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- Publisher Website: 10.1002/ijc.20951
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- PMID: 15723309
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Article: Fecal and urinary excretion of aflatoxin B 1 metabolites (AFQ 1, AFM 1 and AFB-N 7-guanine) in young Chinese males
Title | Fecal and urinary excretion of aflatoxin B 1 metabolites (AFQ 1, AFM 1 and AFB-N 7-guanine) in young Chinese males |
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Authors | |
Keywords | Aflatoxin B1 Aflatoxin B1-N7-guanine Aflatoxin M1 Aflatoxin Q1 Hepatitis B virus |
Issue Date | 2005 |
Publisher | John Wiley & Sons, Inc.. The Journal's web site is located at http://www3.interscience.wiley.com/journal/29331/home |
Citation | International Journal Of Cancer, 2005, v. 115 n. 6, p. 879-884 How to Cite? |
Abstract | Our study was designed to assess the fecal and urinary excretion of 3 aflatoxin B 1 (AFB 1) metabolites, aflatoxins M 1 (AFM 1) and Q 1 (AFQ 1) and aflatoxin B 1-N 7-guanine (AFB-N 7-guanine) that are produced by the predominant forms of cytochrome P450 enzymes responsible for the biotransformation of AFB 1. Fecal and urinary AFM 1, AFQ 1 and urinary AFB-N 7-guanine were assessed in 83 young Chinese males selected from a larger population (n = 300) based on detectable urinary AFM 1. The concentration of fecal AFQ 1 (median 137 ng/g fresh weight, IQR 9.1 to 450) was approximately 60 times higher than that of AFM 1 (2.3 ng/g, IQR 0.0 to 7.3). In urine, the median AFQ 1 was 10.4 ng/ml (IQR 3.4 to 23.3), and the median AFM 1 and AFB-N 7-guanine 0.04 ng/ml (IQR 0.01 to 0.33) and 0.38 ng/ml (IQR 0.0 to 2.15), respectively. A subgroup (n = 14) with hepatitis B virus (HBV) infection had significantly higher fecal concentrations of AFQ 1 (p = 0.043) and AFM 1 (p = 0.001) than those who were hepatitis B-virus antigen (HBsAg) negative, and the respective differences in urinary AFQ 1 and AFM 1 concentrations approached statistical significance (p = 0.054, p = 0.138). Our study demonstrates that AFQ 1 is excreted in urine and feces at higher levels than AFM 1, and feces are an important route of excretion of these AFB 1 metabolites. AFQ 1 should be further assessed for its predictive value as a marker for exposure and risk of dietary aflatoxins. © 2005 Wiley-Liss, Inc. |
Persistent Identifier | http://hdl.handle.net/10722/178889 |
ISSN | 2023 Impact Factor: 5.7 2023 SCImago Journal Rankings: 2.131 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Mykkänen, H | en_US |
dc.contributor.author | Zhu, H | en_US |
dc.contributor.author | Salminen, E | en_US |
dc.contributor.author | Juvonen, RO | en_US |
dc.contributor.author | Ling, W | en_US |
dc.contributor.author | Ma, J | en_US |
dc.contributor.author | Polychronaki, N | en_US |
dc.contributor.author | Kemiläinen, H | en_US |
dc.contributor.author | Mykkänen, O | en_US |
dc.contributor.author | Salminen, S | en_US |
dc.contributor.author | ElNezami, H | en_US |
dc.date.accessioned | 2012-12-19T09:50:29Z | - |
dc.date.available | 2012-12-19T09:50:29Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.citation | International Journal Of Cancer, 2005, v. 115 n. 6, p. 879-884 | en_US |
dc.identifier.issn | 0020-7136 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/178889 | - |
