Effects of Vitamin C Supplementation on Sickle Cell Disease
Abstract:
Sickle cell disease is the general name for a
group of disorders that affect haemoglobin, the red pigment in red blood cells that
delivers oxygen to cells throughout the body. Fortunately, Vitamin C has been found
to be very vital in improving and sustaining health. This study sought to determine
the effect of vitamin C supplementation on the blood pressure and blood count in
sickle cell patients. The study was a randomized double blind, placebo –controlled
study. The treatment group received 300mg of vitamin C per day for 3 months. The
data of 60 subjects were analysed. Vitamin C supplementation increased the mean
haemoglobin concentration and haematocrit of the subjects with SC genotype by 2.4%
and 2.5% respectively compared to baseline (even though not statistically significant).
There was a statistically significant increase in the Mean Copuscular Haemoglobin
Concentration of the subjects with SC genotype on vitamin C (from 29.61 to 31.32
g/dl) compared to those on placebo (from 30.44 to 28.5 g/dl) (P = 0.01). Vitamin
C supplementation therefore has some beneficial effects on some full blood count
parameters of sickle cell patients with SC genotype.
Keywords: Sickle Cell Disease; Vitamin C.
References:
[1].
Adiiboka, F. (2012).
Effects of Vitamin C supplementation on Sickle Cell disease. Thesis submitted to
the university of Ghana, Legon, in partial fulfilment of the requirements for the
award of Mphil. Nutrition degree.
[2].
Cox, M. (2009). Interpreting
Blood Tests and Investigations. RCN Conference (January). USA.
[3].
Harris, Y.R. and Graham,
J.A (2007). The African Child: development. Springer Publishing Company. USA.
[4].
Higdon, J. and Drake,
V. (2011). An Evidence-Based Approach to Vitamins and Minerals: Health Benefits
and Intake Recommendations. Thieme Publishers. Pg. 39.
[5].
Jaja, S.I., Ikotun,
A.R., Gbenebitse, S. and Temiye, E.O. (2002). Blood pressure, hematologic and erythrocyte
fragility changes in children suffering from sickle cell anemia following ascorbic
acid supplementation. Journal of Tropical Pediatrics, 48(6), 366-70.
[6].
Jekel, J.F., Katz,
D.L., Elmore, J.G. (2007). Epidemiology, biostatistics and preventive medicine.
Saunders Elsevier, Philadelphia. Pp. 198-200.
[7].
World Health
Organisation (WHO) (2006). Sickle cell anaemia. Report by the Secretariat. 59th
World Health Assembly.11.4.