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- Publisher Website: 10.1016/j.jhep.2007.02.023
- Scopus: eid_2-s2.0-34347389866
- PMID: 17462782
- WOS: WOS:000248642400006
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Article: Serum adiponectin is increased in advancing liver fibrosis and declines with reduction in fibrosis in chronic hepatitis B
Title | Serum adiponectin is increased in advancing liver fibrosis and declines with reduction in fibrosis in chronic hepatitis B |
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Authors | |
Keywords | Adiponectin Adiponectin oligomeric form Chronic hepatitis B Lamivudine Liver cirrhosis Pegylated interferon alfa-2a Sustained virological response |
Issue Date | 2007 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jhep |
Citation | Journal Of Hepatology, 2007, v. 47 n. 2, p. 191-202 How to Cite? |
Abstract | Background/Aims: Despite the possible role of adiponectin in the pathogenesis of liver cirrhosis, few data have been collected from patients in different stages of liver fibrosis. We studied the role of adiponectin in 2 chronic hepatitis B (CHB)-patient cohorts. Methods: Serum adiponectin was quantified by enzyme-linked immunosorbent assay. One-hundred liver biopsy specimens from CHB patients with different stages of fibrosis and 38 paired liver biopsies from hepatitis B e antigen-positive patients randomized to lamivudine (n = 15), pegylated interferon alfa-2a (n = 15) or pegylated interferon alfa-2a plus lamivudine (n = 8) therapy for 48 weeks were assessed. Results: Serum adiponectin was detected at levels ranging over fourfold magnitude with advancing fibrosis stage and correlated positively with fibrosis stage [r = 0.45, p < 0.001]. CHB patients with stage 0-1 fibrosis had higher composition of high molecular weight (HMW) form of adiponectin when compared with CHB patients with liver cirrhosis [mean ± SEM 51.2 ± 2.1% vs. 40.9 ± 1.7%, respectively, p = 0.001]. After antiviral therapy, patients with fibrosis reduction had marked decline in serum adiponectin level and increase in HMW form of adiponectin [mean ± SEM 43.5 ± 1.2% vs. 37.0 ± 3.0%, respectively, p = 0.04]. Conclusions: Serum adiponectin may have a role in fibrosis progression in CHB infection. A marked decline in serum adiponectin after antiviral therapy is associated with fibrosis reduction. © 2007 European Association for the Study of the Liver. |
Persistent Identifier | http://hdl.handle.net/10722/77676 |
ISSN | 2023 Impact Factor: 26.8 2023 SCImago Journal Rankings: 9.857 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Hui, CK | en_HK |
dc.contributor.author | Zhang, HY | en_HK |
dc.contributor.author | Lee, NP | en_HK |
dc.contributor.author | Chan, W | en_HK |
dc.contributor.author | Yueng, YH | en_HK |
dc.contributor.author | Leung, KW | en_HK |
dc.contributor.author | Lu, L | en_HK |
dc.contributor.author | Leung, N | en_HK |
dc.contributor.author | Lo, CM | en_HK |
dc.contributor.author | Fan, ST | en_HK |
dc.contributor.author | Luk, JM | en_HK |
dc.contributor.author | Xu, A | en_HK |
dc.contributor.author | Lam, KS | en_HK |
dc.contributor.author | Kwong, YL | en_HK |
dc.contributor.author | Lau, GKK | en_HK |
dc.date.accessioned | 2010-09-06T07:34:30Z | - |
dc.date.available | 2010-09-06T07:34:30Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Journal Of Hepatology, 2007, v. 47 n. 2, p. 191-202 | en_HK |
dc.identifier.issn | 0168-8278 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77676 | - |
dc.description.abstract | Background/Aims: Despite the possible role of adiponectin in the pathogenesis of liver cirrhosis, few data have been collected from patients in different stages of liver fibrosis. We studied the role of adiponectin in 2 chronic hepatitis B (CHB)-patient cohorts. Methods: Serum adiponectin was quantified by enzyme-linked immunosorbent assay. One-hundred liver biopsy specimens from CHB patients with different stages of fibrosis and 38 paired liver biopsies from hepatitis B e antigen-positive patients randomized to lamivudine (n = 15), pegylated interferon alfa-2a (n = 15) or pegylated interferon alfa-2a plus lamivudine (n = 8) therapy for 48 weeks were assessed. Results: Serum adiponectin was detected at levels ranging over fourfold magnitude with advancing fibrosis stage and correlated positively with fibrosis stage [r = 0.45, p < 0.001]. CHB patients with stage 0-1 fibrosis had higher composition of high molecular weight (HMW) form of adiponectin when compared with CHB patients with liver cirrhosis [mean ± SEM 51.2 ± 2.1% vs. 40.9 ± 1.7%, respectively, p = 0.001]. After antiviral therapy, patients with fibrosis reduction had marked decline in serum adiponectin level and increase in HMW form of adiponectin [mean ± SEM 43.5 ± 1.2% vs. 37.0 ± 3.0%, respectively, p = 0.04]. Conclusions: Serum adiponectin may have a role in fibrosis progression in CHB infection. A marked decline in serum adiponectin after antiviral therapy is associated with fibrosis reduction. © 2007 European Association for the Study of the Liver. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jhep | en_HK |
