Source:http://linkedlifedata.com/resource/pubmed/id/10421643
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
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| pubmed:dateCreated |
1999-8-12
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| pubmed:abstractText |
We followed 145 men with chronic hepatitis B virus (HBV) hepatitis for 10 years to determine whether exposure to aflatoxin, or concomitant exposure to hepatitis C virus (HCV), or family history of hepatocellular carcinoma (HCC) increased the risk of developing HCC. We collected 8 monthly urine samples before beginning follow-up and pooled them to detect aflatoxin metabolite M1 (AFM1). AFM1 was detected in 78 (54%) of the subjects. The risk of HCC was increased 3.3-fold (with a 95% confidence interval of 1.2-8.7) in those with detectable AFM1 (above 3.6 ng/L). This relative risk was adjusted for age and for HCV status. The attributable risk from exposure to detectable AFM1 was 0.553 (0.087, 0.94). The relative risk of fatal cirrhosis for those with elevated AFM1 was 2.8 (0.6, 14.3), and the odds of having a persistently elevated alanine transaminase (ALT) were 2.5-fold greater in those with detectable AFM1 (P =.007). Concomitant infection with HCV increased the risk of HCC 5.8-fold (2. 0-17), adjusted for age and AFM1 status. A family history of HCC increased the risk of HCC 5.6-fold, adjusted for age and AFM1. Four men with detectable AFM1 and HCC all had missense mutation in codon 249 of the p53 gene in cancer tissues. This study shows that exposure to AFM1 can account for a substantial part of the risk of HCC in men with chronic HBV hepatitis and adds importantly to the evidence that HCV and family history of HCC increase the risk of HCC in men with chronic HBV hepatitis.
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| pubmed:commentsCorrections | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Aug
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| pubmed:issn |
0270-9139
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
30
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
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| pubmed:pagination |
379-83
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| pubmed:dateRevised |
2006-11-15
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| pubmed:meshHeading |
pubmed-meshheading:10421643-Adolescent,
pubmed-meshheading:10421643-Adult,
pubmed-meshheading:10421643-Aflatoxin M1,
pubmed-meshheading:10421643-Aged,
pubmed-meshheading:10421643-Carcinoma, Hepatocellular,
pubmed-meshheading:10421643-Carrier State,
pubmed-meshheading:10421643-Child,
pubmed-meshheading:10421643-Child, Preschool,
pubmed-meshheading:10421643-Cohort Studies,
pubmed-meshheading:10421643-Hepatitis B, Chronic,
pubmed-meshheading:10421643-Hepatitis B Surface Antigens,
pubmed-meshheading:10421643-Humans,
pubmed-meshheading:10421643-Infant,
pubmed-meshheading:10421643-Infant, Newborn,
pubmed-meshheading:10421643-Liver Neoplasms,
pubmed-meshheading:10421643-Male,
pubmed-meshheading:10421643-Middle Aged,
pubmed-meshheading:10421643-Prospective Studies,
pubmed-meshheading:10421643-Risk
|
| pubmed:year |
1999
|
| pubmed:articleTitle |
Increased risk of hepatocellular carcinoma in male hepatitis B surface antigen carriers with chronic hepatitis who have detectable urinary aflatoxin metabolite M1.
|
| pubmed:affiliation |
Cancer Institute, National Laboratory of Molecular Oncology, Chinese Academy of Medical Sciences, Beijing, China. ztsun@public3.bta.net.cn
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|