“…Genotype B is associated with milder disease, is more likely to be HBeAg negative and have less risk of development of hepatocellular carcinoma compared to genotype C. [4][5][6] The studies comparing the clinical outcomes and clinical severity of the disease between genotypes A and D have presented conflicting results without any clear result on which genotype is associated with more severe disease. 1 There is a gradation of e-antigen clearance/e-antigen seroconversion response when treated with pegylated interferon (IFN) according to the genotypes: SVR was 44.3%, 31.5%, 29.1%, and 24.4% among genotypes A-D-infected patients, respectively. In addition, long-term HBsAg loss/seroconversion was also significantly higher among genotype A infected chronic hepatitis B patients [both e-antigen-positive (15.3%, 1.7%, 2.2%, and 1.6% for genotypes A-D, respectively) and e-antigen-negative (20%, 6%, 9%, and 6% for genotypes A-D, respectively)] when treated with pegylated IFNs.…”