Assessment of the anthelmintic efficacy of albendazole in school children in seven countries where soil-transmitted helminths are endemic

Jozef Vercruysse, Jerzy M Behnke, Marco Albonico, Shaali Makame Ame, Cécile Angebault, Jeffrey M Bethony, Dirk Engels, Bertrand Guillard, Thi Viet Hoa Nguyen, Gagandeep Kang, Deepthi Kattula, Andrew C Kotze, James S McCarthy, Zeleke Mekonnen, Antonio Montresor, Maria Victoria Periago, Laurentine Sumo, Louis-Albert Tchuem Tchuenté, Thi Cam Thach Dang, Ahmed Zeynudin, Bruno Levecke, Jozef Vercruysse, Jerzy M Behnke, Marco Albonico, Shaali Makame Ame, Cécile Angebault, Jeffrey M Bethony, Dirk Engels, Bertrand Guillard, Thi Viet Hoa Nguyen, Gagandeep Kang, Deepthi Kattula, Andrew C Kotze, James S McCarthy, Zeleke Mekonnen, Antonio Montresor, Maria Victoria Periago, Laurentine Sumo, Louis-Albert Tchuem Tchuenté, Thi Cam Thach Dang, Ahmed Zeynudin, Bruno Levecke

Abstract

Background: The three major soil-transmitted helminths (STH) Ascaris lumbricoides, Trichuris trichiura and Necator americanus/Ancylostoma duodenale are among the most widespread parasites worldwide. Despite the global expansion of preventive anthelmintic treatment, standard operating procedures to monitor anthelmintic drug efficacy are lacking. The objective of this study, therefore, was to define the efficacy of a single 400 milligram dose of albendazole (ALB) against these three STH using a standardized protocol.

Methodology/principal findings: Seven trials were undertaken among school children in Brazil, Cameroon, Cambodia, Ethiopia, India, Tanzania and Vietnam. Efficacy was assessed by the Cure Rate (CR) and the Fecal Egg Count Reduction (FECR) using the McMaster egg counting technique to determine fecal egg counts (FEC). Overall, the highest CRs were observed for A. lumbricoides (98.2%) followed by hookworms (87.8%) and T. trichiura (46.6%). There was considerable variation in the CR for the three parasites across trials (country), by age or the pre-intervention FEC (pre-treatment). The latter is probably the most important as it had a considerable effect on the CR of all three STH. Therapeutic efficacies, as reflected by the FECRs, were very high for A. lumbricoides (99.5%) and hookworms (94.8%) but significantly lower for T. trichiura (50.8%), and were affected to different extents among the 3 species by the pre-intervention FEC counts and trial (country), but not by sex or age.

Conclusions/significance: Our findings suggest that a FECR (based on arithmetic means) of >95% for A. lumbricoides and >90% for hookworms should be the expected minimum in all future surveys, and that therapeutic efficacy below this level following a single dose of ALB should be viewed with concern in light of potential drug resistance. A standard threshold for efficacy against T. trichiura has yet to be established, as a single-dose of ALB is unlikely to be satisfactory for this parasite.

Trial registration: ClinicalTrials.gov NCT01087099.

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1. The participation, occurrence of STH…
Figure 1. The participation, occurrence of STH and sample submission compliance for pre- and post-intervention surveys.
Subjects who were not able to provide a sample for the follow-up, or who were experiencing a severe current medical condition or had diarrhea at the time of the first sampling were excluded from the trial.
Figure 2. The estimated impact of age,…
Figure 2. The estimated impact of age, fecal egg count and trial on the cure rate.
The estimated impact of age, fecal egg count (FEC) and trial (country) on the cure rate of A. lumbricoides (A), T. trichiura (B) and hookworms (C) derived from a generalized linear models (binomial error).
Figure 3. The distribution of the fecal…
Figure 3. The distribution of the fecal egg count of soil-transmitted helminths.
The distribution of the fecal egg count (FEC) of A. lumbricoides (A), T. trichiura (B) and hookworms (C). The absolute values of the median, the 2.5th and 97.5th percentile (%) are provided. In addition, these values are represented as solid (median) and dashed lines (2.5 and 97.5%).

