Table 2. Post-treatment malaria transmission in relation to mutations in the dhfr and dhps genes.
Double mutation * | ≥ three mutations * | p-value | |
Median gametocyte density/µL ¥ on day of feeding, (IQR) | |||
Non-ACT | 10.40 (3.83–30.33) | 4.96 (0.51–22.47) | 0.27 |
ACT | 0.84 (0.03–1.94) | 0.17 (0.04–1.01) | 0.66 |
Proportion of children infecting at least one mosquito, % (n/N) | |||
Non-ACT | 77.8 (7/9) | 73.5 (25/34) | 1.00 |
ACT | 50.0 (3/6) | 62.5 (5/8) | 1.00 |
Proportion of infected mosquitoes, % (n/N)§ | |||
Non-ACT | 7.0 (19/270) | 6.0 (61/1020) | 0.79 |
ACT | 3.2 (6/180) | 3.3 (8/240) | 0.65 |
IQR = interquartile range; Non-ACT = treatment with sulphadoxine-pyrimethamine (SP) alone or in combination with amodiaquine; ACT = treatment with SP and artesunate (3 days).
Gametocyte densities were measured by Pfs25 QT-NASBA.
Mutations were determined at enrolment: double mutation = mutations in c108+c59 or c108+c51; ≥ three mutations = mutations in c51+c59+c108 and possible additional mutations;
estimates were adjusted for correlation between observations from the same individual.