As. Prasad et al., Effect of zinc supplementation on incidence of infections and hospital admissions in sickle cell disease (SCD), AM J HEMAT, 61(3), 1999, pp. 194-202
Zinc deficiency is a common nutritional problem in adult sickle-cell diseas
e (SCD) patients, Hyperzincuria and increased requirement of zinc due to co
ntinued hemolysis in SCD are probable bases for zinc deficiency in these pa
tients. Zinc deficiency affects adversely T-helper(1) (TH1) functions and c
ell mediated immunity and interleukin (IL)-2 production is decreased in zin
c deficient subjects. We hypothesized that zinc supplementation will improv
e T-helper, function and decrease incidence of infections in patients with
SCD. We tested this hypothesis in 32 SCD subjects who were divided in three
groups (Grs A, B, and C). Grs A (n = 11)and B (n = 10)were zinc deficient
based on cellular zinc criteria and Gr C (n = 11) were zinc sufficient. Gr
A subjects were observed for 1 year (baseline), following which they receiv
ed zinc acetate (50 to 75 mg of elemental zinc orally daily) for 3 years. G
r B subjects were observed for 1 year(baseline), following which they recei
ved placebo for 1 year and then switched to zinc supplementation (50 to 75
mg of elemental zinc orally daily) for 2 years. Gr C subjects did not recei
ve any intervention inasmuch as they were zinc sufficient. Prolonged zinc s
upplementation resulted in an increase in lymphocyte and granulocyte zinc(P
= 0.0001), and an increase in interleukin-a production (P = 0.0001), decre
ased incidence of documented bacteriologically positive infections (P = 0.0
026), decreased number of hospitalizations and decreased number of vaso-occ
lusive pain crisis (P = 0.0001). The predominant pathogens isolated were st
aphylococci and streptococci involving the respiratory tract and aerobic gr
am-negative bacteria, particularly Escherichia coli, involving the urinary
tract, Further confirmation of our observations will require prospective st
udies of zinc supplementation in a larger number of SCD patients. Am. J. He
matol. 61:194-202, 1999. (C) 1999 Wiley-Liss, Inc.