Evidence map›Paper›PMID 38725027›Full record

ArticleMalaria journal2024

Kinetics of glucose-6-phosphate dehydrogenase (G6PD) activity during Plasmodium vivax infection: implications for early radical malaria treatment.

Laureen Dahuron, Juste Goungounga, Moustapha Drame, Maylis Douine, Mathieu Nacher, Théo Blaise, Emilie Mosnier, Lise Musset, Marie Fouillet, Félix Djossou and 1 more

Abstract read
In one paragraph

Article in Malaria journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

11 authors.

Laureen DahuronInfectious and Tropical Diseases Department, Centre Hospitalier de Cayenne Andrée Rosemon, French Guiana, Cayenne, France. laureen.dahuron@gmail.com.
Juste GoungoungaUniversité de Rennes, EHESP, CNRS, Inserm, Arènes-UMR 6051, RSMS-U 1309, 35000, Rennes, France.
Moustapha DrameDepartment of Clinical Research and Innovation, University Hospital of Martinique, Fort-de-France, Martinique, France.
Maylis DouineCentre d'Investigation Clinique Antilles-Guyane (CIC Inserm 1424), Centre Hospitalier de Cayenne Andrée Rosemon, French Guiana, Cayenne, France.
Mathieu NacherCentre d'Investigation Clinique Antilles-Guyane (CIC Inserm 1424), Centre Hospitalier de Cayenne Andrée Rosemon, French Guiana, Cayenne, France.
Théo BlaiseCentre d'Investigation Clinique Antilles-Guyane (CIC Inserm 1424), Centre Hospitalier de Cayenne Andrée Rosemon, French Guiana, Cayenne, France.
Emilie MosnierSciences Economiques et Sociales de la Santé et Traitement de l'Information Médicale, UMR1252, Aix Marseille Univ, INSERM, IRD, SESSTIM, Marseille, France.
Lise MussetLaboratoire de parasitologie, Centre Nationale de Référence du Paludisme, World Health Organization Collaborating Centre for Surveillance of Antimalarial Drug Resistance, Institut Pasteur de la Guyane, French Guiana, Cayenne, France.
Marie FouilletInfectious and Tropical Diseases Department, Centre Hospitalier de Cayenne Andrée Rosemon, French Guiana, Cayenne, France.
Félix DjossouInfectious and Tropical Diseases Department, Centre Hospitalier de Cayenne Andrée Rosemon, French Guiana, Cayenne, France.
Loïc EpelboinInfectious and Tropical Diseases Department, Centre Hospitalier de Cayenne Andrée Rosemon, French Guiana, Cayenne, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlasmodium vivax relapses due to dormant liver hypnozoites can be prevented with primaquine. However, the dose must be adjusted in individuals with glucose-6-phosphate-dehydrogenase (G6PD) deficiency. In French Guiana, assessment of G6PD activity is typically delayed until day (D)14 to avoid the risk if misclassification. This study assessed the kinetics of G6PD activity throughout P. vivax infection to inform the timing of treatment.

methodsFor this retrospective monocentric study, data on G6PD activity between D1 and D28 after treatment initiation with chloroquine or artemisinin-based combination therapy were collected for patients followed at Cayenne Hospital, French Guiana, between January 2018 and December 2020. Patients were divided into three groups based on the number of available G6PD activity assessments: (i) at least two measurements during the P. vivax malaria infection; (ii) two measurements: one during the current infection and one previously; (iii) only one measurement during the malaria infection.

resultsIn total, 210 patients were included (80, 20 and 110 in groups 1, 2 and 3, respectively). Data from group 1 showed that G6PD activity remained stable in each patient over time (D1, D3, D7, D14, D21, D28). None of the patients with normal G6PD activity during the initial phase (D1-D3) of the malaria episode (n = 44) was categorized as G6PD-deficient at D14. Patients with G6PD activity < 80% at D1 or D3 showed normal activity at D14. Sex and reticulocyte count were statistically associated with G6PD activity variation. In the whole sample (n = 210), no patient had severe G6PD deficiency (< 10%) and only three between 10 and 30%, giving a G6PD deficiency prevalence of 1.4%. Among the 100 patients from group 1 and 2, 30 patients (26.5%) were lost to follow-up before primaquine initiation.

conclusionsIn patients treated for P. vivax infection, G6PD activity did not vary over time. Therefore, G6PD activity on D1 instead of D14 could be used for primaquine dose-adjustment. This could allow earlier radical treatment with primaquine, that could have a public health impact by decreasing early recurrences and patients lost to follow-up before primaquine initiation. This hypothesis needs to be confirmed in larger prospective studies.

Indexed as

AntimalarialsGlucosephosphate DehydrogenaseMalaria, VivaxAdultAgedAged, 80 and overArtemisininsChloroquineFemaleFrench GuianaGlucosephosphate Dehydrogenase DeficiencyHumansKineticsMaleMiddle AgedPlasmodium vivaxAntimalarialsartemisininArtemisininsChloroquineG6PD protein, humanGlucosephosphate DehydrogenasePrimaquineFrench GuianaG6PD/Glucose-6-phosphase dehydrogenaseMalariaPlasmodium vivaxPrimaquine

Identifiers

PMID38725027
PMCPMC11080303

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Registered trials

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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.