Skeletal muscle protein turnover responses to parenteral nutrition in patients with alcoholic liver cirrhosis and sarcopenia

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Standard

Skeletal muscle protein turnover responses to parenteral nutrition in patients with alcoholic liver cirrhosis and sarcopenia. / Iepsen, Ulrik Winning; Rinnov, Anders Rasmussen; Munch, Gregers Winding; Rugbjerg, Mette; Winding, Kamilla Munch; Lauridsen, Carsten; Berg, Ronan M G; Pedersen, Bente Klarlund; Gluud, Lise Lotte; van Hall, Gerrit.

I: American Journal of Physiology: Gastrointestinal and Liver Physiology, Bind 325, Nr. 2, 2023, s. G174–G183.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Iepsen, UW, Rinnov, AR, Munch, GW, Rugbjerg, M, Winding, KM, Lauridsen, C, Berg, RMG, Pedersen, BK, Gluud, LL & van Hall, G 2023, 'Skeletal muscle protein turnover responses to parenteral nutrition in patients with alcoholic liver cirrhosis and sarcopenia', American Journal of Physiology: Gastrointestinal and Liver Physiology, bind 325, nr. 2, s. G174–G183. https://doi.org/10.1152/ajpgi.00242.2022

APA

Iepsen, U. W., Rinnov, A. R., Munch, G. W., Rugbjerg, M., Winding, K. M., Lauridsen, C., Berg, R. M. G., Pedersen, B. K., Gluud, L. L., & van Hall, G. (2023). Skeletal muscle protein turnover responses to parenteral nutrition in patients with alcoholic liver cirrhosis and sarcopenia. American Journal of Physiology: Gastrointestinal and Liver Physiology, 325(2), G174–G183. https://doi.org/10.1152/ajpgi.00242.2022

Vancouver

Iepsen UW, Rinnov AR, Munch GW, Rugbjerg M, Winding KM, Lauridsen C o.a. Skeletal muscle protein turnover responses to parenteral nutrition in patients with alcoholic liver cirrhosis and sarcopenia. American Journal of Physiology: Gastrointestinal and Liver Physiology. 2023;325(2):G174–G183. https://doi.org/10.1152/ajpgi.00242.2022

Author

Iepsen, Ulrik Winning ; Rinnov, Anders Rasmussen ; Munch, Gregers Winding ; Rugbjerg, Mette ; Winding, Kamilla Munch ; Lauridsen, Carsten ; Berg, Ronan M G ; Pedersen, Bente Klarlund ; Gluud, Lise Lotte ; van Hall, Gerrit. / Skeletal muscle protein turnover responses to parenteral nutrition in patients with alcoholic liver cirrhosis and sarcopenia. I: American Journal of Physiology: Gastrointestinal and Liver Physiology. 2023 ; Bind 325, Nr. 2. s. G174–G183.

Bibtex

@article{260fb3aa27d34b048f325fc74de3daac,
title = "Skeletal muscle protein turnover responses to parenteral nutrition in patients with alcoholic liver cirrhosis and sarcopenia",
abstract = "Alcoholic liver cirrhosis (ALC) is accompanied by sarcopenia. The aim of this study was to investigate the acute effects of balanced parenteral nutrition (PN) on skeletal muscle protein turnover in ALC. Eight male patients with ALC and seven age- and sex-matched healthy controls were studied for three hours of fasting followed by three hours of intravenous PN (SmofKabiven 1206 mL: Amino acid 38 g, carbohydrates 85 g, fat 34 g) 4 ml/kg/hour. We measured leg blood flow, sampled paired femoral arterio-venous concentrations and quadriceps muscle biopsies while providing a primed continuous infusion of [ring-2D5]-phenylalanine to quantify muscle protein synthesis and breakdown. Patients with ALC exhibited shorter 6-min walking distance (ALC: 487 ± 38 vs. controls: 722 ± 14 m, p<0.05), lower hand-grip strength (ALC: 34 ± 2 vs. controls: 52 ± 2 kg, p<0.05), and CT-verified leg muscle loss (ALC: 5922 ± 246 vs. controls: 8110 ± 345 mm2, p<0.05). Net leg muscle phenylalanine uptake changed from negative (muscle loss) during fasting to positive (muscle gain) in response to PN (ALC: -0.18 ± +0.01 vs. 0.24 ± 0.03 µmol/kg muscle*min-1; p <0.001 and controls: -0.15 ± 0.01 vs. 0.09 ± 0.01 µmol/kg muscle*min-1; p <0.001), but with higher net muscle phenylalanine uptake in ALC than controls (p <0.001). Insulin concentrations were substantially higher in ALC patients during PN. Our results suggest a higher net muscle phenylalanine uptake during a single infusion of PN in stable ALC patients with sarcopenia compared with healthy controls.",
author = "Iepsen, {Ulrik Winning} and Rinnov, {Anders Rasmussen} and Munch, {Gregers Winding} and Mette Rugbjerg and Winding, {Kamilla Munch} and Carsten Lauridsen and Berg, {Ronan M G} and Pedersen, {Bente Klarlund} and Gluud, {Lise Lotte} and {van Hall}, Gerrit",
year = "2023",
doi = "10.1152/ajpgi.00242.2022",
language = "English",
volume = "325",
pages = "G174–G183",
journal = "American Journal of Physiology: Gastrointestinal and Liver Physiology",
issn = "0193-1857",
publisher = "American Physiological Society",
number = "2",

