Evidence map›Paper›PMID 35725456›Full record

ArticleMalaria journal2022

Maintenance of high temporal Plasmodium falciparum genetic diversity and complexity of infection in asymptomatic and symptomatic infections in Kilifi, Kenya from 2007 to 2018.

Kelvin M Kimenyi, Kevin Wamae, Joyce M Ngoi, Zaydah R de Laurent, Leonard Ndwiga, Victor Osoti, George Obiero, Abdirahman I Abdi, Philip Bejon, Lynette Isabella Ochola-Oyier

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 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 3 institutions in 3 countries.

Kelvin M KimenyiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. kmuteru@kemri-wellcome.org.ORCID http://orcid.org/0000-0002-7157-1041
Kevin WamaeKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Joyce M NgoiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Zaydah R de LaurentKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Leonard NdwigaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Victor OsotiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
George ObieroDepartment of Biochemistry, University of Nairobi, Nairobi, Kenya.
Abdirahman I AbdiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Philip BejonKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Lynette Isabella Ochola-OyierKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Kenya Medical Research Institute · KEAfrica Center · USUniversity of Nairobi · KE

Funding

DELGEME 107740/Z/15/ZWellcome TrustWellcome Trust 107568/Z/15/ZWellcome Trust 209289/Z/17/Z
6 · The paper itself

Abstract

backgroundHigh levels of genetic diversity are common characteristics of Plasmodium falciparum parasite populations in high malaria transmission regions. There has been a decline in malaria transmission intensity over 12 years of surveillance in the community in Kilifi, Kenya. This study sought to investigate whether there was a corresponding reduction in P. falciparum genetic diversity, using msp2 as a genetic marker.

methodsBlood samples were obtained from children (< 15 years) enrolled into a cohort with active weekly surveillance between 2007 and 2018 in Kilifi, Kenya. Asymptomatic infections were defined during the annual cross-sectional blood survey and the first-febrile malaria episode was detected during the weekly follow-up. Parasite DNA was extracted and successfully genotyped using allele-specific nested polymerase chain reactions for msp2 and capillary electrophoresis fragment analysis.

resultsBased on cross-sectional surveys conducted in 2007-2018, there was a significant reduction in malaria prevalence (16.2-5.5%: P-value < 0.001), however msp2 genetic diversity remained high. A high heterozygosity index (He) (> 0.95) was observed in both asymptomatic infections and febrile malaria over time. About 281 (68.5%) asymptomatic infections were polyclonal (> 2 variants per infection) compared to 46 (56%) polyclonal first-febrile infections. There was significant difference in complexity of infection (COI) between asymptomatic 2.3 [95% confidence interval (CI) 2.2-2.5] and febrile infections 2.0 (95% CI 1.7-2.3) (P = 0.016). Majority of asymptomatic infections (44.2%) carried mixed alleles (i.e., both FC27 and IC/3D7), while FC27 alleles were more frequent (53.3%) among the first-febrile infections.

conclusionsPlasmodium falciparum infections in Kilifi are still highly diverse and polyclonal, despite the reduction in malaria transmission in the community.

Indexed as

Malaria, FalciparumPlasmodium falciparumAntigens, ProtozoanAsymptomatic InfectionsChildCross-Sectional StudiesFeverGenetic VariationGenotypeHumansKenyaProtozoan ProteinsAntigens, ProtozoanProtozoan ProteinsComplexity of infectionsGenetic diversityKenyaMalariamsp2P. falciparum

Identifiers

PMID35725456
PMCPMC9207840
OpenAlexW4283155876

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.