dc.relation.ispartof | Journal of Hepatology | en_HK |
dc.rights | Journal of Hepatology. Copyright © Elsevier BV. | en_HK |
dc.subject | Adiponectin | en_HK |
dc.subject | Adiponectin oligomeric form | en_HK |
dc.subject | Chronic hepatitis B | en_HK |
dc.subject | Lamivudine | en_HK |
dc.subject | Liver cirrhosis | en_HK |
dc.subject | Pegylated interferon alfa-2a | en_HK |
dc.subject | Sustained virological response | en_HK |
dc.subject.mesh | Adiponectin - blood - chemistry - genetics | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Aged, 80 and over | en_HK |
dc.subject.mesh | Antiviral Agents - therapeutic use | en_HK |
dc.subject.mesh | Cohort Studies | en_HK |
dc.subject.mesh | Disease Progression | en_HK |
dc.subject.mesh | Enzyme-Linked Immunosorbent Assay | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Hepatitis B, Chronic - complications - drug therapy - pathology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Immunohistochemistry | en_HK |
dc.subject.mesh | Liver - metabolism | en_HK |
dc.subject.mesh | Liver Cirrhosis - blood - metabolism - pathology - virology | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Molecular Weight | en_HK |
dc.subject.mesh | RNA, Messenger - metabolism | en_HK |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_HK |
dc.subject.mesh | Severity of Illness Index | en_HK |
dc.title | Serum adiponectin is increased in advancing liver fibrosis and declines with reduction in fibrosis in chronic hepatitis B | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0168-8278&volume=47&issue=2&spage=191&epage=202&date=2007&atitle=Serum+adiponectin+is+increased+in+advancing+liver+fibrosis+and+declines+with+reduction+in+fibrosis+in+chronic+hepatitis+B | en_HK |
dc.identifier.email | Lee, NP: nikkilee@hku.hk | en_HK |
dc.identifier.email | Lo, CM: chungmlo@hkucc.hku.hk | en_HK |
dc.identifier.email | Fan, ST: stfan@hku.hk | en_HK |
dc.identifier.email | Luk, JM: jmluk@hkucc.hku.hk | en_HK |
dc.identifier.email | Xu, A: amxu@hkucc.hku.hk | en_HK |
dc.identifier.email | Lam, KS: ksllam@hku.hk | en_HK |
dc.identifier.email | Kwong, YL: ylkwong@hku.hk | en_HK |
dc.identifier.authority | Lee, NP=rp00263 | en_HK |
dc.identifier.authority | Lo, CM=rp00412 | en_HK |
dc.identifier.authority | Fan, ST=rp00355 | en_HK |
dc.identifier.authority | Luk, JM=rp00349 | en_HK |
dc.identifier.authority | Xu, A=rp00485 | en_HK |
dc.identifier.authority | Lam, KS=rp00343 | en_HK |
dc.identifier.authority | Kwong, YL=rp00358 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jhep.2007.02.023 | en_HK |
dc.identifier.pmid | 17462782 | - |
dc.identifier.scopus | eid_2-s2.0-34347389866 | en_HK |
dc.identifier.hkuros | 133098 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34347389866&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 47 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 191 | en_HK |
dc.identifier.epage | 202 | en_HK |
dc.identifier.isi | WOS:000248642400006 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Hui, CK=35082057900 | en_HK |
dc.identifier.scopusauthorid | Zhang, HY=8965962000 | en_HK |
dc.identifier.scopusauthorid | Lee, NP=7402722690 | en_HK |
dc.identifier.scopusauthorid | Chan, W=55040807500 | en_HK |
dc.identifier.scopusauthorid | Yueng, YH=8965962100 | en_HK |
dc.identifier.scopusauthorid | Leung, KW=23097859100 | en_HK |
dc.identifier.scopusauthorid | Lu, L=26326922300 | en_HK |
dc.identifier.scopusauthorid | Leung, N=26643107200 | en_HK |
dc.identifier.scopusauthorid | Lo, CM=7401771672 | en_HK |
dc.identifier.scopusauthorid | Fan, ST=7402678224 | en_HK |
dc.identifier.scopusauthorid | Luk, JM=7006777791 | en_HK |
dc.identifier.scopusauthorid | Xu, A=7202655409 | en_HK |
dc.identifier.scopusauthorid | Lam, KS=8082870600 | en_HK |
dc.identifier.scopusauthorid | Kwong, YL=7102818954 | en_HK |
dc.identifier.scopusauthorid | Lau, GKK=7102301257 | en_HK |
dc.identifier.issnl | 0168-8278 | - |