Evidence map›Paper›PMID 41073974›Full record

ArticleBMC infectious diseases2025

Cycle threshold values and SARS-CoV-2 variant associations with breakthrough infections: a retrospective study in Accra, Ghana.

Frank Twum Aboagye, Lawrence Annison, Ebenezer Krampah Aidoo, Maame Ekua Acquah, Yvonne Aryeetey Ashong, Betty Bandoh Oppong, Lawrencia Osae-Nyarko, Isaac Owusu-Frimpong, Henry Kwadwo Hackman, Sharon Annison and 5 more

Erratum issuedAbstract read
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Frank Twum AboagyeDepartment of Medical Laboratory Technology, Faculty of Applied Sciences, Accra Technical University, Accra, Ghana. frankaboagye71@gmail.com.
Lawrence AnnisonDepartment of Medical Laboratory Technology, Faculty of Applied Sciences, Accra Technical University, Accra, Ghana.
Ebenezer Krampah AidooDepartment of Medical Laboratory Technology, Faculty of Applied Sciences, Accra Technical University, Accra, Ghana.
Maame Ekua AcquahWest African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Yvonne Aryeetey AshongDepartment of Parasitology, College of Medical Sciences, Noguchi Memorial Institute of Medical Research, University of Ghana, Legon, Accra, Ghana.
Betty Bandoh OppongBiomedical and Public Health Research Unit, Council for Scientific and Industrial Research - Water Research Institute, Accra, Ghana.
Lawrencia Osae-NyarkoBiomedical and Public Health Research Unit, Council for Scientific and Industrial Research - Water Research Institute, Accra, Ghana.
Isaac Owusu-FrimpongDepartment of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, United States of America.
Henry Kwadwo HackmanDepartment of Medical Laboratory Technology, Faculty of Applied Sciences, Accra Technical University, Accra, Ghana.
Sharon AnnisonDepartment of Epidemiology and Disease Control, School of Public Health, University of Ghana, Legon, Accra, Ghana.
Queenstar Dedei QuarshieBiomedical and Public Health Research Unit, Council for Scientific and Industrial Research - Water Research Institute, Accra, Ghana.
Abena Konadu Owusu-Senyah EnninfulBiomedical and Public Health Research Unit, Council for Scientific and Industrial Research - Water Research Institute, Accra, Ghana.
Naa Adjeley KumaBiomedical and Public Health Research Unit, Council for Scientific and Industrial Research - Water Research Institute, Accra, Ghana.
Bill Clinton EgyamDepartment of Molecular Biology, MDS Lancet Laboratories Ghana Limited, East Legon, Accra, Ghana.
Mike Y Osei-AtweneboanaBiomedical and Public Health Research Unit, Council for Scientific and Industrial Research - Water Research Institute, Accra, Ghana. oseiatweneboana@yahoo.co.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreakthrough infections are defined as SARS-CoV-2 infections occurring ≥ 14 days after completing the primary COVID-19 vaccination series and remain a public health challenge, particularly in regions where immune-evasive variants are circulating. However, data on their virological and clinical profiles in low-resource settings are limited.

methodsThis retrospective study was conducted from July to December 2022 in Accra, Ghana, among individuals testing positive for SARS-CoV-2. Real-time Reverse Transcription Polymerase Chain Reaction (RT-PCR) was performed using the Allplex™ 2019-nCoV Assay. Cycle threshold (Ct) values for the nucleocapsid (N), RNA-dependent RNA polymerase (RdRP), and envelope (E) genes, categorised as < 25, 25–30, or > 30. Variant identification targeted Alpha, Delta, and Omicron mutations using mutation-specific RT-PCR. Logistic regression was used to assess associations between vaccination status and demographic, clinical, and virological factors.

resultsOf the 268 samples analysed, 81 tested positive; 43.20% [n = 35] were vaccinated individuals. Median Ct-values for the N [27.13, IQR: 21.59–31.96] and E [24.57, IQR: 19.43–29.43] genes were significantly higher among vaccinated cases, indicating lower viral loads. Breakthrough infections were strongly associated with the Omicron variant [aOR = 4.38, p = 0.034]. Diarrhoea [aOR = 9.67, p = 0.022], sore throat [aOR = 8.99, p = 0.038], headache [aOR = 10.156, p = 0.039] and chills [aOR = 3.316, p = 0.046] were mostly associated with breakthrough infections. Ct-values of 25–30 [aOR = 11.33, p = 0.012] and > 30 [aOR = 4.01, p = 0.047] were significantly associated with breakthrough infection compared to Ct < 25 in breakthrough infections.

conclusionVaccinated individuals with SARS-CoV-2 infection had lower viral loads and were more likely to be infected with the Omicron variant. These findings reinforce the role of vaccination in reducing viral load and support the adoption of practical surveillance strategies, such as Ct value-based surveillance and variant screening in low middle-income countries facing similar constraints in genomic capacity and vaccine deployment.

Indexed as

COVID-19SARS-CoV-2AdolescentAdultAgedBreakthrough InfectionsCOVID-19 VaccinesFemaleGhanaHumansMaleMiddle AgedRetrospective StudiesVaccinationYoung AdultCOVID-19 VaccinesBreakthrough infectionCOVID-19 vaccinationGhanaSARS-CoV-2Variants

Identifiers

PMID41073974
PMCPMC12513011

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.