Research Article

Vitamin D and Nonskeletal Complications among Egyptian Sickle Cell Disease Patients

Table 3

Demographic and laboratory data of the 2 groups.

VariableNormal Group (n=32)Deficient Group (n=48)P-value

Age: in years:median (IQR)8 (9.235)11(5)0.043

Sex: n (%)0.732
 Male (%)17 (53.1%)30 (62.5%)
 Female (%)15 (46.9%)18 (37.5%)

Weight percentile: mean ± SD29.7±20.222.1±18.20.072

Height percentile: mean ± SD33.8±26.522.2±24.80.024

Hemoglobin genotype: n (%)0.635
HBSS (%)26 (81.3%)33 (68.7%)
HBSB+ (%)5 (15.6%)11 (20.8%)
HBSB0 (%)1 (3.1%)4 (10.5%)

Splenomegaly: n (%) (n= 28)12 (37.5)16 (33.4)0.655

Splenectomy: n (%) (n=22)7 (31.8)15 (68.2)0.156

Pallor: n (%) (n=38)12 (31.5)26 (68.5)0.267

Jaundice: n (%) (n=21)1 (4.8)20 (95.2)0.001

Osseous changes: n (%) (n=13)3 (23)10 (76)0.015

Hemoglobin (g/dL): mean ± SD8.6±1.17.9±1.60.022

Hematocrit (%): mean ± SD26.9±423.9±5.10.004

Reticulocyte count (%): mean ± SD4.8±2.96.5±4.10.063

Corrected Reticulocyte count (%): mean ± SD2.6±1.43±2.10.401

AST (IU/L): mean ± SD43.3±23.354.4±20.10.006

ALT (IU/L): mean ± SD25.1±20.327.1±18.80.540

LDH (IU/L): mean ± SD454.8±279.4634.9±277.80.001

TSB (mg/dL): mean ± SD4.2±2.45.9±3.50.038

Indirect bilirubin (mg/dL): mean ± SD2±1.82.6±1.40.016

n = number. IQR = interquartile range. SD = standard deviation. HBSS= homozygous hemoglobin S; HBSβ+ = Sβ+ thalassemia; HBSβ0 = Sβ0 thalassemia; AST = aspartate aminotransferase; ALT = alanine aminotransferase; LDH = lactate dehydrogenase; TSB = total serum bilirubin. Bold values indicate statistical significance.