Literature DB >> 15997258

The influence of foetal haemoglobin on the frequency of vaso-occlusive crisis in sickle cell anaemia patients.

M E Enosolease1, O A Ejele, O A Awodu.   

Abstract

OBJECTIVE: Several biological and environmental factors are presumed to account for the morbidity pattern in patients with sickle cell anaemia. Foetal haemoglobin is one of the biological factors thought to decrease morbidity in these patients. We studied the relationship between the foetal haemoglobin levels and vaso-occlusive crisis (VOC) as a measure of the morbidity pattern in this category of patients.
RESULTS: The mean foetal haemoglobin level was 6.4+0.40% (SEM). Vaso-occlusive crisis was more common at lower levels of foetal haemoglobin particularly when lower than 12% (P=0.01). There was a negative correlation between foetal haemoglobin and vaso-occlusive crisis (r=0.561). These variables were also associated in linear regression and both showed statistical significance (p=0.001).
CONCLUSION: We conclude that higher levels of foetal haemoglobin positively influence the occurrence of vaso-occlusive crisis in sickle cell anaemia patients.

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Year:  2005        PMID: 15997258

Source DB:  PubMed          Journal:  Niger Postgrad Med J


  5 in total

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Journal:  OMICS       Date:  2016-10

2.  Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients.

Authors:  Tite Minga Mikobi; Prosper Lukusa Tshilobo; Michel Ntetani Aloni; Georges Mvumbi Lelo; Pierre Zalagile Akilimali; Jean Jacques Muyembe-Tamfum; Valérie Race; Gert Matthijs; Jean Marie Mbuyi Mwamba
Journal:  PLoS One       Date:  2015-05-06       Impact factor: 3.240

3.  Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.

Authors:  Titilope Adeyemo; Oyesola Ojewunmi; Ajoke Oyetunji
Journal:  Pan Afr Med J       Date:  2014-05-22

4.  FOETAL HAEMOGLOBIN (HbF) STATUS IN ADULT SICKLE CELL ANAEMIA PATIENTS IN IBADAN, NIGERIA.

Authors:  J A Olaniyi; O G Arinola; A B Odetunde
Journal:  Ann Ib Postgrad Med       Date:  2010-06

5.  Comparison of patients from Nigeria and the USA highlights modifiable risk factors for sickle cell anemia complications.

Authors:  Titilola S Akingbola; Bamidele O Tayo; Babatunde Salako; Jennifer E Layden; Lewis L Hsu; Richard S Cooper; Victor R Gordeuk; Santosh L Saraf
Journal:  Hemoglobin       Date:  2014-06-18       Impact factor: 0.849

  5 in total

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