Rodriguez-Frias F, Jardi R, Buti M, Schaper M, Hermosilla E, Valdes A, Allende H, Martell M, Esteban R, Guardia J
Department of Biochemistry, Hospital Universitario Vall d'Hebron, Barcelona, Spain.
J Viral Hepat. 2006 May;13(5):343-50. doi: 10.1111/j.1365-2893.2005.00691.x.
This study aims to determine the prevalence of hepatitis B virus (HBV) genotypes (A-F) and their association with the G1896A precore mutation in 486 patients positive for HBV surface antigen. Genotypes were determined by RFLP and precore mutation by real-time PCR. Genotypes D (48.1%) and A (39.5%) were the most common, followed by F (4.1%) and B, C and E (<1%). The A to D ratio (A:D) was 1.4 in HBeAg+ chronic hepatitis B (CHB), 0.6 in HBeAg- CHB and 1.4 in HBeAg- inactive carriers. Distribution of these genotypes was different between HBeAg+ CHB and HBeAg- CHB (P = 0.02), and between HBeAg- CHB and HBeAg- inactive carriers (P = 0.009). Genotype A was the most prevalent in HBeAg+ CHB with elevated alanine aminotransferase (ALT) (68.6%) and genotype D in HBeAg+ CHB with fluctuating ALT (60.7%). There was a difference in genotype prevalence between chronic and acute infection (P = 0.03). The precore mutant correlated with high levels of HBV-DNA in genotype d HBeAg- CHB. Genotype D is not as highly prevalent in Spanish patients as would be expected in a Mediterranean area. The unequal prevalence of genotypes between acute and chronic infection suggests that genotype A is associated with a higher tendency to cause chronic infection.
本研究旨在确定486例乙肝表面抗原阳性患者中乙型肝炎病毒(HBV)基因型(A - F)的流行情况及其与G1896A前核心突变的关联。通过限制性片段长度多态性(RFLP)确定基因型,通过实时聚合酶链反应(PCR)确定前核心突变。基因型D(48.1%)和A(39.5%)最为常见,其次是F(4.1%)以及B、C和E(<1%)。在HBeAg阳性的慢性乙型肝炎(CHB)中A与D的比例(A:D)为1.4,在HBeAg阴性的CHB中为0.6,在HBeAg阴性的非活动性携带者中为1.4。这些基因型的分布在HBeAg阳性CHB和HBeAg阴性CHB之间存在差异(P = 0.02),在HBeAg阴性CHB和HBeAg阴性非活动性携带者之间也存在差异(P = 0.009)。在丙氨酸氨基转移酶(ALT)升高的HBeAg阳性CHB中,基因型A最为普遍(68.6%),而在ALT波动的HBeAg阳性CHB中,基因型D最为普遍(60.7%)。慢性感染和急性感染之间的基因型流行情况存在差异(P = 0.03)。在前核心突变体与基因型D的HBeAg阴性CHB中高水平的HBV - DNA相关。基因型D在西班牙患者中的流行率不像在地中海地区预期的那么高。急性感染和慢性感染之间基因型的不均衡流行表明基因型A与导致慢性感染的更高倾向相关。