Evidence map›Paper›PMID 29381699›Full record

ArticlePLoS genetics2018

Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania.

Matt Ravenhall, Susana Campino, Nuno Sepúlveda, Alphaxard Manjurano, Behzad Nadjm, George Mtove, Hannah Wangai, Caroline Maxwell, Raimos Olomi, Hugh Reyburn and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 84 citations in OpenAlex.

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  9. A novel locus inFrontiers in genetics · 2024
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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

14 authors at 3 institutions in 4 countries.

Matt RavenhallPathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-7818-2348
Susana CampinoPathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Nuno SepúlvedaDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-8542-1706
Alphaxard ManjuranoJoint Malaria Programme, Kilimanjaro Christian Medical College, Moshi, Tanzania.ORCID 0000-0001-7583-6425
Behzad NadjmJoint Malaria Programme, Kilimanjaro Christian Medical College, Moshi, Tanzania.ORCID 0000-0002-7704-3629
George MtoveJoint Malaria Programme, Kilimanjaro Christian Medical College, Moshi, Tanzania.
Hannah WangaiJoint Malaria Programme, Kilimanjaro Christian Medical College, Moshi, Tanzania.
Caroline MaxwellJoint Malaria Programme, Kilimanjaro Christian Medical College, Moshi, Tanzania.
Raimos OlomiJoint Malaria Programme, Kilimanjaro Christian Medical College, Moshi, Tanzania.
Hugh ReyburnDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0003-4186-8861
Christopher J DrakeleyDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Eleanor M RileyDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Taane G ClarkPathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0001-8985-9265
MalariaGEN
Christian Medical College, Vellore · INUniversity of London · GBUniversity of Lisbon · PT

Funding

Medical Research Council G0600230Medical Research Council G0600718Medical Research Council MC_PC_15103Medical Research Council MR/K000551/1Medical Research Council MR/M01360X/1Medical Research Council MR/N010469/1Wellcome Trust
6 · The paper itself

Abstract

Significant selection pressure has been exerted on the genomes of human populations exposed to Plasmodium falciparum infection, resulting in the acquisition of mechanisms of resistance against severe malarial disease. Many host genetic factors, including sickle cell trait, have been associated with reduced risk of developing severe malaria, but do not account for all of the observed phenotypic variation. Identification of novel inherited risk factors relies upon high-resolution genome-wide association studies (GWAS). We present findings of a GWAS of severe malaria performed in a Tanzanian population (n = 914, 15.2 million SNPs). Beyond the expected association with the sickle cell HbS variant, we identify protective associations within two interleukin receptors (IL-23R and IL-12RBR2) and the kelch-like protein KLHL3 (all P<10-6), as well as near significant effects for Major Histocompatibility Complex (MHC) haplotypes. Complementary analyses, based on detecting extended haplotype homozygosity, identified SYNJ2BP, GCLC and MHC as potential loci under recent positive selection. Through whole genome sequencing of an independent Tanzanian cohort (parent-child trios n = 247), we confirm the allele frequencies of common polymorphisms underlying associations and selection, as well as the presence of multiple structural variants that could be in linkage with these SNPs. Imputation of structural variants in a region encompassing the glycophorin genes on chromosome 4, led to the characterisation of more than 50 rare variants, and individually no strong evidence of associations with severe malaria in our primary dataset (P>0.3). Our approach demonstrates the potential of a joint genotyping-sequencing strategy to identify as-yet unknown susceptibility loci in an African population with well-characterised malaria phenotypes. The regions encompassing these loci are potential targets for the design of much needed interventions for preventing or treating malarial disease.

Indexed as

Polymorphism, Single NucleotideSelection, GeneticCase-Control StudiesChildChild, PreschoolFemaleGene FrequencyGenetic Predisposition to DiseaseGenome-Wide Association StudyHaplotypesHumansInfantMalaria, FalciparumMalePhenotypeSeverity of Illness Index

Identifiers

PMID29381699
PMCPMC5806895
OpenAlexW2785373513

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.