Characteristics of included studies.

<div><p>Introduction</p><p>Sickle Cell Anemia (SCA) is a significant genetic disorder in Africa; however, comprehensive data on its prevalence and geographic distribution remain limited. We aimed to estimate the pooled prevalence of SCA (HbSS) in African populations and exami...

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Autor principal: Bwambale Jonani (21156747) (author)
Outros Autores: Emmanuel Charles Kasule (21156750) (author), Bwire Roman Herman (21168941) (author), Joel Fredrick Arturo (21156756) (author), Mwesigwa Calvin Mugambwa (22683322) (author), Ssebulime Stephen (21156771) (author), John Bosco Mundaka (20309196) (author), Richard Kwizera (606632) (author), Gerald Mboowa (770601) (author), Felix Bongomin (5081681) (author)
Publicado em: 2025
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_version_ 1849927629027672064
author Bwambale Jonani (21156747)
author2 Emmanuel Charles Kasule (21156750)
Bwire Roman Herman (21168941)
Joel Fredrick Arturo (21156756)
Mwesigwa Calvin Mugambwa (22683322)
Ssebulime Stephen (21156771)
John Bosco Mundaka (20309196)
Richard Kwizera (606632)
Gerald Mboowa (770601)
Felix Bongomin (5081681)
author2_role author
author
author
author
author
author
author
author
author
author_facet Bwambale Jonani (21156747)
Emmanuel Charles Kasule (21156750)
Bwire Roman Herman (21168941)
Joel Fredrick Arturo (21156756)
Mwesigwa Calvin Mugambwa (22683322)
Ssebulime Stephen (21156771)
John Bosco Mundaka (20309196)
Richard Kwizera (606632)
Gerald Mboowa (770601)
Felix Bongomin (5081681)
author_role author
dc.creator.none.fl_str_mv Bwambale Jonani (21156747)
Emmanuel Charles Kasule (21156750)
Bwire Roman Herman (21168941)
Joel Fredrick Arturo (21156756)
Mwesigwa Calvin Mugambwa (22683322)
Ssebulime Stephen (21156771)
John Bosco Mundaka (20309196)
Richard Kwizera (606632)
Gerald Mboowa (770601)
Felix Bongomin (5081681)
dc.date.none.fl_str_mv 2025-11-25T18:27:01Z
dc.identifier.none.fl_str_mv 10.1371/journal.pone.0337090.t001
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/Characteristics_of_included_studies_/30713614
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Biotechnology
Science Policy
Infectious Diseases
Biological Sciences not elsewhere classified
three decades despite
systematically searched pubmed
sickle cell anemia
electrophoretic techniques predominated
21 %– 8
1994 &# 8211
improved diagnostic accessibility
southern africa showed
sensitivity analysis showed
central africa showed
74 %; p
significant genetic disorder
including geographic region
08 %– 1
analysis </ p
2 </ sup
males 2
diagnostic method
xlink ">
temporal variations
systematic review
subgroup analyses
study variability
study design
specific interventions
significantly moderated
research output
remained stable
quality assurance
quality assessments
prediction interval
marginally significant
logit transformation
google scholar
fold increase
findings highlight
examine regional
continued surveillance
comprehensive data
children exhibited
cases ).
care technologies
base databases
african populations
91 %.
88 %),
839 participants
694 ).
65 %)
6 %).
dc.title.none.fl_str_mv Characteristics of included studies.
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description <div><p>Introduction</p><p>Sickle Cell Anemia (SCA) is a significant genetic disorder in Africa; however, comprehensive data on its prevalence and geographic distribution remain limited. We aimed to estimate the pooled prevalence of SCA (HbSS) in African populations and examine regional, demographic, and temporal variations from 1994–2024.</p><p>Methods</p><p>We systematically searched PubMed, Scopus, Google Scholar, and BASE databases for studies reporting SCA prevalence in African populations. Screening and quality assessments were performed using JBI tools. A random-effects meta-analysis with logit transformation was performed, with subgroup analyses by region, age, sex, and study design. Meta-regression explored heterogeneity sources, including geographic region, age category, diagnostic method, study design, and publication year.</p><p>Results</p><p>From 115 studies with 1,203,839 participants and 17,458 confirmed HbSS cases, the pooled prevalence was 1.43% (95% CI: 1.08%–1.88%), with substantial heterogeneity (I<sup>2</sup> = 99.1%) and a prediction interval of 0.21%–8.91%. Central Africa showed the highest prevalence (1.99%), and Southern Africa showed the lowest (0.59%). Children exhibited a higher prevalence (1.65%) than adults (0.45%), while sex differences were non-significant (males 2.71%, females 1.74%; p = 0.694). The prevalence has remained stable over three decades despite a six-fold increase in research output, although wide prediction intervals indicated substantial between-study variability. Electrophoretic techniques predominated (86.4% of cases). Diagnostic method (χ² = 16.73, p = 0.033) and age category (χ² = 33.66, p < 0.0001) significantly moderated the prevalence. The multivariable meta-regression was marginally significant (χ² = 29.01, p = 0.066), but substantial residual heterogeneity persisted (I<sup>2</sup> = 98.6%). Leave-one-out sensitivity analysis showed that no single study significantly impacted the pooled estimates.</p><p>Conclusion</p><p>SCA represents a substantial and geographically variable public health challenge across Africa. These findings highlight the need for region-specific interventions, expanded newborn screening programs, improved diagnostic accessibility with quality assurance for point-of-care technologies, and continued surveillance to address geographic gaps.</p></div>
eu_rights_str_mv openAccess
id Manara_a15746ea1fdecbd79a3bbfe5337efc9d
identifier_str_mv 10.1371/journal.pone.0337090.t001
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30713614
publishDate 2025