dc.description.abstract | Our study was designed to assess the fecal and urinary excretion of 3 aflatoxin B 1 (AFB 1) metabolites, aflatoxins M 1 (AFM 1) and Q 1 (AFQ 1) and aflatoxin B 1-N 7-guanine (AFB-N 7-guanine) that are produced by the predominant forms of cytochrome P450 enzymes responsible for the biotransformation of AFB 1. Fecal and urinary AFM 1, AFQ 1 and urinary AFB-N 7-guanine were assessed in 83 young Chinese males selected from a larger population (n = 300) based on detectable urinary AFM 1. The concentration of fecal AFQ 1 (median 137 ng/g fresh weight, IQR 9.1 to 450) was approximately 60 times higher than that of AFM 1 (2.3 ng/g, IQR 0.0 to 7.3). In urine, the median AFQ 1 was 10.4 ng/ml (IQR 3.4 to 23.3), and the median AFM 1 and AFB-N 7-guanine 0.04 ng/ml (IQR 0.01 to 0.33) and 0.38 ng/ml (IQR 0.0 to 2.15), respectively. A subgroup (n = 14) with hepatitis B virus (HBV) infection had significantly higher fecal concentrations of AFQ 1 (p = 0.043) and AFM 1 (p = 0.001) than those who were hepatitis B-virus antigen (HBsAg) negative, and the respective differences in urinary AFQ 1 and AFM 1 concentrations approached statistical significance (p = 0.054, p = 0.138). Our study demonstrates that AFQ 1 is excreted in urine and feces at higher levels than AFM 1, and feces are an important route of excretion of these AFB 1 metabolites. AFQ 1 should be further assessed for its predictive value as a marker for exposure and risk of dietary aflatoxins. © 2005 Wiley-Liss, Inc. | en_US |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc.. The Journal's web site is located at http://www3.interscience.wiley.com/journal/29331/home | en_US |
dc.relation.ispartof | International Journal of Cancer | en_US |
dc.subject | Aflatoxin B1 | - |
dc.subject | Aflatoxin B1-N7-guanine | - |
dc.subject | Aflatoxin M1 | - |
dc.subject | Aflatoxin Q1 | - |
dc.subject | Hepatitis B virus | - |
dc.subject.mesh | Aflatoxin B1 - Analogs & Derivatives - Metabolism - Urine | en_US |
dc.subject.mesh | Aflatoxin M1 - Urine | en_US |
dc.subject.mesh | Aflatoxins - Urine | en_US |
dc.subject.mesh | China | en_US |
dc.subject.mesh | Feces - Chemistry | en_US |
dc.subject.mesh | Guanine - Analogs & Derivatives - Urine | en_US |
dc.subject.mesh | Hepatitis B - Complications - Urine | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.title | Fecal and urinary excretion of aflatoxin B 1 metabolites (AFQ 1, AFM 1 and AFB-N 7-guanine) in young Chinese males | en_US |
dc.type | Article | en_US |
dc.identifier.email | ElNezami, H: elnezami@hkucc.hku.hk | en_US |
dc.identifier.authority | ElNezami, H=rp00694 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/ijc.20951 | en_US |
dc.identifier.pmid | 15723309 | - |
dc.identifier.scopus | eid_2-s2.0-20344404714 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-20344404714&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 115 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.spage | 879 | en_US |
dc.identifier.epage | 884 | en_US |
dc.identifier.isi | WOS:000229689700004 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Mykkänen, H=7003915985 | en_US |
dc.identifier.scopusauthorid | Zhu, H=9237388600 | en_US |
dc.identifier.scopusauthorid | Salminen, E=7006341181 | en_US |
dc.identifier.scopusauthorid | Juvonen, RO=7005331813 | en_US |
dc.identifier.scopusauthorid | Ling, W=14054110400 | en_US |
dc.identifier.scopusauthorid | Ma, J=36079484000 | en_US |
dc.identifier.scopusauthorid | Polychronaki, N=6505944468 | en_US |
dc.identifier.scopusauthorid | Kemiläinen, H=8581939400 | en_US |
dc.identifier.scopusauthorid | Mykkänen, O=17346640500 | en_US |
dc.identifier.scopusauthorid | Salminen, S=7102912002 | en_US |
dc.identifier.scopusauthorid | ElNezami, H=6603690577 | en_US |
dc.identifier.issnl | 0020-7136 | - |