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Human Cytomegalovirus Infant Infection Adversely Affects Growth and Development in Maternally HIV-Exposed and Unexposed Infants in Zambia

Identifieur interne : 003A31 ( Main/Exploration ); précédent : 003A30; suivant : 003A32

Human Cytomegalovirus Infant Infection Adversely Affects Growth and Development in Maternally HIV-Exposed and Unexposed Infants in Zambia

Auteurs : U. A. Gompels [Royaume-Uni] ; N. Larke [Royaume-Uni] ; M. Sanz-Ramos [Royaume-Uni] ; M. Bates [Royaume-Uni] ; K. Musonda [Royaume-Uni, Zambie] ; D. Manno [Royaume-Uni] ; J. Siame [Zambie] ; M. Monze [Zambie] ; S. Filteau [Royaume-Uni]

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RBID : Pascal:12-0145271

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English descriptors

Abstract

Background. Human immunodeficiency virus (HIV) and human cytomegalovirus (HCMV) coinfections have been shown to increase infant morbidity, mortality, and AIDS progression. In HIV-endemic regions, maternal HIV-exposed but HIV-uninfected infants, which is the majority of children affected by HIV, also show poor growth and increased morbidity. Although nutrition has been examined, the effects of HCMV infection have not been evaluated. We studied the effects of HCMV infection on the growth, development, and health of maternally HIV-exposed and unexposed infants in Zambia. Methods. Infants were examined in a cohort recruited to a trial of micronutrient-fortified complementary foods. HIV-infected mothers and infants had received perinatal antiretroviral therapy to prevent mother-to-child HIV transmission. Growth, development, and morbidity were analyzed by linear regression analyses in relation to maternal HIV exposure and HCMV infection, as screened by sera DNA for viremia at 6 months of age and by antibody for infection at 18 months. Results. All HCMV-seropositive infants had decreased length-for-age by 18 months compared with seronegative infants (standard deviation [z]-score difference: -0.44 [95% confidence interval {CI}, -.72 to -.17]; P = .002). In HIV-exposed infants, those who were HCMV positive compared with those who were negative, also had reduced head size (mean z-score difference: -0.72 [95% CI, -1.23 to -.22]; P = .01; P interaction = .02 for greater HCMV effect in HIV-exposed vs -unexposed) and lower psychomotor development (Bayley test score difference: -4.1 [95% CI, -7.8 to -.5]; P = .03). HIV-exposed, HCMV-viremic infants were more commonly referred for hospital treatment than HCMV-negative infants. The effects of HCMV were unaffected by micronutrient fortification. Conclusion. HCMV affects child growth, development, and morbidity of African infants, particularly in those maternally exposed to HIV. HCMV is therefore a risk factor for child health in this region.

