Liver and renal biochemical profiles of people with sickle cell disease in Africa: a systematic review and meta‑analysis of case‑control studies

dc.contributor.authorAwor, Silvia
dc.contributor.authorBongomin, Felix
dc.contributor.authorKaggwa, Mark Mohan
dc.contributor.authorPebolo, Francis Pebalo
dc.contributor.authorEpila, Jackie
dc.contributor.authorMalinga, Geoffrey Maxwell
dc.contributor.authorOryema, Christine
dc.contributor.authorNnamuyomba, Proscovia
dc.contributor.authorAbola, Benard
dc.contributor.authorOngwech, Acaye
dc.contributor.authorMusoke, David
dc.date.accessioned2026-03-06T09:21:11Z
dc.date.issued2024
dc.description.abstractBackground Sickle cell disease (SCD) is a genetic blood disorder characterized by a painful vaso-occlusive crisis due to the sickling of red blood cells in capillaries. Complications often lead to liver and renal dysfunctions, contributing to morbidity and mortality, particularly for children under 5. This systematic review and meta-analysis aimed to evaluate the liver and renal functions of people with SCD (HbSS) compared to those without it (HbAA) in Africa. Methods The protocol was registered with PROSPERO (CRD42022346771). We searched PubMed, Embase, Web of Science, and Google Scholar using the keywords “liver function”, “renal function”, “sickle cell disease”, and “Africa” on 6th May 2023 for peer-reviewed articles with abstracts in English. We included case-control studies comparing SCD (HbSS) with controls without hemoglobinopathies (HbAA). We used the random-effect model to calculate the pooled average values for the blood tests of people with SCD in RStudio version 4.2.2. Results Overall, 17 articles were analyzed from five African countries involving 1312 people with SCD and 1558 controls. The pooled mean difference of liver enzymes aspartate transaminase (AST) was 8.62 (95% CI − 2.99–20.23, I2 = 97.0%, p < 0.01), alanine transaminase (ALT) 7.82 (95% CI − 0.16–15.80, I2 = 99%, p < 0.01) and alkaline phosphatase (ALP) − 2.54 (95% CI − 64.72 – 59.64, I2 = 99%, p < 0.01) compared to controls. The pooled mean difference for the renal biochemical profiles creatinine − 3.15 (95% CI − 15.02; 8.72, I2=99%, p < 0.01) with a funnel plot asymmetry of t = 1.09, df = 9, p = 0.3048 and sample estimates bias of 6.0409. The pooled mean difference for serum urea was − 0.57 (95% CI − 3.49; 2.36, I2 = 99%, p < 0.01), and the estimated glomerular filtration (eGFR) rate was 19.79 (95% CI 10.89–28.68 mL/min/1.73 m2, I2 = 87%, p < 0.01) compared to controls. Conclusion People with SCD have slightly elevated liver enzymes and estimated glomerular filtration rates compared to controls in Africa. With all the heterogeneity (I2) > 50%, there was substantial variation in the reported articles’ results.
dc.identifier.citationAwor S., Bongomin F., Kaggwa, M. M., Pebolo, F.P., Epila, J., Malinga, G. M., Oryema, C., Nnamuyomba, P., Abola, B., Ongwech, A., & Musoke, D. (2024). Liver and renal biochemical profiles of people with sickle cell disease in Africa: a systematic review and meta-analysis of case-control studies.
dc.identifier.urihttps://doi.org/10.1186/s13643-024-02662-6
dc.identifier.urihttps://ir.lirauni.ac.ug/handle/123456789/1060
dc.language.isoen
dc.publisherBMC
dc.subjectSickle cell
dc.subjectLiver function
dc.subjectRenal function
dc.subjectSystematic review
dc.subjectAfrica
dc.titleLiver and renal biochemical profiles of people with sickle cell disease in Africa: a systematic review and meta‑analysis of case‑control studies
dc.typeArticle

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