2010
DOI: 10.1016/j.trstmh.2010.08.006
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Seroprevalence of antibodies to hepatitis E virus in two large communities in Havana, Cuba

Abstract: Hepatitis E virus (HEV) infection is an important cause of acute viral hepatitis in tropical and sub-tropical regions that occurs both as epidemic episodes and sporadic cases. The aim of this investigation was to estimate the prevalence of total immunoglobulin (Ig) anti-hepatitis E virus (anti-HEV) and the risk factors associated to two communities in Havana City. Serum samples (n=469) obtained from healthy individuals with no history of viral hepatitis were screened for total anti-HEV by enzyme immunoassay (E… Show more

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Cited by 18 publications
(13 citation statements)
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“…The seroprevalence of HEV in a population generally increases with age [15][18], [22], [25]. In our study, the seroprevalence of HEV increased throughout the whole age range, the first marked increase in seropositivity occurred at 15 to 29 years in males and 20 to 39 years in females.…”
Section: Discussionsupporting
confidence: 58%
“…The seroprevalence of HEV in a population generally increases with age [15][18], [22], [25]. In our study, the seroprevalence of HEV increased throughout the whole age range, the first marked increase in seropositivity occurred at 15 to 29 years in males and 20 to 39 years in females.…”
Section: Discussionsupporting
confidence: 58%
“…However, the positivity of HEV antibodies in Northeastern China, South Korea and Japan, was 50.7% in Korean Chinese, 47.7% in native Chinese, 34% in South Koreans, 14.3% in Koreans living in Japan and 6% in native Japanese (Taniguchi et al., 2009). Villalba et al. (2010) stated the prevalence of anti‐HEV in 47 of total 469 randomly selected humans in Havana, Cuba.…”
Section: Discussionmentioning
confidence: 99%
“…The antigen source for the fourth‐generation total antibody assay (solid phase and the conjugate) is the recombinant protein (ET2.1) from the C‐terminal ORF‐2 (Chinese strain) having 96% homology to all HEV strains in GenBank including avian and swine strains. Testing was performed as outlined by Villalba et al Briefly, test samples and controls were diluted 1 in 5 and added to antigen‐coated wells and incubated for 30 minutes at 37°C. After washing six times, 100 µL of peroxidase‐labeled conjugate was added and incubated for 30 minutes at 37°C.…”
Section: Methodsmentioning
confidence: 99%