Evidence map›Paper›PMID 42241421›Full record

ArticlePloS one2026

Trends in the burden of sickle cell disorders in Sierra Leone, 1990-2023: An analysis of Global Burden of Disease Study 2023 estimates.

Monalisa M J Faulkner, Fatima Jalloh, Foray Mohamed Foray, Sahr L Gborie, Mohamed B Jalloh

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Article in PloS one, 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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5 · Who and what money

Authors and funding

5 authors.

Monalisa M J FaulknerUniversity of Sierra Leone Teaching Hospitals Complex, Ola During Children's Hospital, Freetown, Sierra Leone.
Fatima JallohCollege of Medicine and Allied Health Sciences, University of Sierra Leone, Freetown, Sierra Leone.
Foray Mohamed ForayCollege of Health Sciences and Public Policy, Walden University, Minneapolis, Minnesota, United States of America.
Sahr L GborieUniversity of Sierra Leone Teaching Hospitals Complex, Ola During Children's Hospital, Freetown, Sierra Leone.
Mohamed B JallohCollege of Medicine and Allied Health Sciences, University of Sierra Leone, Freetown, Sierra Leone.ORCID https://orcid.org/0000-0002-3172-2749

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSickle cell disease is a major cause of childhood mortality in sub-Saharan Africa, yet country-specific burden estimates for high-prevalence settings in West Africa remain limited.

objectiveTo describe Global Burden of Disease (GBD) 2023 modeled estimates of sickle cell disorders burden in Sierra Leone from 1990 through 2023, including temporal trends, age and sex patterns, and demographic contributors to mortality change.

methodsWe analyzed GBD 2023 modeled estimates for sickle cell disorders in Sierra Leone, including prevalence, deaths, years lived with disability (YLDs), years of life lost (YLLs), and disability-adjusted life-years (DALYs) as absolute counts and age-standardized rates. Temporal trends in age-standardized rates were assessed using log-linear regression. The Kitagawa-Das Gupta decomposition partitioned the change in estimated deaths into population growth, age-structure change, and age-specific mortality-rate changes.

resultsEstimated prevalent cases increased from 48,689 (95% UI, 42,588-56,140) in 1990-90,498 (78,126-105,815) in 2023. Estimated deaths increased from 408 (288-579) to 635 (438-862), while the estimated age-standardized mortality rate declined from 10.2 to 7.9 per 100,000 (APC, -0.46%; 95% CI, -0.64 to -0.29). Decomposition attributed 159.6% of the net increase in deaths to population growth, -7.8% to age-structure change, and -51.8% to lower modeled age-specific rates. In 2023, an estimated 49.5% of deaths occurred before age 20. Point estimates suggested possible higher male mortality, but uncertainty intervals were wide and compatible with no clear sex difference.

conclusionsGBD estimates suggest that Sierra Leone's absolute burden of sickle cell disorders increased substantially between 1990 and 2023, while modeled rates declined. These modeled estimates highlight a growing absolute burden and persistent early-life mortality, supporting the need for improved surveillance, newborn screening, infection prophylaxis, hydroxyurea access, and longitudinal care systems.

Indexed as

Anemia, Sickle CellGlobal Burden of DiseaseAdolescentAdultChildChild, PreschoolDisability-Adjusted Life YearsFemaleHumansInfantInfant, NewbornMaleMiddle AgedPrevalenceSierra LeoneYoung Adult

Identifiers

PMID42241421
PMCPMC13235869

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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 OpenQuestion graph.