Pancreatic function in Crohn's disease

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Standard

Pancreatic function in Crohn's disease. / Hegnhøj, J; Hansen, C P; Rannem, T; Sobirk, H; Bjerglund Andersen, L; Andersen, Jens Rikardt.

I: Gut, Bind 31, Nr. 9, 1990, s. 1076-1079.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hegnhøj, J, Hansen, CP, Rannem, T, Sobirk, H, Bjerglund Andersen, L & Andersen, JR 1990, 'Pancreatic function in Crohn's disease', Gut, bind 31, nr. 9, s. 1076-1079. https://doi.org/10.1136/gut.31.9.1076

APA

Hegnhøj, J., Hansen, C. P., Rannem, T., Sobirk, H., Bjerglund Andersen, L., & Andersen, J. R. (1990). Pancreatic function in Crohn's disease. Gut, 31(9), 1076-1079. https://doi.org/10.1136/gut.31.9.1076

Vancouver

Hegnhøj J, Hansen CP, Rannem T, Sobirk H, Bjerglund Andersen L, Andersen JR. Pancreatic function in Crohn's disease. Gut. 1990;31(9):1076-1079. https://doi.org/10.1136/gut.31.9.1076

Author

Hegnhøj, J ; Hansen, C P ; Rannem, T ; Sobirk, H ; Bjerglund Andersen, L ; Andersen, Jens Rikardt. / Pancreatic function in Crohn's disease. I: Gut. 1990 ; Bind 31, Nr. 9. s. 1076-1079.

Bibtex

@article{2af1e3a404f04ab18b2fd17399317acc,
title = "Pancreatic function in Crohn's disease",
abstract = "We investigated exocrine pancreatic function in a population of patients with Crohn's disease in order to correlate the pancreatic function with clinical and laboratory variables. A total of 143 patients affected by Crohn's disease and 115 control subjects were studied. All had a Lundh meal test. As a group patients with Crohn's disease had significantly decreased activity of both amylase (p < 0.02) and lipase (p < 0.001) in duodenal aspirates. In patients with Crohn's disease enzyme activities were not correlated to duration of disease or to extent or localisation of previous bowel resection. The lowest enzyme values were found in patients with the most extensive bowel involvement, and they were significantly lower (p < 0.05) than in patients with disease confined to the terminal ileum. The differences between enzyme values in other subgroups of patients were not significant. For the patient group as a whole no correlation was found between disease activity and enzyme values, but for the most uniform group of patients, those with terminal ileitis, pancreatic function was significantly lower (p < 0.05) in patients with moderate and severe disease compared with patients with mild disease. Thus at least two factors seem to be responsible for impaired pancreatic function in Crohn's disease: firstly disease activity and secondly localisation or extent of disease.",
author = "J Hegnh{\o}j and Hansen, {C P} and T Rannem and H Sobirk and {Bjerglund Andersen}, L and Andersen, {Jens Rikardt}",
note = "(Ekstern)",
year = "1990",
doi = "10.1136/gut.31.9.1076",
language = "English",
volume = "31",
pages = "1076--1079",
journal = "Gut",
issn = "0017-5749",
publisher = "B M J Group",
number = "9",

}

RIS

TY - JOUR

T1 - Pancreatic function in Crohn's disease

AU - Hegnhøj, J

AU - Hansen, C P

AU - Rannem, T

AU - Sobirk, H

AU - Bjerglund Andersen, L

AU - Andersen, Jens Rikardt

N1 - (Ekstern)

PY - 1990

Y1 - 1990

N2 - We investigated exocrine pancreatic function in a population of patients with Crohn's disease in order to correlate the pancreatic function with clinical and laboratory variables. A total of 143 patients affected by Crohn's disease and 115 control subjects were studied. All had a Lundh meal test. As a group patients with Crohn's disease had significantly decreased activity of both amylase (p < 0.02) and lipase (p < 0.001) in duodenal aspirates. In patients with Crohn's disease enzyme activities were not correlated to duration of disease or to extent or localisation of previous bowel resection. The lowest enzyme values were found in patients with the most extensive bowel involvement, and they were significantly lower (p < 0.05) than in patients with disease confined to the terminal ileum. The differences between enzyme values in other subgroups of patients were not significant. For the patient group as a whole no correlation was found between disease activity and enzyme values, but for the most uniform group of patients, those with terminal ileitis, pancreatic function was significantly lower (p < 0.05) in patients with moderate and severe disease compared with patients with mild disease. Thus at least two factors seem to be responsible for impaired pancreatic function in Crohn's disease: firstly disease activity and secondly localisation or extent of disease.

AB - We investigated exocrine pancreatic function in a population of patients with Crohn's disease in order to correlate the pancreatic function with clinical and laboratory variables. A total of 143 patients affected by Crohn's disease and 115 control subjects were studied. All had a Lundh meal test. As a group patients with Crohn's disease had significantly decreased activity of both amylase (p < 0.02) and lipase (p < 0.001) in duodenal aspirates. In patients with Crohn's disease enzyme activities were not correlated to duration of disease or to extent or localisation of previous bowel resection. The lowest enzyme values were found in patients with the most extensive bowel involvement, and they were significantly lower (p < 0.05) than in patients with disease confined to the terminal ileum. The differences between enzyme values in other subgroups of patients were not significant. For the patient group as a whole no correlation was found between disease activity and enzyme values, but for the most uniform group of patients, those with terminal ileitis, pancreatic function was significantly lower (p < 0.05) in patients with moderate and severe disease compared with patients with mild disease. Thus at least two factors seem to be responsible for impaired pancreatic function in Crohn's disease: firstly disease activity and secondly localisation or extent of disease.

UR - http://www.scopus.com/inward/record.url?scp=0025125117&partnerID=8YFLogxK

U2 - 10.1136/gut.31.9.1076

DO - 10.1136/gut.31.9.1076

M3 - Journal article

C2 - 1698692

AN - SCOPUS:0025125117

VL - 31

SP - 1076

EP - 1079

JO - Gut

JF - Gut

SN - 0017-5749

IS - 9

ER -

ID: 251991069