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Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal

INTRODUCTION: Asymptomatic persons infected with the parasites causing visceral leishmaniasis (VL) usually outnumber clinically apparent cases by a ratio of 4–10 to 1. We assessed the risk of progression from infection to disease as a function of DAT and rK39 serological titers. METHODS: We used ava...

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Autores principales: Hasker, Epco, Malaviya, Paritosh, Gidwani, Kamlesh, Picado, Albert, Ostyn, Bart, Kansal, Sangeeta, Singh, Rudra Pratap, Singh, Om Prakash, Chourasia, Ankita, Singh, Abhishek Kumar, Shankar, Ravi, Wilson, Mary E., Khanal, Basudha, Rijal, Suman, Boelaert, Marleen, Sundar, Shyam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900391/
https://www.ncbi.nlm.nih.gov/pubmed/24466361
http://dx.doi.org/10.1371/journal.pntd.0002657
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author Hasker, Epco
Malaviya, Paritosh
Gidwani, Kamlesh
Picado, Albert
Ostyn, Bart
Kansal, Sangeeta
Singh, Rudra Pratap
Singh, Om Prakash
Chourasia, Ankita
Singh, Abhishek Kumar
Shankar, Ravi
Wilson, Mary E.
Khanal, Basudha
Rijal, Suman
Boelaert, Marleen
Sundar, Shyam
author_facet Hasker, Epco
Malaviya, Paritosh
Gidwani, Kamlesh
Picado, Albert
Ostyn, Bart
Kansal, Sangeeta
Singh, Rudra Pratap
Singh, Om Prakash
Chourasia, Ankita
Singh, Abhishek Kumar
Shankar, Ravi
Wilson, Mary E.
Khanal, Basudha
Rijal, Suman
Boelaert, Marleen
Sundar, Shyam
author_sort Hasker, Epco
collection PubMed
description INTRODUCTION: Asymptomatic persons infected with the parasites causing visceral leishmaniasis (VL) usually outnumber clinically apparent cases by a ratio of 4–10 to 1. We assessed the risk of progression from infection to disease as a function of DAT and rK39 serological titers. METHODS: We used available data on four cohorts from villages in India and Nepal that are highly endemic for Leishmania donovani. In each cohort two serosurveys had been conducted. Based on results of initial surveys, subjects were classified as seronegative, moderately seropositive or strongly seropositive using both DAT and rK39. Based on the combination of first and second survey results we identified seroconvertors for both markers. Seroconvertors were subdivided in high and low titer convertors. Subjects were followed up for at least one year following the second survey. Incident VL cases were recorded and verified. RESULTS: We assessed a total of 32,529 enrolled subjects, for a total follow-up time of 72,169 person years. Altogether 235 incident VL cases were documented. The probability of progression to disease was strongly associated with initial serostatus and with seroconversion; this was particularly the case for those with high titers and most prominently among seroconvertors. For high titer DAT convertors the hazard ratio reached as high as 97.4 when compared to non-convertors. The strengths of the associations varied between cohorts and between markers but similar trends were observed between the four cohorts and the two markers. DISCUSSION: There is a strongly increased risk of progressing to disease among DAT and/or rK39 seropositives with high titers. The options for prophylactic treatment for this group merit further investigation, as it could be of clinical benefit if it prevents progression to disease. Prophylactic treatment might also have a public health benefit if it can be corroborated that these asymptomatically infected individuals are infectious for sand flies.
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spelling pubmed-39003912014-01-24 Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal Hasker, Epco Malaviya, Paritosh Gidwani, Kamlesh Picado, Albert Ostyn, Bart Kansal, Sangeeta Singh, Rudra Pratap Singh, Om Prakash Chourasia, Ankita Singh, Abhishek Kumar Shankar, Ravi Wilson, Mary E. Khanal, Basudha Rijal, Suman Boelaert, Marleen Sundar, Shyam PLoS Negl Trop Dis Research Article INTRODUCTION: Asymptomatic persons infected with the parasites causing visceral leishmaniasis (VL) usually outnumber clinically apparent cases by a ratio of 4–10 to 1. We assessed the risk of progression from infection to disease as a function of DAT and rK39 serological titers. METHODS: We used available data on four cohorts from villages in India and Nepal that are highly endemic for Leishmania donovani. In each cohort two serosurveys had been conducted. Based on results of initial surveys, subjects were classified as seronegative, moderately seropositive or strongly seropositive using both DAT and rK39. Based on the combination of first and second survey results we identified seroconvertors for both markers. Seroconvertors were subdivided in high and low titer convertors. Subjects were followed up for at least one year following the second survey. Incident VL cases were recorded and verified. RESULTS: We assessed a total of 32,529 enrolled subjects, for a total follow-up time of 72,169 person years. Altogether 235 incident VL cases were documented. The probability of progression to disease was strongly associated with initial serostatus and with seroconversion; this was particularly the case for those with high titers and most prominently among seroconvertors. For high titer DAT convertors the hazard ratio reached as high as 97.4 when compared to non-convertors. The strengths of the associations varied between cohorts and between markers but similar trends were observed between the four cohorts and the two markers. DISCUSSION: There is a strongly increased risk of progressing to disease among DAT and/or rK39 seropositives with high titers. The options for prophylactic treatment for this group merit further investigation, as it could be of clinical benefit if it prevents progression to disease. Prophylactic treatment might also have a public health benefit if it can be corroborated that these asymptomatically infected individuals are infectious for sand flies. Public Library of Science 2014-01-23 /pmc/articles/PMC3900391/ /pubmed/24466361 http://dx.doi.org/10.1371/journal.pntd.0002657 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Hasker, Epco
Malaviya, Paritosh
Gidwani, Kamlesh
Picado, Albert
Ostyn, Bart
Kansal, Sangeeta
Singh, Rudra Pratap
Singh, Om Prakash
Chourasia, Ankita
Singh, Abhishek Kumar
Shankar, Ravi
Wilson, Mary E.
Khanal, Basudha
Rijal, Suman
Boelaert, Marleen
Sundar, Shyam
Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal
title Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal
title_full Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal
title_fullStr Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal
title_full_unstemmed Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal
title_short Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal
title_sort strong association between serological status and probability of progression to clinical visceral leishmaniasis in prospective cohort studies in india and nepal
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900391/
https://www.ncbi.nlm.nih.gov/pubmed/24466361
http://dx.doi.org/10.1371/journal.pntd.0002657
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