Prognostic value of lectin pathway molecules and complement proteins in ascitic fluid and blood in patients with liver cirrhosis

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

Standard

Prognostic value of lectin pathway molecules and complement proteins in ascitic fluid and blood in patients with liver cirrhosis. / Glargaard, Signe; Boysen, Trine; Pilely, Katrine; Garred, Peter; Ytting, Henriette.

In: Scandinavian Journal of Gastroenterology, Vol. 53, No. 1, 2018, p. 64-69.

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

Harvard

Glargaard, S, Boysen, T, Pilely, K, Garred, P & Ytting, H 2018, 'Prognostic value of lectin pathway molecules and complement proteins in ascitic fluid and blood in patients with liver cirrhosis', Scandinavian Journal of Gastroenterology, vol. 53, no. 1, pp. 64-69. https://doi.org/10.1080/00365521.2017.1386710

APA

Glargaard, S., Boysen, T., Pilely, K., Garred, P., & Ytting, H. (2018). Prognostic value of lectin pathway molecules and complement proteins in ascitic fluid and blood in patients with liver cirrhosis. Scandinavian Journal of Gastroenterology, 53(1), 64-69. https://doi.org/10.1080/00365521.2017.1386710

Vancouver

Glargaard S, Boysen T, Pilely K, Garred P, Ytting H. Prognostic value of lectin pathway molecules and complement proteins in ascitic fluid and blood in patients with liver cirrhosis. Scandinavian Journal of Gastroenterology. 2018;53(1):64-69. https://doi.org/10.1080/00365521.2017.1386710

Author

Glargaard, Signe ; Boysen, Trine ; Pilely, Katrine ; Garred, Peter ; Ytting, Henriette. / Prognostic value of lectin pathway molecules and complement proteins in ascitic fluid and blood in patients with liver cirrhosis. In: Scandinavian Journal of Gastroenterology. 2018 ; Vol. 53, No. 1. pp. 64-69.

Bibtex

@article{1d0034687e4d4f9288608a96abff4393,
title = "Prognostic value of lectin pathway molecules and complement proteins in ascitic fluid and blood in patients with liver cirrhosis",
abstract = "BACKGROUND AND AIM: Patients with liver cirrhosis and ascites have a poor prognosis with increased risk of infection related death, as advanced stages of cirrhosis are associated with immunodeficiency. We aimed to investigate immunologically active molecules in ascitic fluid and blood and their potential association to survival.MATERIALS AND METHODS: In an exploratory pilot study; blood and ascitic fluid from 34 patients with liver cirrhosis of different etiology were analyzed for pattern recognition molecules (ficolin-1, ficolin-2, ficolin-3 and MBL) and complement proteins (C4 and C3). An observational follow-up study (minimum 17 months) was conducted to assess the association to all-cause mortality or liver transplantation.RESULTS: Ficolin-1, ficolin-2, MBL, C4 and C3 in ascitic fluid and ficolin-1, C4 and C3 in blood were significantly (p = .001-.027) lower in patients with Child-Pugh stage C (n = 16, 47%) compared to Child-Pugh stage B cirrhosis (n = 18, 53%). In multivariate COX-regression analysis low levels of ficolin-1(p = .036) and C3 (p = .025) in ascitic fluid and C4(p = .005) and C3 (p = .032) in serum were associated with all-cause mortality or liver transplantation independent of Child-Pugh score.CONCLUSION: Levels of lectin-complement pathway molecules in ascitic fluid and blood are lower in patients with more advanced stage of cirrhosis. Low C4 and C3 in serum and C3 and ficolin-1 in ascitic fluid are risk factors for all-cause mortality or liver transplantation independently of liver function in patients with cirrhosis and ascites.",
keywords = "Adult, Aged, Ascites/metabolism, Ascitic Fluid/chemistry, Complement System Proteins/analysis, Denmark, Female, Follow-Up Studies, Humans, Lectins/analysis, Liver Cirrhosis/complications, Liver Transplantation, Male, Middle Aged, Multivariate Analysis, Pilot Projects, Prognosis, Proportional Hazards Models, Severity of Illness Index",
author = "Signe Glargaard and Trine Boysen and Katrine Pilely and Peter Garred and Henriette Ytting",
year = "2018",
doi = "10.1080/00365521.2017.1386710",
language = "English",
volume = "53",
pages = "64--69",
journal = "Scandinavian Journal of Gastroenterology",
issn = "0036-5521",
publisher = "Taylor & Francis",
number = "1",

