Evidence map›Paper›PMID 42060623›Full record

ArticlePloS one2026

Persistent proteinuria among a cohort of Nigerian children with sickle cell anaemia.

Angela Esohe Adeoti-Lawani, Gabriel Obiorah Ezeh, Elizabeth Eberechi Oyenusi, Chris Imokhuede Esezobor

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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

4 authors.

Angela Esohe Adeoti-LawaniDepartment of Paediatrics, National Hospital, Abuja, Nigeria.ORCID https://orcid.org/0009-0001-3379-4164
Gabriel Obiorah EzehDepartment of Paediatrics, National Hospital, Abuja, Nigeria.
Elizabeth Eberechi OyenusiDepartment of Paediatrics, Faculty of Clinical Sciences, College of Medicine, University of Lagos, Lagos, Nigeria.
Chris Imokhuede EsezoborDepartment of Paediatrics, Faculty of Clinical Sciences, College of Medicine, University of Lagos, Lagos, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPersistent proteinuria is an early and modifiable marker of kidney damage. Although Nigeria has the highest burden of sickle cell anaemia (SCA) globally, the prevalence of proteinuria is unknown largely because many of the studies only determined proteinuria in a single urine sample or used less sensitive methods, such as dipstick. Unlike dipstick screening, quantitative urine protein-creatinine ratio allows more accurate detection of low-grade proteinuria.

objectivesTo determine the prevalence and determinants of persistent proteinuria among children with SCA.

methodsChildren with SCA and age and sex-matched controls attending a publicly funded hospital in central Nigeria were consecutively enrolled. Proteinuria was determined at the first visit using the spot urine protein creatinine ratio and repeated at least 3 months afterwards for those with proteinuria. In addition, serum creatinine, full blood count, and fetal hemoglobin were determined at the first visit. Persistent proteinuria was defined as a urine protein-to-creatinine ratio ≥0.2 at both visits over a follow-up period of at least 3 months. Participants were classified based on the presence or absence of persistent proteinuria, and baseline characteristics were compared using within-group distributions for categorical variables with appropriate statistical tests.

resultsOne hundred and forty-nine children, each with SCA and controls, were enrolled, respectively. The median (IQR) age of the study participants was 9.0 (6.0) years for both groups, with 65% being males. Persistent proteinuria occurred in 35 (23.5%) children with SCA versus 4 (2.7%) controls (p-value < 0.01). Children with persistent proteinuria had a lower level of fetal hemoglobin. (adjusted OR 0.583, 95% C.I 0.473-0.719).

conclusionAbout a quarter of children with SCA had persistent proteinuria, an early and modifiable marker of chronic kidney disease.

Indexed as

Anemia, Sickle CellProteinuriaAdolescentCase-Control StudiesChildChild, PreschoolCohort StudiesCreatinineFemaleHumansMaleNigeriaPrevalenceCreatinine

Identifiers

PMID42060623
PMCPMC13132187

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