Evidence map›Paper›PMID 25885177›Full record

ArticleMalaria journal2015

G6PD gene variants and its association with malaria in a Sri Lankan population.

Rajika L Dewasurendra, Kirk A Rockett, S Deepika Fernando, Richard Carter, Dominic P Kwiatkowski, Nadira D Karunaweera, MalariaGEN Consortium

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 8% 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

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

  1. Pooled it
  2. Article
  3. No G6PD A- (G202A) variant detected amongMalariaWorld journal · 2026
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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 2 countries.

Rajika L DewasurendraDepartment of Parasitology, Faculty of Medicine, University of Colombo, 25, Kynsey Road, Colombo 08, Sri Lanka. rdewasurendra@yahoo.com.
Kirk A RockettTheWellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3, 7BN, UK. kirk.rockett@well.ox.ac.uk.
S Deepika FernandoDepartment of Parasitology, Faculty of Medicine, University of Colombo, 25, Kynsey Road, Colombo 08, Sri Lanka. ferndeep@gmail.com.
Richard CarterDivision of Biological Sciences, Ashworth Laboratories, University of Edinburgh, West Mains Rd, Edinburgh, EH9 3JT, UK. r.carter@ed.ac.uk.
Dominic P KwiatkowskiTheWellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3, 7BN, UK. dominic@well.ox.ac.uk.
Nadira D KarunaweeraDepartment of Parasitology, Faculty of Medicine, University of Colombo, 25, Kynsey Road, Colombo 08, Sri Lanka. nadira@parasit.cmb.ac.lk.
MalariaGEN Consortium
University of Colombo · LKUniversity of Oxford · GBUniversity of Edinburgh · GB

Funding

Medical Research Council G0600230Medical Research Council G0600718Medical Research Council MR/M006212/1Wellcome Trust 075491/Z04Wellcome Trust 090532/Z/09/Z)Wellcome Trust 090770Wellcome Trust 090770/Z/09/ZWellcome Trust WT077383/Z/05/Z
6 · The paper itself

Abstract

backgroundGlucose-6-phosphate dehydrogenase (G6PD) is an enzyme that plays an important role in many cellular functions. Deficiency of this enzyme results from point mutations in the coding region of the G6PD gene. G6PD-deficiency is important in malaria, as certain anti-malarial drugs could induce haemolysis in such patients and mutations in this gene may influence the susceptibility or resistance to the disease. Detailed information on genetic variations in the G6PD gene for Sri Lankan populations is yet to be revealed. This study describes a set of G6PD mutations present in a Sri Lankan population and their association with uncomplicated malaria.

methodsDNA was extracted from 1,051 individuals. Sixty-eight SNPs in the region of the G6PD gene were genotyped. A database created during the 1992-1993 malaria epidemic for the same individuals was used to assess the associations between the G6PD SNPs and parasite density or disease severity of uncomplicated malaria infections. Linkage disequilibrium for SNPs and haplotype structures were identified.

resultsSeventeen genetic variants were polymorphic in this population. The mutant allele was the major allele in 9 SNPs. Common G6PD variants already described in Asians or South-Asians seemed to be absent or rare in this population. Both the severity of disease in uncomplicated malaria infections and parasitaemia were significantly lower in males infected with Plasmodium falciparum carrying the ancestral allele of rs915942 compared to those carrying the mutant allele. The parasite density of males infected with P. falciparum was significantly lower also in those who possessed the mutant alleles of rs5986877, rs7879049 and rs7053878. Two haplotype blocks were identified, where the recombination rates were higher in males with no history of malaria when compared to those who have experienced the disease in the past.

conclusionsThis is the most detailed survey of G6PD SNPs in a Sri Lankan population undertaken so far that enabled novel description of single nucleotide polymorphisms within the G6PD gene. A few of these genetic variations identified, demonstrated a tendency to be associated with either disease severity or parasite density in uncomplicated disease in males. Known G6PD gene polymorphisms already described from elsewhere were either absent or rare in the local study population.

Indexed as

AdolescentAdultAgedAged, 80 and overFemaleGlucosephosphate DehydrogenaseHaplotypesHumansMalariaMaleMiddle AgedPolymorphism, Single NucleotideSri LankaYoung AdultGlucosephosphate Dehydrogenase

Identifiers

PMID25885177
PMCPMC4343272
OpenAlexW2129931260

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.