Risk factors for gametocyte carriage in uncomplicated falciparum malaria

被引:191
作者
Price, R [1 ]
Nosten, F
Simpson, JA
Luxemburger, C
Phaipun, L
Ter Kuile, F
Van Vugt, M
Chongsuphajaisiddhi, T
White, NJ
机构
[1] Shoklo Malaria Res Unit, Mae Sot 63110, Tak, Thailand
[2] Mahidol Univ, Fac Trop Med, Bangkok 10400, Thailand
[3] Univ Amsterdam, Div Infect Dis Trop Med & AIDS, Acad Med Ctr, Amsterdam, Netherlands
[4] John Radcliffe Hosp, Nuffield Dept Clin Med, Ctr Trop Med, Oxford OX3 9D4, England
基金
英国惠康基金;
关键词
D O I
10.4269/ajtmh.1999.60.1019
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The factors affecting the development of patent Plasmodium falciparum gametocytemia were assessed in 5,682 patients entered prospectively into a series of antimalarial drug trials conducted in an area of low and seasonal transmission on the western border of Thailand. Of the 4,565 patients with admission thick smear assessments, 110 (2.4%) had gametocytemia. During the follow-up period 170 (3%) of all patients developed patent gametocytemia, which in 89% had developed by day 14 following treatment. In a multiple logistic regression model five factors were found to be independent risk factors at presentation for the development or persistence of gametocytemia during follow up; patent gametocytemia on admission (adjusted odds ratio [AOR] = 7.8, 95% confidence interval [CI] = 3.7-16, P < 0.001), anemia (hematocrit <30%) (AOR = 3.9, 95% CI = 2.3-6.5, P < 0.001),no coincident P. vivax malaria (AOR = 3.5, 95% CI = 1.04-11.5, P < 0.04), presentation with a recrudescent infection (AOR = 2.3, 95% CI = 1.3-4.1, P < 0.004), and a history of illness longer than two days (AOR = 3.3, 95% CI = 1.7-6.6, P < 0.001). Patients whose infections responded slowly to treatment or recrudesced subsequently were also more likely to carry gametocytes than those who responded rapidly or were cured (relative risks = 1.9, 95% CI = 1.3-2.7 and 2.8, 95% CI = 2.0-4.0, respectively; P < 0.001). These data provide further evidence of important epidemiologic interactions between P. falciparum and P. vivax, and drug resistance and transmission potential.
引用
收藏
页码:1019 / 1023
页数:5
相关论文
共 18 条
[1]  
Carter R, 1979, Bull World Health Organ, V57 Suppl 1, P37
[2]   EVIDENCE FOR CYCLIC DEVELOPMENT AND SHORT-LIVED MATURITY IN GAMETOCYTES OF PLASMODIUM-FALCIPARUM [J].
HAWKING, F ;
WILSON, ME ;
GAMMAGE, K .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1971, 65 (05) :549-&
[3]  
JEFFERY GM, 1956, AM J HYG, V64, P1
[4]   The epidemiology of malaria in a Karen population on the western border of Thailand [J].
Luxemburger, C ;
Thwai, KL ;
White, NJ ;
Webster, HK ;
Kyle, DE ;
Maelankirri, L ;
Chongsuphajaisiddhi, T ;
Nosten, F .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1996, 90 (02) :105-111
[5]   Plasmodium vivax and P-falciparum: Biological interactions and the possibility of cross-species immunity [J].
Maitland, K ;
Williams, TN ;
Newbold, CI .
PARASITOLOGY TODAY, 1997, 13 (06) :227-231
[6]  
MILLER M. J., 1958, TRANS ROY SOC TROP MED AND HYG, V52, P152, DOI 10.1016/0035-9203(58)90036-1
[7]   THE PRODUCTION OF MATURE GAMETOCYTES OF PLASMODIUM-FALCIPARUM IN CONTINUOUS CULTURES OF DIFFERENT ISOLATES INFECTIVE TO MOSQUITOS [J].
PONNUDURAI, T ;
MEUWISSEN, JHET ;
LEEUWENBERG, ADEM ;
VERHAVE, JP ;
LENSEN, AHW .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1982, 76 (02) :242-250
[8]   Effects of artemisinin derivatives on malaria transmissibility [J].
Price, RN ;
Nosten, F ;
Luxemburger, C ;
terKuile, FO ;
Paiphun, L ;
Chongsuphajaisiddhi, T ;
White, NJ .
LANCET, 1996, 347 (9016) :1654-1658
[9]  
RIECKMANN KH, 1969, MIL MED, V134, P802
[10]   HEMOLYSIS OF INFECTED ERYTHROCYTES - A TRIGGER FOR FORMATION OF PLASMODIUM-FALCIPARUM GAMETOCYTES [J].
SCHNEWEIS, S ;
MAIER, WA ;
SEITZ, HM .
PARASITOLOGY RESEARCH, 1991, 77 (05) :458-460