ArticleScientific reports2026
Temporal patterns of haemoglobin phenotypes among Nigerian university students based on ten years of surveillance data.
Article in Scientific reports, 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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Abstract
Haemoglobinopathies remain among the most common monogenic disorders worldwide, with sickle cell disease (SCD) and various forms of thalassemia posing significant challenges to public health systems, particularly in low- and middle-income countries. This study presents a ten-year retrospective analysis of haemoglobin phenotype surveillance data, encompassing multiple regions and demographic strata. This retrospective work was conducted at Bowen University Hospital, Iwo, Osun State, southwestern Nigeria between January 2015 and December 2024. Data were extracted and analyzed using machine learning from 8890 medical records of undergraduate annual phenotype screening spanning ten years (2015-2024). HbAA was the most common genotype at 75.11% (n = 6,677). SCD genotypes (HbSS and HbSC) showed a non-significant downward trend over the ten-year period (slope = - 0.03 percentage points/year; R
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