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Antimicrobial Agents and Chemotherapy, April 2000, p. 835-839, Vol. 44, No. 4
Institute of Tropical Medicine and Medical
Faculty Charité, Humboldt-University, Berlin,
Germany1; Dalarna University College,
Borlänge, Sweden2; and
Postgraduate Institute for Medical Research and Training,
University of Ibadan, Ibadan, Nigeria3
Received 6 July 1999/Returned for modification 30 November
1999/Accepted 27 December 1999
Consumption of chloroquine (CQ) and subtherapeutic drug levels in
blood are considered to be widespread in areas where malaria is
endemic. A cross-sectional study was performed with 405 Nigerian children to assess factors associated with the presence of CQ in blood
and to examine correlations of drug levels with malaria parasite
species and densities. Infections with Plasmodium species and parasite densities were determined by microscopy and PCR assays. Whole-blood CQ concentrations were measured by high-performance liquid
chromatography. Plasmodium falciparum, P. malariae, and P. ovale were observed in 80, 16, and
9% of the children, respectively, and CQ was detected in 52% of the
children. CQ concentrations were >17 and <100 nmol/liter in 25% of
the children, 100 to 499 nmol/liter in 14% of the children, and
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Concentrations of Chloroquine and Malaria Parasites
in Blood in Nigerian Children
500
nmol/liter in 13% of the children. Young age, attendance at health
posts, and absence of parasitemia were factors independently associated
with CQ in blood. With increasing concentrations of CQ, the prevalence
of P. falciparum infection and parasite densities
decreased. However, at concentrations corresponding to those usually
attained during regular prophylaxis (
500 nmol/liter), 62% of
children were still harboring P. falciparum parasites. In
contrast, no infection with P. malariae and only one
infection with P. ovale were observed in children with CQ
concentrations of
100 nmol/liter. These data show the high prevalence
of subcurative CQ concentrations in Nigerian children and confirm the
considerable degree of CQ resistance in that country. Subtherapeutic
drug levels are likely to further promote CQ resistance and may impair
the development and maintenance of premunition in areas where malaria
is endemic.
*
Corresponding author. Mailing address: Institut
für Tropenmedizin, Spandauer Damm 130, 14050 Berlin, Germany.
Phone: 49-30-30116-750. Fax: 49-30-30116-888. E-mail:
frank.mockenhaupt{at}charite.de.
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