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A serum metabonomic study on the difference between alcohol- and HBV-induced liver cirrhosis by ultraperformance liquid chromatography coupled to mass spectrometry plus quadrupole time-of-flight mass spectrometry
Liver cirrhosis is the fatal consequence of chronic hepatitis, making early diagnosis of liver cirrhosis critical. Liver biopsy is still the standard diagnostic method for liver cirrhosis, although its use in a broad population with alcoholism or hepatitis B virus (HBV) infection remains difficult....
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Published in: | Chinese medical journal 2011-05, Vol.124 (9), p.1367-1373 |
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creator | Lian, Jiang-shan Liu, Wei Hao, Shao-rui Guo, Yong-zheng Huang, Hai-jun Chen, De-ying Xie, Qing Pan, Xiao-ping Xu, Wei Yuan, Wen-xia Li, Lan-juan Huang, Jian-rong |
description | Liver cirrhosis is the fatal consequence of chronic hepatitis, making early diagnosis of liver cirrhosis critical. Liver biopsy is still the standard diagnostic method for liver cirrhosis, although its use in a broad population with alcoholism or hepatitis B virus (HBV) infection remains difficult. In this study, we used a metabonomic approach to detect potential biomarkers for early diagnosis of liver cirrhosis.
Serum specimens were collected prospectively from normal control subjects (n = 22) and patients with alcoholic cirrhosis (n = 18) or HBV-induced cirrhosis (n = 19). The serum metabonome was analyzed using ultraperformance liquid chromatography (LC)/time-of-flight mass spectrometry (MS) integrated with chemometrics. The acquired LC-MS data were normalized and processed using principal component analysis (PCA) and partial least squares discrimination analysis (PLS-DA).
Significant differences in the metabonomics among the three groups were observed. Lysophosphatidyl cholines (LPCs) (LPC C16:0, LPC C18:0, LPC C18:2, LPC C18:3, LPC C20:3, LPC C20:5) were decreased in the serum of patients with hepatic cirrhosis, whereas bile acids (glycocholic acid, glycochenodeoxycholic acid), hypoxanthine, and stearamide were increased in the serum of patients with hepatic cirrhosis. These metabolites are considered "common" biomarkers for hepatic cirrhosis. Oleamide and myristamide were increased in the serum of patients with alcoholic cirrhosis but decreased in those with HBV-induced cirrhosis. These could be specific biomarkers for differential diagnosis between alcohol- and HBV-induced hepatic cirrhosis.
There are significant metabonomic differences between alcohol- and HBV-induced liver cirrhosis. Metabonomics is a top-down systems biology tool for conducting research on clinical problems. |
doi_str_mv | 10.3760/cma.j.issn.0366-6999.2011.09.018 |
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Serum specimens were collected prospectively from normal control subjects (n = 22) and patients with alcoholic cirrhosis (n = 18) or HBV-induced cirrhosis (n = 19). The serum metabonome was analyzed using ultraperformance liquid chromatography (LC)/time-of-flight mass spectrometry (MS) integrated with chemometrics. The acquired LC-MS data were normalized and processed using principal component analysis (PCA) and partial least squares discrimination analysis (PLS-DA).
Significant differences in the metabonomics among the three groups were observed. Lysophosphatidyl cholines (LPCs) (LPC C16:0, LPC C18:0, LPC C18:2, LPC C18:3, LPC C20:3, LPC C20:5) were decreased in the serum of patients with hepatic cirrhosis, whereas bile acids (glycocholic acid, glycochenodeoxycholic acid), hypoxanthine, and stearamide were increased in the serum of patients with hepatic cirrhosis. These metabolites are considered "common" biomarkers for hepatic cirrhosis. Oleamide and myristamide were increased in the serum of patients with alcoholic cirrhosis but decreased in those with HBV-induced cirrhosis. These could be specific biomarkers for differential diagnosis between alcohol- and HBV-induced hepatic cirrhosis.
