Infectious Diseases of Poverty (Aug 2019)

Declining responsiveness of childhood Plasmodium falciparum infections to artemisinin-based combination treatments ten years following deployment as first-line antimalarials in Nigeria

  • Akintunde Sowunmi,
  • Godwin Ntadom,
  • Kazeem Akano,
  • Folasade O. Ibironke,
  • Adejumoke I. Ayede,
  • Chimere Agomo,
  • Onikepe A. Folarin,
  • Grace O. Gbotosho,
  • Christian Happi,
  • Stephen Oguche,
  • Henrietta U. Okafor,
  • Martin Meremikwu,
  • Philip Agomo,
  • William Ogala,
  • Ismaila Watila,
  • Olugbenga Mokuolu,
  • Finomo Finomo,
  • Joy C. Ebenebe,
  • Nma Jiya,
  • Jose Ambe,
  • Robinson Wammanda,
  • George Emechebe,
  • Wellington Oyibo,
  • Francis Useh,
  • Temitope Aderoyeje,
  • Titilope M. Dokunmu,
  • Omobolaji T. Alebiosu,
  • Sikiru Amoo,
  • Oluwabunmi K. Basorun,
  • Olubunmi A. Wewe,
  • Chukwuebuka Okafor,
  • Odafe Akpoborie,
  • Bayo Fatunmbi,
  • Elsie O. Adewoye,
  • Nnenna M. Ezeigwe,
  • Ayoade Oduola

DOI
https://doi.org/10.1186/s40249-019-0577-x
Journal volume & issue
Vol. 8, no. 1
pp. 1 – 18

Abstract

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Abstract Background The development and spread of artemisinin-resistant Plasmodium falciparum malaria in Greater Mekong Subregion has created impetus for continuing global monitoring of efficacy of artemisinin-based combination therapies (ACTs). This post analyses is aimed to evaluate changes in early treatment response markers 10 years after the adoption of ACTs as first-line treatments of uncomplicated falciparum malaria in Nigeria. Methods At 14 sentinel sites in six geographical areas of Nigeria, we evaluated treatment responses in 1341 children under 5 years and in additional 360 children under 16 years with uncomplicated malaria enrolled in randomized trials of artemether-lumefantrine versus artesunate-amodiaquine at 5-year interval in 2009–2010 and 2014–2015 and at 2-year interval in 2009–2010 and 2012–2015, respectively after deployment in 2005. Results Asexual parasite positivity 1 day after treatment initiation (APPD1) rose from 54 to 62% and 2 days after treatment initiation from 5 to 26% in 2009–2010 to 2014–2015 (P = 0.002 and P 75 000 μl− 1, haematocrit > 27% 1 day post-treatment initiation, treatment with artemether-lumefantrine and enrolment in 2014–2015 independently predicted APPD1. In parallel, Kaplan-Meier estimated risk of recurrent infections by day 28 rose from 8 to 14% (P = 0.005) and from 9 to 15% (P = 0.02) with artemether-lumefantrine and artesunate-amodiaquine, respectively. Mean asexual parasitaemia half-life increased significantly from 1.1 h to 1.3 h within 2 years (P < 0.0001). Conclusions These data indicate declining parasitological responses through time to the two ACTs may be due to emergence of parasites with reduced susceptibility or decrease in immunity to the infections in these children. Trial registration Pan African Clinical Trial Registration PACTR201508001188143, 3 July 2015; PACTR201508001191898, 7 July 2015 and PACTR201508001193368, 8 July 2015 PACTR201510001189370, 3 July 2015; PACTR201709002064150, 1 March 2017; https://www.pactr.samrca.ac.za

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