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Use of High-Dose, Twice-Yearly Albendazole and Ivermectin to Suppress Wuchereria bancrofti Microfilarial Levels

Identifieur interne : 002D52 ( Pmc/Curation ); précédent : 002D51; suivant : 002D53

Use of High-Dose, Twice-Yearly Albendazole and Ivermectin to Suppress Wuchereria bancrofti Microfilarial Levels

Auteurs : Benoit Dembele ; Yaya I. Coulibaly ; Housseini Dolo ; Siaka Konate ; Siaka Y. Coulibaly ; Dramane Sanogo ; Lamine Soumaoro ; Michel E. Coulibaly ; Salif Seriba Doumbia ; Abdallah A. Diallo ; Sekou F. Traore ; Adama Diaman Keita ; Michael P. Fay ; Thomas B. Nutman ; Amy D. Klion

Source :

RBID : PMC:3106228

Abstract

Background. Annual mass treatment with albendazole and ivermectin is the mainstay of current strategies to interrupt transmission of Wuchereria bancrofti in Africa. More-effective microfilarial suppression could potentially reduce the time necessary to interrupt transmission, easing the economic burden of mass treatment programs in countries with limited resources.

Methods. To determine the effect of increased dose and frequency of albendazole-ivermectin treatment on microfilarial clearance, 51 W. bancrofti microfilaremic residents of an area of W. bancrofti endemicity in Mali were randomized to receive 2 doses of annual, standard-dose albendazole-ivermectin therapy (400 mg and 150 µg/kg; n = 26) or 4 doses of twice-yearly, increased-dose albendazole-ivermectin therapy (800 mg and 400 µg/kg; n = 25).

Results. Although microfilarial levels decreased significantly after therapy in both groups, levels were significantly lower in the high-dose, twice-yearly group at 12, 18, and 24 months. Furthermore, there was complete clearance of detectable microfilariae at 12 months in the 19 patients in the twice-yearly therapy group with data available at 12 months, compared with 9 of 21 patients in the annual therapy group (P<.001 , by Fisher's exact test). This difference between the 2 groups was sustained at 18 and 24 months, with no detectable microfilariae in the patients receiving twice-yearly treatment. Worm nests detectable by ultrasonography and W. bancrofti circulating antigen levels, as measured by enzyme-linked immunosorbent assay, were decreased to the same degree in both groups at 24 months, compared with baseline.

Conclusions. These findings suggest that increasing the dosage and frequency of albendazole-ivermectin treatment enhances suppression of microfilariae but that this effect may not be attributable to improved adulticidal activity.


