Evidence map›Paper›PMID 42084624›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

Prevalence and determinants of early markers of kidney damage in homozygotic sickle cell patients in the DR Congo: Update.

Dieumerci Betukumesu Kabasele, Michel Aloni, Arriel Makembi Bunkete, François Kajingulu, Paul Lumbala Kabuyi, Orly Kazadi, Mireille Solange Nganga Nkanga, Joseph Bodi Mabiala, Tite Mikobi, Benjamin Longo Mbenza and 2 more

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Article in Pediatric nephrology (Berlin, Germany), 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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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Dieumerci Betukumesu KabaseleDepartment of Pediatrics, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Michel AloniDepartment of Pediatrics, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Arriel Makembi BunketeDepartment of Nephrology and Dialysis, University of Kinshasa, Kinshasa, Democratic Republic of the Congo. docteur.makarriel2017@gmail.com.ORCID http://orcid.org/0000-0001-9651-437X
François KajinguluDepartment of Nephrology and Dialysis, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Paul Lumbala KabuyiDepartment of Pediatrics, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Orly KazadiDepartment of Pediatrics, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Mireille Solange Nganga NkangaDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Joseph Bodi MabialaDepartment of Pediatrics, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Tite MikobiDepartment of Genetics, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Benjamin Longo MbenzaDepartment of Cardiology, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Pipo Michel TshiasumaDepartment of Pulmonology, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Jean Lambert Gini EhunguDepartment of Pediatrics, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSickle cell nephropathy is a common complication of sickle cell disease that begins in childhood and can progress silently to chronic kidney disease. In the Democratic Republic of Congo (DRC), data on early kidney damage in children with sickle cell disease remain limited. In 2017, studies conducted in the same context reported separately on the prevalence of microalbuminuria and glomerular hyperfiltration (GHF). This study aimed to update the prevalence of albuminuria and GHF and to determine their associated factors in children with sickle cell disease in the DRC.

methodsWe conducted a cross-sectional study including 175 children with sickle cell disease, followed up in four hospitals in Kinshasa. High albuminuria and GHF, the main evaluation criteria, were defined respectively by an albuminuria/creatinine ratio (ACR) ≥ 30 mg/g and an estimated glomerular filtration rate (eGFR) > 130 ml/min/1.73 m

resultsAmong the 175 children included, 28.5% had high albuminuria and 38.3% had GHF. Factors significantly associated with early renal involvement were frequent blood transfusions (≥ 9/year), recurrent vaso-occlusive crises (≥ 3/year), low fetal hemoglobin levels (< 15%), and markers of hemolysis (LDH > 400 IU/L and elevated indirect bilirubin). These results reflect a high persistence of early renal impairment nearly nine years after the first data were published.

conclusionsEarly markers of kidney damage remain very common in children with homozygous sickle cell disease in the DRC. This persistence highlights the lack of effective kidney prevention strategies and the urgent need for systematic screening using simple and accessible tools in resource-limited settings.

Indexed as

AlbuminuriaAnemia, Sickle CellRenal Insufficiency, ChronicAdolescentBiomarkersBlood TransfusionChildChild, PreschoolCreatinineCross-Sectional StudiesDemocratic Republic of the CongoFemaleGlomerular Filtration RateHumansKidneyMaleBiomarkersCreatinineAlbuminuriaCongolese childrenHyperfiltrationSickle cell disease

Identifiers

PMID42084624
PMCPMC13481430

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