4.5 Article

Temporal changes in HCV genotype distribution in three different high risk populations in San Francisco, California

期刊

BMC INFECTIOUS DISEASES
卷 11, 期 -, 页码 -

出版社

BIOMED CENTRAL LTD
DOI: 10.1186/1471-2334-11-208

关键词

hepatitis C virus; HCV; GT; injection drug use; HIV; birth cohort; African-American

资金

  1. U.S. National Institutes for Health (NIH) [R01-DA016017-03A1, U19-AI40034-13, K01-DA023365, UL1-RR024131, P30-AI27763, R01-DA09532, R01-DA12109, R01-DA13245, R01-DA021550, N01-CO-12400]
  2. Substance Abuse and Mental Health Services Administration [H79-TI12103]
  3. San Francisco Department of Public Health [POHC99001316]
  4. NIDA [2 R01 DA016017-03A1]

向作者/读者索取更多资源

Background: Hepatitis C virus (HCV) genotype (GT) has become an important measure in the diagnosis and monitoring of HCV infection treatment. In the United States (U. S.) HCV GT 1 is reported as the most common infecting GT among chronically infected patients. In Europe, however, recent studies have suggested that the epidemiology of HCV GTs is changing. Methods: We assessed HCV GT distribution in 460 patients from three HCV-infected high risk populations in San Francisco, and examined patterns by birth cohort to assess temporal trends. Multiple logistic regression was used to assess factors independently associated with GT 1 infection compared to other GTs (2, 3, and 4). Results: Overall, GT 1 was predominant (72.4%), however younger injection drug users (IDU) had a lower proportion of GT 1 infections (54.7%) compared to older IDU and HIV-infected patients (80.5% and 76.6%, respectively). Analysis by birth cohort showed increasing proportions of non-GT 1 infections associated with year of birth: birth before 1970 was independently associated with higher adjusted odds of GT 1: AOR 2.03 (95% CI: 1.23, 3.34). African-Americans as compared to whites also had higher adjusted odds of GT 1 infection (AOR: 3.37; 95% CI: 1.89, 5.99). Conclusions: Although, HCV GT 1 remains the most prevalent GT, especially among older groups, changes in GT distribution could have significant implications for how HCV might be controlled on a population level and treated on an individual level.

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