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Effect of intensive versus standard anthelminthic treatment on growth and cognition among children living in a high Schistosoma mansoni transmission setting: a study nested within a cluster-randomised trial

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Effect of intensive versus standard anthelminthic treatment on growth and cognition among children living in a high Schistosoma mansoni transmission setting: a study nested within a cluster-randomised trial . / Nampijja, Margaret; Lubyayi, Lawrence; Tumusiime, Josephine et al.
In: Wellcome Open Research, Vol. 5, 258, 29.10.2020.

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Harvard

Nampijja, M, Lubyayi, L, Tumusiime, J, Nabulime, J, Kizindo, R, Kabuubi, P, Sanya, RE, Kabagenyi, J, Akurut, H, Muhangi, L, Webb, EL, Alcock, K, Elliott, AM & Team, FTLIISWAT 2020, 'Effect of intensive versus standard anthelminthic treatment on growth and cognition among children living in a high Schistosoma mansoni transmission setting: a study nested within a cluster-randomised trial ', Wellcome Open Research, vol. 5, 258. https://doi.org/10.12688/wellcomeopenres.16092.1

APA

Nampijja, M., Lubyayi, L., Tumusiime, J., Nabulime, J., Kizindo, R., Kabuubi, P., Sanya, R. E., Kabagenyi, J., Akurut, H., Muhangi, L., Webb, E. L., Alcock, K., Elliott, A. M., & Team, F. T. LIISWA. T. (2020). Effect of intensive versus standard anthelminthic treatment on growth and cognition among children living in a high Schistosoma mansoni transmission setting: a study nested within a cluster-randomised trial . Wellcome Open Research, 5, Article 258. https://doi.org/10.12688/wellcomeopenres.16092.1

Vancouver

Nampijja M, Lubyayi L, Tumusiime J, Nabulime J, Kizindo R, Kabuubi P et al. Effect of intensive versus standard anthelminthic treatment on growth and cognition among children living in a high Schistosoma mansoni transmission setting: a study nested within a cluster-randomised trial . Wellcome Open Research. 2020 Oct 29;5:258. doi: 10.12688/wellcomeopenres.16092.1

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Bibtex

@article{f19da9b127df4f838793f1dbe3a68427,
title = "Effect of intensive versus standard anthelminthic treatment on growth and cognition among children living in a high Schistosoma mansoni transmission setting: a study nested within a cluster-randomised trial ",
abstract = "Background: Schistosomiasis and other worm infections have been associated with growth and cognitive impairments; however, whether treatment reverses these effects is uncertain. Moreover, mechanisms linking these infections to cognition are not clear. We aimed to compare growth and cognitive benefits of intensive versus standard anthelminthic treatment in school-aged-children and explore processes that might be involved. We hypothesised that intensive treatment would have greater benefits than standard treatment.Methods: The study was nested within a cluster-randomised trial of either quarterly single-dose praziquantel of 40mg/kg to treat Schistosoma mansoni plus triple dose albendazole of 400mg (intensive treatment) to treat soil-transmitted worms including Ascaris lumbricoides, hookworm and Trichuris trichiura, or annual single-dose praziquantel 40mg/kg plus six-monthly single-dose albendazole 400mg (standard treatment) conducted in the Koome islands in Lake Victoria, Uganda (ISRCTN47196031). Children aged 5-9 years (N=384) were assessed on primary outcomes (height, weight and eight measures of cognitive ability), worm infection, and proposed mediators of worm effects (cytokines, iron status, physical activity) at one year (intensive n=85; standard n=64) and at two years (intensive n=158; standard n=128) of the intervention. Linear regression was used to examine intervention effects on height, weight and cognitive performance. Linear mixed effects models were used to study changes in growth and cognitive performance between the two arms across the two time-points.Results: Intensive treatment resulted in lower Schistosoma mansoni prevalence than standard treatment (at one year, 41% versus 70%; adjusted odds ratio (aOR)=0.24, 95% CI: 0.12, 0.49; at two years, 39% versus 69%; aOR=0.27; 95% CI: 0.16, 0.43) but there were no significant differences in growth and cognitive outcomes at either time-point. Worms and treatment showed no consistent association with the proposed mediators of worm effects.Conclusion: Reduction in worm burden may not improve growth and cognitive outcomes in high S. mansoni transmission settings. Possible implications are discussed.",
keywords = "growth, cognitive performance, anthelminthic treatment, praziquantel, albendazole, Schistosoma mansoni",
author = "Margaret Nampijja and Lawrence Lubyayi and Josephine Tumusiime and Juliet Nabulime and Robert Kizindo and Prossy Kabuubi and Sanya, {Richard E.} and Joy Kabagenyi and Hellen Akurut and Lawrence Muhangi and Webb, {Emily L.} and Katie Alcock and Elliott, {Alison M.} and Team, {for the LaVIISWA Trial}",
year = "2020",
month = oct,
day = "29",
doi = "10.12688/wellcomeopenres.16092.1",
language = "English",
volume = "5",
journal = "Wellcome Open Research",
issn = "2398-502X",
publisher = "F1000 Research Ltd.",

}

RIS

TY - JOUR

T1 - Effect of intensive versus standard anthelminthic treatment on growth and cognition among children living in a high Schistosoma mansoni transmission setting

T2 - a study nested within a cluster-randomised trial

AU - Nampijja, Margaret

AU - Lubyayi, Lawrence

AU - Tumusiime, Josephine

AU - Nabulime, Juliet

AU - Kizindo, Robert

AU - Kabuubi, Prossy

AU - Sanya, Richard E.

