Activities of Artesunate and Primaquine against Asexual- and Sexual-Stage Parasites in Falciparum Malaria

ABSTRACT The activities of primaquine in combination with quinine or artesunate against asexual- and sexual-stage parasites were assessed in 176 adult Thai patients with uncomplicated Plasmodium falciparum malaria. Patients were randomized to one of the six following 7-day oral treatment regimens: (i) quinine alone, (ii) quinine with tetracycline, (iii) quinine with primaquine at 15 mg/day, (iv) quinine with primaquine at 30 mg/day, (v) artesunate alone, or (vi) artesunate with primaquine. Clinical recovery occurred in all patients. There were no significant differences in fever clearance times, rates of P. falciparum reappearance, or recurrent vivax malaria between the six treatment groups. Patients treated with artesunate alone or in combination with primaquine had significantly shorter parasite clearance times (mean ± standard deviation = 65± 18 versus 79 ± 21 h) and lower gametocyte carriage rates (40 versus 62.7%) than those treated with quinine (P ≤ 0.007). Primaquine did not affect the therapeutic response (P > 0.2). Gametocytemia was detected in 98 patients (56% [22% before treatment and 34% after treatment]). Artesunate reduced the appearance of gametocytemia (relative risk [95% confidence interval] = 0.34 [0.17 to 0.70]), whereas combinations containing primaquine resulted in shorter gametocyte clearance times (medians of 66 versus 271 h for quinine groups and 73 versus 137 h for artesunate groups; P≤ 0.038). These results suggest that artesunate predominantly inhibits gametocyte development whereas primaquine accelerates gametocyte clearance in P. falciparum malaria.

[1]  N. White,et al.  Therapeutic Responses to Quinine and Clindamycin in Multidrug-Resistant Falciparum Malaria , 2000, Antimicrobial Agents and Chemotherapy.

[2]  N. White,et al.  Randomized comparison of quinine-clindamycin versus artesunate in the treatment of falciparum malaria in pregnancy. , 2001, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[3]  J. Simpson,et al.  Therapeutic Responses to Different Antimalarial Drugs in Vivax Malaria , 2000, Antimicrobial Agents and Chemotherapy.

[4]  L. H. Schmidt Chemotherapy of the drug-resistant malarias. , 1969, Annual review of microbiology.

[5]  Y. Fu,et al.  The infectivity of gametocytes of Plasmodium falciparum from patients treated with artemisinin. , 1994, Chinese medical journal.

[6]  C. Drakeley,et al.  Artesunate reduces but does not prevent posttreatment transmission of Plasmodium falciparum to Anopheles gambiae. , 2001, The Journal of infectious diseases.

[7]  R. Price,et al.  Effects of artemisinin derivatives on malaria transmissibility , 1996, The Lancet.

[8]  J. Baird,et al.  Can primaquine therapy for vivax malaria be improved? , 2003, Trends in parasitology.

[9]  Richard N. Price,et al.  Effects of artesunate-mefloquine combination on incidence of Plasmodium falciparum malaria and mefloquine resistance in western Thailand: a prospective study , 2000, The Lancet.

[10]  C. Murray,et al.  Adult mortality in developing countries. , 1990, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[11]  N. White,et al.  Use of artemisinin derivatives for the control of malaria. , 1998, Medecine tropicale : revue du Corps de sante colonial.

[12]  D. Kyle,et al.  Efficacy of quinine-tetracycline for acute uncomplicated falciparum malaria in Thailand , 1992, The Lancet.

[13]  C. Dolea,et al.  World Health Organization , 1949, International Organization.

[14]  G. Coatney,et al.  Studies in human malaria. XXXI. Comparison of primaquine, isopentaquine, SN-3883, and pamaquine as curative agents against Chesson strain vivax malaria. , 1953, The American journal of tropical medicine and hygiene.

[15]  W. Wernsdorfer,et al.  In vitro activity of tafenoquine alone and in combination with artemisinin against Plasmodium falciparum. , 2002, The American journal of tropical medicine and hygiene.

[16]  S. Looareesuwan,et al.  HIGH RATE OF PLASMODIUM VIVAX RELAPSE FOLLOWING TREATMENT OF FALCIPARUM MALARIA IN THAILAND , 1987, The Lancet.

[17]  R. Grewal Pharmacology of 8-aminoquinolines. , 1981, Bulletin of the World Health Organization.

[18]  Y. Suputtamongkol,et al.  The efficacy of combined mefloquine-artesunate versus mefloquine-primaquine on subsequent development of Plasmodium falciparum gametocytemia. , 2003, The American journal of tropical medicine and hygiene.

[19]  A. Mr Severe and complicated malaria. , 2002 .

[20]  S. Pukrittayakamee,et al.  Blood stage antimalarial efficacy of primaquine in Plasmodium vivax malaria. , 1994, The Journal of infectious diseases.

[21]  M R Prabha Adhikari,et al.  Severe and complicated malaria. , 2002, Indian journal of medical sciences.

[22]  N. Mehra,et al.  In vitro gametocytocidal activity of artemisinin and its derivatives on Plasmodium falciparum. , 1993, Japanese journal of medical science & biology.

[23]  Nirbhay Kumar,et al.  Stage-specific gametocytocidal effect in vitro of the antimalaria drug qinghaosu onPlasmodium falciparum , 2004, Parasitology Research.

[24]  P. Olliaro,et al.  Averting a malaria disaster , 1999, The Lancet.

[25]  T. Harinasuta,et al.  EFFECT OF PRIMAQUINE ON GAMETOCYTES OF PLASMODIUM FALCIPARUM IN THAILAND , 1980, The Lancet.

[26]  R. J. Dern,et al.  The antimalarial action of primaquine against the blood and tissue stages of falciparum malaria (Panama, P-F-6 strain). , 1955, The Journal of laboratory and clinical medicine.

[27]  M. D. Young,et al.  Studies in Human Malaria. I. The Protective Action of Sulfadiazine and Sulfapyrazine against Sporozoite-induced Falciparum Malaria. , 1949 .