Url:
DOI: 10.1086/657063
PubMed: 21039220
PubMed Central: 3106228

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PMC:3106228

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Microfilarial Levels</title>
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<name sortKey="Keita, Adama Diaman" sort="Keita, Adama Diaman" uniqKey="Keita A" first="Adama Diaman" last="Keita">Adama Diaman Keita</name>
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<name sortKey="Nutman, Thomas B" sort="Nutman, Thomas B" uniqKey="Nutman T" first="Thomas B." last="Nutman">Thomas B. Nutman</name>
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<name sortKey="Klion, Amy D" sort="Klion, Amy D" uniqKey="Klion A" first="Amy D." last="Klion">Amy D. Klion</name>
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<title xml:lang="en" level="a" type="main">Use of High-Dose, Twice-Yearly Albendazole and Ivermectin to Suppress
<italic>Wuchereria bancrofti</italic>
Microfilarial Levels</title>
<author>
<name sortKey="Dembele, Benoit" sort="Dembele, Benoit" uniqKey="Dembele B" first="Benoit" last="Dembele">Benoit Dembele</name>
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<author>
<name sortKey="Coulibaly, Yaya I" sort="Coulibaly, Yaya I" uniqKey="Coulibaly Y" first="Yaya I." last="Coulibaly">Yaya I. Coulibaly</name>
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<nlm:aff id="a1"></nlm:aff>
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<name sortKey="Dolo, Housseini" sort="Dolo, Housseini" uniqKey="Dolo H" first="Housseini" last="Dolo">Housseini Dolo</name>
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<nlm:aff id="a1"></nlm:aff>
</affiliation>
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<author>
<name sortKey="Konate, Siaka" sort="Konate, Siaka" uniqKey="Konate S" first="Siaka" last="Konate">Siaka Konate</name>
<affiliation>
<nlm:aff id="a1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Coulibaly, Siaka Y" sort="Coulibaly, Siaka Y" uniqKey="Coulibaly S" first="Siaka Y." last="Coulibaly">Siaka Y. Coulibaly</name>
<affiliation>
<nlm:aff id="a1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Sanogo, Dramane" sort="Sanogo, Dramane" uniqKey="Sanogo D" first="Dramane" last="Sanogo">Dramane Sanogo</name>
<affiliation>
<nlm:aff id="a1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Soumaoro, Lamine" sort="Soumaoro, Lamine" uniqKey="Soumaoro L" first="Lamine" last="Soumaoro">Lamine Soumaoro</name>
<affiliation>
<nlm:aff id="a1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Coulibaly, Michel E" sort="Coulibaly, Michel E" uniqKey="Coulibaly M" first="Michel E." last="Coulibaly">Michel E. Coulibaly</name>
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<nlm:aff id="a1"></nlm:aff>
</affiliation>
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<author>
<name sortKey="Doumbia, Salif Seriba" sort="Doumbia, Salif Seriba" uniqKey="Doumbia S" first="Salif Seriba" last="Doumbia">Salif Seriba Doumbia</name>
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<nlm:aff id="a1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Diallo, Abdallah A" sort="Diallo, Abdallah A" uniqKey="Diallo A" first="Abdallah A." last="Diallo">Abdallah A. Diallo</name>
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<nlm:aff id="a1"></nlm:aff>
</affiliation>
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<name sortKey="Traore, Sekou F" sort="Traore, Sekou F" uniqKey="Traore S" first="Sekou F." last="Traore">Sekou F. Traore</name>
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</affiliation>
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<name sortKey="Keita, Adama Diaman" sort="Keita, Adama Diaman" uniqKey="Keita A" first="Adama Diaman" last="Keita">Adama Diaman Keita</name>
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<nlm:aff id="a2"></nlm:aff>
</affiliation>
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<name sortKey="Fay, Michael P" sort="Fay, Michael P" uniqKey="Fay M" first="Michael P." last="Fay">Michael P. Fay</name>
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<nlm:aff id="a3"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Nutman, Thomas B" sort="Nutman, Thomas B" uniqKey="Nutman T" first="Thomas B." last="Nutman">Thomas B. Nutman</name>
<affiliation>
<nlm:aff id="a4"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Klion, Amy D" sort="Klion, Amy D" uniqKey="Klion A" first="Amy D." last="Klion">Amy D. Klion</name>
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</affiliation>
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<series>
<title level="j">Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America</title>
<idno type="ISSN">1058-4838</idno>
<idno type="eISSN">1537-6591</idno>
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<date when="2010">2010</date>
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<front>
<div type="abstract" xml:lang="en">
<p>
<bold>
<italic>Background.</italic>
</bold>
Annual mass treatment with albendazole and ivermectin is the mainstay of current strategies to interrupt transmission of
<italic>Wuchereria bancrofti</italic>
in Africa. More-effective microfilarial suppression could potentially reduce the time necessary to interrupt transmission, easing the economic burden of mass treatment programs in countries with limited resources.</p>
<p>
<bold>
<italic>Methods.</italic>
</bold>
To determine the effect of increased dose and frequency of albendazole-ivermectin treatment on microfilarial clearance, 51
<italic>W. bancrofti</italic>
microfilaremic residents of an area of
<italic>W. bancrofti</italic>
endemicity in Mali were randomized to receive 2 doses of annual, standard-dose albendazole-ivermectin therapy (400 mg and 150 µg/kg;
<italic>n</italic>
= 26) or 4 doses of twice-yearly, increased-dose albendazole-ivermectin therapy (800 mg and 400 µg/kg;
<italic>n</italic>
= 25).</p>
<p>
<bold>
<italic>Results.</italic>
</bold>
Although microfilarial levels decreased significantly after therapy in both groups, levels were significantly lower in the high-dose, twice-yearly group at 12, 18, and 24 months. Furthermore, there was complete clearance of detectable microfilariae at 12 months in the 19 patients in the twice-yearly therapy group with data available at 12 months, compared with 9 of 21 patients in the annual therapy group (
<italic>P</italic>
<.001 , by Fisher's exact test). This difference between the 2 groups was sustained at 18 and 24 months, with no detectable microfilariae in the patients receiving twice-yearly treatment. Worm nests detectable by ultrasonography and
<italic>W. bancrofti</italic>
circulating antigen levels, as measured by enzyme-linked immunosorbent assay, were decreased to the same degree in both groups at 24 months, compared with baseline.</p>
<p>
