Evidence map›Paper›PMID 23614351›Full record

ArticleEpilepsia2013

The genetic risk of acute seizures in African children with falciparum malaria.

Symon M Kariuki, Kirk Rockett, Taane G Clark, Hugh Reyburn, Tsiri Agbenyega, Terrie E Taylor, Gretchen L Birbeck, Thomas N Williams, Charles R J C Newton

Open access · hybridAbstract read
In one paragraph

Article in Epilepsia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.6field-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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  4. Article
  5. Epileptogenesis in Common Parasitic Infections.Current neurology and neuroscience reports · 2022
    Review
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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

9 authors at 5 institutions in 4 countries.

Symon M KariukiKenya Medical Research Institute, Centre for Geographic Medicine Research Coast, Kilifi, Kenya. skariuki@kemri-wellcome.org
Kirk Rockett
Taane G Clark
Hugh Reyburn
Tsiri Agbenyega
Terrie E Taylor
Gretchen L Birbeck
Thomas N Williams
Charles R J C Newton
Kenya Medical Research Institute · KELondon School of Hygiene & Tropical Medicine · GBMichigan State University · USCentre for Human Genetics · GBKwame Nkrumah University of Science and Technology · GH

Funding

Medical Research Council G0600230Wellcome Trust 075491/Z/04Wellcome Trust 077012/Z/05/ZWellcome Trust 083744Wellcome Trust 090532/Z/09/ZWellcome Trust 091758Wellcome Trust 092654Wellcome Trust 099782/Z/12/ZWellcome Trust WT077383/Z/05/Z
6 · The paper itself

Abstract

purposeIt is unclear why some children with falciparum malaria develop acute seizures and what determines the phenotype of seizures. We sought to determine if polymorphisms of malaria candidate genes are associated with acute seizures.

methodsLogistic regression was used to investigate genetic associations with malaria-associated seizures (MAS) and complex MAS (repetitive, prolonged, or focal seizures) in four MalariaGEN African sites, namely: Blantyre, Malawi; Kilifi, Kenya; Kumasi, Ghana; and Muheza, Tanzania. The analysis was repeated for five inheritance models (dominant, heterozygous, recessive, additive, and general) and adjusted for potential confounders and multiple testing. KEY

findingsComplex phenotypes of seizures constituted 71% of all admissions with MAS across the sites. MAS were strongly associated with cluster of differentiation-ligand-rs3092945 in females in Kilifi (p = 0.00068) and interleukin (IL)-17 receptor E-rs708567 in the pooled analysis across the sites (p = 0.00709). Complex MAS were strongly associated with epidermal growth factor module-containing mucin-like hormone receptor (EMR)1-rs373533 in Kumasi (p = 0.00033), but none in the pooled analysis. Focal MAS were strongly associated with IL-20 receptor A-rs1555498 in Muheza (p = 0.00016), but none in the pooled analysis. Prolonged MAS were strongly associated with complement receptor 1-rs17047660 in Kilifi (p = 0.00121) and glucose-6-phosphate dehydrogenase-rs1050828 in females in the pooled analysis (p = 0.00155). Repetitive MAS were strongly associated with EMR1-rs373533 in Kumasi (p = 0.00003) and cystic fibrosis transmembrane conductance receptor-rs17140229 in the pooled analysis (p = 0.00543). MAS with coma/cerebral malaria were strongly associated with EMR1-rs373533 in Kumasi (p = 0.00019) and IL10-rs3024500 in the pooled analysis across the sites (p = 0.00064). SIGNIFICANCE: We have identified a number of genetic associations that may explain the risk of seizures in >2,000 cases admitted to hospitals with MAS across four sites in Africa. These associations differed according to phenotype of seizures and site.

Indexed as

Africa South of the SaharaCalcium-Binding ProteinsChild, PreschoolCystic Fibrosis Transmembrane Conductance RegulatorFemaleGene FrequencyGenetic Association StudiesGenotypeGlucosephosphate DehydrogenaseHumansLogistic ModelsMalaria, FalciparumMaleMembrane GlycoproteinsMucinsPhenotypeADGRE1 protein, humanCalcium-Binding ProteinsCystic Fibrosis Transmembrane Conductance RegulatorGlucosephosphate DehydrogenaseMembrane GlycoproteinsMucinsReceptors, ComplementReceptors, G-Protein-Coupled

Identifiers

PMID23614351
PMCPMC3734649
OpenAlexW2096497657

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LicenceCC BY
Read underepoch 390

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.