Evidence map›Paper›PMID 36352480›Full record

ArticleParasites & vectors2022

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

Jérémy T Campillo, Frédéric Louya, Paul Bikita, François Missamou, Sébastien D S Pion, Michel Boussinesq, Cédric B Chesnais

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Jérémy T CampilloInstitut de Recherche Pour le Développement (IRD), TransVIHMI, Université de Montpellier, INSERM Unité 1175, Montpellier, France. jeremy.campillo@ird.fr.
Frédéric LouyaProgramme National de Lutte Contre L'Onchocercose, Direction de l'Épidémiologie et de la Lutte Contre la Maladie, Ministère de la Santé et de la Population, Brazzaville, Republic of Congo.
Paul BikitaProgramme National de Lutte Contre L'Onchocercose, Direction de l'Épidémiologie et de la Lutte Contre la Maladie, Ministère de la Santé et de la Population, Brazzaville, Republic of Congo.
François MissamouProgramme National de Lutte Contre L'Onchocercose, Direction de l'Épidémiologie et de la Lutte Contre la Maladie, Ministère de la Santé et de la Population, Brazzaville, Republic of Congo.
Sébastien D S PionInstitut de Recherche Pour le Développement (IRD), TransVIHMI, Université de Montpellier, INSERM Unité 1175, Montpellier, France.
Michel BoussinesqInstitut de Recherche Pour le Développement (IRD), TransVIHMI, Université de Montpellier, INSERM Unité 1175, Montpellier, France.
Cédric B ChesnaisInstitut de Recherche Pour le Développement (IRD), TransVIHMI, Université de Montpellier, INSERM Unité 1175, Montpellier, France.
Inserm · FRInstitut de Recherche pour le Développement · FRRecherches Translationnelles sur le VIH et les Maladies Infectieuses

Funding

Agence Nationale de la Recherche 18-CE17-0008
6 · The paper itself

Abstract

backgroundLoa 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.

methodsMicrofilaremia 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.

resultsAll 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.

conclusionsWe 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.

Indexed as

LoaLoiasisAnimalsCongoHumansMicrofilariaeLoa loaMicrofilaremiaPeriodicityRepublic of the CongoTemperature

Identifiers

PMID36352480
PMCPMC9647901
OpenAlexW4308627663

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.