}

RIS

TY - JOUR

T1 - Skeletal muscle protein turnover responses to parenteral nutrition in patients with alcoholic liver cirrhosis and sarcopenia

AU - Iepsen, Ulrik Winning

AU - Rinnov, Anders Rasmussen

AU - Munch, Gregers Winding

AU - Rugbjerg, Mette

AU - Winding, Kamilla Munch

AU - Lauridsen, Carsten

AU - Berg, Ronan M G

AU - Pedersen, Bente Klarlund

AU - Gluud, Lise Lotte

AU - van Hall, Gerrit

PY - 2023

Y1 - 2023

N2 - Alcoholic liver cirrhosis (ALC) is accompanied by sarcopenia. The aim of this study was to investigate the acute effects of balanced parenteral nutrition (PN) on skeletal muscle protein turnover in ALC. Eight male patients with ALC and seven age- and sex-matched healthy controls were studied for three hours of fasting followed by three hours of intravenous PN (SmofKabiven 1206 mL: Amino acid 38 g, carbohydrates 85 g, fat 34 g) 4 ml/kg/hour. We measured leg blood flow, sampled paired femoral arterio-venous concentrations and quadriceps muscle biopsies while providing a primed continuous infusion of [ring-2D5]-phenylalanine to quantify muscle protein synthesis and breakdown. Patients with ALC exhibited shorter 6-min walking distance (ALC: 487 ± 38 vs. controls: 722 ± 14 m, p<0.05), lower hand-grip strength (ALC: 34 ± 2 vs. controls: 52 ± 2 kg, p<0.05), and CT-verified leg muscle loss (ALC: 5922 ± 246 vs. controls: 8110 ± 345 mm2, p<0.05). Net leg muscle phenylalanine uptake changed from negative (muscle loss) during fasting to positive (muscle gain) in response to PN (ALC: -0.18 ± +0.01 vs. 0.24 ± 0.03 µmol/kg muscle*min-1; p <0.001 and controls: -0.15 ± 0.01 vs. 0.09 ± 0.01 µmol/kg muscle*min-1; p <0.001), but with higher net muscle phenylalanine uptake in ALC than controls (p <0.001). Insulin concentrations were substantially higher in ALC patients during PN. Our results suggest a higher net muscle phenylalanine uptake during a single infusion of PN in stable ALC patients with sarcopenia compared with healthy controls.

AB - Alcoholic liver cirrhosis (ALC) is accompanied by sarcopenia. The aim of this study was to investigate the acute effects of balanced parenteral nutrition (PN) on skeletal muscle protein turnover in ALC. Eight male patients with ALC and seven age- and sex-matched healthy controls were studied for three hours of fasting followed by three hours of intravenous PN (SmofKabiven 1206 mL: Amino acid 38 g, carbohydrates 85 g, fat 34 g) 4 ml/kg/hour. We measured leg blood flow, sampled paired femoral arterio-venous concentrations and quadriceps muscle biopsies while providing a primed continuous infusion of [ring-2D5]-phenylalanine to quantify muscle protein synthesis and breakdown. Patients with ALC exhibited shorter 6-min walking distance (ALC: 487 ± 38 vs. controls: 722 ± 14 m, p<0.05), lower hand-grip strength (ALC: 34 ± 2 vs. controls: 52 ± 2 kg, p<0.05), and CT-verified leg muscle loss (ALC: 5922 ± 246 vs. controls: 8110 ± 345 mm2, p<0.05). Net leg muscle phenylalanine uptake changed from negative (muscle loss) during fasting to positive (muscle gain) in response to PN (ALC: -0.18 ± +0.01 vs. 0.24 ± 0.03 µmol/kg muscle*min-1; p <0.001 and controls: -0.15 ± 0.01 vs. 0.09 ± 0.01 µmol/kg muscle*min-1; p <0.001), but with higher net muscle phenylalanine uptake in ALC than controls (p <0.001). Insulin concentrations were substantially higher in ALC patients during PN. Our results suggest a higher net muscle phenylalanine uptake during a single infusion of PN in stable ALC patients with sarcopenia compared with healthy controls.

U2 - 10.1152/ajpgi.00242.2022

DO - 10.1152/ajpgi.00242.2022

M3 - Journal article

C2 - 37339940

VL - 325

SP - G174–G183

JO - American Journal of Physiology: Gastrointestinal and Liver Physiology

JF - American Journal of Physiology: Gastrointestinal and Liver Physiology

SN - 0193-1857

IS - 2

ER -

ID: 360394230