AU - Kabagenyi, Joy

AU - Akurut, Hellen

AU - Muhangi, Lawrence

AU - Webb, Emily L.

AU - Alcock, Katie

AU - Elliott, Alison M.

AU - Team, for the LaVIISWA Trial

PY - 2020/10/29

Y1 - 2020/10/29

N2 - Background: Schistosomiasis and other worm infections have been associated with growth and cognitive impairments; however, whether treatment reverses these effects is uncertain. Moreover, mechanisms linking these infections to cognition are not clear. We aimed to compare growth and cognitive benefits of intensive versus standard anthelminthic treatment in school-aged-children and explore processes that might be involved. We hypothesised that intensive treatment would have greater benefits than standard treatment.Methods: The study was nested within a cluster-randomised trial of either quarterly single-dose praziquantel of 40mg/kg to treat Schistosoma mansoni plus triple dose albendazole of 400mg (intensive treatment) to treat soil-transmitted worms including Ascaris lumbricoides, hookworm and Trichuris trichiura, or annual single-dose praziquantel 40mg/kg plus six-monthly single-dose albendazole 400mg (standard treatment) conducted in the Koome islands in Lake Victoria, Uganda (ISRCTN47196031). Children aged 5-9 years (N=384) were assessed on primary outcomes (height, weight and eight measures of cognitive ability), worm infection, and proposed mediators of worm effects (cytokines, iron status, physical activity) at one year (intensive n=85; standard n=64) and at two years (intensive n=158; standard n=128) of the intervention. Linear regression was used to examine intervention effects on height, weight and cognitive performance. Linear mixed effects models were used to study changes in growth and cognitive performance between the two arms across the two time-points.Results: Intensive treatment resulted in lower Schistosoma mansoni prevalence than standard treatment (at one year, 41% versus 70%; adjusted odds ratio (aOR)=0.24, 95% CI: 0.12, 0.49; at two years, 39% versus 69%; aOR=0.27; 95% CI: 0.16, 0.43) but there were no significant differences in growth and cognitive outcomes at either time-point. Worms and treatment showed no consistent association with the proposed mediators of worm effects.Conclusion: Reduction in worm burden may not improve growth and cognitive outcomes in high S. mansoni transmission settings. Possible implications are discussed.

AB - Background: Schistosomiasis and other worm infections have been associated with growth and cognitive impairments; however, whether treatment reverses these effects is uncertain. Moreover, mechanisms linking these infections to cognition are not clear. We aimed to compare growth and cognitive benefits of intensive versus standard anthelminthic treatment in school-aged-children and explore processes that might be involved. We hypothesised that intensive treatment would have greater benefits than standard treatment.Methods: The study was nested within a cluster-randomised trial of either quarterly single-dose praziquantel of 40mg/kg to treat Schistosoma mansoni plus triple dose albendazole of 400mg (intensive treatment) to treat soil-transmitted worms including Ascaris lumbricoides, hookworm and Trichuris trichiura, or annual single-dose praziquantel 40mg/kg plus six-monthly single-dose albendazole 400mg (standard treatment) conducted in the Koome islands in Lake Victoria, Uganda (ISRCTN47196031). Children aged 5-9 years (N=384) were assessed on primary outcomes (height, weight and eight measures of cognitive ability), worm infection, and proposed mediators of worm effects (cytokines, iron status, physical activity) at one year (intensive n=85; standard n=64) and at two years (intensive n=158; standard n=128) of the intervention. Linear regression was used to examine intervention effects on height, weight and cognitive performance. Linear mixed effects models were used to study changes in growth and cognitive performance between the two arms across the two time-points.Results: Intensive treatment resulted in lower Schistosoma mansoni prevalence than standard treatment (at one year, 41% versus 70%; adjusted odds ratio (aOR)=0.24, 95% CI: 0.12, 0.49; at two years, 39% versus 69%; aOR=0.27; 95% CI: 0.16, 0.43) but there were no significant differences in growth and cognitive outcomes at either time-point. Worms and treatment showed no consistent association with the proposed mediators of worm effects.Conclusion: Reduction in worm burden may not improve growth and cognitive outcomes in high S. mansoni transmission settings. Possible implications are discussed.

KW - growth

KW - cognitive performance

KW - anthelminthic treatment

KW - praziquantel

KW - albendazole

KW - Schistosoma mansoni

U2 - 10.12688/wellcomeopenres.16092.1

DO - 10.12688/wellcomeopenres.16092.1

M3 - Journal article

VL - 5

JO - Wellcome Open Research

JF - Wellcome Open Research

SN - 2398-502X

M1 - 258

ER -