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Cystatin C-derived estimated glomerular filtration rate in children with sickle cell anaemia

BACKGROUND: Sickle cell disease is the most common inherited blood disorder in humans and constitutes a major public health burden. It is a multisystemic condition with long-term renal complications. Early detection of sickle cell nephropathy and initiation of appropriate interventions are associate...

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Autores principales: Babatunde, Hakeem Edun, Bello, Afeez Oyesola, Adeboye, Muhammed A. Nurudeen, Folayan, Olumuyiwa Shola, Ojewole, Olugoke Ezekiel, Abubakar, Usman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688062/
https://www.ncbi.nlm.nih.gov/pubmed/38031035
http://dx.doi.org/10.1186/s12882-023-03393-x
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author Babatunde, Hakeem Edun
Bello, Afeez Oyesola
Adeboye, Muhammed A. Nurudeen
Folayan, Olumuyiwa Shola
Ojewole, Olugoke Ezekiel
Abubakar, Usman
author_facet Babatunde, Hakeem Edun
Bello, Afeez Oyesola
Adeboye, Muhammed A. Nurudeen
Folayan, Olumuyiwa Shola
Ojewole, Olugoke Ezekiel
Abubakar, Usman
author_sort Babatunde, Hakeem Edun
collection PubMed
description BACKGROUND: Sickle cell disease is the most common inherited blood disorder in humans and constitutes a major public health burden. It is a multisystemic condition with long-term renal complications. Early detection of sickle cell nephropathy and initiation of appropriate interventions are associated with improved survival and quality of life. This study aimed to compare the cystatin C-derived estimated glomerular filtration rate (GFR) of the study groups and also, to correlate the clinical features of chronic kidney disease (CKD) with decreased GFR in children with sickle cell anaemia (SCA). METHODS: This hospital-based cross-sectional analytic study recruited 86 SCA subjects in steady-state and 86 age and sex-matched healthy HbAA controls aged 1–14 years who attended the Paediatric Haematology and Outpatient clinics of Federal Medical Centre Bida over six months. Data were collected using a semi-structured questionnaire, and participants’ length/height, weight, and blood pressure were measured using standard procedures. Blood samples were drawn for serum cystatin C assay via the sandwich enzyme-linked immunosorbent assay (ELISA) technique. Filler’s equation was used to calculate the glomerular filtration rate. RESULTS: There was a significant difference in the mean cystatin C-derived GFR between the two groups, i.e. 116 ± 30mL/min/1.73m(2) vs. 106 ± 24mL/min/1.73m(2) for the SCA and control groups, respectively (p = 0.017). The prevalence of supernormal GFR (i.e. GFR > 140mL/min/1.73m(2)) and decreased GFR (i.e. GFR < 90mL/min/1.73m(2)) was 19.8% and 22.1%, respectively, in children with SCA. There was no significant association between the age at diagnosis of SCA, blood transfusions, blood pressure, packed cell volume and presence of peripheral oedema with decreased GFR in the study subjects. CONCLUSIONS: Supernormal GFR is common in children with SCA and there is no significant association between clinical features of CKD with decreased GFR. Regular evaluation of renal function is, however, recommended in children with SCA for early detection and treatment of renal complications in order to halt the progression to end-stage kidney disease (ESKD).
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spelling pubmed-106880622023-11-30 Cystatin C-derived estimated glomerular filtration rate in children with sickle cell anaemia Babatunde, Hakeem Edun Bello, Afeez Oyesola Adeboye, Muhammed A. Nurudeen Folayan, Olumuyiwa Shola Ojewole, Olugoke Ezekiel Abubakar, Usman BMC Nephrol Research BACKGROUND: Sickle cell disease is the most common inherited blood disorder in humans and constitutes a major public health burden. It is a multisystemic condition with long-term renal complications. Early detection of sickle cell nephropathy and initiation of appropriate interventions are associated with improved survival and quality of life. This study aimed to compare the cystatin C-derived estimated glomerular filtration rate (GFR) of the study groups and also, to correlate the clinical features of chronic kidney disease (CKD) with decreased GFR in children with sickle cell anaemia (SCA). METHODS: This hospital-based cross-sectional analytic study recruited 86 SCA subjects in steady-state and 86 age and sex-matched healthy HbAA controls aged 1–14 years who attended the Paediatric Haematology and Outpatient clinics of Federal Medical Centre Bida over six months. Data were collected using a semi-structured questionnaire, and participants’ length/height, weight, and blood pressure were measured using standard procedures. Blood samples were drawn for serum cystatin C assay via the sandwich enzyme-linked immunosorbent assay (ELISA) technique. Filler’s equation was used to calculate the glomerular filtration rate. RESULTS: There was a significant difference in the mean cystatin C-derived GFR between the two groups, i.e. 116 ± 30mL/min/1.73m(2) vs. 106 ± 24mL/min/1.73m(2) for the SCA and control groups, respectively (p = 0.017). The prevalence of supernormal GFR (i.e. GFR > 140mL/min/1.73m(2)) and decreased GFR (i.e. GFR < 90mL/min/1.73m(2)) was 19.8% and 22.1%, respectively, in children with SCA. There was no significant association between the age at diagnosis of SCA, blood transfusions, blood pressure, packed cell volume and presence of peripheral oedema with decreased GFR in the study subjects. CONCLUSIONS: Supernormal GFR is common in children with SCA and there is no significant association between clinical features of CKD with decreased GFR. Regular evaluation of renal function is, however, recommended in children with SCA for early detection and treatment of renal complications in order to halt the progression to end-stage kidney disease (ESKD). BioMed Central 2023-11-29 /pmc/articles/PMC10688062/ /pubmed/38031035 http://dx.doi.org/10.1186/s12882-023-03393-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Babatunde, Hakeem Edun
Bello, Afeez Oyesola
Adeboye, Muhammed A. Nurudeen
Folayan, Olumuyiwa Shola
Ojewole, Olugoke Ezekiel
Abubakar, Usman
Cystatin C-derived estimated glomerular filtration rate in children with sickle cell anaemia
title Cystatin C-derived estimated glomerular filtration rate in children with sickle cell anaemia
title_full Cystatin C-derived estimated glomerular filtration rate in children with sickle cell anaemia
title_fullStr Cystatin C-derived estimated glomerular filtration rate in children with sickle cell anaemia
title_full_unstemmed Cystatin C-derived estimated glomerular filtration rate in children with sickle cell anaemia
title_short Cystatin C-derived estimated glomerular filtration rate in children with sickle cell anaemia
title_sort cystatin c-derived estimated glomerular filtration rate in children with sickle cell anaemia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688062/
https://www.ncbi.nlm.nih.gov/pubmed/38031035
http://dx.doi.org/10.1186/s12882-023-03393-x
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