Author/Authors :
Rezaei-Tavirani Mostafa نويسنده , Sharifian Afsaneh نويسنده , Mohebbi Seyed Reza نويسنده Research Center for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran , Safaei Akram نويسنده Gastroentrology and Liver Diseases Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran Safaei Akram , Arefi Oskouie Afsaneh نويسنده Department of Basic Science, Faculty of Paramedical Sciences , SHABANI Mahtab نويسنده
Abstract :
Background Cirrhosis is recognized by a reduction in hepatocyte
proliferation with an increase in fibrous tissue, which may ultimately
lead to the development of cancerous nodules. Liver biopsy has remained
the gold standard for confirming liver fibrosis stages, but there are
not any nonreversible and specific therapeutic targets in advanced
cirrhosis. In the present study, we used the NMR method to find
potential therapeutic markers in serum of HCV - cirrhotic patients with
advanced stage. Methods A metabolic profiling study was conducted using
2 groups: decompensated HCV-cirrhosis patients (n = 21) and healthy
controls (n = 18). 1H nuclear magnetic resonance (NMR) approach was used
to obtain the serum metabolic profiles of the samples. The acquired data
were processed by the multivariate principal component analysis (PCA)
and orthogonal partial least squares discriminant analysis (OPLS-DA).
Moreover, metabolic pathways were determined using MetaboAnalyst 3.0.
Results Specifically, 16 metabolites showed alteration between the 2
groups. Compared with healthy controls, a number of metabolites showed
increased concentration in serum of decompensated HCV-cirrhosis such as
succinic acid, isovaleraldehyde, citrulline, propanal and
cinnamaldehyde, while several others were observed in decreased levels
in the decompensated HCV-cirrhosis such as valine, glutamine,
trimethylamine, lactate, proline, aspartate, lipid, VLDL, isoleucine,
fucose, and glutamate. Aminoacyl-tRNA biosynthesis, alanine, aspartate,
glutamate metabolism and arginine, and proline metabolism are the most
significant pathways associated with advanced HCV- cirrhosis.
Conclusions Metabolomic profiling through NMR can identify the metabolic
disturbances in advanced HCV-cirrhosis. Aberrant amino acid biosynthesis
may be the hallmark with increasing severity of cirrhosis as well as
alterations in energetic metabolism.