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<name sortKey="Manno, D" sort="Manno, D" uniqKey="Manno D" first="D." last="Manno">D. Manno</name>
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<orgName type="university">Université de Londres</orgName>
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<name sortKey="Siame, J" sort="Siame, J" uniqKey="Siame J" first="J." last="Siame">J. Siame</name>
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<name sortKey="Monze, M" sort="Monze, M" uniqKey="Monze M" first="M." last="Monze">M. Monze</name>
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<s1>Virology Unit and, University Teaching Hospital</s1>
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<name sortKey="Filteau, S" sort="Filteau, S" uniqKey="Filteau S" first="S." last="Filteau">S. Filteau</name>
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<s1>Department of Nutrition and Public Health Interventions, and, University of London</s1>
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<country>Royaume-Uni</country>
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<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
<orgName type="university">Université de Londres</orgName>
</affiliation>
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<title level="j" type="main">Clinical infectious diseases</title>
<title level="j" type="abbreviated">Clin. infect. dis.</title>
<idno type="ISSN">1058-4838</idno>
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<date when="2012">2012</date>
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<title level="j" type="main">Clinical infectious diseases</title>
<title level="j" type="abbreviated">Clin. infect. dis.</title>
<idno type="ISSN">1058-4838</idno>
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<keywords scheme="KwdEn" xml:lang="en">
<term>AIDS</term>
<term>Growth</term>
<term>Human cytomegalovirus</term>
<term>Human immunodeficiency virus</term>
<term>Infant</term>
<term>Viral disease</term>
<term>Zambia</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Virose</term>
<term>SIDA</term>
<term>Nourrisson</term>
<term>Croissance</term>
<term>Zambie</term>
<term>Cytomegalovirus humain</term>
<term>Virus immunodéficience humaine</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>Zambie</term>
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<div type="abstract" xml:lang="en">Background. Human immunodeficiency virus (HIV) and human cytomegalovirus (HCMV) coinfections have been shown to increase infant morbidity, mortality, and AIDS progression. In HIV-endemic regions, maternal HIV-exposed but HIV-uninfected infants, which is the majority of children affected by HIV, also show poor growth and increased morbidity. Although nutrition has been examined, the effects of HCMV infection have not been evaluated. We studied the effects of HCMV infection on the growth, development, and health of maternally HIV-exposed and unexposed infants in Zambia. Methods. Infants were examined in a cohort recruited to a trial of micronutrient-fortified complementary foods. HIV-infected mothers and infants had received perinatal antiretroviral therapy to prevent mother-to-child HIV transmission. Growth, development, and morbidity were analyzed by linear regression analyses in relation to maternal HIV exposure and HCMV infection, as screened by sera DNA for viremia at 6 months of age and by antibody for infection at 18 months. Results. All HCMV-seropositive infants had decreased length-for-age by 18 months compared with seronegative infants (standard deviation [z]-score difference: -0.44 [95% confidence interval {CI}, -.72 to -.17]; P = .002). In HIV-exposed infants, those who were HCMV positive compared with those who were negative, also had reduced head size (mean z-score difference: -0.72 [95% CI, -1.23 to -.22]; P = .01; P interaction = .02 for greater HCMV effect in HIV-exposed vs -unexposed) and lower psychomotor development (Bayley test score difference: -4.1 [95% CI, -7.8 to -.5]; P = .03). HIV-exposed, HCMV-viremic infants were more commonly referred for hospital treatment than HCMV-negative infants. The effects of HCMV were unaffected by micronutrient fortification. Conclusion. HCMV affects child growth, development, and morbidity of African infants, particularly in those maternally exposed to HIV. HCMV is therefore a risk factor for child health in this region.</div>
</front>
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<affiliations>
<list>
<country>
<li>Royaume-Uni</li>
<li>Zambie</li>
</country>
<region>
<li>Angleterre</li>
<li>Grand Londres</li>
</region>
<settlement>
<li>Londres</li>
</settlement>
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<li>Université de Londres</li>
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<country name="Royaume-Uni">
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<name sortKey="Gompels, U A" sort="Gompels, U A" uniqKey="Gompels U" first="U. A." last="Gompels">U. A. Gompels</name>
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<name sortKey="Bates, M" sort="Bates, M" uniqKey="Bates M" first="M." last="Bates">M. Bates</name>
<name sortKey="Filteau, S" sort="Filteau, S" uniqKey="Filteau S" first="S." last="Filteau">S. Filteau</name>
<name sortKey="Larke, N" sort="Larke, N" uniqKey="Larke N" first="N." last="Larke">N. Larke</name>
<name sortKey="Manno, D" sort="Manno, D" uniqKey="Manno D" first="D." last="Manno">D. Manno</name>
<name sortKey="Musonda, K" sort="Musonda, K" uniqKey="Musonda K" first="K." last="Musonda">K. Musonda</name>
<name sortKey="Sanz Ramos, M" sort="Sanz Ramos, M" uniqKey="Sanz Ramos M" first="M." last="Sanz-Ramos">M. Sanz-Ramos</name>
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<noRegion>
<name sortKey="Musonda, K" sort="Musonda, K" uniqKey="Musonda K" first="K." last="Musonda">K. Musonda</name>
</noRegion>
<name sortKey="Monze, M" sort="Monze, M" uniqKey="Monze M" first="M." last="Monze">M. Monze</name>
<name sortKey="Siame, J" sort="Siame, J" uniqKey="Siame J" first="J." last="Siame">J. Siame</name>
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