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Article: Serum lipid alterations identified in chronic hepatitis B, hepatitis B virus-associated cirrhosis and carcinoma patients

TitleSerum lipid alterations identified in chronic hepatitis B, hepatitis B virus-associated cirrhosis and carcinoma patients
Authors
Issue Date2017
Citation
Scientific Reports, 2017, v. 7, article no. 42710 How to Cite?
AbstractThe incidences of chronic hepatitis B (CHB), Hepatitis B virus (HBV)-associated cirrhosis and HBV-associated carcinoma are high and increasing. This study was designed to evaluate serum lipid metabolite changes that are associated with the progression from CHB to HBV-associated cirrhosis and ultimately to HBV-associated HCC. A targeted metabolomic assay was performed in fasting sera from 136 CHB patients, 104 HBV-associated cirrhosis, and 95 HBV-associated HCC using ultra-performance liquid chromatography triple quadrupole mass spectrometry. A total of 140 metabolites were identified. Clear separations between each two groups were obtained using the partial least squares discriminate analysis of 9 lipid metabolites. Progressively lower levels of long-chain lysophosphatidylcholines (lysoPC a C18:2, lysoPC a C20:3, lysoPC a C20:4) were observed from CHB to cirrhosis to carcinoma; lower levels of lysoPC a C20:4 were found in patients with higher model for end-stage liver disease in the same disease group; and lysoPC a C20:3 levels were lower in Child-Pugh Class C than in Class A and Class B in HBV-associated cirrhosis and HBV-associated HCC groups. The octadecadienyl carnitine level was higher in HBV-associated cirrhosis group than in other two groups. Serum levels of selected long-chain lysoPCs are promising markers for the progression of HBV-associated liver diseases.
Persistent Identifierhttp://hdl.handle.net/10722/342535
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWu, Tao-
dc.contributor.authorZheng, Xiaojiao-
dc.contributor.authorYang, Ming-
dc.contributor.authorZhao, Aihua-
dc.contributor.authorLi, Meng-
dc.contributor.authorChen, Tianlu-
dc.contributor.authorPanee, Jun-
dc.contributor.authorJia, Wei-
dc.contributor.authorJi, Guang-
dc.date.accessioned2024-04-17T07:04:30Z-
dc.date.available2024-04-17T07:04:30Z-
dc.date.issued2017-
dc.identifier.citationScientific Reports, 2017, v. 7, article no. 42710-
dc.identifier.urihttp://hdl.handle.net/10722/342535-
dc.description.abstractThe incidences of chronic hepatitis B (CHB), Hepatitis B virus (HBV)-associated cirrhosis and HBV-associated carcinoma are high and increasing. This study was designed to evaluate serum lipid metabolite changes that are associated with the progression from CHB to HBV-associated cirrhosis and ultimately to HBV-associated HCC. A targeted metabolomic assay was performed in fasting sera from 136 CHB patients, 104 HBV-associated cirrhosis, and 95 HBV-associated HCC using ultra-performance liquid chromatography triple quadrupole mass spectrometry. A total of 140 metabolites were identified. Clear separations between each two groups were obtained using the partial least squares discriminate analysis of 9 lipid metabolites. Progressively lower levels of long-chain lysophosphatidylcholines (lysoPC a C18:2, lysoPC a C20:3, lysoPC a C20:4) were observed from CHB to cirrhosis to carcinoma; lower levels of lysoPC a C20:4 were found in patients with higher model for end-stage liver disease in the same disease group; and lysoPC a C20:3 levels were lower in Child-Pugh Class C than in Class A and Class B in HBV-associated cirrhosis and HBV-associated HCC groups. The octadecadienyl carnitine level was higher in HBV-associated cirrhosis group than in other two groups. Serum levels of selected long-chain lysoPCs are promising markers for the progression of HBV-associated liver diseases.-
dc.languageeng-
dc.relation.ispartofScientific Reports-
dc.titleSerum lipid alterations identified in chronic hepatitis B, hepatitis B virus-associated cirrhosis and carcinoma patients-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/srep42710-
dc.identifier.pmid28198443-
dc.identifier.scopuseid_2-s2.0-85013173817-
dc.identifier.volume7-
dc.identifier.spagearticle no. 42710-
dc.identifier.epagearticle no. 42710-
dc.identifier.eissn2045-2322-
dc.identifier.isiWOS:000394292400001-

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