Evidence map›Paper›PMID 39164542›Full record

ArticleActa parasitologica2024

Glucose-6-phosphate Dehydrogenase Variants: Analysing in Indian Plasmodium vivax Patients.

Jahnvi Jakhan, Loick Pradel Kojom Foko, Geetika Narang, Vineeta Singh

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Article in Acta parasitologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Jahnvi JakhanICMR-National Institute of Malaria Research (NIMR), Dwarka, Sector-8, New Delhi, 110077, India.ORCID http://orcid.org/0000-0001-9443-558X
Loick Pradel Kojom FokoICMR-National Institute of Malaria Research (NIMR), Dwarka, Sector-8, New Delhi, 110077, India.ORCID http://orcid.org/0000-0002-4286-147X
Geetika NarangICMR-National Institute of Malaria Research (NIMR), Dwarka, Sector-8, New Delhi, 110077, India.ORCID http://orcid.org/0000-0002-9905-1857
Vineeta SinghICMR-National Institute of Malaria Research (NIMR), Dwarka, Sector-8, New Delhi, 110077, India. vineetas_2000@yahoo.com.ORCID http://orcid.org/0000-0003-0113-7394

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePrimaquine (PQ) is recommended for radical cure of Plasmodium vivax (Pv) malaria, but its utilization is still limited due to high risk of severe haemolytic anaemia in patients with glucose-6-phosphate dehydrogenase deficiency (G6PD-d). The aim of the present study is to assess the different genotypic variants leading to G6PD-d in Delhi and Goa regions of India.

methodsA total of 46 samples (34 retrospective Pv-mono-infected samples and 12 Pv-uninfected samples) were included in the study. Various genetic variants leading to G6PD-d were analysed by PCR amplification and DNA sequencing of different targeted exons of G6PD gene.

resultsMolecular analysis showed presence of four mutations in study population viz. 1311 C > T, 34.1% & IVSXI 93T > C, 45.5% and two novel mutations 1388G > T, 2.3% and 1398 C > T, 2.3% (silent mutation). The bioinformatics and computational analysis demonstrate that the slight conformational changes caused by R643L mutation in protein are deleterious in nature.

conclusionThe observed mutations do not clarify the role or association between G6PD-d and Pv-infected cases. Further investigation is required in order to fully comprehend and analyse the precise role of these mutations with context to malaria infections.

Indexed as

Glucosephosphate DehydrogenaseGlucosephosphate Dehydrogenase DeficiencyMalaria, VivaxPlasmodium vivaxAdultFemaleGenetic VariationGenotypeHumansIndiaMaleMutationRetrospective StudiesG6PD protein, humanGlucosephosphate DehydrogenaseG6PD-deficiencyGenetic polymorphismIndiaPlasmodium vivax

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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.