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Article: Plasma fibronectin levels identified via quantitative proteomics profiling predicts hepatitis B surface antigen seroclearance in chronic hepatitis B

TitlePlasma fibronectin levels identified via quantitative proteomics profiling predicts hepatitis B surface antigen seroclearance in chronic hepatitis B
Authors
KeywordsBiomarker
Functional cure
HBsAg
HBV
iTRAQ
Issue Date2019
PublisherOxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org
Citation
The Journal of Infectious Diseases, 2019, v. 220 n. 6, p. 940-950 How to Cite?
AbstractBackground: Seroclearance of hepatitis B surface antigen (HBsAg) is a potentially achievable target of chronic hepatitis B (CHB). Plasma proteins relevant to HBsAg seroclearance remain undetermined. Methods: We prospectively recruited treatment-naive CHB patients with spontaneous HBsAg seroclearance and matched HBsAg-positive controls. Plasma protein profiling was performed using isobaric tags for relative and absolute quantitation-based proteomics, with the expression of candidate proteins validated in a separate cohort. The predictive value of fibronectin was assessed at 3 years, 1 year (Year -1) before, and at the time (Year 0) of HBsAg seroclearance. Results: Four hundred eighty-seven plasma proteins were identified via proteomics, with 97 proteins showing altered expression. In the verification cohort (n = 90), median plasma fibronectin levels in patients with HBsAg seroclearance was higher than in controls (P = .009). In the longitudinal cohort (n = 164), patients with HBsAg seroclearance, compared with controls, had a higher median fibronectin levels at Year -1 (413.26 vs 227.95 µg/mL) and Year 0 (349.45 vs 208.72 µg/mL) (both P < .001). In patients with an annual HBsAg log reduction >0.5, Year -1 fibronectin level achieved an area under the receiving operator characteristic of 0.884 in predicting HBsAg seroclearance. Conclusions: Using proteomics-based technology, plasma fibronectin may be associated with HBsAg seroclearance and a potential predictor of “functional cure”.
Persistent Identifierhttp://hdl.handle.net/10722/270088
ISSN
2021 Impact Factor: 7.759
2020 SCImago Journal Rankings: 2.690
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiu, F-
dc.contributor.authorSeto, WK-
dc.contributor.authorWong, DKH-
dc.contributor.authorHuang, FY-
dc.contributor.authorCheung, KS-
dc.contributor.authorMak, LY-
dc.contributor.authorSharma, R-
dc.contributor.authorZhang, S-
dc.contributor.authorFung, J-
dc.contributor.authorLai, CL-
dc.contributor.authorYuen, MF-
dc.date.accessioned2019-05-20T05:09:18Z-
dc.date.available2019-05-20T05:09:18Z-
dc.date.issued2019-
dc.identifier.citationThe Journal of Infectious Diseases, 2019, v. 220 n. 6, p. 940-950-
dc.identifier.issn0022-1899-
dc.identifier.urihttp://hdl.handle.net/10722/270088-
dc.description.abstractBackground: Seroclearance of hepatitis B surface antigen (HBsAg) is a potentially achievable target of chronic hepatitis B (CHB). Plasma proteins relevant to HBsAg seroclearance remain undetermined. Methods: We prospectively recruited treatment-naive CHB patients with spontaneous HBsAg seroclearance and matched HBsAg-positive controls. Plasma protein profiling was performed using isobaric tags for relative and absolute quantitation-based proteomics, with the expression of candidate proteins validated in a separate cohort. The predictive value of fibronectin was assessed at 3 years, 1 year (Year -1) before, and at the time (Year 0) of HBsAg seroclearance. Results: Four hundred eighty-seven plasma proteins were identified via proteomics, with 97 proteins showing altered expression. In the verification cohort (n = 90), median plasma fibronectin levels in patients with HBsAg seroclearance was higher than in controls (P = .009). In the longitudinal cohort (n = 164), patients with HBsAg seroclearance, compared with controls, had a higher median fibronectin levels at Year -1 (413.26 vs 227.95 µg/mL) and Year 0 (349.45 vs 208.72 µg/mL) (both P < .001). In patients with an annual HBsAg log reduction >0.5, Year -1 fibronectin level achieved an area under the receiving operator characteristic of 0.884 in predicting HBsAg seroclearance. Conclusions: Using proteomics-based technology, plasma fibronectin may be associated with HBsAg seroclearance and a potential predictor of “functional cure”.-
dc.languageeng-
dc.publisherOxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org-
dc.relation.ispartofThe Journal of Infectious Diseases-
dc.rightsThis is a pre-copyedited, author-produced version of an article accepted for publication in The Journal of Infectious Diseases following peer review. The version of record The Journal of Infectious Diseases, 2019, v. 220 n. 6, p. 940-950 is available online at: https://doi.org/10.1093/infdis/jiz223-
dc.subjectBiomarker-
dc.subjectFunctional cure-
dc.subjectHBsAg-
dc.subjectHBV-
dc.subjectiTRAQ-
dc.titlePlasma fibronectin levels identified via quantitative proteomics profiling predicts hepatitis B surface antigen seroclearance in chronic hepatitis B-
dc.typeArticle-
dc.identifier.emailSeto, WK: wkseto@hku.hk-
dc.identifier.emailWong, DKH: danywong@hku.hk-
dc.identifier.emailHuang, FY: fungyu@hkucc.hku.hk-
dc.identifier.emailCheung, KS: cks634@hku.hk-
dc.identifier.emailMak, LY: lungyi@hku.hk-
dc.identifier.emailSharma, R: rasharma@hku.hk-
dc.identifier.emailFung, J: jfung@hkucc.hku.hk-
dc.identifier.emailLai, CL: hrmelcl@hkucc.hku.hk-
dc.identifier.emailYuen, MF: mfyuen@hku.hk-
dc.identifier.authoritySeto, WK=rp01659-
dc.identifier.authorityWong, DKH=rp00492-
dc.identifier.authorityCheung, KS=rp02532-
dc.identifier.authorityMak, LY=rp02668-
dc.identifier.authorityFung, J=rp00518-
dc.identifier.authorityLai, CL=rp00314-
dc.identifier.authorityYuen, MF=rp00479-
dc.description.naturepostprint-
dc.identifier.doi10.1093/infdis/jiz223-
dc.identifier.pmid31056649-
dc.identifier.scopuseid_2-s2.0-85071350128-
dc.identifier.hkuros297818-
dc.identifier.volume220-
dc.identifier.issue6-
dc.identifier.spage940-
dc.identifier.epage950-
dc.identifier.isiWOS:000490985400004-
dc.publisher.placeUnited States-
dc.identifier.issnl0022-1899-

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