Article: A new model using routinely available clinical parameters to predict significant liver fibrosis in chronic hepatitis B
| Title | A new model using routinely available clinical parameters to predict significant liver fibrosis in chronic hepatitis B |
|---|---|
| Authors | Seto, WK3 Lee, CF1 2 Lai, CL3 Ip, PPC3 Fong, YT3 Fung, J3 Wong, KH3 Yuen, MF3 |
| Issue Date | 2011 |
| Publisher | Public Library of Science. The Journal's web site is located at http://www.plosone.org/home.action |
| Citation | Plos One, 2011, v. 6 n. 8 [How to Cite?] DOI: http://dx.doi.org/10.1371/journal.pone.0023077 |
| Abstract | Objective: We developed a predictive model for significant fibrosis in chronic hepatitis B (CHB) based on routinely available clinical parameters. Methods: 237 treatment-naïve CHB patients [58.4% hepatitis B e antigen (HBeAg)-positive] who had undergone liver biopsy were randomly divided into two cohorts: training group (n = 108) and validation group (n = 129). Liver histology was assessed for fibrosis. All common demographics, viral serology, viral load and liver biochemistry were analyzed. Results: Based on 12 available clinical parameters (age, sex, HBeAg status, HBV DNA, platelet, albumin, bilirubin, ALT, AST, ALP, GGT and AFP), a model to predict significant liver fibrosis (Ishak fibrosis score ≥3) was derived using the five best parameters (age, ALP, AST, AFP and platelet). Using the formula log(index+1) = 0.025+0.0031(age)+0.1483 log(ALP)+0.004 log(AST)+0.0908 log(AFP+1)-0.028 log(platelet), the PAPAS (Platelet/Age/Phosphatase/AFP/AST) index predicts significant fibrosis with an area under the receiving operating characteristics (AUROC) curve of 0.776 [0.797 for patients with ALT <2×upper limit of normal (ULN)] The negative predictive value to exclude significant fibrosis was 88.4%. This predictive power is superior to other non-invasive models using common parameters, including the AST/platelet/GGT/AFP (APGA) index, AST/platelet ratio index (APRI), and the FIB-4 index (AUROC of 0.757, 0.708 and 0.723 respectively). Using the PAPAS index, 67.5% of liver biopsies for patients being considered for treatment with ALT <2×ULN could be avoided. Conclusion: The PAPAS index can predict and exclude significant fibrosis, and may reduce the need for liver biopsy in CHB patients. © 2011 Seto et al. |
| ISSN | 1932-6203 2011 Impact Factor: 4.092 2011 SCImago Journal Rankings: 0.519 |
| DOI | http://dx.doi.org/10.1371/journal.pone.0023077 |
| PubMed Central ID | PMC3154931 |
| References | References in Scopus |
| dc.contributor.author | Seto, WK |
|---|---|
| dc.contributor.author | Lee, CF |
| dc.contributor.author | Lai, CL |
| dc.contributor.author | Ip, PPC |
| dc.contributor.author | Fong, YT |
| dc.contributor.author | Fung, J |
| dc.contributor.author | Wong, KH |
| dc.contributor.author | Yuen, MF |
| dc.date.accessioned | 2011-10-28T02:44:55Z |
| dc.date.available | 2011-10-28T02:44:55Z |
| dc.date.issued | 2011 |
| dc.description.abstract | Objective: We developed a predictive model for significant fibrosis in chronic hepatitis B (CHB) based on routinely available clinical parameters. Methods: 237 treatment-naïve CHB patients [58.4% hepatitis B e antigen (HBeAg)-positive] who had undergone liver biopsy were randomly divided into two cohorts: training group (n = 108) and validation group (n = 129). Liver histology was assessed for fibrosis. All common demographics, viral serology, viral load and liver biochemistry were analyzed. Results: Based on 12 available clinical parameters (age, sex, HBeAg status, HBV DNA, platelet, albumin, bilirubin, ALT, AST, ALP, GGT and AFP), a model to predict significant liver fibrosis (Ishak fibrosis score ≥3) was derived using the five best parameters (age, ALP, AST, AFP and platelet). Using the formula log(index+1) = 0.025+0.0031(age)+0.1483 log(ALP)+0.004 log(AST)+0.0908 log(AFP+1)-0.028 log(platelet), the PAPAS (Platelet/Age/Phosphatase/AFP/AST) index predicts significant fibrosis with an area under the receiving operating characteristics (AUROC) curve of 0.776 [0.797 for patients with ALT <2×upper limit of normal (ULN)] The negative predictive value to exclude significant fibrosis was 88.4%. This predictive power is superior to other non-invasive models using common parameters, including the AST/platelet/GGT/AFP (APGA) index, AST/platelet ratio index (APRI), and the FIB-4 index (AUROC of 0.757, 0.708 and 0.723 respectively). Using the PAPAS index, 67.5% of liver biopsies for patients being considered for treatment with ALT <2×ULN could be avoided. Conclusion: The PAPAS index can predict and exclude significant fibrosis, and may reduce the need for liver biopsy in CHB patients. © 2011 Seto et al. |
| dc.description.nature | published_or_final_version |
| dc.identifier.citation | Plos One, 2011, v. 6 n. 8 [How to Cite?] DOI: http://dx.doi.org/10.1371/journal.pone.0023077 |
| dc.identifier.doi | http://dx.doi.org/10.1371/journal.pone.0023077 |
| dc.identifier.epage | e23077 |
| dc.identifier.hkuros | 196658 |
| dc.identifier.hkuros | 213690 |
| dc.identifier.isi | WOS:000293953400025 |
| dc.identifier.issn | 1932-6203 2011 Impact Factor: 4.092 2011 SCImago Journal Rankings: 0.519 |
| dc.identifier.issue | 8 |
| dc.identifier.pmcid | PMC3154931 |
| dc.identifier.pmid | 21853071 |
| dc.identifier.scopus | eid_2-s2.0-80051604371 |
| dc.identifier.spage | e23077 |
| dc.identifier.uri | http://hdl.handle.net/10722/142388 |
| dc.identifier.volume | 6 |
| dc.language | eng |
| dc.publisher | Public Library of Science. The Journal's web site is located at http://www.plosone.org/home.action |
| dc.publisher.place | United States |
| dc.relation.ispartof | PLoS ONE |
| dc.relation.references | References in Scopus |
| dc.subject.mesh | Hepatitis B, Chronic - complications - diagnosis |
| dc.subject.mesh | Liver Cirrhosis - complications - diagnosis |
| dc.subject.mesh | Models, Biological |
| dc.subject.mesh | Predictive Value of Tests |
| dc.subject.mesh | Reproducibility of Results |
| dc.title | A new model using routinely available clinical parameters to predict significant liver fibrosis in chronic hepatitis B |
| dc.type | Article |
Author Affiliations
- Duke-NUS Graduate Medical School Singapore
- Singapore Clinical Research Institute
- The University of Hong Kong

