Serum fibrinogen alpha C‐chain 5.9 kDa fragment as a biomarker for early detection of hepatic fibrosis related to hepatitis C virus. Issue 5 (17th May 2013)
- Record Type:
- Journal Article
- Title:
- Serum fibrinogen alpha C‐chain 5.9 kDa fragment as a biomarker for early detection of hepatic fibrosis related to hepatitis C virus. Issue 5 (17th May 2013)
- Main Title:
- Serum fibrinogen alpha C‐chain 5.9 kDa fragment as a biomarker for early detection of hepatic fibrosis related to hepatitis C virus
- Authors:
- Sogawa, Kazuyuki
Noda, Kenta
Umemura, Hiroshi
Seimiya, Masanori
Kuga, Takahisa
Tomonaga, Takeshi
Nishimura, Motoi
Kanai, Fumihiko
Imazeki, Fumio
Takizawa, Hirotaka
Yoneda, Masato
Nakajima, Atsushi
Tsutsumi, Mikihiro
Yokosuka, Osamu
Nomura, Fumio
Semmes, O. John
Conrads, Thomas P. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="prca1461-sec-0010" sec-type="section"> <title>Purpose</title> <p>Clinical application of biomarker candidates discovered by proteomic analysis is challenging. The purpose of this study was to standardize preanalytical conditions for measurement of serum levels of fibrinogen alpha C‐chain 5.9 kDa fragment (FIC 5.9) and to test the diagnostic value of this peptide for detection of early hepatic fibrosis in patients with hepatitis C virus (HCV)‐related chronic hepatitis.</p> </sec> <sec id="prca1461-sec-0020" sec-type="section"> <title>Experimental design</title> <p>Serum FIC 5.9 levels were measured by a sandwich ELISA. Effects on the serum FIC 5.9 level of temperature, the time between venipuncture and serum separation, and the types of collection tubes used were examined. The diagnostic value of serum FIC 5.9 as an early indicator of hepatic fibrosis due to HCV was then assessed.</p> </sec> <sec id="prca1461-sec-0030" sec-type="section"> <title>Results</title> <p>FIC 5.9 was produced in a time‐ and temperature‐dependent manner after venipuncture. Abnormal FIC 5.9 values were found in 89.5% of FI stage patients. Receiver operating characteristic analyses confirmed the superiority of FIC 5.9 over other conventional markers for early detection of fibrosis.</p> </sec> <sec id="prca1461-sec-0040" sec-type="section"> <title>Conclusions and clinical relevance</title> <p>The serum FIC 5.9<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="prca1461-sec-0010" sec-type="section"> <title>Purpose</title> <p>Clinical application of biomarker candidates discovered by proteomic analysis is challenging. The purpose of this study was to standardize preanalytical conditions for measurement of serum levels of fibrinogen alpha C‐chain 5.9 kDa fragment (FIC 5.9) and to test the diagnostic value of this peptide for detection of early hepatic fibrosis in patients with hepatitis C virus (HCV)‐related chronic hepatitis.</p> </sec> <sec id="prca1461-sec-0020" sec-type="section"> <title>Experimental design</title> <p>Serum FIC 5.9 levels were measured by a sandwich ELISA. Effects on the serum FIC 5.9 level of temperature, the time between venipuncture and serum separation, and the types of collection tubes used were examined. The diagnostic value of serum FIC 5.9 as an early indicator of hepatic fibrosis due to HCV was then assessed.</p> </sec> <sec id="prca1461-sec-0030" sec-type="section"> <title>Results</title> <p>FIC 5.9 was produced in a time‐ and temperature‐dependent manner after venipuncture. Abnormal FIC 5.9 values were found in 89.5% of FI stage patients. Receiver operating characteristic analyses confirmed the superiority of FIC 5.9 over other conventional markers for early detection of fibrosis.</p> </sec> <sec id="prca1461-sec-0040" sec-type="section"> <title>Conclusions and clinical relevance</title> <p>The serum FIC 5.9 level may be an early indicator of hepatic fibrosis in HCV‐related chronic liver diseases. This study provides an example of a pipeline from biomarker discovery by proteome analysis to assay optimization and preliminary clinical validation.</p> </sec> </abstract> … (more)
- Is Part Of:
- Proteomics. Volume 7:Issue 5/6(2013)
- Journal:
- Proteomics
- Issue:
- Volume 7:Issue 5/6(2013)
- Issue Display:
- Volume 7, Issue 5/6 (2013)
- Year:
- 2013
- Volume:
- 7
- Issue:
- 5/6
- Issue Sort Value:
- 2013-0007-NaN-0000
- Page Start:
- 424
- Page End:
- 431
- Publication Date:
- 2013-05-17
- Subjects:
- Proteomics -- Periodicals
572.605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1862-8354 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/prca.201200094 ↗
- Languages:
- English
- ISSNs:
- 1862-8346
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.178500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3115.xml