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Therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in four malaria endemic states of India

BACKGROUND: Malaria is a major public health problem in India and accounts for about 88% of malaria burden in South-East Asia. India alone accounted for 2% of total malaria cases globally. Anti-malarial drug resistance is one of the major problems for malaria control and elimination programme. Artem...

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Autores principales: Krishna, Sri, Mishra, Sweta, Tiwari, Prakash, Vishwakarma, Anup K., Khandai, Sushrikanta, Shrivastava, Suyesh, Verma, Anil K., Tiwari, Shashikant, Barman, Hari, Jhariya, Surendra, Tiwari, Pradeep, Tidgam, Anup S., Varun, Brij M., Singh, Sunil, Yerane, Naresh, Tembhurne, Chintaman R., Mandavi, Prem L., Tekam, Shyam S., Malik, Manas, Behera, Kali P., Jayswar, Himanshu, Sonwani, Khemraj, Diggikar, Mukund S., Pradhan, Madan M., Khasotiya, Sher S., Kumar, Avdhesh, Dhingra, Neeraj, Bustos, Maria Dorina G., Christophel, Eva-Maria, Ringwald, Pascal, Kumari, Roop, Shukla, Man M., Singh, Neeru, Das, Aparup, Bharti, Praveen K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139028/
https://www.ncbi.nlm.nih.gov/pubmed/34020652
http://dx.doi.org/10.1186/s12936-021-03762-7
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author Krishna, Sri
Mishra, Sweta
Tiwari, Prakash
Vishwakarma, Anup K.
Khandai, Sushrikanta
Shrivastava, Suyesh
Verma, Anil K.
Tiwari, Shashikant
Barman, Hari
Jhariya, Surendra
Tiwari, Pradeep
Tidgam, Anup S.
Varun, Brij M.
Singh, Sunil
Yerane, Naresh
Tembhurne, Chintaman R.
Mandavi, Prem L.
Tekam, Shyam S.
Malik, Manas
Behera, Kali P.
Jayswar, Himanshu
Sonwani, Khemraj
Diggikar, Mukund S.
Pradhan, Madan M.
Khasotiya, Sher S.
Kumar, Avdhesh
Dhingra, Neeraj
Bustos, Maria Dorina G.
Christophel, Eva-Maria
Ringwald, Pascal
Kumari, Roop
Shukla, Man M.
Singh, Neeru
Das, Aparup
Bharti, Praveen K.
author_facet Krishna, Sri
Mishra, Sweta
Tiwari, Prakash
Vishwakarma, Anup K.
Khandai, Sushrikanta
Shrivastava, Suyesh
Verma, Anil K.
Tiwari, Shashikant
Barman, Hari
Jhariya, Surendra
Tiwari, Pradeep
Tidgam, Anup S.
Varun, Brij M.
Singh, Sunil
Yerane, Naresh
Tembhurne, Chintaman R.
Mandavi, Prem L.
Tekam, Shyam S.
Malik, Manas
Behera, Kali P.
Jayswar, Himanshu
Sonwani, Khemraj
Diggikar, Mukund S.
Pradhan, Madan M.
Khasotiya, Sher S.
Kumar, Avdhesh
Dhingra, Neeraj
Bustos, Maria Dorina G.
Christophel, Eva-Maria
Ringwald, Pascal
Kumari, Roop
Shukla, Man M.
Singh, Neeru
Das, Aparup
Bharti, Praveen K.
author_sort Krishna, Sri
collection PubMed
description BACKGROUND: Malaria is a major public health problem in India and accounts for about 88% of malaria burden in South-East Asia. India alone accounted for 2% of total malaria cases globally. Anti-malarial drug resistance is one of the major problems for malaria control and elimination programme. Artemether-lumefantrine (AL) is the first-line treatment of uncomplicated Plasmodium falciparum in north eastern states of India since 2013 after confirming the resistance against sulfadoxine-pyrimethamine. In the present study, therapeutic efficacy of artemether-lumefantrine and k13 polymorphism was assessed in uncomplicated P. falciparum malaria. METHODS: This study was conducted at four community health centres located in Koraput district of Odisha, Bastar district of Chhattisgarh, Balaghat district of Madhya Pradesh and Gondia district of Maharashtra state. Patients with uncomplicated P. falciparum malaria were administered with fixed dose combination (6 doses) of artemether-lumefantrine for 3days and clinical and parasitological response was recorded up to 28days as per World Health Organization protocol. Nucleotide sequencing of msp1 and msp2 gene was performed to differentiate between recrudescence and reinfection. Amplification and sequencing of k13 propeller gene region covering codon 450680 was also carried out to identify the polymorphism. RESULTS: A total 376 malaria patients who fulfilled the enrolment criteria as well as consented for the study were enrolled. Total 356 patients were followed up successfully up to 28days. Overall, the adequate clinical and parasitological response was 98.9% and 99.4% with and without PCR correction respectively. No case of early treatment failure was observed. However, four cases (1.1%) of late parasitological failure were found from the Bastar district of Chhattisgarh. Genotyping of msp1 and msp2 confirmed 2 cases each of recrudescence and reinfection, respectively. Mutation analysis of k13 propeller gene showed one non-synonymous mutation Q613H in one isolate from Bastar. CONCLUSIONS: The study results showed that artemether-lumefantrine is highly effective in the treatment of uncomplicated P. falciparum malaria among all age groups. No functional mutation in k13 was found in the study area. The data from this study will be helpful in implementation of artemether-lumefantrine in case of treatment failure by artesunate plus sulfadoxine-pyrimethamine.
