 Use 
                of ribavirin in combination with pegylated interferon reduces 
                the risk of HCV relapse and improves the likelihood of achieving 
                sustained virological response (SVR) to treatment for chronic 
                hepatitis C. Ribavirin doses are typically adjusted according 
                to weight, especially for people with HCV genotype 1, usually 
                ranging from 800 or 1000 to 1200 or 1400 mg/day.
Use 
                of ribavirin in combination with pegylated interferon reduces 
                the risk of HCV relapse and improves the likelihood of achieving 
                sustained virological response (SVR) to treatment for chronic 
                hepatitis C. Ribavirin doses are typically adjusted according 
                to weight, especially for people with HCV genotype 1, usually 
                ranging from 800 or 1000 to 1200 or 1400 mg/day.
                
                Many previous studies have found that body weight or BMI predicts 
                treatment outcomes, with heavier people being less likely to achieve 
                SVR. While obesity and related metabolic problems are known to 
                have an effect on hepatitis C and liver health in general, poorer 
                treatment response among heavier patients may also indicate that 
                they did not receive enough ribavirin to do the job.
                
                To further explore this issue, Jenny Heathcote from the University 
                of Toronto and colleagues conducted a study to determine whether 
                patient weight influences early viral kinetics (changes in HCV 
                levels soon after starting therapy) and subsequent SVR.
                
                This retrospective analysis included 134 chronic hepatitis C patients 
                -- 57% with hard-to-treat HCV genotype 1 -- who received pegyalted 
                interferon plus ribavirin. The average BMI was 26.7 (classified 
                as overweight) and the average ribavirin dose was 13.9 mg/kg/day.
                
                The researchers looked at HCV viral load measurements taken at 
                week 4 of treatment using 2 tests with different sensitivities. 
                The first RVR assessment used a PCR test with a limit of detection 
                of 50 IU/mL. Heathcote's team later re-tested stored blood samples 
                using the Taqman assay with a lower limit of 15 IU/mL.
                
                Results 
                 
                   
                    |  | Overall, 
                      59% of study participants achieved SVR, or continued undetectable 
                      HCV viral load 6 months after completing treatment. | 
                   
                    |  | 39.6% 
                      of these patients achieved RVR at week 4 according to the 
                      50 IU/mL test. | 
                   
                    |  | Fewer 
                      patients -- 27.6% -- achieved RVR according to the more 
                      sensitive 15 IU/mL assay. | 
                   
                    |  | Neither 
                      body weight nor BMI influenced likelihood SVR or RVR by 
                      either test. | 
                   
                    |  | The 
                      positive predictive value of RVR for SVR was 88.7% for the 
                      50 IU/mL test and 97.3% for the 15 IU/mL test. | 
                   
                    |  | RVR 
                      according to either the 50 or 15 IU/mL cutoff was a better 
                      independent predictor of SVR that HCV genotype and viral 
                      load. | 
                
                "RVR 
                  is the strongest predictor of SVR," the study authors concluded. 
                  "Early viral kinetics is not influenced by body weight 
                  or BMI when weight-based ribavirin is prescribed."
                  
                  Investigator affiliations: Department of Medicine, Toronto Western 
                  Hospital, University Health Network, Toronto, ON, Canada; University 
                  of Sydney, Sydney, NSW, Australia; Division of Gastroenterology 
                  and Department of Microbiology, Laboratory Medicine & Pathobiology, 
                  Mt. Sinai Hospital, University of Toronto, Toronto, ON, Canada
                  
                  1/25/11
                Reference
                  V Pattullo, NC Ravindran, T Mazzulli, DK Wong, and EJ Heathcote. 
                  Pegylated interferon plus optimized weight-based ribavirin dosing 
                  negate the influence of weight and body mass index on early 
                  viral kinetics and sustained virological response in chronic 
                  hepatitis C. Journal of Viral Hepatitis 17(12): 834-838 
                  (Abstract). 
                  December 2010.