Research Article

Haptoglobin Gene Polymorphism among Sickle Cell Patients in West Cameroon: Hematological and Clinical Implications

Table 5

Haptoglobin genotype and allele frequency distribution in the study population.

GroupsSS (n = 102)AS (n = 55)AA (n = 60) value

Hp genotypesHp 1-132 (31.4%)a16 (29.1%)a,b21 (35%)a,b≤0.001
Hp 2-115 (14.7%)b23 (41.8%)a23 (38.3%)a
Hp 2-255 (53.9%)a16 (29.1%)b16 (26.7%)b
Hp1S-1S25 (24.5%)a,b8 (14.5%)a9 (15%)a≤0.001
Hp1F-1F6 (5.9%)a,b,c6 (10.9%)a9 (15%)a
Hp1S-1F1 (1%)a,b,c2 (3.6%)a3 (5%)a
Hp2-1S11 (10.8%)a,c13 (23.6%)a13 (21.7%)a
Hp2-1F4 (3.9%)c10 (18.2%)a10 (16.7%)a
Hp2-255 (53.9%)a,b16 (29.1%)a16 (26.7%)a

Hp allele frequenciesHp1S0.3040.2820.283
Hp1F0.0840.2180.258
Hp20.6130.50.458

a, b, and c: values with different letters in the same line are significantly different at  < 0.05; SD: standard deviation; ∗: chi2 test with the Bonferroni adjustment and Fischer test for small size groups.