There are significant metabonomic differences between alcohol- and HBV-induced liver cirrhosis. Metabonomics is a top-down systems biology tool for conducting research on clinical problems.</description><identifier>ISSN: 0366-6999</identifier><identifier>DOI: 10.3760/cma.j.issn.0366-6999.2011.09.018</identifier><identifier>PMID: 21740750</identifier><language>eng</language><publisher>China</publisher><subject>Adult ; Aged ; Alcohols - adverse effects ; Chromatography, Liquid - methods ; Female ; Hepatitis B virus - pathogenicity ; Humans ; Liver Cirrhosis - blood ; Liver Cirrhosis - etiology ; Liver Cirrhosis - metabolism ; Liver Cirrhosis - virology ; Male ; Mass Spectrometry - methods ; Middle Aged ; Principal Component Analysis</subject><ispartof>Chinese medical journal, 2011-05, Vol.124 (9), p.1367-1373</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c273t-493b80679ab70c5471cd2ebb7ceff19a870160c4b1d15adb65921a3d5bf51fd53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21740750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lian, Jiang-shan</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><creatorcontrib>Hao, Shao-rui</creatorcontrib><creatorcontrib>Guo, Yong-zheng</creatorcontrib><creatorcontrib>Huang, Hai-jun</creatorcontrib><creatorcontrib>Chen, De-ying</creatorcontrib><creatorcontrib>Xie, Qing</creatorcontrib><creatorcontrib>Pan, Xiao-ping</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Yuan, Wen-xia</creatorcontrib><creatorcontrib>Li, Lan-juan</creatorcontrib><creatorcontrib>Huang, Jian-rong</creatorcontrib><title>A serum metabonomic study on the difference between alcohol- and HBV-induced liver cirrhosis by ultraperformance liquid chromatography coupled to mass spectrometry plus quadrupole time-of-flight mass spectrometry</title><title>Chinese medical journal</title><addtitle>Chin Med J (Engl)</addtitle><description>Liver cirrhosis is the fatal consequence of chronic hepatitis, making early diagnosis of liver cirrhosis critical. Liver biopsy is still the standard diagnostic method for liver cirrhosis, although its use in a broad population with alcoholism or hepatitis B virus (HBV) infection remains difficult. In this study, we used a metabonomic approach to detect potential biomarkers for early diagnosis of liver cirrhosis.
Serum specimens were collected prospectively from normal control subjects (n = 22) and patients with alcoholic cirrhosis (n = 18) or HBV-induced cirrhosis (n = 19). The serum metabonome was analyzed using ultraperformance liquid chromatography (LC)/time-of-flight mass spectrometry (MS) integrated with chemometrics. The acquired LC-MS data were normalized and processed using principal component analysis (PCA) and partial least squares discrimination analysis (PLS-DA).
Significant differences in the metabonomics among the three groups were observed. Lysophosphatidyl cholines (LPCs) (LPC C16:0, LPC C18:0, LPC C18:2, LPC C18:3, LPC C20:3, LPC C20:5) were decreased in the serum of patients with hepatic cirrhosis, whereas bile acids (glycocholic acid, glycochenodeoxycholic acid), hypoxanthine, and stearamide were increased in the serum of patients with hepatic cirrhosis. These metabolites are considered "common" biomarkers for hepatic cirrhosis. Oleamide and myristamide were increased in the serum of patients with alcoholic cirrhosis but decreased in those with HBV-induced cirrhosis. These could be specific biomarkers for differential diagnosis between alcohol- and HBV-induced hepatic cirrhosis.
There are significant metabonomic differences between alcohol- and HBV-induced liver cirrhosis. Metabonomics is a top-down systems biology tool for conducting research on clinical problems.</description><subject>Adult</subject><subject>Aged</subject><subject>Alcohols - adverse effects</subject><subject>Chromatography, Liquid - methods</subject><subject>Female</subject><subject>Hepatitis B virus - pathogenicity</subject><subject>Humans</subject><subject>Liver Cirrhosis - blood</subject><subject>Liver Cirrhosis - etiology</subject><subject>Liver Cirrhosis - metabolism</subject><subject>Liver Cirrhosis - virology</subject><subject>Male</subject><subject>Mass Spectrometry - methods</subject><subject>Middle Aged</subject><subject>Principal Component Analysis</subject><issn>0366-6999</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNplkctu1TAURT0A0VL4BXRmMEmwk2v7ZlgqoEiVmADTKz-OG1d2nOsHKP_JBxFEYcJoS2evsyabkDeM9qMU9K2Jqn_ofSlLT0chOjFNUz9Qxno69ZQdn5DLf_cL8ryUB0oHzqV4Ri4GJg9UcnpJfl5DwdwiRKxKpyVFb6DUZjdIC9QZwXrnMONiEDTWH4gLqGDSnEIHarFw--5b5xfbDFoI_jtmMD7nORVfQG_QQs1qxexSjuq3JPhz8xbMnFNUNd3v7byBSW0Nu6EmiKoUKCuauhNY8wZraAXOTdnc1hQQqo_YJde54O_n-v_DC_LUqVDw5WNeka8f3n-5ue3uPn_8dHN915lBjrU7TKM-UiEnpSU1_CCZsQNqLQ06xyZ1lJQJag6aWcaV1YJPA1Oj5dpx5iwfr8jrP941p3PDUk_RF4MhqAVTK6ejFGzaFxE7-eqRbDqiPa3ZR5W3098hxl94UJTi</recordid><startdate>201105</startdate><enddate>201105</enddate><creator>Lian, Jiang-shan</creator><creator>Liu, Wei</creator><creator>Hao, Shao-rui</creator><creator>Guo, Yong-zheng</creator><creator>Huang, Hai-jun</creator><creator>Chen, De-ying</creator><creator>Xie, Qing</creator><creator>Pan, Xiao-ping</creator><creator>Xu, Wei</creator><creator>Yuan, Wen-xia</creator><creator>Li, Lan-juan</creator><creator>Huang, Jian-rong</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201105</creationdate><title>A