Evidence map›Paper›PMID 36076204›Full record

ArticleMalaria journal2022

Prevalence of G6PD deficiency and distribution of its genetic variants among malaria-suspected patients visiting Metehara health centre, Eastern Ethiopia.

Tassew Tefera Shenkutie, Desalegn Nega, Asrat Hailu, Daniel Kepple, Logan Witherspoon, Eugenia Lo, Meshesha Tsigie Negash, Aderaw Adamu, Shewayiref Geremew Gebremichael, Bokretsion Gidey and 3 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  7. Observational
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  12. Prevalence and characteristics ofmedRxiv : the preprint server for health sciences · 2023
    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

13 authors at 5 institutions in 2 countries.

Tassew Tefera ShenkutieDepartment of Medical Laboratory Sciences, Debre Berhan University, Debre Berhan, Ethiopia. tassewtefera@gmail.com.ORCID http://orcid.org/0000-0003-0281-0456
Desalegn NegaBacterial, Parasitic, and Zoonotic Diseases Research Directorate, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Asrat HailuDepartment of Microbiology, Immunology and Parasitology, Addis Ababa University, Addis Ababa, Ethiopia.
Daniel KeppleDepartment of Biological Sciences, University of North Carolina, Charlotte, NC, USA.
Logan WitherspoonDepartment of Biological Sciences, University of North Carolina, Charlotte, NC, USA.
Eugenia LoDepartment of Biological Sciences, University of North Carolina, Charlotte, NC, USA.
Meshesha Tsigie NegashBacterial, Parasitic, and Zoonotic Diseases Research Directorate, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Aderaw AdamuDepartment of Medical Laboratory Sciences, Wollo University, Dessie, Ethiopia.
Shewayiref Geremew GebremichaelNational Data Management Centre for Health, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Bokretsion GideyBacterial, Parasitic, and Zoonotic Diseases Research Directorate, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Geremew TasewBacterial, Parasitic, and Zoonotic Diseases Research Directorate, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Sindew M FelekeBacterial, Parasitic, and Zoonotic Diseases Research Directorate, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Tadesse KebedeDepartment of Microbiology, Immunology and Parasitology, Addis Ababa University, Addis Ababa, Ethiopia.
Ethiopian Public Health Institute · ETUniversity of North Carolina at Charlotte · USAddis Ababa University · ETDebre Berhan University · ETWollo University · ET

Funding

Plasmodium vivax Erythrocyte Invasion Mechanisms and Humoral Immune Response in Duffy Negative AfricansR01AI162947 · NIAID · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI Eugenia Lo · 2022 to 2026
$3.4M
NIAID NIH HHS R01 AI162947
6 · The paper itself

Abstract

backgroundGlucose-6-phosphate dehydrogenase (G6PD) is cytosolic enzyme, which has a vital role for the integrity and functioning of red blood cells. Lower activity of this enzyme leads to the occurrence of acute haemolytic anaemia after exposure to oxidative stressors like primaquine. Primaquine is an important drug for the radical cure of Plasmodium vivax and blocking transmission of Plasmodium falciparum, and thereby enhancing malaria elimination. However, there is a need to identify G6PD deficient individuals and administer the drug with caution due to its haemolytic side effects. The main objective of this study is to determine the prevalence of G6PD deficiency among malaria-suspected individuals.

methodsA facility-based cross-sectional study was conducted from September 2020 to September 2021 in Metehara Health Centre, Eastern Ethiopia. A structured questionnaire was used to collect the socio-demographic and clinical information of the study participants. Capillary and venous blood samples were collected based on standard procedures for onsite screening, dried blood spot preparation, and malaria microscopy. The G6PD enzyme activity was measured by careSTART™ G6PD biosensor analyzer. Data was entered and analysed by SPSS.

resultsA total of 498 study participants were included in the study, of which 62% (309) were males. The overall prevalence of G6PD deficiency based on the biosensor screening was 3.6% (18/498), of which 2.9% and 4.8% were males and females, respectively. Eleven of the G6PD deficient samples had mutations confirmed by G6PD gene sequencing analysis. Mutations were detected in G267 + 119C/T, A376T, and ChrX:154535443. A significant association was found in sex and history of previous malaria infection with G6PD deficiency.

conclusionsThe study showed that the G6PD deficient phenotype exists in Metehara even if the prevalence is not very high. G267 + 119C/T mutation is the predominant G6PD variant in this area. Therefore, malaria patient treatment using primaquine should be monitored closely for any adverse effects.

Indexed as

AntimalarialsGlucosephosphate Dehydrogenase DeficiencyMalariaMalaria, VivaxCross-Sectional StudiesEthiopiaFemaleHemolysisHumansMalePrevalencePrimaquineAntimalarialsPrimaquineEthiopiaGlucose-6-phosphate dehydrogenaseMeteharaPlasmodium falciparumPlasmodium vivaxPrimaquine

Identifiers

PMID36076204
PMCPMC9461287
OpenAlexW4295083617

What OpenQuestion holds

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LicenceCC BY
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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.