IDL-BNC @ IDRC >
IDRC / CRDI >
IDRC Research Results / Résultats de recherches du CRDI >
Please use this identifier to cite or link to this item:
|Title: ||Identification of malaria transmission and epidemic hotspots in the western Kenya highlands : its application to malaria epidemic prediction|
|Authors: ||Wanjala, Christine L.|
Githeko, Andrew K.
|Issue Date: ||2011|
|Publisher: ||BioMed Central, London, GB|
|Abstract: ||Background: Malaria in the western Kenya highlands is characterized by unstable and high transmission variability
which results in epidemics during periods of suitable climatic conditions. The sensitivity of a site to malaria
epidemics depends on the level of immunity of the human population. This study examined how terrain in the
highlands affects exposure and sensitivity of a site to malaria.
Methods: The study was conducted in five sites in the western Kenya highlands, two U-shaped valleys (Iguhu,
Emutete), two V-shaped valleys (Marani, Fort-Ternan) and one plateau (Shikondi) for 16 months among 6-15 years
old children. Exposure to malaria was tested using circum-sporozoite protein (CSP) and merozoite surface protein
(MSP) immunochromatographic antibody tests; malaria infections were tested by microscopic examination of thick
and thin smears, the children’s homes were georeferenced using a global positioning system. Paired t-test was
used to compare the mean prevalence rates of the sites, K-function was use to determine if the clustering of
malaria infections was significant.
Results and Discussion: The mean antibody prevalence was 22.6% in Iguhu, 24% in Emutete, 11.5% in Shikondi,
8.3% in Fort-Ternan and 9.3% in Marani. The mean malaria infection prevalence was 23.3% in Iguhu, 21.9% in
Emutete, 4.7% in Shikondi, 2.9% in Fort-Ternan and 2.4% in Marani. There was a significant difference in the
antibodies and malaria infection prevalence between the two valley systems, and between the two valley systems
and the plateau (P < 0.05). There was no significant difference in the antibodies and malaria infection prevalence
in the two U-shaped valleys (Iguhu and Emutete) and in the V-shaped valleys (Marani and Fort Ternan) (P > 0.05).
There was 8.5- fold and a 2-fold greater parasite and antibody prevalence respectively, in the U-shaped compared
to the V-shaped valleys. The plateau antibody and parasite prevalence was similar to that of the V-shaped valleys.
There was clustering of malaria antibodies and infections around flat areas in the U-shaped valleys, the infections
were randomly distributed in the V-shaped valleys and less clustered at the plateau.
Conclusion: This study showed that the V-shaped ecosystems have very low malaria prevalence and few
individuals with an immune response to two major malaria antigens and they can be considered as epidemic
hotspots. These populations are at higher risk of severe forms of malaria during hyper-transmission seasons. The
plateau ecosystem has a similar infection and immune response to the V-shaped ecosystems. The U-shaped
ecosystems are transmission hotspots.|
|Project Number: ||104707|
|Project Title: ||Transferring the Malaria Epidemic Prediction Model to Users in East Africa|
|Appears in Collections:||East Africa / Afrique de l'Est|
Health / Santé
Research Results (CCAA) / Résultats de recherches (ACCA)
IDRC Research Results / Résultats de recherches du CRDI
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.