Accelereret urinstofsyntese hos patienter med aktiv inflammatorisk tarmsygdom

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Accelereret urinstofsyntese hos patienter med aktiv inflammatorisk tarmsygdom. / Lundsgaard, Charlotte; Hamberg, Ole; Thomsen, Ole Østergaard; Nielsen, Ole Haagen; Vilstrup, Hendrik.

In: Ugeskrift for Laeger, Vol. 159, No. 44, 27.10.1997, p. 6519-6522.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Lundsgaard, C, Hamberg, O, Thomsen, OØ, Nielsen, OH & Vilstrup, H 1997, 'Accelereret urinstofsyntese hos patienter med aktiv inflammatorisk tarmsygdom', Ugeskrift for Laeger, vol. 159, no. 44, pp. 6519-6522.

APA

Lundsgaard, C., Hamberg, O., Thomsen, O. Ø., Nielsen, O. H., & Vilstrup, H. (1997). Accelereret urinstofsyntese hos patienter med aktiv inflammatorisk tarmsygdom. Ugeskrift for Laeger, 159(44), 6519-6522.

Vancouver

Lundsgaard C, Hamberg O, Thomsen OØ, Nielsen OH, Vilstrup H. Accelereret urinstofsyntese hos patienter med aktiv inflammatorisk tarmsygdom. Ugeskrift for Laeger. 1997 Oct 27;159(44):6519-6522.

Author

Lundsgaard, Charlotte ; Hamberg, Ole ; Thomsen, Ole Østergaard ; Nielsen, Ole Haagen ; Vilstrup, Hendrik. / Accelereret urinstofsyntese hos patienter med aktiv inflammatorisk tarmsygdom. In: Ugeskrift for Laeger. 1997 ; Vol. 159, No. 44. pp. 6519-6522.

Bibtex

@article{63f96b0ba42046749e74faada4fe0842,
title = "Accelereret urinstofsyntese hos patienter med aktiv inflammatorisk tarmsygdom",
abstract = "Patients with active inflammatory bowel disease are often reported to be in negative nitrogen balance. Therefore, we examined basal and amino acid stimulated urea synthesis in 11 patients with active inflammatory bowel disease and in 10 patients with non-active disease. A primed continuous infusion of an amino acid mixture was given from t=1 h to t=5 h; during the first and the last two hours no amino acid infusion was given. Urea nitrogen synthesis rate was quantified independently of changes in blood amino acid concentration by means of the functional hepatic nitrogen clearance, i.e. the linear slope of the regression of urea nitrogen synthesis rate on blood amino acid concentration. Basal and amino acid stimulated urea nitrogen synthesis rate as well as functional hepatic nitrogen clearance were elevated two-fold in the patients with active disease. No differences between the two groups were observed as regards basal or stimulated plasma glucagon, cortisol, catecholamines and serum levels of interleukin-1α, interleukin-1β, tumor necrosis factor-alpha and interleukin-6. The results show that liver function related to conversion of.",
author = "Charlotte Lundsgaard and Ole Hamberg and Thomsen, {Ole {\O}stergaard} and Nielsen, {Ole Haagen} and Hendrik Vilstrup",
year = "1997",
month = oct,
day = "27",
language = "Dansk",
volume = "159",
pages = "6519--6522",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "44",

}

RIS

TY - JOUR

T1 - Accelereret urinstofsyntese hos patienter med aktiv inflammatorisk tarmsygdom

AU - Lundsgaard, Charlotte

AU - Hamberg, Ole

AU - Thomsen, Ole Østergaard

AU - Nielsen, Ole Haagen

AU - Vilstrup, Hendrik

PY - 1997/10/27

Y1 - 1997/10/27

N2 - Patients with active inflammatory bowel disease are often reported to be in negative nitrogen balance. Therefore, we examined basal and amino acid stimulated urea synthesis in 11 patients with active inflammatory bowel disease and in 10 patients with non-active disease. A primed continuous infusion of an amino acid mixture was given from t=1 h to t=5 h; during the first and the last two hours no amino acid infusion was given. Urea nitrogen synthesis rate was quantified independently of changes in blood amino acid concentration by means of the functional hepatic nitrogen clearance, i.e. the linear slope of the regression of urea nitrogen synthesis rate on blood amino acid concentration. Basal and amino acid stimulated urea nitrogen synthesis rate as well as functional hepatic nitrogen clearance were elevated two-fold in the patients with active disease. No differences between the two groups were observed as regards basal or stimulated plasma glucagon, cortisol, catecholamines and serum levels of interleukin-1α, interleukin-1β, tumor necrosis factor-alpha and interleukin-6. The results show that liver function related to conversion of.

AB - Patients with active inflammatory bowel disease are often reported to be in negative nitrogen balance. Therefore, we examined basal and amino acid stimulated urea synthesis in 11 patients with active inflammatory bowel disease and in 10 patients with non-active disease. A primed continuous infusion of an amino acid mixture was given from t=1 h to t=5 h; during the first and the last two hours no amino acid infusion was given. Urea nitrogen synthesis rate was quantified independently of changes in blood amino acid concentration by means of the functional hepatic nitrogen clearance, i.e. the linear slope of the regression of urea nitrogen synthesis rate on blood amino acid concentration. Basal and amino acid stimulated urea nitrogen synthesis rate as well as functional hepatic nitrogen clearance were elevated two-fold in the patients with active disease. No differences between the two groups were observed as regards basal or stimulated plasma glucagon, cortisol, catecholamines and serum levels of interleukin-1α, interleukin-1β, tumor necrosis factor-alpha and interleukin-6. The results show that liver function related to conversion of.

UR - http://www.scopus.com/inward/record.url?scp=0031588198&partnerID=8YFLogxK

M3 - Tidsskriftartikel

C2 - 9411971

AN - SCOPUS:0031588198

VL - 159

SP - 6519

EP - 6522

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 44

ER -

ID: 218718081