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Prevalence of sickle cell trait and its association to renal dysfunction among blood donors at University of Medical Sciences Teaching Hospital, Ondo, Nigeria
INTRODUCTION: Prospective blood donors are routinely screened for blood borne infections but medical illnesses and haemoglobin genotype are overlooked despite a high prevalence of haemoglobin AS among Nigerian donors. OBJECTIVE: To determine the prevalence of haemoglobin AS and its association to re...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Makerere Medical School
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843258/ https://www.ncbi.nlm.nih.gov/pubmed/35222587 http://dx.doi.org/10.4314/ahs.v21i3.33 |
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author | Akinbodewa, Akinwumi Ayodeji Ogunleye, Adeyemi Adejumo, Oluseyi Ademola |
author_facet | Akinbodewa, Akinwumi Ayodeji Ogunleye, Adeyemi Adejumo, Oluseyi Ademola |
author_sort | Akinbodewa, Akinwumi Ayodeji |
collection | PubMed |
description | INTRODUCTION: Prospective blood donors are routinely screened for blood borne infections but medical illnesses and haemoglobin genotype are overlooked despite a high prevalence of haemoglobin AS among Nigerian donors. OBJECTIVE: To determine the prevalence of haemoglobin AS and its association to renal function, if any. METHOD: Apparently healthy donors were studied between February and December 2018. Their haemoglobin genotype and, estimated glomerular filtration rates were determined. RESULTS: There were 96 males (94.1%) and 6 (5.9%) females with mean age of 26.7±4.5 years (range 19–44 years) and mean eGFR of 103.97±19.00ml/min/1.73m2. Eighty one (79.4%) and 21 (20.6%) subjects had haemoglobin AA and AS genotypes respectively. The mean eGFR for subjects with haemoglobin AA and AS were 105.2±18.6ml/min/1.73m(2) and 99.9 ± 21.2ml/min/1.73m(2) respectively (p value = 0.270). Eighty one (79.4%), 20 (19.6%) and 1 (1.0%) subjects had renal function at >90ml/min/1.73m(2), 60–89ml/min/1.73m(2) and 30–59ml/min/m(2) respectively. There was no significant difference in the mean eGFR between subjects with haemoglobin AA and AS (mean difference 5.3, p = 0.265, 95%CI = -4.07 to 14.60). CONCLUSION: The prevalence of sickle cell trait among Nigerian blood donors is high. There is no significant difference in the renal function status of blood donors with SCT and normal haemoglobin genotype. |
format | Online Article Text |
id | pubmed-8843258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Makerere Medical School |
record_format | MEDLINE/PubMed |
spelling | pubmed-88432582022-02-24 Prevalence of sickle cell trait and its association to renal dysfunction among blood donors at University of Medical Sciences Teaching Hospital, Ondo, Nigeria Akinbodewa, Akinwumi Ayodeji Ogunleye, Adeyemi Adejumo, Oluseyi Ademola Afr Health Sci Articles INTRODUCTION: Prospective blood donors are routinely screened for blood borne infections but medical illnesses and haemoglobin genotype are overlooked despite a high prevalence of haemoglobin AS among Nigerian donors. OBJECTIVE: To determine the prevalence of haemoglobin AS and its association to renal function, if any. METHOD: Apparently healthy donors were studied between February and December 2018. Their haemoglobin genotype and, estimated glomerular filtration rates were determined. RESULTS: There were 96 males (94.1%) and 6 (5.9%) females with mean age of 26.7±4.5 years (range 19–44 years) and mean eGFR of 103.97±19.00ml/min/1.73m2. Eighty one (79.4%) and 21 (20.6%) subjects had haemoglobin AA and AS genotypes respectively. The mean eGFR for subjects with haemoglobin AA and AS were 105.2±18.6ml/min/1.73m(2) and 99.9 ± 21.2ml/min/1.73m(2) respectively (p value = 0.270). Eighty one (79.4%), 20 (19.6%) and 1 (1.0%) subjects had renal function at >90ml/min/1.73m(2), 60–89ml/min/1.73m(2) and 30–59ml/min/m(2) respectively. There was no significant difference in the mean eGFR between subjects with haemoglobin AA and AS (mean difference 5.3, p = 0.265, 95%CI = -4.07 to 14.60). CONCLUSION: The prevalence of sickle cell trait among Nigerian blood donors is high. There is no significant difference in the renal function status of blood donors with SCT and normal haemoglobin genotype. Makerere Medical School 2021-09 /pmc/articles/PMC8843258/ /pubmed/35222587 http://dx.doi.org/10.4314/ahs.v21i3.33 Text en © 2021 Akinbodewa AA et al. https://creativecommons.org/licenses/by/4.0/Licensee African Health Sciences. This is an Open Access article distributed under the terms of the Creative commons Attribution License (https://creativecommons.org/licenses/BY/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Akinbodewa, Akinwumi Ayodeji Ogunleye, Adeyemi Adejumo, Oluseyi Ademola Prevalence of sickle cell trait and its association to renal dysfunction among blood donors at University of Medical Sciences Teaching Hospital, Ondo, Nigeria |
title | Prevalence of sickle cell trait and its association to renal dysfunction among blood donors at University of Medical Sciences Teaching Hospital, Ondo, Nigeria |
title_full | Prevalence of sickle cell trait and its association to renal dysfunction among blood donors at University of Medical Sciences Teaching Hospital, Ondo, Nigeria |
title_fullStr | Prevalence of sickle cell trait and its association to renal dysfunction among blood donors at University of Medical Sciences Teaching Hospital, Ondo, Nigeria |
title_full_unstemmed | Prevalence of sickle cell trait and its association to renal dysfunction among blood donors at University of Medical Sciences Teaching Hospital, Ondo, Nigeria |
title_short | Prevalence of sickle cell trait and its association to renal dysfunction among blood donors at University of Medical Sciences Teaching Hospital, Ondo, Nigeria |
title_sort | prevalence of sickle cell trait and its association to renal dysfunction among blood donors at university of medical sciences teaching hospital, ondo, nigeria |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843258/ https://www.ncbi.nlm.nih.gov/pubmed/35222587 http://dx.doi.org/10.4314/ahs.v21i3.33 |
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