Molecular tracing of the global hepatitis C virus epidemic predicts regional patterns of hepatocellular carcinoma mortality

被引:91
作者
Tanaka, Y
Kurbanov, F
Mano, S
Orito, E
Vargas, V
Esteban, JI
Yuen, MF
Lai, CL
Kramvis, A
Kew, MC
Smuts, HE
Netesov, SV
Alter, HJ
Mizokami, M [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Clin Mol Informat Med, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Nagoya City Univ, Grad Sch Nat Sci, Nagoya, Aichi, Japan
[3] Nagoya City Univ, Grad Sch Med Sci, Dept Internal Med & Mol Sci, Nagoya, Aichi 4678601, Japan
[4] Hosp Gen Univ Vall Hebron, Dept Internal Med, Barcelona, Spain
[5] Univ Hong Kong, Queen Mary Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
[6] Univ Witwatersrand, Dept Med, Univ Mol Hepatol Res Unit, MRC CANSA, ZA-2001 Johannesburg, South Africa
[7] Univ Cape Town, Natl Hlth Lab Serv, Div Med Virol, ZA-7925 Cape Town, South Africa
[8] VECTOR Koltsovo, State Res Ctr Virol & Biotechnol, Novosibirsk, Russia
[9] NIH, Warren Grant Magnuson Clin Ctr, Dept Transfus Med, Bethesda, MD 20892 USA
关键词
D O I
10.1053/j.gastro.2006.01.032
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Molecular evolutionary analysis based on coalescent theory can provide important insights into epidemiologic processes worldwide. This approach was combined with analyses of the hepatitis C virus (HCV) epidemiologic-historical background and HCV-related hepatocellular carcinoma (HCC) in different countries. Methods: The HCV gene sequences of :13:1 genotype 1b (HCV-1b) strains from Japan, 38 HCV-1a strains from the United States, 33 HCV-1b strains from Spain, 27 HCV-3a strains from the former Soviet Union (FSU), 47 HCV-4a strains from Egypt, 25 HCV-5a strains from South Africa, and 24 HCV-6a strains from Hong Kong isolated in this study and previous studies were analyzed. Results: The coalescent analysis indicated that a transition from constant size to rapid exponential growth (spread time) occurred in Japan in the 1920s (HCV-1b), but not until the 1940s for the same genotype in Spain and other European countries. The spread time of HCV-1a in the United States was estimated to be in the 1960s; HCV-3a in the FSU, HCV-5a in South Africa, and HCV-6a in Hong Kong in the 1960s, mid-1950s, and late 1970s, respectively. Three different linear progression curves were determined by analysis of the relationship between HCV seroprevalence and HCC mortality in different geographic regions; a steep ascent indicated the greatest progression to HCC in Japan, a near horizontal line indicated the least progression in the United States and the FSU, and an intermediate slope was observed in Europe. Conclusions: These findings strongly suggest that the initial spread time of HCV is associated with the progression dynamics of HCC in each area, irrespective of genotype.
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页码:703 / 714
页数:12
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