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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Trieb, M; Horvath, A; Birner-Gruenberger, R; Spindelboeck, W; Stadlbauer, V; Taschler, U; Curcic, S; Stauber, RE; Holzer, M; Pasterk, L; Heinemann, A; Marsche, G.
Liver disease alters high-density lipoprotein composition, metabolism and function.
Biochim Biophys Acta. 2016; 1861(7):630-638 Doi: 10.1016/j.bbalip.2016.04.013 [OPEN ACCESS]
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Führende Autor*innen der Med Uni Graz
Marsche Gunther
Stadlbauer-Köllner Vanessa
Trieb Markus
Co-Autor*innen der Med Uni Graz
Birner-Grünberger Ruth
Curcic Sanja
Heinemann Akos
Holzer Michael
Horvath Angela
Spindelböck Walter Johann
Stauber Rudolf
Taschler Ulrike
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Abstract:
High-density lipoproteins (HDL) are important endogenous inhibitors of inflammatory responses. Functional impairment of HDL might contribute to the excess mortality experienced by patients with liver disease, but the effect of cirrhosis on HDL metabolism and function remain elusive. To get an integrated measure of HDL quantity and quality, we assessed several metrics of HDL function using apolipoprotein (apo) B-depleted sera from patients with compensated cirrhosis, patients with acutely decompensated cirrhosis and healthy controls. We observed that sera of cirrhotic patients showed reduced levels of HDL-cholesterol and profoundly suppressed activities of several enzymes involved in HDL maturation and metabolism. Native gel electrophoresis analyses revealed that cirrhotic serum HDL shifts towards the larger HDL2 subclass. Proteomic assessment of isolated HDL identified several proteins, including apoA-I, apoC-III, apoE, paraoxonase 1 and acute phase serum amyloid A to be significantly altered in cirrhotic patients. With regard to function, these alterations in levels, composition and structure of HDL were strongly associated with metrics of function of apoB-depleted sera, including cholesterol efflux capability, paraoxonase activity, the ability to inhibit monocyte production of cytokines and endothelial regenerative activities. Of particular interest, cholesterol efflux capacity appeared to be strongly associated with liver disease mortality. Our findings may be clinically relevant and improve our ability to monitor cirrhotic patients at high risk. Copyright © 2016 Elsevier B.V. All rights reserved.
Find related publications in this database (using NLM MeSH Indexing)
Aged -
Apolipoprotein A-I - blood
Apolipoprotein C-III - blood
Apolipoproteins B - blood
Apolipoproteins E - blood
Aryldialkylphosphatase - blood
Bilirubin - blood
Cholesterol, HDL - blood
Cholesterol, LDL - blood
Creatinine - blood
Cross-Sectional Studies -
Cytokines - biosynthesis
Cytokines - secretion
Female -
Humans -
Liver - metabolism
Liver - pathology
Liver - physiopathology
Liver Cirrhosis - blood
Liver Cirrhosis - pathology
Liver Cirrhosis - physiopathology
Male -
Middle Aged -
Monocytes - metabolism
Monocytes - pathology
Serum Albumin - metabolism
Serum Amyloid A Protein -
Survival Analysis -
Triglycerides - blood

Find related publications in this database (Keywords)
Liver disease
HDL-function
HDL-proteome
Cholesterol efflux
Paraoxonase
LCAT
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