HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via ISI Web of Science (2) Citing Articles via Google Scholar Google Scholar Articles by MÉNDEZ, F. Articles by PLOWE, C. V. Search for Related Content PubMed PubMed Citation Articles by MÉNDEZ, F. Articles by PLOWE, C. V. Related Collections Drug-Resistance Malaria

USE OF AREA UNDER THE CURVE TO CHARACTERIZE TRANSMISSION POTENTIAL AFTER ANTIMALARIAL TREATMENT

To evaluate transmission potential of Plasmodium falciparum, we use the area under the curve (AUC) of gametocyte levels after treatment as an approach to combine their duration and magnitude. Analysis of determinants of AUC was based on two main exposures: parasite clearance time (PCT) and presence of dihydrofolate reductase and dihydropteroate synthase mutations associated with sulfadoxine-pyrimethamine (SP) resistance in vitro. Exposures were determined based on the first three days after treatment with SP of 96 individuals who had malaria, cleared parasitemia by days 1–3, and were followed-up for 21 days. Using regression methods, we characterized both the heterogeneity of the presence of gametocytes (AUC > 0) and the magnitude of the AUC among those with an AUC > 0. A PCT of two or three days was associated with a substantial and highly significant odds ratio for presence of gametocytes. Among those who developed gametocytes, if their clearance time was 3 days or if they had any mutations (1 or 2) the magnitude of gametocytemia was 3-fold. Methods presented are applicable to both observational studies and clinical trials assessing the effect of therapies on transmission potential.

Received January 25, 2006. Accepted for publication May 31, 2006.

Financial support: This research was supported in part by a grant AI055687-02 from the National Institutes of Health, and the Universidad del Valle, Cali, Colombia.

^* Address correspondence to Fabián Méndez, Escuela de Salud Pública, Universidad del Valle, San Fernando, Calle 4B No. 36-140, Edificio 118, Cali, Colombia. E-mail: famendez{at}univalle.edu.co

Authors’ addresses: Fabián Méndez, Escuela de Salud Pública, Universidad del Valle, San Fernando, Calle 4B No. 36-140, Edificio 118, Cali, Colombia, Fax: 57-2-557-0425, E-mail: famendez{at}univalle.edu.co. Álvaro Muñoz, Department of Epidemiology, The Johns Hopkins Bloomberg School of Public Health, 615 North Wolfe Street, E-7648, Baltimore, MD 21205, E-mail: jvaldez{at}jhsph.edu. Christopher V. Plowe, Center for Vaccine Development, University of Maryland School of Medicine, 685 West Baltimore Street, HSF 480, Baltimore, MD 21201, E-mail: cplowe{at}medicine.umaryland.edu.

This article has been cited by other articles:

				J. T. Bousema, C. J. Drakeley, P. F. Mens, T. Arens, R. Houben, S. A. Omar, L. C. Gouagna, H. Schallig, and R. W. Sauerwein Increased Plasmodium falciparum Gametocyte Production in Mixed Infections with P. malariae Am J Trop Med Hyg, March 1, 2008; 78(3): 442 - 448. [Abstract] [Full Text] [PDF]