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Recent Molecular Assessment of Plasmodium vivax and Plasmodium falciparum Asymptomatic Infections in Botswana

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Abstract.In 2016, we reported the presence of Plasmodium vivax in Botswana through active case detection. A real-time PCR was used during a similar study in 10 districts to assess changes in the P. vivax prevalence. We assessed 1,614 children (2–13 years of age) for hemoglobin (Hb; g/dL) and Plasmodium parasites. The median age of all participants was 5.0 years (25th percentile, 3 years; 75th percentile, 8 years). The median Hb (g/dL) level was 12.1, but 18.3% of the participants had anemia (Hb < 11.0 g/dL); these participants were clustered in the younger than 5 years age group in all districts (P < 0.001). The risk of anemia decreased with age 5 years or older (odds ratio [OR], 0.26; 95% confidence interval [CI], 0.197–0.34; P < 0.001). The prevalence rates of Plasmodium parasites were as follows: P. vivax, 12.7%; P. falciparum, 12.7%; P. malariae, 0.74%; and P. ovale (P. ovale curtisi), 0.68%. Mixed infection rates were as follows: P. falciparum and P. vivax, 2.35%; P. falciparum and P. ovale curtisi, 0.56%; P. vivax and P. malariae, 0.06%; and P. falciparum and P. malariae, 0.68%. The infections were largely asymptomatic (99.6%). Using logistic regression, the risk of infection with P. vivax was highest in Kweneng East (OR, 6.2; 95% CI, 2.9–13.1), followed by South East (OR, 5.6; 95% CI, 2.5–12.3) and Ngami (OR, 5.1; 95% CI, 2.2–12.0). Compared to the risk of infection for children younger than 5 years, the risk of infection decreased for children 5 years or older in regions with high rates of P. vivax and P. falciparum infections. P. vivax and P. falciparum have expanded within the asymptomatic population in Botswana; therefore, careful attention is required for their elimination.
Title: Recent Molecular Assessment of Plasmodium vivax and Plasmodium falciparum Asymptomatic Infections in Botswana
Description:
Abstract.
In 2016, we reported the presence of Plasmodium vivax in Botswana through active case detection.
A real-time PCR was used during a similar study in 10 districts to assess changes in the P.
vivax prevalence.
We assessed 1,614 children (2–13 years of age) for hemoglobin (Hb; g/dL) and Plasmodium parasites.
The median age of all participants was 5.
0 years (25th percentile, 3 years; 75th percentile, 8 years).
The median Hb (g/dL) level was 12.
1, but 18.
3% of the participants had anemia (Hb < 11.
0 g/dL); these participants were clustered in the younger than 5 years age group in all districts (P < 0.
001).
The risk of anemia decreased with age 5 years or older (odds ratio [OR], 0.
26; 95% confidence interval [CI], 0.
197–0.
34; P < 0.
001).
The prevalence rates of Plasmodium parasites were as follows: P.
vivax, 12.
7%; P.
falciparum, 12.
7%; P.
malariae, 0.
74%; and P.
ovale (P.
ovale curtisi), 0.
68%.
Mixed infection rates were as follows: P.
falciparum and P.
vivax, 2.
35%; P.
falciparum and P.
ovale curtisi, 0.
56%; P.
vivax and P.
malariae, 0.
06%; and P.
falciparum and P.
malariae, 0.
68%.
The infections were largely asymptomatic (99.
6%).
Using logistic regression, the risk of infection with P.
vivax was highest in Kweneng East (OR, 6.
2; 95% CI, 2.
9–13.
1), followed by South East (OR, 5.
6; 95% CI, 2.
5–12.
3) and Ngami (OR, 5.
1; 95% CI, 2.
2–12.
0).
Compared to the risk of infection for children younger than 5 years, the risk of infection decreased for children 5 years or older in regions with high rates of P.
vivax and P.
falciparum infections.
P.
vivax and P.
falciparum have expanded within the asymptomatic population in Botswana; therefore, careful attention is required for their elimination.

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