HIV/HBV 
                            Coinfected Patients with Elevated ALT and AST Are 
                            at Greater Risk for Liver Disease Progression
                          
                          By 
                            Liz Highleyman
                            
                             Due 
                            to overlapping risk factors, many people are coinfected 
                            with both HIV and 
                            HBV. Research suggests 
                            that such individuals tend to experience more rapid 
                            liver disease, but the natural history of disease 
                            in this population is not fully understood.
Due 
                            to overlapping risk factors, many people are coinfected 
                            with both HIV and 
                            HBV. Research suggests 
                            that such individuals tend to experience more rapid 
                            liver disease, but the natural history of disease 
                            in this population is not fully understood.
                            
                            P. Sellier and colleagues from France performed a 
                            study to characterize liver-related morbidity, mortality, 
                            and related risk factors in 107 HIV/HBV coinfected 
                            patients. A majority (61%) were from sub-Saharan Africa, 
                            while most of the rest (33%) were European. With regard 
                            to hepatitis B management, 78% were treated with lamivudine 
                            (3TC, Epivir-HBV) and 44% underwent liver biopsies.
                            
                            The researchers collected clinical, biological, and 
                            virological data every 3 months. Liver-related mortality 
                            and a composite score were used to define advanced 
                            liver disease. 
                            
                             
                            Results
                          
                             
                              |  | 19 
                                of the 107 patients (18%) were diagnosed with 
                                advanced liver disease during a mean follow-up 
                                period of 4.8 years: | 
                             
                              |  | 
                                   
                                    |  | 10 
                                      with extensive fibrosis; |   
                                    |  | 5 
                                      with cirrhosis; |   
                                    |  | 3 
                                      with hepatocellular carcinoma resulting 
                                      from cirrhosis; |   
                                    |  | 1 
                                      with fulminant hepatitis following lamivudine 
                                      discontinuation. |  | 
                             
                              |  | 11 
                                patients died overall, 4 of them from HBV-related 
                                liver disease. | 
                             
                              |  | In 
                                a univariate analysis, factors associated with 
                                increased risk of advanced liver disease were 
                                male sex, higher mean HIV and HBV viral loads, 
                                and elevated levels of alanine and aspartate transaminase 
                                (ALT and AST). | 
                             
                              |  | In 
                                a multivariate analysis adjusting for other factors, 
                                the strongest associations were mean AST level 
                                and cumulative time on lamivudine. | 
                             
                              |  | 39% 
                                of patients with elevated mean AST developed advanced 
                                liver disease, compared with just 7% of those 
                                with normal mean AST (relative risk 5.5). | 
                          
                           
                            "During HIV/HBV coinfection, transaminase levels 
                            are strongly associated with advanced liver disease," 
                            the study authors wrote. "Normal mean AST has 
                            a high negative predictive value, contrary to previously 
                            reported data in HIV/HCV patients."
                            
                            Elevated ALT and AST are biomarkers of liver inflammation, 
                            not fibrosis. Other researchers have shown that hepatitis 
                            B monoinfected, hepatitis C monoinfected, and HIV/HCV 
                            coinfected patients may develop advanced liver damage 
                            despite persistently normal ALT levels.
                            
                            Service de Médecine Interne, Service de 
                            Bactériologie - Virologie & Centre d'Informations 
                            et de Soins de l'Immunodéficience Humaine, 
                            A, Hôpital Lariboisière, Assistance Publique-Hôpitaux 
                            de Paris, Paris, France; Immeuble SCOR, 1, avenue 
                            du General de Gaulle, Paris la Défense Cedex, 
                            France.
                            
                            1/19/10
                          Reference
                            P Sellier, N Schnepf, I Jarrin, and others. Description 
                            of liver disease in a cohort of HIV/HBV coinfected 
                            patients. Journal of Clinical Virology 47(1): 
                            13-17 (Abstract). 
                            January 2010.