Evidence map›Paper›PMID 42605415›Full record

ReviewNigerian medical journal : journal of the Nigeria Medical Association

Predictors of nephropathy in sickle cell disease: A cross-sectional analysis across age and clinical phenotypes in Zaria, Nigeria.

M M Abdulrasheed, R M Akuse, S Awwalu, A Ibrahim, M A Bugaje, I B Bosan, I N Ibrahim, Faruk Ja, A Yakubu, H R Ahmad and 4 more

Abstract readReview
In one paragraph

Review in Nigerian medical journal : journal of the Nigeria Medical Association. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

M M AbdulrasheedDepartments of Medicine, Ahmadu Bello University Teaching Hospital, Zaria.
R M AkusePaediatrics, Ahmadu Bello University Teaching Hospital, Zaria.
S AwwaluHaematology, Ahmadu Bello University Teaching Hospital, Zaria.
A IbrahimDepartments of Medicine, Ahmadu Bello University Teaching Hospital, Zaria.
M A BugajePaediatrics, Ahmadu Bello University Teaching Hospital, Zaria.
I B BosanDepartments of Medicine, Ahmadu Bello University Teaching Hospital, Zaria.
I N IbrahimHaematology, Ahmadu Bello University Teaching Hospital, Zaria.
Faruk JaPaediatrics, Ahmadu Bello University Teaching Hospital, Zaria.
A YakubuPaediatrics, Ahmadu Bello University Teaching Hospital, Zaria.
H R AhmadPaediatrics, Ahmadu Bello University Teaching Hospital, Zaria.
R YusufChemical Pathology, Ahmadu Bello University Teaching Hospital, Zaria.
H M SuleimanChemical Pathology, Ahmadu Bello University Teaching Hospital, Zaria.
S B LawalRadiology, Ahmadu Bello University Teaching Hospital, Zaria.
A U IbrahimRadiology, Ahmadu Bello University Teaching Hospital, Zaria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sickle cell disease (SCD) is associated with significant complications, including nephropathy, which can progress to end-stage renal disease. While risks for SCD nephropathy have been identified globally, their specific prevalence and predictors in Nigerian, especially across age and clinical phenotypes, are less well understood. This study assessed the prevalence and predictors of nephropathy among Nigerian SCD patients. Methods: This was a cross-sectional study among paediatrics, adolescent, and adult patients with SCD attending hematology clinics of Ahmadu Bello University Teaching Hospital (ABUTH), Zaria. Interviewer-administered questionnaires were utilised to collect demographic and clinical data. Nephropathy was defined by the presence of proteinuria, haematuria, or eGFR <60 ml/min. Patients were classified into hyper-haemolytic and vaso-occlusive sub-phenotypes. Statistical analyses involved Mann-Whitney U tests, chi-square tests, and logistic regression, with a significance level set at p < 0.05. Results: A total of 311 SCD patients were enrolled, with a median age of 17 (IQR 9-25) years and 65% female. Nephropathy was present in 13.8% of patients, with significantly higher prevalence among adults (23.7%) compared to adolescents (9.1%) and paediatrics patients (3.8%) respectively (X Conclusion: The prevalence of nephropathy in Nigerian SCD patients increases with age and is more common in females, with hyper-hemolytic sub-phenotypes showing a higher risk profile.

Indexed as

NephropathyNigeriaPhenotypesSickle cell diseaseZaria

Identifiers

PMID42605415
PMCPMC13477709

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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.