AJTMH Tropical Medicine and Hygiene News
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 68(1), 2003, pp. 107-110
Copyright © 2003 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (10)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by PILLAI, D. R.
Right arrow Articles by KAIN, K. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by PILLAI, D. R.
Right arrow Articles by KAIN, K. C.
Related Collections
Right arrow Malaria

LACK OF PREDICTION OF MEFLOQUINE AND MEFLOQUINE-ARTESUNATE TREATMENT OUTCOME BY MUTATIONS IN THE PLASMODIUM FALCIPARUM MULTIDRUG RESISTANCE 1 (PFMDR1) GENE FOR PLASMODIUM FALCIPARUM MALARIA IN PERU

DYLAN R. PILLAI, GISELY HIJAR, YSABEL MONTOYA, WILMER MARQUIÑO, TRENTON K. RUEBUSH, II, CHANSUDA WONGSRICHANALAI, AND KEVIN C. KAIN
Tropical Disease Unit, Toronto General Hospital and University of Toronto, Toronto, Ontario, Canada; Instituto Nacional de Salud, Lima, Peru; U.S. Naval Medical Research Center Detachment, Lima, Peru; Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand

We assessed whether mutations in the Plasmodium falciparum multidrug-resistance gene 1 (pfmdr1) (C1034S, D1042N, and Y1246D) would predict treatment outcome during a 28-day in vivo treatment trial in the Peruvian Amazon. Mefloquine (MQ) was compared with mefloquine-artesunate (MQ-AS) in a randomized, multi-clinic protocol for the first time in the Americas. Of 115 patients enrolled in the in vivo arm, 97 patients were eligible for molecular analysis. All 97 patients remained parasite-free during 28 days of follow-up (MQ, n = 46; MQ-AS, n = 51), indicating 100% clinical efficacy of the MQ and MQ-AS treatment regimens. The reported MQ-sensitive alleles (C1034, D1042, and Y1246) were present in 48.5% (n = 47) of the cases, whereas 49 isolates (50.5%) contained the D1246 mutation reported to confer MQ resistance in vitro. However, neither this mutation nor a double mutation (S1034, D1246; n = 16) was predictive of MQ treatment outcome.


Received May 4, 2002. Accepted for publication August 15, 2002.

Acknowledgments: We are indebted to the Peruvian Ministerio de Salud and Instituto Nacional de Salud for facilitating all stages of this study. Expert technical assistance was provided by Nancy Arróspide, Sonia Gutierrez, Carmen Lucas, and Carola Salas (Instituto Nacional de Salud and Naval Medical Research Center Detachment), as well as Kathleen Zhong (University of Toronto).

Financial support: This study was supported in part by a Canadian International Development Agency award from the Canadian Bureau for International Education (Dylan R. Pillai), the Canadian Institutes of Health Research (grant MT-13721 to Keven C. Kain), a Career Scientist Award from the Ontario Ministry of Health (Kevin C. Kain), and a Canada Research Chair from the Canadian Institutes of Health (Kevin C. Kain).

Authors’ addresses: Dylan R. Pillai, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305. Gisely Hijar, Ysabel Montoya, and Wilmer Marquiño, Departments of Molecular Biology and Parasitology, Instituto Nacional de Salud, Lima, Peru. Trenton K. Ruebush II, Center for Disease Control and Prevention, Atlanta, GA. Chansuda Wongsrichanalai, Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand. Kevin C. Kain, Tropical Disease Unit, Toronto General Hospital, 200 Elizabeth Street, EN G-224, Toronto, Ontario, Canada, M5G 2C4, Telephone: 416-340-3535, Fax: 416-595-5826, E-mail: kevin.kain{at}uhn.on.ca




This article has been cited by other articles:


Home page
Am J Trop Med HygHome page
S. Zakeri, M. Afsharpad, T. Kazemzadeh, K. Mehdizadeh, A. Shabani, and N. D. Djadid
Association of pfcrt But Not pfmdr1 Alleles with Chloroquine Resistance in Iranian Isolates of Plasmodium falciparum
Am J Trop Med Hyg, April 1, 2008; 78(4): 633 - 640.
[Abstract] [Full Text] [PDF]


Home page
Am J Trop Med HygHome page
A. P. ALKER, P. LIM, R. SEM, N. K. SHAH, P. YI, D. M. BOUTH, R. TSUYUOKA, J. D. MAGUIRE, T. FANDEUR, F. ARIEY, et al.
PFMDR1 AND IN VIVO RESISTANCE TO ARTESUNATE-MEFLOQUINE IN FALCIPARUM MALARIA ON THE CAMBODIAN-THAI BORDER
Am J Trop Med Hyg, April 1, 2007; 76(4): 641 - 647.
[Abstract] [Full Text] [PDF]


Home page
Am J Trop Med HygHome page
A. L. NELSON, A. PURFIELD, P. MCDANIEL, N. UTHAIMONGKOL, N. BUATHONG, S. SRIWICHAI, R. S. MILLER, C. WONGSRICHANALAI, and S. R. MESHNICK
pfmdr1 GENOTYPING AND IN VIVO MEFLOQUINE RESISTANCE ON THE THAI-MYANMAR BORDER
Am J Trop Med Hyg, May 1, 2005; 72(5): 586 - 592.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
M. Ciach, K. Zong, K. C. Kain, and I. Crandall
Reversal of Mefloquine and Quinine Resistance in Plasmodium falciparum with NP30
Antimicrob. Agents Chemother., August 1, 2003; 47(8): 2393 - 2396.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the American Society of Tropical Medicine and Hygiene.