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling Characteristics of included studies.Bwambale Jonani (21156747)Emmanuel Charles Kasule (21156750)Bwire Roman Herman (21168941)Joel Fredrick Arturo (21156756)Mwesigwa Calvin Mugambwa (22683322)Ssebulime Stephen (21156771)John Bosco Mundaka (20309196)Richard Kwizera (606632)Gerald Mboowa (770601)Felix Bongomin (5081681)BiotechnologyScience PolicyInfectious DiseasesBiological Sciences not elsewhere classifiedthree decades despitesystematically searched pubmedsickle cell anemiaelectrophoretic techniques predominated21 %– 81994 &# 8211improved diagnostic accessibilitysouthern africa showedsensitivity analysis showedcentral africa showed74 %; psignificant genetic disorderincluding geographic region08 %– 1analysis </ p2 </ supmales 2diagnostic methodxlink ">temporal variationssystematic reviewsubgroup analysesstudy variabilitystudy designspecific interventionssignificantly moderatedresearch outputremained stablequality assurancequality assessmentsprediction intervalmarginally significantlogit transformationgoogle scholarfold increasefindings highlightexamine regionalcontinued surveillancecomprehensive datachildren exhibitedcases ).care technologiesbase databasesafrican populations91 %.88 %),839 participants694 ).65 %)6 %).<div><p>Introduction</p><p>Sickle Cell Anemia (SCA) is a significant genetic disorder in Africa; however, comprehensive data on its prevalence and geographic distribution remain limited. We aimed to estimate the pooled prevalence of SCA (HbSS) in African populations and examine regional, demographic, and temporal variations from 1994–2024.</p><p>Methods</p><p>We systematically searched PubMed, Scopus, Google Scholar, and BASE databases for studies reporting SCA prevalence in African populations. Screening and quality assessments were performed using JBI tools. A random-effects meta-analysis with logit transformation was performed, with subgroup analyses by region, age, sex, and study design. Meta-regression explored heterogeneity sources, including geographic region, age category, diagnostic method, study design, and publication year.</p><p>Results</p><p>From 115 studies with 1,203,839 participants and 17,458 confirmed HbSS cases, the pooled prevalence was 1.43% (95% CI: 1.08%–1.88%), with substantial heterogeneity (I<sup>2</sup> = 99.1%) and a prediction interval of 0.21%–8.91%. Central Africa showed the highest prevalence (1.99%), and Southern Africa showed the lowest (0.59%). Children exhibited a higher prevalence (1.65%) than adults (0.45%), while sex differences were non-significant (males 2.71%, females 1.74%; p = 0.694). The prevalence has remained stable over three decades despite a six-fold increase in research output, although wide prediction intervals indicated substantial between-study variability. Electrophoretic techniques predominated (86.4% of cases). Diagnostic method (χ² = 16.73, p = 0.033) and age category (χ² = 33.66, p < 0.0001) significantly moderated the prevalence. The multivariable meta-regression was marginally significant (χ² = 29.01, p = 0.066), but substantial residual heterogeneity persisted (I<sup>2</sup> = 98.6%). Leave-one-out sensitivity analysis showed that no single study significantly impacted the pooled estimates.</p><p>Conclusion</p><p>SCA represents a substantial and geographically variable public health challenge across Africa. These findings highlight the need for region-specific interventions, expanded newborn screening programs, improved diagnostic accessibility with quality assurance for point-of-care technologies, and continued surveillance to address geographic gaps.</p></div>2025-11-25T18:27:01ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.1371/journal.pone.0337090.t001https://figshare.com/articles/dataset/Characteristics_of_included_studies_/30713614CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/307136142025-11-25T18:27:01Z
spellingShingle Characteristics of included studies.
Bwambale Jonani (21156747)
Biotechnology
Science Policy
Infectious Diseases
Biological Sciences not elsewhere classified
three decades despite
systematically searched pubmed
sickle cell anemia
electrophoretic techniques predominated
21 %– 8
1994 &# 8211
improved diagnostic accessibility
southern africa showed
sensitivity analysis showed
central africa showed
74 %; p
significant genetic disorder
including geographic region
08 %– 1
analysis </ p
2 </ sup
males 2
diagnostic method
xlink ">
temporal variations
systematic review
subgroup analyses
study variability
study design
specific interventions
significantly moderated
research output
remained stable
quality assurance
quality assessments
prediction interval
marginally significant
logit transformation
google scholar
fold increase
findings highlight
examine regional
continued surveillance
comprehensive data
children exhibited
cases ).
care technologies
base databases
african populations
91 %.
88 %),
839 participants
694 ).
65 %)
6 %).
status_str publishedVersion
title Characteristics of included studies.
title_full Characteristics of included studies.
title_fullStr Characteristics of included studies.
title_full_unstemmed Characteristics of included studies.
title_short Characteristics of included studies.
title_sort Characteristics of included studies.
topic Biotechnology
Science Policy
Infectious Diseases
Biological Sciences not elsewhere classified
three decades despite
systematically searched pubmed
sickle cell anemia
electrophoretic techniques predominated
21 %– 8
1994 &# 8211
improved diagnostic accessibility
southern africa showed
sensitivity analysis showed
central africa showed
74 %; p
significant genetic disorder
including geographic region
08 %– 1
analysis </ p
2 </ sup
males 2
diagnostic method
xlink ">
temporal variations
systematic review
subgroup analyses
study variability
study design
specific interventions
significantly moderated
research output
remained stable
quality assurance
quality assessments
prediction interval
marginally significant
logit transformation
google scholar
fold increase
findings highlight
examine regional
continued surveillance
comprehensive data
children exhibited
cases ).
care technologies
base databases
african populations
91 %.
88 %),
839 participants
694 ).
65 %)
6 %).