The concentration of total sialic acid in chronic hepatitis B and C.


Journal

Annals of clinical biochemistry
ISSN: 1758-1001
Titre abrégé: Ann Clin Biochem
Pays: England
ID NLM: 0324055

Informations de publication

Date de publication:
01 2019
Historique:
pubmed: 22 7 2018
medline: 4 12 2019
entrez: 21 7 2018
Statut: ppublish

Résumé

The synthesis and glycosylation of glycoproteins and glycolipids take place in the liver. Thus, liver diseases may affect serum concentrations of some carbohydrate derivatives, especially the concentration of sialic acid which is attached to the end of oligosaccharide chains. The aim of this study was to measure and compare the serum concentration of total sialic acid in chronic hepatitis B and C. The hypothesis is that both viruses responsible for the development of inflammation work differently at the cellular level. Serum samples were obtained from 90 patients suffering from liver diseases: 50 from chronic hepatitis B and 40 from chronic hepatitis C at the time of diagnosis. The total sialic acid concentration in the serum was measured according to the enzymatic method using a colorimetric procedure. The mean total sialic acid concentration in patients with chronic hepatitis B was significantly lower than the mean concentration in the healthy group, while in patients with chronic hepatitis C, it was significantly higher than that in healthy people and in patients suffering from chronic hepatitis B. There were no significant differences in total sialic acid concentrations in patients with chronic hepatitis B and C according to the grade of portal/periportal activity, the grade of lobular activity and the stage of fibrosis. We conclude that chronic viral hepatitis affects the total serum concentration of sialic acid. Moreover, the concentration of total sialic acid may be a useful marker to differentiate between chronic hepatitis B and C but is not useful for evaluation of the progression of these diseases.

Sections du résumé

BACKGROUND
The synthesis and glycosylation of glycoproteins and glycolipids take place in the liver. Thus, liver diseases may affect serum concentrations of some carbohydrate derivatives, especially the concentration of sialic acid which is attached to the end of oligosaccharide chains. The aim of this study was to measure and compare the serum concentration of total sialic acid in chronic hepatitis B and C. The hypothesis is that both viruses responsible for the development of inflammation work differently at the cellular level.
METHODS
Serum samples were obtained from 90 patients suffering from liver diseases: 50 from chronic hepatitis B and 40 from chronic hepatitis C at the time of diagnosis. The total sialic acid concentration in the serum was measured according to the enzymatic method using a colorimetric procedure.
RESULTS
The mean total sialic acid concentration in patients with chronic hepatitis B was significantly lower than the mean concentration in the healthy group, while in patients with chronic hepatitis C, it was significantly higher than that in healthy people and in patients suffering from chronic hepatitis B. There were no significant differences in total sialic acid concentrations in patients with chronic hepatitis B and C according to the grade of portal/periportal activity, the grade of lobular activity and the stage of fibrosis.
CONCLUSIONS
We conclude that chronic viral hepatitis affects the total serum concentration of sialic acid. Moreover, the concentration of total sialic acid may be a useful marker to differentiate between chronic hepatitis B and C but is not useful for evaluation of the progression of these diseases.

Identifiants

pubmed: 30027776
doi: 10.1177/0004563218792292
doi:

Substances chimiques

Biomarkers 0
N-Acetylneuraminic Acid GZP2782OP0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

118-122

Auteurs

Ewa Gruszewska (E)

1 Department of Biochemical Diagnostics, Medical University of Bialystok, Bialystok, Poland.

Bogdan Cylwik (B)

2 Department of Pediatric Laboratory Diagnostics, Medical University of Bialystok, Bialystok, Poland.

Monika Gudowska (M)

1 Department of Biochemical Diagnostics, Medical University of Bialystok, Bialystok, Poland.

Anatol Panasiuk (A)

3 Department of Infectious Diseases and Hepatology, Medical University of Bialystok, Bialystok, Poland.

Robert Flisiak (R)

3 Department of Infectious Diseases and Hepatology, Medical University of Bialystok, Bialystok, Poland.

Lech Chrostek (L)

1 Department of Biochemical Diagnostics, Medical University of Bialystok, Bialystok, Poland.

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Classifications MeSH