<bold>
<italic>Conclusions.</italic>
</bold>
These findings suggest that increasing the dosage and frequency of albendazole-ivermectin treatment enhances suppression of microfilariae but that this effect may not be attributable to improved adulticidal activity.</p>
</div>
</front>
</TEI>
<pmc article-type="research-article">
<pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Clin Infect Dis</journal-id>
<journal-id journal-id-type="hwp">cid</journal-id>
<journal-id journal-id-type="publisher-id">clinids</journal-id>
<journal-title-group>
<journal-title>Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America</journal-title>
</journal-title-group>
<issn pub-type="ppub">1058-4838</issn>
<issn pub-type="epub">1537-6591</issn>
<publisher>
<publisher-name>The University of Chicago Press</publisher-name>
</publisher>
</journal-meta>
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<article-id pub-id-type="pmid">21039220</article-id>
<article-id pub-id-type="pmc">3106228</article-id>
<article-id pub-id-type="doi">10.1086/657063</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Articles and Commentaries</subject>
<subj-group subj-group-type="heading">
<subject>Major Articles</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Use of High-Dose, Twice-Yearly Albendazole and Ivermectin to Suppress
<italic>Wuchereria bancrofti</italic>
Microfilarial Levels</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Dembele</surname>
<given-names>Benoit</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Coulibaly</surname>
<given-names>Yaya I.</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Dolo</surname>
<given-names>Housseini</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Konate</surname>
<given-names>Siaka</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Coulibaly</surname>
<given-names>Siaka Y.</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sanogo</surname>
<given-names>Dramane</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Soumaoro</surname>
<given-names>Lamine</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Coulibaly</surname>
<given-names>Michel E.</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Doumbia</surname>
<given-names>Salif Seriba</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Diallo</surname>
<given-names>Abdallah A.</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Traore</surname>
<given-names>Sekou F.</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Keita</surname>
<given-names>Adama Diaman</given-names>
</name>
<xref ref-type="aff" rid="a2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fay</surname>
<given-names>Michael P.</given-names>
</name>
<xref ref-type="aff" rid="a3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Nutman</surname>
<given-names>Thomas B.</given-names>
</name>
<xref ref-type="aff" rid="a4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Klion</surname>
<given-names>Amy D.</given-names>
</name>
<xref ref-type="aff" rid="a4">4</xref>
<xref ref-type="corresp" rid="cor1"></xref>
</contrib>
<aff id="a1">
<label>
<sup>1</sup>
</label>
<institution>Faculty of Medicine, Pharmacy and Dentistry, Filariasis Unit, University of Bamako</institution>
,
<addr-line>Bamako, Mali</addr-line>
</aff>
<aff id="a2">
<label>
<sup>2</sup>
</label>
<institution>Department of Radiology, Hospital of Point G</institution>
,
<addr-line>Bamako, Mali</addr-line>
</aff>
<aff id="a3">
<label>
<sup>3</sup>
</label>
<institution>Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases</institution>
,
<addr-line>Bethesda, Maryland</addr-line>
</aff>
<aff id="a4">
<label>
<sup>4</sup>
</label>
<institution>Laboratory of Parasitic Diseases, National Institutes of Health</institution>
,
<addr-line>Bethesda, Maryland</addr-line>
</aff>
</contrib-group>
<author-notes>
<corresp id="cor1">Reprints or correspondence: Dr. Amy D. Klion Laboratory of Parasitic Diseases Bldg 50 Rm 6351 National Institutes of Health Bethesda MD 20892 (
<email>aklion@nih.gov</email>
).</corresp>
</author-notes>
<pub-date pub-type="ppub">
<day>1</day>
<month>12</month>
<year>2010</year>
</pub-date>
<volume>51</volume>
<issue>11</issue>
<fpage>1229</fpage>
<lpage>1235</lpage>
<history>
<date date-type="received">
<day>9</day>
<month>3</month>
<year>2010</year>
</date>
<date date-type="accepted">
<day>13</day>
<month>5</month>
<year>2010</year>
</date>
</history>
<permissions>
<copyright-statement>© 2010 by the Infectious Diseases Society of America</copyright-statement>
<copyright-year>2010</copyright-year>
</permissions>
<abstract>
<p>
<bold>
<italic>Background.</italic>
</bold>
Annual mass treatment with albendazole and ivermectin is the mainstay of current strategies to interrupt transmission of
<italic>Wuchereria bancrofti</italic>
in Africa. More-effective microfilarial suppression could potentially reduce the time necessary to interrupt transmission, easing the economic burden of mass treatment programs in countries with limited resources.</p>
<p>
<bold>
<italic>Methods.</italic>
</bold>
To determine the effect of increased dose and frequency of albendazole-ivermectin treatment on microfilarial clearance, 51
<italic>W. bancrofti</italic>
microfilaremic residents of an area of
<italic>W. bancrofti</italic>
endemicity in Mali were randomized to receive 2 doses of annual, standard-dose albendazole-ivermectin therapy (400 mg and 150 µg/kg;
<italic>n</italic>
= 26) or 4 doses of twice-yearly, increased-dose albendazole-ivermectin therapy (800 mg and 400 µg/kg;
<italic>n</italic>
= 25).</p>
<p>
<bold>
<italic>Results.</italic>
</bold>
Although microfilarial levels decreased significantly after therapy in both groups, levels were significantly lower in the high-dose, twice-yearly group at 12, 18, and 24 months. Furthermore, there was complete clearance of detectable microfilariae at 12 months in the 19 patients in the twice-yearly therapy group with data available at 12 months, compared with 9 of 21 patients in the annual therapy group (
<italic>P</italic>
<.001 , by Fisher's exact test). This difference between the 2 groups was sustained at 18 and 24 months, with no detectable microfilariae in the patients receiving twice-yearly treatment. Worm nests detectable by ultrasonography and
<italic>W. bancrofti</italic>
circulating antigen levels, as measured by enzyme-linked immunosorbent assay, were decreased to the same degree in both groups at 24 months, compared with baseline.</p>
<p>
<bold>
<italic>Conclusions.</italic>
</bold>
These findings suggest that increasing the dosage and frequency of albendazole-ivermectin treatment enhances suppression of microfilariae but that this effect may not be attributable to improved adulticidal activity.</p>
</abstract>
</article-meta>
</front>
</pmc>
</record>

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