forearm blood flow response to ADN and ACH was less in FDR vs CON (P < .05); systemic hyperinsulinemia added to the FBF effect of ADN in CON (P < .05) but not in FDR. In addition, FDR demonstrated impaired FBF to hyperinsulinemia (2.1 +/- 0.2 vs 4.0 +/- 0.6 mL 100 mL(-1) min(-1)) in FDR and CON, respectively (P < .05). Both M-value (5.0 +/- 0.7 vs 7.0 +/- 0.5 mg min(-1) kg(-1)) and forearm glucose clearance (0.6 +/- 0.1 vs 1.4 +/- 0.4 mL 100 mL(-1)min(-1)) were diminished in FDR compared with CON (all P < .05). FDR demonstrated endothelial dysfunction of the resistance vessels in addition to impaired insulin-stimulated increase in bulk flow. Moreover, FDR demonstrated whole-body insulin resistance as well as decreased basal and insulin-stimulated forearm glucose uptake. It remains to be established whether FDR also demonstrate impaired insulin-stimulated microvascular function.

U2 - 10.1016/j.metabol.2008.08.011

DO - 10.1016/j.metabol.2008.08.011

M3 - Journal article

C2 - 19059536

VL - 58

SP - 93

EP - 101

JO - Metabolism

JF - Metabolism

SN - 0026-0495

IS - 1

ER -

ID: 12771858