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Table 2 Comparison of patients characteristics according to the sickle cell haplotypes

From: High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte

 

Homozygous Bantu

Heterozygous Bantu

Homozygous Benin

Heterozygous Benin

Bantu/Bantu (n = 95)

P

Bantu/− (n = 46)

P

Benin/Benin (n = 4)

P

Benin/− (n = 35)

p

Mean (±SD) or n (%)

Mean (±SD) or n (%)

Mean (±SD) or n (%)

Mean (±SD) or n (%)

Age (years)

         

7,98 (±0,82)

11,23 (±0,55)

0,002

Hématocrit (%)

24,18 (±0,38)

26,26(±0,51)

0,001

      

26,26 (±0,6)

24,43 (±0,36)

0,01

MCV (fL)

81,27 (±1)

67,78 (±1,23)

< 0,001

      

66,72 (±1,42)

80,04 (±0,97)

< 0,001

MCHC (g/dL)

32,75 (±0,13)

31,43 (±0,24)

< 0,001

32,22 (±0,13)

33,72 (±0,74)

0,023

34,25 (±1,04)

32,23 (±0,13)

0,011

   

HbF (%)

   

13,11 (±0,7)

6,08 (±2,3)

0,044

4,01 (±2,7)

13,07 (±0,7)

0,034

12 (±0,75)

15,1 (±1,52)

0,048

HbS (%)

85,9 (±1,1)

79,67 (±1,36)

0,001

      

78,68 (±1,62)

85,48 (±0,98)

0,001

TCD

        

0,041

   

Normal

      

1 (33,3)

101 (83,4)

    

Limit

      

0

10 (8,3)

    

Pathological

      

2 (66,7)

10 (8,3)

    

Duration of follow-up (months)

   

87,57 (±5,03)

143,7 (±30,43)

0,032

153 (±37,4)

87,7 (±5)

0,025

   

Newborn screening

         

29 (74,3)

8 (7,3)

0,001

Treatment Iron chelator

      

2 (50%)

9 (6,3)

0,028

   

Hospitalization/year

  

0,012

        

0,002

No

9 (9,6)

13 (25,5)

       

12 (30,7)

10 (9,5)

 

1 à 2

75 (79,8)

37 (72,5)

       

27 (69,3)

85 (80)

 

≥3

10 (10,6)

1 (2)

       

0

11 (10,5)

 

RBC transfusion

  

0,046

         

Never

18 (18,9)

19 (37,3)

          

Occasionnally

63 (66,4)

28 (54,9)

          

chronic transfusion

14 (14,7)

4 (7,8)