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Quantification of the natural history of visceral leishmaniasis and consequences for control

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Quantification of the natural history of visceral leishmaniasis and consequences for control. / Chapman, Lloyd A.C.; Dyson, Louise; Courtenay, Orin et al.
In: Parasites and Vectors, Vol. 8, No. 1, 521, 22.10.2015.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Chapman, LAC, Dyson, L, Courtenay, O, Chowdhury, R, Bern, C, Medley, GF & Hollingsworth, TD 2015, 'Quantification of the natural history of visceral leishmaniasis and consequences for control', Parasites and Vectors, vol. 8, no. 1, 521. https://doi.org/10.1186/s13071-015-1136-3

APA

Chapman, L. A. C., Dyson, L., Courtenay, O., Chowdhury, R., Bern, C., Medley, G. F., & Hollingsworth, T. D. (2015). Quantification of the natural history of visceral leishmaniasis and consequences for control. Parasites and Vectors, 8(1), Article 521. https://doi.org/10.1186/s13071-015-1136-3

Vancouver

Chapman LAC, Dyson L, Courtenay O, Chowdhury R, Bern C, Medley GF et al. Quantification of the natural history of visceral leishmaniasis and consequences for control. Parasites and Vectors. 2015 Oct 22;8(1):521. doi: 10.1186/s13071-015-1136-3

Author

Chapman, Lloyd A.C. ; Dyson, Louise ; Courtenay, Orin et al. / Quantification of the natural history of visceral leishmaniasis and consequences for control. In: Parasites and Vectors. 2015 ; Vol. 8, No. 1.

Bibtex

@article{cc3c68319ddf45568921a190eaa264f4,
title = "Quantification of the natural history of visceral leishmaniasis and consequences for control",
abstract = "Background: Visceral leishmaniasis has been targeted for elimination as a public health problem (less than 1 case per 10,000 people per year) in the Indian sub-continent by 2017. However, there is still a high degree of uncertainty about the natural history of the disease, in particular about the duration of asymptomatic infection and the proportion of asymptomatically infected individuals that develop clinical visceral leishmaniasis. Quantifying these aspects of the disease is key for guiding efforts to eliminate visceral leishmaniasis and maintaining elimination once it is reached. Methods: Data from a detailed epidemiological study in Bangladesh in 2002-2004 was analysed to estimate key epidemiological parameters. The role of diagnostics in determining the probability and rate of progression to clinical disease was estimated by fitting Cox proportional hazards models. A multi-state Markov model of the natural history of visceral leishmaniasis was fitted to the data to estimate the asymptomatic infection period and the proportion of asymptomatic individuals going on to develop clinical symptoms. Results: At the time of the study, individuals were taking several months to be diagnosed with visceral leishmaniasis, leading to many opportunities for ongoing transmission. The probability of progression to clinical disease was strongly associated with initial seropositivity and even more strongly with seroconversion, with most clinical symptoms developing within a year. The estimated average durations of asymptomatic infection and symptomatic infection for our model of the natural history are 147 days (95 % CI 130-166) and 140 days (95 % CI 123-160), respectively, and are significantly longer than previously reported estimates. We estimate from the data that 14.7 % (95 % CI 12.6-20.0 %) of asymptomatic individuals develop clinical symptoms - a greater proportion than previously estimated. Conclusions: Extended periods of asymptomatic infection could be important for visceral leishmaniasis transmission, but this depends critically on the relative infectivity of asymptomatic and symptomatic individuals to sandflies. These estimates could be informed by similar analysis of other datasets. Our results highlight the importance of reducing times from onset of symptoms to diagnosis and treatment to reduce opportunities for transmission.",
keywords = "Control, Diagnostics, Indian sub-continent, Multi-state Markov model, Natural history, Visceral leishmaniasis",
author = "Chapman, {Lloyd A.C.} and Louise Dyson and Orin Courtenay and Rajib Chowdhury and Caryn Bern and Medley, {Graham F.} and Hollingsworth, {T. Deirdre}",
note = "Publisher Copyright: {\textcopyright} 2015 Chapman et al.",
year = "2015",
month = oct,
day = "22",
doi = "10.1186/s13071-015-1136-3",
language = "English",
volume = "8",
journal = "Parasites and Vectors",
issn = "1756-3305",
publisher = "BioMed Central",
number = "1",

}

RIS

TY - JOUR

T1 - Quantification of the natural history of visceral leishmaniasis and consequences for control

AU - Chapman, Lloyd A.C.

