Evidence map›Paper›PMID 38374470›Full record

ArticleEuropean journal of human genetics : EJHG2024

Perceptions and preferences for genetic testing for sickle cell disease or trait: a qualitative study in Cameroon, Ghana and Tanzania.

Nchangwi Syntia Munung, Karen Kengne Kamga, Marsha J Treadwell, Jemima Dennis-Antwi, Kofi A Anie, Daima Bukini, Julie Makani, Ambroise Wonkam

Open access · hybridAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
7.0field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
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  12. Genomic testing in Low- and Middle-Income Countries (LMIC).European journal of human genetics : EJHG · 2024
    Article
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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

8 authors at 5 institutions in 5 countries.

Nchangwi Syntia MunungDivision of Human Genetics, University of Cape Town, Capetown, South Africa. munung.nchangwi@uct.ac.za.ORCID 0000-0003-1498-3602
Karen Kengne KamgaDivision of Human Genetics, University of Cape Town, Capetown, South Africa.
Marsha J TreadwellUniversity of California San Francisco Department of Pediatrics/Division of Hematology, Oakland, CA, USA.
Jemima Dennis-AntwiCentre for Health Development and Research, Accra, Ghana.
Kofi A AnieLondon Northwest University HealthCare (NHS) Trust, London, UK.ORCID 0000-0003-0513-3331
Daima BukiniMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Julie MakaniMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Ambroise WonkamDivision of Human Genetics, University of Cape Town, Capetown, South Africa. awonkam1@jhmi.edu.ORCID 0000-0003-1420-9051
Muhimbili University of Health and Allied Sciences · TZUniversity of Cape Town · ZAImperial College London · GBJohns Hopkins University · USUniversity of California, San Francisco · US

Funding

Sickle Africa Data Coordinating CenterU24HL135600 · NHLBI · UNIVERSITY OF CAPE TOWN · PI MULDER, NICOLA, WONKAM, AMBROISE · 2017 to 2025
$8.6M
Public Understanding of Big data in Genomics Medicine in Africa (PUBGEM-Africa)U01MH127692 · NIMH · UNIVERSITY OF CAPE TOWN · PI MUNUNG, NCHANGWI SYNTIA, WONKAM, AMBROISE · 2021 to 2025
$1.9M
Sickle Pan African Research Consortium NigEria (SPARC-NEt)U01HL156942 · NHLBI · UNIVERSITY OF ABUJA · PI NNODU, OBIAGELI EUNICE · 2021 to 2025
$1.3M
Exploring Perspectives on Genomics and Sickle Cell Public Health InterventionsU01HG007459 · NHGRI · UNIVERSITY OF CAPE TOWN · PI WONKAM, AMBROISE · 2013 to 2016
$622k
NHGRI NIH HHS U01 HG007459NHLBI NIH HHS U01 HL156942NHLBI NIH HHS U24 HL135600NIMH NIH HHS U01 MH127692U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) U24HL135600U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) 1U01MH127692U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) U01HG007459U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) U24HL135600
6 · The paper itself

Abstract

Sickle cell disease (SCD) is a single gene blood disorder characterised by frequent episodes of pain, chronic anaemic, acute chest syndrome, severe disease complications and lifelong debilitating multi-system organ damage. Genetic testing and screening programs for SCD and the sickle cell trait (SCT) are valuable for early diagnosis and management of children living with SCD, and in the identification of carriers of SCT. People with SCT are for the most part asymptomatic and mainly identified as through genetic testing or when they have a child with SCD. This qualitative study explored perceptions towards genetic testing for SCD and SCT in Cameroon, Ghana, and Tanzania. The results show a general preference for newborn screening for SCD over prenatal and premarital/preconception testing, primarily due to its simpler decision-making process and lower risk for stigmatization. Premarital testing for SCT was perceived to be of low public health value, as couples are unlikely to alter their marriage plans despite being aware of their risk of having a child with SCD. Adolescents were identified as a more suitable population for SCT testing. In the case of prenatal testing, major concerns were centred on cultural, religious, and personal values on pregnancy termination. The study revealed a gender dimension to SCD/SCT testing. Participants mentionned that women bear a heightened burden of decision making in SCD/SCT testing, face a higher risk of rejection by potential in-laws/partners if the carriers of SCT, as well as the possibility of  divorce if they have a child with SCD. The study highlights the complex cultural, ethical, religious and social dynamics surrounding genetic testing for SCD and emphasises the need for public education on SCD and the necessity of incorporating genetic and psychosocial counselling into SCD/SCT testing programs.

Indexed as

Anemia, Sickle CellGenetic TestingSickle Cell TraitAdolescentAdultCameroonFemaleGhanaHumansMaleMiddle AgedNeonatal ScreeningPregnancyPrenatal DiagnosisTanzania

Identifiers

PMID38374470
PMCPMC11499917
OpenAlexW4391930122

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.