TY - JOUR
T1 - Variation in neutrophil levels and artemisinin-based combination therapy efficacy in West-Africa
AU - Djimde, Moussa
AU - Kayentao, Kassoum
AU - Tshiongo, Japhet Kabalu
AU - Fofana, Bakary
AU - Arama, Charles
AU - Sirima, Sodiomon B.
AU - Ouedraogo, Jean Bosco
AU - Beavogui, Abdoul Habib
AU - Sagara, Issaka
AU - Dicko, Alassane
AU - Mens, Petra F.
AU - Schallig, Henk D. F. H.
AU - Djimde, Abdoulaye
N1 - Funding Information: The main clinical trial [Phase IIIb/IV, randomized, open, parallel to 3 arms and multicenter comparative clinical study comparing the efficacy and tolerance in repeated treatment of pyronaridine-artesunate and dihydroartemisinin-piperaquine with those of artesunate-amodiaquine and artemether-lumefantrine over a two-year period in children and adults with uncomplicated Plasmodium sp.] work was supported by the European and Developing Countries Clinical Trial Partnership (EDCTP), Medicines for Malaria Venture (MMV), the UK Medical Research Council, the Swedish International Development Cooperation Agency, German Ministry for Education and Research, University Claude Bernard (Lyon, France), University of Science, Techniques and Technologies of Bamako (Bamako, Mali), the Centre National de Recherche et de Formation sur le Paludisme (Burkina Faso), Institut de Recherche en Sciences de la Santé (Bobo-Dioulasso, Burkina Faso), and Centre National de Formation et de Recherche en Santé Rurale (Republic of Guinea). This analysis was supported through the PYRAPREG project capacity building activities (PhD training). The PYRAPREG project is part of the EDCTP2 programme supported by the European Union (grant number RIA2017MC-2025-PYRAPREG). Publisher Copyright: Copyright © 2023 Djimde et al.
PY - 2023/9/1
Y1 - 2023/9/1
N2 - Introduction: Polymorphonuclear neutrophils (PMN) are involved in pathogen clearance by phagocytosis. However, the role of PMNs in the efficacy of artemisinin-based combination therapy (ACT) is poorly understood. Methodology: In a prospective longitudinal in vivo study, neutrophil rates were compared with malaria carriage after treatment with different ACTs: Artemether - lumefantrine (AL), Artesunate - amodiaquine (ASAQ), Dihydroartemisinin - piperaquine (DP) or Pyronaridine artesunate (PA). The study cases were classified as having neutropenia, normal neutrophil levels or neutrophilia depending on the level of neutrophils in the blood. This study included 3148 patients and was analyzed using R. Results: On day 7, only four patients in the neutropenia group and treated with AL had a malaria positive blood smear based on microscopy. On day 28, the rate of recurrent parasitemia in the AL arm was significantly higher in neutropenia patients (50.9%) than in patients with normal rates of neutrophils (43.1%) or in those with neutrophilia (6.0%) (p < 0.001). In ASAQ arm, the rate of recurrent Plasmodium falciparum parasitemia was 58.8% in the neutropenia group versus 29.4% in patients with normal rates of neutrophils and 11.8% in patients with neutrophilia (p < 0.001). No patient treated with DP with normal neutrophil counts or neutrophilia was carrying malaria parasites on day 28. Among the 15 patients with parasitemia on day 28 in the PA arm, 11 (73.33%) had neutropenia while 4 (26.67%) had a normal neutrophil count (p < 0.001). Conclusions: Patients with neutropenia had higher rates of recurrent P. falciparum parasitemia after ACT.
AB - Introduction: Polymorphonuclear neutrophils (PMN) are involved in pathogen clearance by phagocytosis. However, the role of PMNs in the efficacy of artemisinin-based combination therapy (ACT) is poorly understood. Methodology: In a prospective longitudinal in vivo study, neutrophil rates were compared with malaria carriage after treatment with different ACTs: Artemether - lumefantrine (AL), Artesunate - amodiaquine (ASAQ), Dihydroartemisinin - piperaquine (DP) or Pyronaridine artesunate (PA). The study cases were classified as having neutropenia, normal neutrophil levels or neutrophilia depending on the level of neutrophils in the blood. This study included 3148 patients and was analyzed using R. Results: On day 7, only four patients in the neutropenia group and treated with AL had a malaria positive blood smear based on microscopy. On day 28, the rate of recurrent parasitemia in the AL arm was significantly higher in neutropenia patients (50.9%) than in patients with normal rates of neutrophils (43.1%) or in those with neutrophilia (6.0%) (p < 0.001). In ASAQ arm, the rate of recurrent Plasmodium falciparum parasitemia was 58.8% in the neutropenia group versus 29.4% in patients with normal rates of neutrophils and 11.8% in patients with neutrophilia (p < 0.001). No patient treated with DP with normal neutrophil counts or neutrophilia was carrying malaria parasites on day 28. Among the 15 patients with parasitemia on day 28 in the PA arm, 11 (73.33%) had neutropenia while 4 (26.67%) had a normal neutrophil count (p < 0.001). Conclusions: Patients with neutropenia had higher rates of recurrent P. falciparum parasitemia after ACT.
KW - West Africa
KW - artemisinin-based combination therapy
KW - malaria
KW - neutrophils
UR - http://www.scopus.com/inward/record.url?scp=85174237175&partnerID=8YFLogxK
U2 - https://doi.org/10.3855/jidc.17089
DO - https://doi.org/10.3855/jidc.17089
M3 - Article
C2 - 37824364
SN - 2036-6590
VL - 17
SP - 1337
EP - 1345
JO - Journal of infection in developing countries
JF - Journal of infection in developing countries
IS - 9
ER -