serum metabonomic study on the difference between alcohol- and HBV-induced liver cirrhosis by ultraperformance liquid chromatography coupled to mass spectrometry plus quadrupole time-of-flight mass spectrometry</title><author>Lian, Jiang-shan ; Liu, Wei ; Hao, Shao-rui ; Guo, Yong-zheng ; Huang, Hai-jun ; Chen, De-ying ; Xie, Qing ; Pan, Xiao-ping ; Xu, Wei ; Yuan, Wen-xia ; Li, Lan-juan ; Huang, Jian-rong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c273t-493b80679ab70c5471cd2ebb7ceff19a870160c4b1d15adb65921a3d5bf51fd53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Alcohols - adverse effects</topic><topic>Chromatography, Liquid - methods</topic><topic>Female</topic><topic>Hepatitis B virus - pathogenicity</topic><topic>Humans</topic><topic>Liver Cirrhosis - blood</topic><topic>Liver Cirrhosis - etiology</topic><topic>Liver Cirrhosis - metabolism</topic><topic>Liver Cirrhosis - virology</topic><topic>Male</topic><topic>Mass Spectrometry - methods</topic><topic>Middle Aged</topic><topic>Principal Component Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lian, Jiang-shan</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><creatorcontrib>Hao, Shao-rui</creatorcontrib><creatorcontrib>Guo, Yong-zheng</creatorcontrib><creatorcontrib>Huang, Hai-jun</creatorcontrib><creatorcontrib>Chen, De-ying</creatorcontrib><creatorcontrib>Xie, Qing</creatorcontrib><creatorcontrib>Pan, Xiao-ping</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Yuan, Wen-xia</creatorcontrib><creatorcontrib>Li, Lan-juan</creatorcontrib><creatorcontrib>Huang, Jian-rong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lian, Jiang-shan</au><au>Liu, Wei</au><au>Hao, Shao-rui</au><au>Guo, Yong-zheng</au><au>Huang, Hai-jun</au><au>Chen, De-ying</au><au>Xie, Qing</au><au>Pan, Xiao-ping</au><au>Xu, Wei</au><au>Yuan, Wen-xia</au><au>Li, Lan-juan</au><au>Huang, Jian-rong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A serum metabonomic study on the difference between alcohol- and HBV-induced liver cirrhosis by ultraperformance liquid chromatography coupled to mass spectrometry plus quadrupole time-of-flight mass spectrometry</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chin Med J (Engl)</addtitle><date>2011-05</date><risdate>2011</risdate><volume>124</volume><issue>9</issue><spage>1367</spage><epage>1373</epage><pages>1367-1373</pages><issn>0366-6999</issn><abstract>Liver cirrhosis is the fatal consequence of chronic hepatitis, making early diagnosis of liver cirrhosis critical. Liver biopsy is still the standard diagnostic method for liver cirrhosis, although its use in a broad population with alcoholism or hepatitis B virus (HBV) infection remains difficult. In this study, we used a metabonomic approach to detect potential biomarkers for early diagnosis of liver cirrhosis.
Serum specimens were collected prospectively from normal control subjects (n = 22) and patients with alcoholic cirrhosis (n = 18) or HBV-induced cirrhosis (n = 19). The serum metabonome was analyzed using ultraperformance liquid chromatography (LC)/time-of-flight mass spectrometry (MS) integrated with chemometrics. The acquired LC-MS data were normalized and processed using principal component analysis (PCA) and partial least squares discrimination analysis (PLS-DA).
Significant differences in the metabonomics among the three groups were observed. Lysophosphatidyl cholines (LPCs) (LPC C16:0, LPC C18:0, LPC C18:2, LPC C18:3, LPC C20:3, LPC C20:5) were decreased in the serum of patients with hepatic cirrhosis, whereas bile acids (glycocholic acid, glycochenodeoxycholic acid), hypoxanthine, and stearamide were increased in the serum of patients with hepatic cirrhosis. These metabolites are considered "common" biomarkers for hepatic cirrhosis. Oleamide and myristamide were increased in the serum of patients with alcoholic cirrhosis but decreased in those with HBV-induced cirrhosis. These could be specific biomarkers for differential diagnosis between alcohol- and HBV-induced hepatic cirrhosis.
There are significant metabonomic differences between alcohol- and HBV-induced liver cirrhosis. Metabonomics is a top-down systems biology tool for conducting research on clinical problems.</abstract><cop>China</cop><pmid>21740750</pmid><doi>10.3760/cma.j.issn.0366-6999.2011.09.018</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Alcohols - adverse effects Chromatography, Liquid - methods Female Hepatitis B virus - pathogenicity Humans Liver Cirrhosis - blood Liver Cirrhosis - etiology Liver Cirrhosis - metabolism Liver Cirrhosis - virology Male Mass Spectrometry - methods Middle Aged Principal Component Analysis |
title | A serum metabonomic study on the difference between alcohol- and HBV-induced liver cirrhosis by ultraperformance liquid chromatography coupled to mass spectrometry plus quadrupole time-of-flight mass spectrometry |
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