Skip to main content
. Author manuscript; available in PMC: 2021 Jan 1.
Published in final edited form as: J Hum Genet. 2019 Oct 29;65(2):99–113. doi: 10.1038/s10038-019-0692-3

Table 3.

Impact of COX-2 variants on malaria and SMA at enrollment

Variants Malaria SMA
Events OR 95% CI P value Events OR 95% CI P value
−512
 CC n = 704 REF n = 126 REF
 CT n = 97 0.648 0.419–1.000 0.050 n = 21 1.368 0.771–2.247 0.284
 TT n = 19 2.427 0.497–11.859 0.273 n = 3 1.106 0.287–4.265 0.883
−608
 TT n = 562 REF n = 105 REF
 TC n = 218 1.155 0.790–1.689 0.456 n = 39 1.141 0.720–1.809 0.574
 CC n = 40 0.644 0.326–1.275 0.207 n = 6 0.904 0.324–2.522 0.848
−765
 GG n = 362 REF n = 65 REF
 GC n = 347 1.076 0.759–1.528 0.681 n = 72 0.859 0.562–1.313 0.483
 CC n = 111 0.966 0.595–1.569 0.890 n = 13 1.805 0.902–3.610 0.095
−1195
 AA n = 730 REF n = 135 REF
 AG n = 74 0.753 0.230–2.463 0.638 n = 11 0.851 0.422–1.716 0.652
 GG n = 12 0.672 0.184–2.453 0.547 n = 0
Haplotypes
 CTGA n = 529 1.167 0.840–1.623 0.358 n = 107 1.533 0.998–2.354 0.051
 CCGA n = 238 1.022 0.716 – 1.458 0.906 n = 44 1.021 0.655–1.590 0.927
 CTCA n = 367 0.980 0.709 – 1.355 0.903 n = 64 0.827 0.554–1.234 0.352
 CTCG n = 8 2.474 0.307 –19.936 0.395 n = 0
 TTCA n = 96 1.254 0.796 –1.974 0.329 n = 23 1.486 0.850–2.597 0.164
 TTGG n = 4 1.611 0.127 –20.406 0.713 n = 2 5.780 0.735–45.457 0.095
 CCCA n = 24 0.882 0.342 –2.275 0.795 n = 2 0.479 0.107–2.142 0.335
 TTGA n = 15 0.796 0.252 –2.513 0.697 n = 2 0.956 0.198–4.618 0.955
 CTGG n = 69 0.949 0.548 –1.641 0.850 n = 9 0.701 0.330–1.491 0.356
 TCGA n = 2 0.146 0.013 –1.691 0.124 n = 0
 CCGG n = 5 1.348 0.154 –11.820 0.787 n = 0
 TTCG n = 5 1.611 0.127 –20.406 0.713 n = 0

Data are presented as odds (OR) and 95% confidence intervals (CI) determined using binary logistic regression with the following covariates in the models: age at enrollment, sex, HIV-1 and bacteremia (presence/absence), and sickle cell trait, α+-thalassemia, and G6PD status. Children (n = 1081) were categorized into either malaria negative (n = 261; aparasitemic) or positive (n = 820; parasitemic) for determining susceptibility to malaria, and into either non-SMA (n = 670; Hb ≥ 5.0 g/dL) or SMA (n = 150; Hb < 5.0 g/dL) for determining susceptibility to SMA. Homozygous wild-type genotypes and non-carriers of haplotypes were used as references in the analyses. Bold indicates a P value ≤ 0.050