Serum markers for predicting significant necroinflammatory activity in patients with chronic hepatitis B

The aim of this study was to determine the serum markers that predict significant inflammation in patients with chronic hepatitis B (CHB). Between October 2005 and June 2009, 384 subjects with CHB were enrolled. Multiple logistic regression analysis identified the ALT, hyaluronic acid (HA) and proco...

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Veröffentlicht in:Clinical biochemistry 2012-12, Vol.45 (18), p.1564-1567
Hauptverfasser: Cho, Hyo Jung, Kim, Soon Sun, Ahn, Seun Joo, Bae, Chang Bum, Kim, Han Gyeol, Kim, Young Jip, Lee, Seung Kyung, Song, Ga Won, Kim, Dong Joon, Hwang, Seong Gyu, Yang, Jin Mo, Kim, Young Bae, Park, Young Nyun, Cho, Sung Won, Cheong, Jae Youn
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Sprache:eng
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Zusammenfassung:The aim of this study was to determine the serum markers that predict significant inflammation in patients with chronic hepatitis B (CHB). Between October 2005 and June 2009, 384 subjects with CHB were enrolled. Multiple logistic regression analysis identified the ALT, hyaluronic acid (HA) and procollagen III N-terminal peptide (PIIINP) as independent predictors of significant inflammation (grade≥3). We constructed a formula for predicting significant inflammation. A significant inflammation (SI) score=1.773×ALT score+1.599×PIIINP score+0.677×HA score−1.962. The area under receiver operating characteristic curve of the SI score was 0.831. The sensitivity, specificity, positive predictive value and negative predictive value of the SI score were 79.5%, 70.8%, 76.8% and 74.3%, respectively. A simple scoring system including ALT, PIIINP and HA is an accurate non-invasive predictor of significant inflammatory activities in patients with CHB. ► ALT, HA and PIIINP as predictors of significant inflammation in chronic hepatitis B. ► We constructed a formula predicting significant inflammation in chronic hepatitis B. ► The area under receiver operating characteristic curve of the SI score was 0.831. ► A simple scoring system is an accurate predictor of significant inflammation.
ISSN:0009-9120
1873-2933
DOI:10.1016/j.clinbiochem.2012.07.107