A case-control study for differences among hepatitis B virus infections of genotypes A (Subtypes Aa and Ae) and D

被引:131
作者
Tanaka, Y
Hasegawa, I
Kato, T
Orito, E
Hirashima, N
Acharya, SK
Gish, RG
Kramvis, A
Kew, MC
Yoshihara, N
Shrestha, SM
Khan, M
Miyakawa, Y
Mizokami, M [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Clin Mol Informat Med, Nagoya, Aichi 4678601, Japan
[2] Nagoya City Univ, Grad Sch Med Sci, Dept Internal Med & Mol Sci, Nagoya, Aichi, Japan
[3] Chukyo Hosp, Dept Gastroenterol, Nagoya, Aichi, Japan
[4] All India Inst Med Sci, Dept Gastroenterol, New Delhi, India
[5] Calif Pacific Med Ctr, San Francisco, CA USA
[6] Univ Witwatersrand, Dept Med, Univ Mol Hepatol Res Unit, MRC,CANSA, ZA-2001 Johannesburg, South Africa
[7] Natl Inst Hlth, AIDS Res Ctr, Tokyo 141, Japan
[8] Liver Fdn, Kathmandu, Nepal
[9] Bangabandhu Sheikh Mujib Med Univ, Dept Hepatol, Dhaka, Bangladesh
[10] Miyakawa Mem Res Fdn, Tokyo, Japan
关键词
D O I
10.1002/hep.20365
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
There are two subtypes of hepatitis B virus genotype A (HBV/A) and they are provisionally designated Aa ("a" standing for Africa/Asia) and Ae ("e" for Europe). In a case-control study, 78 HBV/Aa, 78HBV/Ae, and 78HBV/D carriers from several countries were compared. The prevalence of HBe antigen (HBeAg) in serum was significantly lower in carriers of HBV/Aa than in carriers of HBV/Ae (31% vs. 49%; P =.033), with a difference more obvious in the carriers aged 30 years or younger (34% vs. 67%; P =.029). HBV DNA levels in the carriers of HBV/Aa (median, 3.46 log copies/mL; 95% Cl, 2.93-3.95) were significantly lower than those of carriers of HBV/Ae (6.09 log copies/mL; 95% Cl, 4.24-7.64) or of carriers of HBV/D (5.48 log copies/ nil, 95% CI, 4.06-7.02), regardless of the HBeAg status (P <.001). The most specific and frequent substitutions in 54 HBV/Aa isolates were double substitutions for T1809 (100%) and T1812 (96%) immediately upstream of the precore initiation codon, which would interfere with the translation of HBeAg in HBV/Aa infections. They were not detected in 57 HBV/Ae or 61 HBV/D isolates examined. The double mutation in the core promoter (T1762/A1764) was more frequent in both HBV/Aa (50%) and HBV/Ae (44%) than in HBV/D isolates (25%; P <.01), whereas the precore mutation (A1896) occurred in HBV/D isolates only (48%; P <.0001). I conclusion, the clearance of HBeAg from serum may occur by different mechanisms in HBV/Aa, HBV/Ae, and HBV/D infections, which may influence clinical manifestations in the Western countries where both genotypes A and D are prevalent.
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页码:747 / 755
页数:9
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