AU - Dyson, Louise

AU - Courtenay, Orin

AU - Chowdhury, Rajib

AU - Bern, Caryn

AU - Medley, Graham F.

AU - Hollingsworth, T. Deirdre

N1 - Publisher Copyright: © 2015 Chapman et al.

PY - 2015/10/22

Y1 - 2015/10/22

N2 - Background: Visceral leishmaniasis has been targeted for elimination as a public health problem (less than 1 case per 10,000 people per year) in the Indian sub-continent by 2017. However, there is still a high degree of uncertainty about the natural history of the disease, in particular about the duration of asymptomatic infection and the proportion of asymptomatically infected individuals that develop clinical visceral leishmaniasis. Quantifying these aspects of the disease is key for guiding efforts to eliminate visceral leishmaniasis and maintaining elimination once it is reached. Methods: Data from a detailed epidemiological study in Bangladesh in 2002-2004 was analysed to estimate key epidemiological parameters. The role of diagnostics in determining the probability and rate of progression to clinical disease was estimated by fitting Cox proportional hazards models. A multi-state Markov model of the natural history of visceral leishmaniasis was fitted to the data to estimate the asymptomatic infection period and the proportion of asymptomatic individuals going on to develop clinical symptoms. Results: At the time of the study, individuals were taking several months to be diagnosed with visceral leishmaniasis, leading to many opportunities for ongoing transmission. The probability of progression to clinical disease was strongly associated with initial seropositivity and even more strongly with seroconversion, with most clinical symptoms developing within a year. The estimated average durations of asymptomatic infection and symptomatic infection for our model of the natural history are 147 days (95 % CI 130-166) and 140 days (95 % CI 123-160), respectively, and are significantly longer than previously reported estimates. We estimate from the data that 14.7 % (95 % CI 12.6-20.0 %) of asymptomatic individuals develop clinical symptoms - a greater proportion than previously estimated. Conclusions: Extended periods of asymptomatic infection could be important for visceral leishmaniasis transmission, but this depends critically on the relative infectivity of asymptomatic and symptomatic individuals to sandflies. These estimates could be informed by similar analysis of other datasets. Our results highlight the importance of reducing times from onset of symptoms to diagnosis and treatment to reduce opportunities for transmission.

AB - Background: Visceral leishmaniasis has been targeted for elimination as a public health problem (less than 1 case per 10,000 people per year) in the Indian sub-continent by 2017. However, there is still a high degree of uncertainty about the natural history of the disease, in particular about the duration of asymptomatic infection and the proportion of asymptomatically infected individuals that develop clinical visceral leishmaniasis. Quantifying these aspects of the disease is key for guiding efforts to eliminate visceral leishmaniasis and maintaining elimination once it is reached. Methods: Data from a detailed epidemiological study in Bangladesh in 2002-2004 was analysed to estimate key epidemiological parameters. The role of diagnostics in determining the probability and rate of progression to clinical disease was estimated by fitting Cox proportional hazards models. A multi-state Markov model of the natural history of visceral leishmaniasis was fitted to the data to estimate the asymptomatic infection period and the proportion of asymptomatic individuals going on to develop clinical symptoms. Results: At the time of the study, individuals were taking several months to be diagnosed with visceral leishmaniasis, leading to many opportunities for ongoing transmission. The probability of progression to clinical disease was strongly associated with initial seropositivity and even more strongly with seroconversion, with most clinical symptoms developing within a year. The estimated average durations of asymptomatic infection and symptomatic infection for our model of the natural history are 147 days (95 % CI 130-166) and 140 days (95 % CI 123-160), respectively, and are significantly longer than previously reported estimates. We estimate from the data that 14.7 % (95 % CI 12.6-20.0 %) of asymptomatic individuals develop clinical symptoms - a greater proportion than previously estimated. Conclusions: Extended periods of asymptomatic infection could be important for visceral leishmaniasis transmission, but this depends critically on the relative infectivity of asymptomatic and symptomatic individuals to sandflies. These estimates could be informed by similar analysis of other datasets. Our results highlight the importance of reducing times from onset of symptoms to diagnosis and treatment to reduce opportunities for transmission.

KW - Control

KW - Diagnostics

KW - Indian sub-continent

KW - Multi-state Markov model

KW - Natural history

KW - Visceral leishmaniasis

U2 - 10.1186/s13071-015-1136-3

DO - 10.1186/s13071-015-1136-3

M3 - Journal article

C2 - 26490668

AN - SCOPUS:84945193709

VL - 8

JO - Parasites and Vectors

JF - Parasites and Vectors

SN - 1756-3305

IS - 1

M1 - 521

ER -