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Factors associated with the periodicity of Loa loa microfilaremia in the Republic of the Congo

BACKGROUND: Loa loa microfilariae circulate in the peripheral blood of human hosts following a diurnal periodicity, with maximal microfilaremia levels generally observed between 10:00 am and 3:00 pm. Few studies have assessed factors potentially associated with this periodicity. METHODS: Microfilare...

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Autores principales: Campillo, Jérémy T., Louya, Frédéric, Bikita, Paul, Missamou, François, Pion, Sébastien D. S., Boussinesq, Michel, Chesnais, Cédric B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647901/
https://www.ncbi.nlm.nih.gov/pubmed/36352480
http://dx.doi.org/10.1186/s13071-022-05541-y
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author Campillo, Jérémy T.
Louya, Frédéric
Bikita, Paul
Missamou, François
Pion, Sébastien D. S.
Boussinesq, Michel
Chesnais, Cédric B.
author_facet Campillo, Jérémy T.
Louya, Frédéric
Bikita, Paul
Missamou, François
Pion, Sébastien D. S.
Boussinesq, Michel
Chesnais, Cédric B.
author_sort Campillo, Jérémy T.
collection PubMed
description BACKGROUND: Loa loa microfilariae circulate in the peripheral blood of human hosts following a diurnal periodicity, with maximal microfilaremia levels generally observed between 10:00 am and 3:00 pm. Few studies have assessed factors potentially associated with this periodicity. METHODS: Microfilaremia data were collected repeatedly between 9:00 am and 8:00 pm from 13 individuals in the Republic of the Congo. Using local polynomial regression (LOESS), we determined the best models representing the dynamics of microfilaremia over this period. In a second step, using cosinor models, we evaluated the influence of sex, age, and body temperature on the periodicity of L. loa microfilaremia in blood. RESULTS: All subjects reached their maximum microfilaremia between 10:00 am and 4:00 pm. Individual microfilaremia showed different patterns between individuals, and some clearly showed multiple peaks within a day. LOESS provided a good fit to the observed data. Without adjustment, the maximum microfilarial density was reached around 11:00 am. Adjustment revealed three distinct modes of microfilaremia, occurring around 10:00 am, 1:00 pm, and 4:00 pm. Cosinor models also provided good fit to our data. After adjustment on body temperature, the L. loa microfilaremia fluctuation amplitude decreased significantly from 1684.8 to 310.6 microfilariae(mf)/ml and the predicted peak was estimated at 12:02 pm. CONCLUSIONS: We characterized the periodicity of L. loa microfilaremia mathematically with two different approaches: cosinor models and LOESS regression. Both models suggest that body temperature plays a role in the variation in microfilaremia within a day. Further studies are needed to identify individual co-factors affecting microfilaremia. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-96479012022-11-15 Factors associated with the periodicity of Loa loa microfilaremia in the Republic of the Congo Campillo, Jérémy T. Louya, Frédéric Bikita, Paul Missamou, François Pion, Sébastien D. S. Boussinesq, Michel Chesnais, Cédric B. Parasit Vectors Research BACKGROUND: Loa loa microfilariae circulate in the peripheral blood of human hosts following a diurnal periodicity, with maximal microfilaremia levels generally observed between 10:00 am and 3:00 pm. Few studies have assessed factors potentially associated with this periodicity. METHODS: Microfilaremia data were collected repeatedly between 9:00 am and 8:00 pm from 13 individuals in the Republic of the Congo. Using local polynomial regression (LOESS), we determined the best models representing the dynamics of microfilaremia over this period. In a second step, using cosinor models, we evaluated the influence of sex, age, and body temperature on the periodicity of L. loa microfilaremia in blood. RESULTS: All subjects reached their maximum microfilaremia between 10:00 am and 4:00 pm. Individual microfilaremia showed different patterns between individuals, and some clearly showed multiple peaks within a day. LOESS provided a good fit to the observed data. Without adjustment, the maximum microfilarial density was reached around 11:00 am. Adjustment revealed three distinct modes of microfilaremia, occurring around 10:00 am, 1:00 pm, and 4:00 pm. Cosinor models also provided good fit to our data. After adjustment on body temperature, the L. loa microfilaremia fluctuation amplitude decreased significantly from 1684.8 to 310.6 microfilariae(mf)/ml and the predicted peak was estimated at 12:02 pm. CONCLUSIONS: We characterized the periodicity of L. loa microfilaremia mathematically with two different approaches: cosinor models and LOESS regression. Both models suggest that body temperature plays a role in the variation in microfilaremia within a day. Further studies are needed to identify individual co-factors affecting microfilaremia. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2022-11-09 /pmc/articles/PMC9647901/ /pubmed/36352480 http://dx.doi.org/10.1186/s13071-022-05541-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Campillo, Jérémy T.
Louya, Frédéric
Bikita, Paul
Missamou, François
Pion, Sébastien D. S.
Boussinesq, Michel
Chesnais, Cédric B.
Factors associated with the periodicity of Loa loa microfilaremia in the Republic of the Congo
title Factors associated with the periodicity of Loa loa microfilaremia in the Republic of the Congo
title_full Factors associated with the periodicity of Loa loa microfilaremia in the Republic of the Congo
title_fullStr Factors associated with the periodicity of Loa loa microfilaremia in the Republic of the Congo
title_full_unstemmed Factors associated with the periodicity of Loa loa microfilaremia in the Republic of the Congo
title_short Factors associated with the periodicity of Loa loa microfilaremia in the Republic of the Congo
title_sort factors associated with the periodicity of loa loa microfilaremia in the republic of the congo
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647901/
https://www.ncbi.nlm.nih.gov/pubmed/36352480
http://dx.doi.org/10.1186/s13071-022-05541-y
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