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Relationship Between Disease Severity and Folate Status of Children with Sickle Cell Anaemia in Enugu, South East Nigeria

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Journal Afr Health Sci
Date 2021 Nov 19
PMID 34795733
Citations 1
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Abstract

Background: Repeated crises in children with sickle cell anaemia (SCA), which is a manifestation of disease severity, results in depletion of their minimal tissue folate stores, with higher likelihood of folate deficiency. The study aimed to determine the relationship between disease severity and the folate status of children with SCA attending University of Nigeria Teaching Hospital (UNTH), Enugu.

Methods: This was a hospital based, cross-sectional study conducted between September 2018 and March 2019. One hundred participants were recruited, consisting of 50 children having sickle cell crisis and 50 age and gender matched haemoglobin AA genotype controls. Relevant information was documented using a pretested questionnaire. Sickle cell severity score was determined using frequency of crisis, admissions and transfusions in the preceding one year, degree of liver and splenic enlargement, life-time cummulative frequency of specific complications of SCA, leucocyte count and haematocrit.

Results: Folate deficiency was observed in eight percent of the subjects and none of the controls. The difference was not significant (Fisher's exact = 4.167, p=0.117). The odds of being folate deficient was 8.5 times more likely during anaemic crisis than in vaso-occlusive crisis, though not significant (95% C.I 0.05 - 89.750, p = 0.075). The mean SCA severity score was 8.06 ± 3.64, signifying a moderate SCA severity in the study population. There was a no relationship between folate status and severity of SCA (Fisher's exact = 0.054, p = 0.949).

Conclusion: Folate status in children with SCA is not affected by their disease severity. Therefore, there may be no need for additional folate supplementation with increasing severity of sickle cell anaemia.

Citing Articles

Editorial: Infectious diseases and NCDs persist despite concerted effort.

Tumwine J Afr Health Sci. 2021; 21(2):i-v.

PMID: 34795757 PMC: 8568243. DOI: 10.4314/ahs.v21i2.1.

References
1.
Uche E, Adelekan O, Akinbami A, Osunkalu V, Ismail K, Ogbenna A . Serum homocysteine and disease severity in sickle cell anemia patients in Lagos. J Blood Med. 2019; 10:127-134. PMC: 6520594. DOI: 10.2147/JBM.S198316. View

2.
WATSON-WILLIAMS E . Folic acid deficiency in sickle-cell anaemia. East Afr Med J. 1962; 39:213-21. View

3.
Green R . Indicators for assessing folate and vitamin B-12 status and for monitoring the efficacy of intervention strategies. Am J Clin Nutr. 2011; 94(2):666S-72S. PMC: 3142735. DOI: 10.3945/ajcn.110.009613. View

4.
Kennedy T, Fung E, Kawchak D, Zemel B, Ohene-Frempong K, Stallings V . Red blood cell folate and serum vitamin B12 status in children with sickle cell disease. J Pediatr Hematol Oncol. 2001; 23(3):165-9. DOI: 10.1097/00043426-200103000-00009. View

5.
Chinawa J, Emodi I, Ikefuna A, Ocheni S . Coagulation profile of children with sickle cell anemia in steady state and crisis attending the university of Nigeria teaching hospital, Ituku-Ozalla, Enugu. Niger J Clin Pract. 2013; 16(2):159-63. DOI: 10.4103/1119-3077.110132. View