Evidence map›Paper›PMID 37990692›Full record

ArticleGates open research2023

Heterogenous transmission and seroprevalence of SARS-CoV-2 in two demographically diverse populations with low vaccination uptake in Kenya, March and June 2021.

Patrick K Munywoki, Godfrey Bigogo, Carolyne Nasimiyu, Alice Ouma, George Aol, Clifford O Oduor, Samuel Rono, Joshua Auko, George O Agogo, Ruth Njoroge and 12 more

Abstract read
In one paragraph

Article in Gates open research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

22 authors.

Patrick K MunywokiDivision for Global Health Protection, Global Health Center, U.S. Centers for Disease Control and Prevention (CDC)-Kenya, Nairobi, Kenya.ORCID https://orcid.org/0000-0001-9419-7155
Godfrey BigogoCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Kisumu, Kenya.
Carolyne NasimiyuGlobal Health Program, Washington State University - Global Health Kenya (WSU-GH Kenya), Nairobi, Kenya.
Alice OumaCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Kisumu, Kenya.
George AolCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Kisumu, Kenya.
Clifford O OduorCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Samuel RonoCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Joshua AukoCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Kisumu, Kenya.
George O AgogoDivision for Global Health Protection, Global Health Center, U.S. Centers for Disease Control and Prevention (CDC)-Kenya, Nairobi, Kenya.
Ruth NjorogeGlobal Health Program, Washington State University - Global Health Kenya (WSU-GH Kenya), Nairobi, Kenya.
Dismas OketchGlobal Health Program, Washington State University - Global Health Kenya (WSU-GH Kenya), Nairobi, Kenya.
Dennis OdhiamboCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Kisumu, Kenya.
Victor W OdeyoCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Kisumu, Kenya.
Gilbert KikwaiCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Clayton OnyangoDivision for Global Health Protection, Global Health Center, U.S. Centers for Disease Control and Prevention (CDC)-Kenya, Nairobi, Kenya.
Bonventure JumaDivision for Global Health Protection, Global Health Center, U.S. Centers for Disease Control and Prevention (CDC)-Kenya, Nairobi, Kenya.
Elizabeth HunspergerDivision for Global Health Protection, Global Health Center, U.S. Centers for Disease Control and Prevention (CDC)-Kenya, Nairobi, Kenya.ORCID https://orcid.org/0000-0002-4450-621X
Shirley LidechiCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Kisumu, Kenya.
Caroline Apondi OchiengCentre for Global Health Research, Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Terrence Q LoDivision for Global Health Protection, Global Health Center, U.S. Centers for Disease Control and Prevention (CDC)-Kenya, Nairobi, Kenya.
Peninah MunyuaDivision for Global Health Protection, Global Health Center, U.S. Centers for Disease Control and Prevention (CDC)-Kenya, Nairobi, Kenya.
Amy Herman-RoloffDivision for Global Health Protection, Global Health Center, U.S. Centers for Disease Control and Prevention (CDC)-Kenya, Nairobi, Kenya.

Funding

ACL HHS U01GH002143CGH CDC HHS U01 GH002143
6 · The paper itself

Abstract

Background: SARS-CoV-2 has extensively spread in cities and rural communities, and studies are needed to quantify exposure in the population. We report seroprevalence of SARS-CoV-2 in two well-characterized populations in Kenya at two time points. These data inform the design and delivery of public health mitigation measures. Methods: Leveraging on existing population based infectious disease surveillance (PBIDS) in two demographically diverse settings, a rural site in western Kenya in Asembo, Siaya County, and an urban informal settlement in Kibera, Nairobi County, we set up a longitudinal cohort of randomly selected households with serial sampling of all consenting household members in March and June/July 2021. Both sites included 1,794 and 1,638 participants in the March and June/July 2021, respectively. Individual seroprevalence of SARS-CoV-2 antibodies was expressed as a percentage of the seropositive among the individuals tested, accounting for household clustering and weighted by the PBIDS age and sex distribution. Results: Overall weighted individual seroprevalence increased from 56.2% (95%CI: 52.1, 60.2%) in March 2021 to 63.9% (95%CI: 59.5, 68.0%) in June 2021 in Kibera. For Asembo, the seroprevalence almost doubled from 26.0% (95%CI: 22.4, 30.0%) in March 2021 to 48.7% (95%CI: 44.3, 53.2%) in July 2021. Seroprevalence was highly heterogeneous by age and geography in these populations-higher seroprevalence was observed in the urban informal settlement (compared to the rural setting), and children aged <10 years had the lowest seroprevalence in both sites. Only 1.2% and 1.6% of the study participants reported receipt of at least one dose of the COVID-19 vaccine by the second round of serosurvey-none by the first round. Conclusions: In these two populations, SARS-CoV-2 seroprevalence increased in the first 16 months of the COVID-19 pandemic in Kenya. It is important to prioritize additional mitigation measures, such as vaccine distribution, in crowded and low socioeconomic settings.

Indexed as

COVID-19HouseholdsKenyaPopulation-basedRuralSARS-CoV-2SerologyseroprevalenceSerosurveytransmissionurban informal settlement

Identifiers

PMID37990692
PMCPMC10661969

What Socratic 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 Socratic graph.