Evidence map›Paper›PMID 42288892›Full record

ArticleMalaria journal2026

From silent infection to symptomatic malaria: host phenomic determinants of Plasmodium falciparum outcomes in Fanteakwa South District, Ghana.

Enoch Aninagyei, George Abeiku Abbew, Comfort Addo Boatey, Regina Yayra Menu, Ebenezer Tawiah Nyarkotey, Desmond Omane Acheampong

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Article in Malaria journal, 2026. 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Enoch AninagyeiDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, PMB 31, Ho, Volta Region, Ghana. eaninagyei@uhas.edu.gh.
George Abeiku AbbewDepartment of Biomedical Sciences, School of Allied Health Sciences, University of Cape Coast, Cape Coast, Ghana.
Comfort Addo BoateyDepartment of Biomedical Sciences, School of Allied Health Sciences, University of Cape Coast, Cape Coast, Ghana.
Regina Yayra MenuDepartment of Molecular Biology and Biotechnology, School of Biological Sciences, University of Cape Coast, Cape Coast, Ghana.
Ebenezer Tawiah NyarkoteyDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, PMB 31, Ho, Volta Region, Ghana.
Desmond Omane AcheampongDepartment of Biomedical Sciences, School of Allied Health Sciences, University of Cape Coast, Cape Coast, Ghana. dacheampong@ucc.edu.gh.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAsymptomatic Plasmodium falciparum infections sustain malaria transmission in endemic areas, yet progression to symptomatic disease varies among individuals. This study examined asymptomatic infection in Fanteakwa South District, Ghana, focusing on how demographic and host phenomic factors influence progression to symptomatic malaria.

methodsThis study employed a prospective cohort design nested within a cross-sectional survey. Participants of all ages were recruited from four communities using stratified random sampling and screened for malaria using mRDT and PCR. ABO blood group, Rhesus D factor, and haemoglobin phenotype were determined. Individuals with asymptomatic P. falciparum infection were followed weekly for 28 days with repeat mRDT, microscopy, and temperature measurements. Statistical analyses evaluated associations between demographic, phenomic, and infection outcomes.

resultsAmong 353 participants, females constituted 59.8%, and adults aged 18-65 years were the largest age group (42.5%). Blood group O (55.8%), HbAA (85.3%), and Rhesus D positivity (91.8%) predominated. PCR detected more P. falciparum infections (52.1%) than mRDT (42.8%), indicating a substantial burden of submicroscopic asymptomatic malaria. PCR positivity varied across communities and was highest among children (61.9%) and adolescents (68.6%). During follow-up, 131 participants (37.1%) converted to mRDT and microscopy positivity, with 43.5% converting in the first week. Early conversion was most frequent among children (54.5%, p < 0.001), followed by adolescents, while adults and older adults showed fewer early conversions. Individuals with blood groups A and AB progressed earlier, whereas blood group O showed delayed conversion. All conversions occurred among HbAA individuals, with no progression among HbAS carriers. The Rhesus D factor had no significant effect, while gender differences emerged later, with higher conversion among males in Week 3 (p = 0.015).

conclusionProgression from asymptomatic to symptomatic P. falciparum infection is strongly shaped by age and host erythrocyte phenomic traits. Blood groups A and AB and the HbAA phenotype favour early conversion, whereas blood group O and HbAS delay or prevent progression. These findings underscore the importance of molecular surveillance and phenome-informed risk stratification for targeted malaria control in endemic communities.

Indexed as

Asymptomatic InfectionsMalaria, FalciparumPlasmodium falciparumAdolescentAdultAgedChildChild, PreschoolCross-Sectional StudiesDisease ProgressionFemaleGhanaHumansInfantMaleMiddle AgedABO blood groupAsymptomatic malariaGhanaHaemoglobin variantsHost phenomesMolecular epidemiologyPlasmodium falciparum

Identifiers

PMID42288892
PMCPMC13491822

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.