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. 2019 Jul 2;45:290–302. doi: 10.1016/j.ebiom.2019.06.043

Table 1.

Demographic, clinical, and laboratory characteristics upon enrolment.

Characteristics Aparasitemic Non-SMA (Hb ≥ 5.0 g/dL) SMA (Hb < 5.0 g/dL) P
Demographic indices
Sample size (n) 292 986 234
Gender, n (%)
Male 147 (50.34) 502 (50.91) 114 (48.72) 0.834a
Female 145 (49.70) 484 (49.09) 120 (51.28)
Age, (months) 11.28 (13.00) 12.70 (10.46) 9.51 (10.73)*** 0.002b
Haematological and parasitological indices
Haemoglobin, g/dL 10.40 (2.40) 7.70 (2.80) 4.30 (1.00)*** <0.001b
Hematocrit, (Hct. %) 32.90 (6.30) 25.30 (8.90) 14.20 (3.70) *** <0.001b
RBC, (×1012/μL) 4.67 (1.03) 3.78 (1.39) 1.90 (0.63) *** <0.001b
WBC (×103/μL) 10.80 (7.00) 11.70 (6.30) 14.30 (9.90) *** <0.001b
Lymphocytes (×103/μL) 5.90 (4.20) 5.20 (3.60) 6.70 (5.20) *** <0.001b
Monocytes (×103/μL) 0.80 (0.70) 0.90 (0.80) 1.40 (1.30) *** <0.001b
Granulocytes (×103/μL) 3.80 (3.10) 5.12 (4.00) 5.20 (4.80) <0.001b
Platelet counts (×103/μL) 350.00 (220.00) 152.50 (124.00) 142.50 (100.00)* 0.003b
Parasite density/μL 0.00 (0.00) 28,902.75 (78,961) 23,507.85 (62,646) 0.004c
Genetic variants
G6PD gene, n. (%)
 Normal 193 (76.60) 687 (75.40) 181 (79.00)
 Intermediate 49 (19.40) 185 (20.30) 36 (15.70) 0.589a
 Deficient 10 (4.00) 39 (4.30) 12 (5.20)
α-thalassaemia, n. (%)
 αα/αα 109 (45.00) 374 (43.40) 90 (41.90)
 -α/αα 71 (29.30) 331 (38.40) 86 (40.00) 0.031a
 -α/−α 62 (25.60) 157 (18.20) 39 (18.10)
Sickle cell trait, n. (%)
 HbAA 230 (80.40) 807 (82.50) 208 (89.70)***
 HbAS 53 (18.50) 169 (17.30) 20 (8.60) <0.001a
 HbSS 3 (1.00) 2 (0.20) 4 (1.70)
Co-infections
Bacteremia 27 (9.25) 59 (5.98) 20 (8.55) 0.489a
HIV-1 12 (4.11) 25 (2.54) 13 (5.56)* 0.039a

Study participants (n = 1512) were stratified into three groups, aparasitemic, SMA (i.e., Hb < 5.0 g/dL with any density parasitaemia) or non-SMA (Hb ≥ 5.0 g/dL with any density parasitaemia). Data presented are medians (interquartile range, IQR), unless otherwise stated.

a

Statistical significance determined by the chi-square analysis.

b

Differences were determined using Kruskal-Wallis tests, and where significant differences were observed, pairwise comparisons between the non-SMA and SMA groups were performed using Mann-Whitney U tests.

c

Exclusion of the aparasitemic group, differences between the non-SMA and SMA groups determined using Mann-Whitney U tests. Bold indicates P ≤ 0.050. *Represents significant pairwise comparisons between the non-SMA and SMA groups at P < 0.050, **represents P < 0.01, and ***represents P < 0.001. G6PD is presented as absence/presence of G6PD alleles (G202A and A376G), α-thalassaemia is presented as absence/presence of the deletional determinant (−α3.7/−α3.7), and sickle cell trait is presented as the three genotypes. In some samples, we were not able to determine G6PD (n = 120), α-thalassaemia (n = 193), and sickle cell trait (n = 16).