4.7 Article

Hepatitis C virus (HCV) seroprevalence, RNA detection, and genotype distribution across Florida, 2015-2018

期刊

PREVENTIVE MEDICINE
卷 161, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ypmed.2022.107136

关键词

HCV; Seroprevalence; RNA; Genotype

资金

  1. State of Florida
  2. Florida Academic Cancer Center Alliance (FACCA)
  3. American Cancer Society Clinical Research Professor Award
  4. Biostatistics Core Facility at Moffitt Cancer Center(NCI) [P30 CA076292]
  5. OneFlorida Clinical Data Network - Patient -Centered Outcomes Research Institute [CDRN-1501-26692]
  6. One-Florida Cancer Control Alliance - Florida Department of Health's James
  7. Esther King Biomedical Research Program [4KB16]
  8. University of Florida Clinical and Translational Science Institute [UL1TR001427]

向作者/读者索取更多资源

Chronic hepatitis C virus infection is a major cause of hepatocellular carcinoma in the U.S. Screening for HCV is recommended for baby boomers, and this recommendation has expanded to all adults due to increasing rates of HCV infection in younger adults. This study assesses the burden of HCV infection across demographics and supports the shift from age and risk-based screening guidelines to universal adult screening.
Chronic hepatitis C virus (HCV) infection is a leading cause of hepatocellular carcinoma (HCC) in the U.S. Due to high rates of HCV among baby boomers (born 1945-1965), it was recommended they receive universal screening. This was expanded to all U.S. adults in 2020 due to evidence of increasing rates of chronic HCV in younger adults. An assessment of HCV burden across demographics is crucial to understand the future burden of HCC and target under-screened adults for HCV. Using the OneFlorida Clinical Research Consortium, of more than one million individuals in Florida, all HCV antibody and viral RNA tests completed from 2015 to 2018 were identified. HCV seroprevalence, HCV viral load (active infection), and HCV genotype distribution by risk groups were assessed. Overall, HCV seroprevalence and active infection were highest among White non-Hispanic in-dividuals, males, and baby boomers. However, odds of a positive HCV antibody test were higher among Black non-Hispanic individuals born before 1945 (aOR: 2.74; 95% CI: 1.98-3.78) or 1945-1965 (aOR: 1.46; 95% CI: 1.36-1.56) compared to White non-Hispanic individuals. In contrast, among individuals born after 1965, Black non-Hispanics were less likely than White non-Hispanics to test HCV antibody positive (aOR of 0.5-0.28). A similar age/race pattern was observed for active HCV infection. There was a higher prevalence of genotype 1A and 3 and lower prevalence of 1B in younger adults. Patterns of HCV seroprevalence and active HCV infection identified in our study support the recent shift from age and risk-based screening guidelines to universal adult screening.

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