}

RIS

TY - JOUR

T1 - Prognostic value of lectin pathway molecules and complement proteins in ascitic fluid and blood in patients with liver cirrhosis

AU - Glargaard, Signe

AU - Boysen, Trine

AU - Pilely, Katrine

AU - Garred, Peter

AU - Ytting, Henriette

PY - 2018

Y1 - 2018

N2 - BACKGROUND AND AIM: Patients with liver cirrhosis and ascites have a poor prognosis with increased risk of infection related death, as advanced stages of cirrhosis are associated with immunodeficiency. We aimed to investigate immunologically active molecules in ascitic fluid and blood and their potential association to survival.MATERIALS AND METHODS: In an exploratory pilot study; blood and ascitic fluid from 34 patients with liver cirrhosis of different etiology were analyzed for pattern recognition molecules (ficolin-1, ficolin-2, ficolin-3 and MBL) and complement proteins (C4 and C3). An observational follow-up study (minimum 17 months) was conducted to assess the association to all-cause mortality or liver transplantation.RESULTS: Ficolin-1, ficolin-2, MBL, C4 and C3 in ascitic fluid and ficolin-1, C4 and C3 in blood were significantly (p = .001-.027) lower in patients with Child-Pugh stage C (n = 16, 47%) compared to Child-Pugh stage B cirrhosis (n = 18, 53%). In multivariate COX-regression analysis low levels of ficolin-1(p = .036) and C3 (p = .025) in ascitic fluid and C4(p = .005) and C3 (p = .032) in serum were associated with all-cause mortality or liver transplantation independent of Child-Pugh score.CONCLUSION: Levels of lectin-complement pathway molecules in ascitic fluid and blood are lower in patients with more advanced stage of cirrhosis. Low C4 and C3 in serum and C3 and ficolin-1 in ascitic fluid are risk factors for all-cause mortality or liver transplantation independently of liver function in patients with cirrhosis and ascites.

AB - BACKGROUND AND AIM: Patients with liver cirrhosis and ascites have a poor prognosis with increased risk of infection related death, as advanced stages of cirrhosis are associated with immunodeficiency. We aimed to investigate immunologically active molecules in ascitic fluid and blood and their potential association to survival.MATERIALS AND METHODS: In an exploratory pilot study; blood and ascitic fluid from 34 patients with liver cirrhosis of different etiology were analyzed for pattern recognition molecules (ficolin-1, ficolin-2, ficolin-3 and MBL) and complement proteins (C4 and C3). An observational follow-up study (minimum 17 months) was conducted to assess the association to all-cause mortality or liver transplantation.RESULTS: Ficolin-1, ficolin-2, MBL, C4 and C3 in ascitic fluid and ficolin-1, C4 and C3 in blood were significantly (p = .001-.027) lower in patients with Child-Pugh stage C (n = 16, 47%) compared to Child-Pugh stage B cirrhosis (n = 18, 53%). In multivariate COX-regression analysis low levels of ficolin-1(p = .036) and C3 (p = .025) in ascitic fluid and C4(p = .005) and C3 (p = .032) in serum were associated with all-cause mortality or liver transplantation independent of Child-Pugh score.CONCLUSION: Levels of lectin-complement pathway molecules in ascitic fluid and blood are lower in patients with more advanced stage of cirrhosis. Low C4 and C3 in serum and C3 and ficolin-1 in ascitic fluid are risk factors for all-cause mortality or liver transplantation independently of liver function in patients with cirrhosis and ascites.

KW - Adult

KW - Aged

KW - Ascites/metabolism

KW - Ascitic Fluid/chemistry

KW - Complement System Proteins/analysis

KW - Denmark

KW - Female

KW - Follow-Up Studies

KW - Humans

KW - Lectins/analysis

KW - Liver Cirrhosis/complications

KW - Liver Transplantation

KW - Male

KW - Middle Aged

KW - Multivariate Analysis

KW - Pilot Projects

KW - Prognosis

KW - Proportional Hazards Models

KW - Severity of Illness Index

U2 - 10.1080/00365521.2017.1386710

DO - 10.1080/00365521.2017.1386710

M3 - Journal article

C2 - 28982257

VL - 53

SP - 64

EP - 69

JO - Scandinavian Journal of Gastroenterology

JF - Scandinavian Journal of Gastroenterology

SN - 0036-5521

IS - 1

ER -

ID: 213156870