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Table 1 Clinical Characteristics of enrolled subjects by genotype (N = 266).

From: Asymptomatic bacteriuria in sickle cell disease: a cross-sectional study

Clinical characteristics

HbSS N = 148

HbSC N = 85

HbSβ0 N = 6

HbSβ+ N = 22

Sickle variants* N = 5

Age yr

26.4 ± 2.6

27 ± 2.3

25.9 ± 2.3

26.5 ± 2.5

25.1 ± 2.5

†Gender (M:F)

71:77

38:47

2:4

13:9

4:1

#Creatinine μmol/L

45.7 ± 9.4a

63.3 ± 11.7b

70.7 ± 23.1b

61.9 ± 12.4b

62 ± 20.4a

#Uric Acid mmol/L

0.3 ± 0.1a

0.3 ± 0.1a

0.4 ± 0.1a

0.4 ± 0.3b

0.3 ± 0.1a

#Haemoglobin g/L

80.2 ± 9.9a

108.2 ± 8b

91.6 ± 11.8b

109.9 ± 12.4b

124 ± 22.1b

#Nucleated Blood cells × 109/Lc

15.9 ± 3.2a

10.2 ± 2.9b

13.3 ± 2.2b

9.2 ± 2.7b

9.9 ± 2.5b

†Proteinuria ≥ trace : No proteinuria (n = 182)

17

7

0

1

0

†Positive History of gram negative sepsis

2

2

0

0

0

†Positive recorded history of ever having UTI

50

25

2

1

1

  1. Values are means ± sd ; † values are counts. Abbreviations – HbSS = Homozygous sickle cell disease, HbSC= Sickle cell-haemoglobin C, HbSβ0 = Sickle cell-β0 thalassemia, HbSβ+ = Sickle cell-β+ thalassemia; UTI= Urinary Tract Infections.
  2. * Sickle variants include sickle cell-hereditary persistence of foetal haemoglobin, sickle cell -haemoglobin O Arab, sickle cell -haemoglobin Lepore-Boston.
  3. # Significant difference in mean values by genotype. Dissimilar superscript to HbSS values are significantly different (p < 0.03)