Cargando…
Longitudinal evaluation of asymptomatic Leishmania infection in HIV-infected individuals in North-West Ethiopia: A pilot study
BACKGROUND: In endemic regions, asymptomatic Leishmania infection is common. In HIV patients, detection of asymptomatic Leishmania infection could potentially identify those at risk of visceral leishmaniasis (VL). However, data on the prevalence, incidence, and determinants of asymptomatic infection...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799935/ https://www.ncbi.nlm.nih.gov/pubmed/31593563 http://dx.doi.org/10.1371/journal.pntd.0007765 |
_version_ | 1783460400540418048 |
---|---|
author | van Griensven, Johan van Henten, Saskia Mengesha, Bewketu Kassa, Mekibib Adem, Emebet Endris Seid, Mengistu Abdellati, Saïd Asefa, Wondimu Simegn, Tesfa Debasu, Degnachew Bogale, Tadfe Gedamu, Yonas Van Den Bossche, Dorien Adriaensen, Wim Van der Auwera, Gert Cnops, Lieselotte Vogt, Florian Diro, Ermias |
author_facet | van Griensven, Johan van Henten, Saskia Mengesha, Bewketu Kassa, Mekibib Adem, Emebet Endris Seid, Mengistu Abdellati, Saïd Asefa, Wondimu Simegn, Tesfa Debasu, Degnachew Bogale, Tadfe Gedamu, Yonas Van Den Bossche, Dorien Adriaensen, Wim Van der Auwera, Gert Cnops, Lieselotte Vogt, Florian Diro, Ermias |
author_sort | van Griensven, Johan |
collection | PubMed |
description | BACKGROUND: In endemic regions, asymptomatic Leishmania infection is common. In HIV patients, detection of asymptomatic Leishmania infection could potentially identify those at risk of visceral leishmaniasis (VL). However, data on the prevalence, incidence, and determinants of asymptomatic infection, and the risk of VL are lacking. METHODS: We conducted a cross-sectional survey at a single ART centre, followed by a prospective cohort study amongst HIV-infected adults in HIV care in a district hospital in a VL-endemic area in North-West Ethiopia (9/2015-8/2016). Asymptomatic Leishmania infection was detected using the direct agglutination test (DAT), rK39-rapid diagnostic test (RDT)), PCR on peripheral blood and the KAtex urine antigen test, and defined as positivity on any Leishmania marker. All individuals were followed longitudinally (irrespective of the Leishmania test results). Risk factors for asymptomatic Leishmania infection were determined using logistic regression. RESULTS: A total of 534 HIV-infected individuals enrolled in HIV care were included in the study. After excluding 13 patients with a history of VL and an 10 patients with incomplete baseline Leishmania tests, 511 were included in analysis. The median age was 38 years (interquartile range (IQR) 30–45), 62.6% were male. The median follow-up time was 12 months (IQR 9–12). No deaths were reported during the study period. Most (95.5%) were on antiretroviral treatment at enrolment, for a median of 52 months (IQR 27–79). The median CD4 count at enrolment was 377 cells/mm3 (IQR 250–518). The baseline prevalence of Leishmania infection was 12.8% in males and 4.2% in females. Overall, 7.4% tested positive for rK39, 4.3% for DAT, 0.2% for PCR and 0.2% for KAtex. Independent risk factors for a prevalent infection were male sex (odds ratio (OR) 3.2; 95% confidence intervals (CI) 14–7.0) and concurrent malaria infection (OR 6.1; 95% CI 1.9–18.9). Amongst the 49 prevalent (baseline) infections with further follow-up, the cumulative incidence of losing the Leishmania markers by one year was 40.1%. There were 36 incident infections during the course of the study, with a cumulative one-year risk of 9.5%. Only one case of VL was detected during follow-up. CONCLUSIONS: We found a high prevalence of asymptomatic Leishmania infection, persisting in most cases. The incidence was more modest and overt VL was rare. Larger and longer studies with more complete follow-up may help to decide whether a test and treat strategy would be justified in this context. TRIAL REGISTRATION: ClinicalTrials.gov NCT02839603 |
format | Online Article Text |
id | pubmed-6799935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67999352019-10-25 Longitudinal evaluation of asymptomatic Leishmania infection in HIV-infected individuals in North-West Ethiopia: A pilot study van Griensven, Johan van Henten, Saskia Mengesha, Bewketu Kassa, Mekibib Adem, Emebet Endris Seid, Mengistu Abdellati, Saïd Asefa, Wondimu Simegn, Tesfa Debasu, Degnachew Bogale, Tadfe Gedamu, Yonas Van Den Bossche, Dorien Adriaensen, Wim Van der Auwera, Gert Cnops, Lieselotte Vogt, Florian Diro, Ermias PLoS Negl Trop Dis Research Article BACKGROUND: In endemic regions, asymptomatic Leishmania infection is common. In HIV patients, detection of asymptomatic Leishmania infection could potentially identify those at risk of visceral leishmaniasis (VL). However, data on the prevalence, incidence, and determinants of asymptomatic infection, and the risk of VL are lacking. METHODS: We conducted a cross-sectional survey at a single ART centre, followed by a prospective cohort study amongst HIV-infected adults in HIV care in a district hospital in a VL-endemic area in North-West Ethiopia (9/2015-8/2016). Asymptomatic Leishmania infection was detected using the direct agglutination test (DAT), rK39-rapid diagnostic test (RDT)), PCR on peripheral blood and the KAtex urine antigen test, and defined as positivity on any Leishmania marker. All individuals were followed longitudinally (irrespective of the Leishmania test results). Risk factors for asymptomatic Leishmania infection were determined using logistic regression. RESULTS: A total of 534 HIV-infected individuals enrolled in HIV care were included in the study. After excluding 13 patients with a history of VL and an 10 patients with incomplete baseline Leishmania tests, 511 were included in analysis. The median age was 38 years (interquartile range (IQR) 30–45), 62.6% were male. The median follow-up time was 12 months (IQR 9–12). No deaths were reported during the study period. Most (95.5%) were on antiretroviral treatment at enrolment, for a median of 52 months (IQR 27–79). The median CD4 count at enrolment was 377 cells/mm3 (IQR 250–518). The baseline prevalence of Leishmania infection was 12.8% in males and 4.2% in females. Overall, 7.4% tested positive for rK39, 4.3% for DAT, 0.2% for PCR and 0.2% for KAtex. Independent risk factors for a prevalent infection were male sex (odds ratio (OR) 3.2; 95% confidence intervals (CI) 14–7.0) and concurrent malaria infection (OR 6.1; 95% CI 1.9–18.9). Amongst the 49 prevalent (baseline) infections with further follow-up, the cumulative incidence of losing the Leishmania markers by one year was 40.1%. There were 36 incident infections during the course of the study, with a cumulative one-year risk of 9.5%. Only one case of VL was detected during follow-up. CONCLUSIONS: We found a high prevalence of asymptomatic Leishmania infection, persisting in most cases. The incidence was more modest and overt VL was rare. Larger and longer studies with more complete follow-up may help to decide whether a test and treat strategy would be justified in this context. TRIAL REGISTRATION: ClinicalTrials.gov NCT02839603 Public Library of Science 2019-10-08 /pmc/articles/PMC6799935/ /pubmed/31593563 http://dx.doi.org/10.1371/journal.pntd.0007765 Text en © 2019 van Griensven et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article van Griensven, Johan van Henten, Saskia Mengesha, Bewketu Kassa, Mekibib Adem, Emebet Endris Seid, Mengistu Abdellati, Saïd Asefa, Wondimu Simegn, Tesfa Debasu, Degnachew Bogale, Tadfe Gedamu, Yonas Van Den Bossche, Dorien Adriaensen, Wim Van der Auwera, Gert Cnops, Lieselotte Vogt, Florian Diro, Ermias Longitudinal evaluation of asymptomatic Leishmania infection in HIV-infected individuals in North-West Ethiopia: A pilot study |
title | Longitudinal evaluation of asymptomatic Leishmania infection in HIV-infected individuals in North-West Ethiopia: A pilot study |
title_full | Longitudinal evaluation of asymptomatic Leishmania infection in HIV-infected individuals in North-West Ethiopia: A pilot study |
title_fullStr | Longitudinal evaluation of asymptomatic Leishmania infection in HIV-infected individuals in North-West Ethiopia: A pilot study |
title_full_unstemmed | Longitudinal evaluation of asymptomatic Leishmania infection in HIV-infected individuals in North-West Ethiopia: A pilot study |
title_short | Longitudinal evaluation of asymptomatic Leishmania infection in HIV-infected individuals in North-West Ethiopia: A pilot study |
title_sort | longitudinal evaluation of asymptomatic leishmania infection in hiv-infected individuals in north-west ethiopia: a pilot study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799935/ https://www.ncbi.nlm.nih.gov/pubmed/31593563 http://dx.doi.org/10.1371/journal.pntd.0007765 |
work_keys_str_mv | AT vangriensvenjohan longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT vanhentensaskia longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT mengeshabewketu longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT kassamekibib longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT adememebet longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT endrisseidmengistu longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT abdellatisaid longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT asefawondimu longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT simegntesfa longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT debasudegnachew longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT bogaletadfe longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT gedamuyonas longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT vandenbosschedorien longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT adriaensenwim longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT vanderauweragert longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT cnopslieselotte longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT vogtflorian longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy AT diroermias longitudinalevaluationofasymptomaticleishmaniainfectioninhivinfectedindividualsinnorthwestethiopiaapilotstudy |