Estimating malaria transmission intensity from Plasmodium falciparum serological data using antibody density models
Author(s)
Pothin, E
Ferguson, NM
Drakeley, CJ
Ghani, AC
Type
Journal Article
Abstract
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.
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.
Date Issued
2016-02-09
Date Acceptance
2016-01-22
Citation
Malaria Journal, 2016, 15
ISSN
1475-2875
Publisher
BioMed Central
Journal / Book Title
Malaria Journal
Volume
15
Copyright Statement
© 2016 Pothin et al. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License
(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium,
provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/
publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium,
provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/
publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
License URL
Subjects
Science & Technology
Life Sciences & Biomedicine
Infectious Diseases
Parasitology
Tropical Medicine
Malaria
Model
Serology
Measuring transmission intensity
Antibody titre
Cross-sectional data
Force of infection
Plasmodium falciparum
MIXTURE-MODELS
ENDEMICITY
ELIMINATION
PREVALENCE
RESPONSES
ANTIGENS
AGE
INFECTION
TANZANIA
AREAS
Publication Status
Published
Article Number
79