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spelling pubmed-81390282021-05-21 Therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in four malaria endemic states of India Krishna, Sri Mishra, Sweta Tiwari, Prakash Vishwakarma, Anup K. Khandai, Sushrikanta Shrivastava, Suyesh Verma, Anil K. Tiwari, Shashikant Barman, Hari Jhariya, Surendra Tiwari, Pradeep Tidgam, Anup S. Varun, Brij M. Singh, Sunil Yerane, Naresh Tembhurne, Chintaman R. Mandavi, Prem L. Tekam, Shyam S. Malik, Manas Behera, Kali P. Jayswar, Himanshu Sonwani, Khemraj Diggikar, Mukund S. Pradhan, Madan M. Khasotiya, Sher S. Kumar, Avdhesh Dhingra, Neeraj Bustos, Maria Dorina G. Christophel, Eva-Maria Ringwald, Pascal Kumari, Roop Shukla, Man M. Singh, Neeru Das, Aparup Bharti, Praveen K. Malar J Research BACKGROUND: Malaria is a major public health problem in India and accounts for about 88% of malaria burden in South-East Asia. India alone accounted for 2% of total malaria cases globally. Anti-malarial drug resistance is one of the major problems for malaria control and elimination programme. Artemether-lumefantrine (AL) is the first-line treatment of uncomplicated Plasmodium falciparum in north eastern states of India since 2013 after confirming the resistance against sulfadoxine-pyrimethamine. In the present study, therapeutic efficacy of artemether-lumefantrine and k13 polymorphism was assessed in uncomplicated P. falciparum malaria. METHODS: This study was conducted at four community health centres located in Koraput district of Odisha, Bastar district of Chhattisgarh, Balaghat district of Madhya Pradesh and Gondia district of Maharashtra state. Patients with uncomplicated P. falciparum malaria were administered with fixed dose combination (6 doses) of artemether-lumefantrine for 3days and clinical and parasitological response was recorded up to 28days as per World Health Organization protocol. Nucleotide sequencing of msp1 and msp2 gene was performed to differentiate between recrudescence and reinfection. Amplification and sequencing of k13 propeller gene region covering codon 450680 was also carried out to identify the polymorphism. RESULTS: A total 376 malaria patients who fulfilled the enrolment criteria as well as consented for the study were enrolled. Total 356 patients were followed up successfully up to 28days. Overall, the adequate clinical and parasitological response was 98.9% and 99.4% with and without PCR correction respectively. No case of early treatment failure was observed. However, four cases (1.1%) of late parasitological failure were found from the Bastar district of Chhattisgarh. Genotyping of msp1 and msp2 confirmed 2 cases each of recrudescence and reinfection, respectively. Mutation analysis of k13 propeller gene showed one non-synonymous mutation Q613H in one isolate from Bastar. CONCLUSIONS: The study results showed that artemether-lumefantrine is highly effective in the treatment of uncomplicated P. falciparum malaria among all age groups. No functional mutation in k13 was found in the study area. The data from this study will be helpful in implementation of artemether-lumefantrine in case of treatment failure by artesunate plus sulfadoxine-pyrimethamine. BioMed Central 2021-05-21 /pmc/articles/PMC8139028/ /pubmed/34020652 http://dx.doi.org/10.1186/s12936-021-03762-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Krishna, Sri
Mishra, Sweta
Tiwari, Prakash
Vishwakarma, Anup K.
Khandai, Sushrikanta
Shrivastava, Suyesh
Verma, Anil K.
Tiwari, Shashikant
Barman, Hari
Jhariya, Surendra
Tiwari, Pradeep
Tidgam, Anup S.
Varun, Brij M.
Singh, Sunil
Yerane, Naresh
Tembhurne, Chintaman R.
Mandavi, Prem L.
Tekam, Shyam S.
Malik, Manas
Behera, Kali P.
Jayswar, Himanshu
Sonwani, Khemraj
Diggikar, Mukund S.
Pradhan, Madan M.
Khasotiya, Sher S.
Kumar, Avdhesh
Dhingra, Neeraj
Bustos, Maria Dorina G.
Christophel, Eva-Maria
Ringwald, Pascal
Kumari, Roop
Shukla, Man M.
Singh, Neeru
Das, Aparup
Bharti, Praveen K.
Therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in four malaria endemic states of India
title Therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in four malaria endemic states of India
title_full Therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in four malaria endemic states of India
title_fullStr Therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in four malaria endemic states of India
title_full_unstemmed Therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in four malaria endemic states of India
title_short Therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in four malaria endemic states of India
title_sort therapeutic efficacy of artemether-lumefantrine for the treatment of uncomplicated plasmodium falciparum malaria in four malaria endemic states of india
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139028/
https://www.ncbi.nlm.nih.gov/pubmed/34020652
http://dx.doi.org/10.1186/s12936-021-03762-7
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