Background: Serological data are increasingly being used to monitor malaria transmission intensity and have been demonstrated to be particularly useful in areas of low transmission where traditional measures such as EIR and parasite prevalence are limited. The seroconversion rate (SCR) is usually estimated using catalytic models in which the measured antibody levels are used to categorize individuals as seropositive or seronegative. One limitation of this approach is the requirement to impose a fixed cut-off to distinguish seropositive and negative individuals. Furthermore, the continuous variation in antibody levels is ignored thereby potentially reducing the precision of the estimate. Methods: An age-specific density model which mimics antibody acquisition and loss was developed to make full use of the information provided by serological measures of antibody levels. This was fitted to blood-stage antibody density data from 12 villages at varying transmission intensity in Northern Tanzania to estimate the exposure rate as an alternative measure of transmission intensity. Results: The results show a high correlation between the exposure rate estimates obtained and the estimated SCR obtained from a catalytic model (r = 0.95) and with two derived measures of EIR (r = 0.74 and r = 0.81). Estimates of exposure rate obtained with the density model were also more precise than those derived from catalytic models. Conclusion: This approach, if validated across different epidemiological settings, could be a useful alternative framework for quantifying transmission intensity, which makes more complete use of serological data.
机构:
Eijkman Oxford Clin Res Unit, Jakarta 10430, IndonesiaUniv Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
Elyazar, Iqbal R. F.
Johnston, Geoffrey L.
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Columbia Univ, Sch Int & Publ Affairs, New York, NY USA
Columbia Univ, Dept Microbiol & Immunol, Coll Phys & Surg, New York, NY 10032 USAUniv Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
Johnston, Geoffrey L.
Tatem, Andrew J.
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机构:
NIH, Fogarty Int Ctr, Bethesda, MD 20892 USA
Univ Florida, Emerging Pathogens Inst, Gainesville, FL USA
Univ Florida, Dept Geog, Gainesville, FL 32611 USAUniv Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
Tatem, Andrew J.
Hay, Simon I.
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机构:
Univ Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
NIH, Fogarty Int Ctr, Bethesda, MD 20892 USAUniv Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
机构:
Eijkman Oxford Clin Res Unit, Jakarta 10430, IndonesiaUniv Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
Elyazar, Iqbal R. F.
Johnston, Geoffrey L.
论文数: 0引用数: 0
h-index: 0
机构:
Columbia Univ, Sch Int & Publ Affairs, New York, NY USA
Columbia Univ, Dept Microbiol & Immunol, Coll Phys & Surg, New York, NY 10032 USAUniv Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
Johnston, Geoffrey L.
Tatem, Andrew J.
论文数: 0引用数: 0
h-index: 0
机构:
NIH, Fogarty Int Ctr, Bethesda, MD 20892 USA
Univ Florida, Emerging Pathogens Inst, Gainesville, FL USA
Univ Florida, Dept Geog, Gainesville, FL 32611 USAUniv Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
Tatem, Andrew J.
Hay, Simon I.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England
NIH, Fogarty Int Ctr, Bethesda, MD 20892 USAUniv Oxford, Dept Zool, Spatial Ecol & Epidemiol Grp, Oxford, England