Le SIDA au Ghana (serveur d'exploration)

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Association of high viral load and abnormal liver function with high aflatoxin B1–albumin adduct levels in HIV-positive Ghanaians: preliminary observations

Identifieur interne : 000394 ( Pmc/Checkpoint ); précédent : 000393; suivant : 000395

Association of high viral load and abnormal liver function with high aflatoxin B1–albumin adduct levels in HIV-positive Ghanaians: preliminary observations

Auteurs : P. E. Jolly [États-Unis] ; F. M. Shuaib [États-Unis] ; Y. Jiang [États-Unis] ; P. Preko [Ghana] ; J. Baidoo [Ghana] ; J. K. Stiles [États-Unis] ; J.-S. Wang [États-Unis] ; T. D. Phillips [États-Unis] ; J. H. Williams [États-Unis]

Source :

RBID : PMC:3381352

Abstract

We examined the association between certain clinical factors and aflatoxin B1–albumin adduct (AF-ALB) levels in HIV-positive people. Plasma samples collected from 314 (155 HIV-positive and 159 HIV-negative) people were tested for AF-ALB levels, viral load, CD4+ T-cell count, liver function profile, malaria parasitaemia, and hepatitis B and C virus infections. HIV-positive participants were divided into high and low groups based on their median AF-ALB of 0.93 pmol mg−1 albumin and multivariable logistic and linear regression methods used to assess relationships between clinical conditions and AF-ALB levels. Multivariable logistic regression showed statistically significant increased odds of having higher HIV viral loads (OR=2.84; 95% CI=1.17–7.78) and higher direct bilirubin levels (OR=5.47; 95% CI=1.03–22.85) among HIV-positive participants in the high AF-ALB group. There were also higher levels of total bilirubin and lower levels of albumin in association with high AF-ALB. Thus, aflatoxin exposure may contribute to high viral loads and abnormal liver function in HIV-positive people and so promote disease progression.


Url:
DOI: 10.1080/19440049.2011.581698
PubMed: 21749228
PubMed Central: 3381352


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PMC:3381352

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<p id="P1">We examined the association between certain clinical factors and aflatoxin B
<sub>1</sub>
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<sup>−1</sup>
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<surname>Jolly</surname>
<given-names>P.E.</given-names>
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<xref rid="FN1" ref-type="author-notes">*</xref>
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</name>
<xref ref-type="aff" rid="A1">a</xref>
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<name>
<surname>Jiang</surname>
<given-names>Y.</given-names>
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<xref ref-type="aff" rid="A1">a</xref>
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<name>
<surname>Preko</surname>
<given-names>P.</given-names>
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Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA</aff>
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AIDS ALLY and St. Markus Hospital, Kumasi, Ghana</aff>
<aff id="A3">
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Department of Microbiology, Biochemistry and Immunology, Morehouse School of Medicine, Atlanta, GA, USA</aff>
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Department of Environmental Health Science, University of Georgia, Athens, GA, USA</aff>
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Corresponding author.
<email>jollyp@uab.edu</email>
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<p id="P1">We examined the association between certain clinical factors and aflatoxin B
<sub>1</sub>
–albumin adduct (AF-ALB) levels in HIV-positive people. Plasma samples collected from 314 (155 HIV-positive and 159 HIV-negative) people were tested for AF-ALB levels, viral load, CD4+ T-cell count, liver function profile, malaria parasitaemia, and hepatitis B and C virus infections. HIV-positive participants were divided into high and low groups based on their median AF-ALB of 0.93 pmol mg
<sup>−1</sup>
albumin and multivariable logistic and linear regression methods used to assess relationships between clinical conditions and AF-ALB levels. Multivariable logistic regression showed statistically significant increased odds of having higher HIV viral loads (OR=2.84; 95% CI=1.17–7.78) and higher direct bilirubin levels (OR=5.47; 95% CI=1.03–22.85) among HIV-positive participants in the high AF-ALB group. There were also higher levels of total bilirubin and lower levels of albumin in association with high AF-ALB. Thus, aflatoxin exposure may contribute to high viral loads and abnormal liver function in HIV-positive people and so promote disease progression.</p>
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