Cargando…

Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State

BACKGROUND: Sickle cell disease is a genetic haemoglobinopathy with consequent haemolysis and anaemia. It is of interest to study its effect on red cell indices beside haemoglobin concentration. OBJECTIVES: The objective of the study is to determine the values of red cell indices in preschool-age ch...

Descripción completa

Detalles Bibliográficos
Autores principales: Akodu, Samuel Olufemi, Njokanma, Olisamedua Fidelis, AdeoluKehinde, Omolara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369233/
https://www.ncbi.nlm.nih.gov/pubmed/25802694
_version_ 1782362741077442560
author Akodu, Samuel Olufemi
Njokanma, Olisamedua Fidelis
AdeoluKehinde, Omolara
author_facet Akodu, Samuel Olufemi
Njokanma, Olisamedua Fidelis
AdeoluKehinde, Omolara
author_sort Akodu, Samuel Olufemi
collection PubMed
description BACKGROUND: Sickle cell disease is a genetic haemoglobinopathy with consequent haemolysis and anaemia. It is of interest to study its effect on red cell indices beside haemoglobin concentration. OBJECTIVES: The objective of the study is to determine the values of red cell indices in preschool-age children with sickle cell anaemia. METHODS: we conducted a cross-sectional study including 97 children with sickle cell anaemia aged six months to five years and 97 age-and sex-matched healthy controls with haemoglobin genotype AA (Hb AA). The red cell indices such as packed cell volume, haemoglobin concentration, mean corpuscular volume, red blood cell count, mean corpuscular haemoglobin and mean corpuscular haemoglobin concentration were investigated, using an auto analyzer. RESULTS: The mean PCV, haemoglobin concentration and red blood cell count were significantly higher in HbAA controls (p = 0.000 in each case). The mean MCV was higher among HbSS subjects but it was only among females and when the result was analyzed irrespective of gender that the difference was statistically significant (p < 0.05). CONCLUSION: Children with sickle cell anaemia in steady state have lower values of all red cell parameters and higher values of MCV, compared to haemoglobin phenotype AA controls.
format Online
Article
Text
id pubmed-4369233
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Tehran University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-43692332015-03-23 Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State Akodu, Samuel Olufemi Njokanma, Olisamedua Fidelis AdeoluKehinde, Omolara Int J Hematol Oncol Stem Cell Res Original Article BACKGROUND: Sickle cell disease is a genetic haemoglobinopathy with consequent haemolysis and anaemia. It is of interest to study its effect on red cell indices beside haemoglobin concentration. OBJECTIVES: The objective of the study is to determine the values of red cell indices in preschool-age children with sickle cell anaemia. METHODS: we conducted a cross-sectional study including 97 children with sickle cell anaemia aged six months to five years and 97 age-and sex-matched healthy controls with haemoglobin genotype AA (Hb AA). The red cell indices such as packed cell volume, haemoglobin concentration, mean corpuscular volume, red blood cell count, mean corpuscular haemoglobin and mean corpuscular haemoglobin concentration were investigated, using an auto analyzer. RESULTS: The mean PCV, haemoglobin concentration and red blood cell count were significantly higher in HbAA controls (p = 0.000 in each case). The mean MCV was higher among HbSS subjects but it was only among females and when the result was analyzed irrespective of gender that the difference was statistically significant (p < 0.05). CONCLUSION: Children with sickle cell anaemia in steady state have lower values of all red cell parameters and higher values of MCV, compared to haemoglobin phenotype AA controls. Tehran University of Medical Sciences 2015-01-01 /pmc/articles/PMC4369233/ /pubmed/25802694 Text en © 2013 Hematology-Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Akodu, Samuel Olufemi
Njokanma, Olisamedua Fidelis
AdeoluKehinde, Omolara
Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State
title Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State
title_full Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State
title_fullStr Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State
title_full_unstemmed Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State
title_short Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State
title_sort erythrocyte indices in pre-school nigerian children with sickle cell anaemia in steady state
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369233/
https://www.ncbi.nlm.nih.gov/pubmed/25802694
work_keys_str_mv AT akodusamuelolufemi erythrocyteindicesinpreschoolnigerianchildrenwithsicklecellanaemiainsteadystate
AT njokanmaolisameduafidelis erythrocyteindicesinpreschoolnigerianchildrenwithsicklecellanaemiainsteadystate
AT adeolukehindeomolara erythrocyteindicesinpreschoolnigerianchildrenwithsicklecellanaemiainsteadystate