References

    1. World Health Organization. Report of the third global meeting of the partners for parasitic control. WHO/CDS/CPE/PVC/2005.14, World Health Organization, Geneva; 2005. Deworming for health and development.
    1. Albonico M, Allen H, Chitsulo L, Engels D, Gabrielli AF, et al. Controlling soil-transmitted helminthiasis in pre-school-age children through preventive chemotherapy. PLoS Negl Trop Dis. 2008;2:e126.
    1. Bennett A, Guyatt H. Reducing intestinal nematode infection: efficacy of albendazole and mebendazole. Parasitol Today. 2000;16:71–74.
    1. Wolstenholme AJ, Fairweather I, Prichard R, von Samson-Himmelstjerna G, Sangster NC. Drug resistance in veterinary helminths. Trends Parasitol. 2004;20:469–476.
    1. Albonico M, Engels D, Savioli L. Monitoring drug efficacy and early detection of drug resistance in human soil-transmitted nematodes: a pressing public health agenda for helminth control. Int J Parasitol. 2004;34:1205–1210.
    1. Geerts S, Gryseels B. Anthelmintic resistance in human helminths: a review. Trop Med Int Health. 2001;6:915–921.
    1. De Clercq D, Sacko M, Behnke JM, Gilbert F, Dorny P, et al. Failure of mebendazole in treatment of human hookworm infections in the Southern Region of Mali. Am J Trop Med Hyg. 1997;57:25–30.
    1. Keiser J, Utzinger J. Efficacy of current drugs against soil-transmitted helminth infections - systematic review and meta-analysis. JAMA. 2008;299:1937–1948.
    1. Levecke B, De Wilde N, Vandenhoute E, Vercruysse J. Field validity and feasibility of four techniques for the detection of Trichuris in simians: a model for monitoring drug efficacy in public health? PLoS Negl Trop Dis. 2009;3(1):e366.
    1. Coles GC, Bauer C, Borgsteede FH, Geerts S, Klei TR, et al. World Association for the Advancement of Veterinary Parasitology (W.A.A.V.P.) methods for the detection of anthelmintic resistance in nematodes of veterinary importance. Vet Parasitol. 1992;44:35–44.
    1. Coles GC, Jackson F, Pomroy WE, Samson-Himmelstjerna G, Silvestre A, et al. The detection of anthelmintic resistance in nematodes of veterinary importance. Vet Parasitol. 2006;136:167–185.
    1. Ministry of Agriculture, Fisheries and Food. London: Her Majesty's Stationery Office (HMSO); 1986. Manual of veterinary parasitological laboratory techniques (Reference Book; 418), 3rd ed.160
    1. Montresor A, Crompton DWT, Hall H, Bundy DAP, Savioli L. Guidelines for the evaluation of soil-transmitted helminthiasis and schistosomiasis at community level. 1998. A guide for control programme managers. WHO/CTD/SIP98.1, World Health Organization, Geneva.
    1. Crawley MT. Oxford: Blackwell Scientific Press ; 1993. GLIM for Ecologists. p. ix + 380.
    1. Dobson RJ, Sangster NC, Besier RB, Woodgate RG. Geometric means provide a biased efficacy result when conducting a fecal egg count reduction test (FECRT). Vet Parasitol. 2009;161:162–167.
    1. Albonico M, Smith PG, Hall A, Chwaya HM, Alawi KS. A randomised controlled trial comparing mebendazole 500 mg and albendazole 400 mg against Ascaris, Trichuris and the hookworms. Trans R Soc Trop Med Hyg. 1994;88:585–589.
    1. Albonico M, Bickle Q, Ramsan M, Montresor A, Savioli L, et al. Efficacy of mebendazole and levamisole alone or in combination against intestinal nematode infections after repeated targeted mebendazole treatment in Zanzibar. Bull WHO. 2003;81:343–352.
    1. Hu M, Chilton NB, El-Osta YGA, Gasser RB. Comparative analysis of mitochondrial genome data for Necator americanus from two endemic regions reveals substantial genetic variation. Int J Parasitol. 2003;33:955–963.
    1. Leles D, Araújo A, Vicente AC, Iñiguez AM. Molecular diagnosis of ascariasis from human feces and description of a new Ascaris sp. genotype in Brazil. Vet Parasitol. 2009;163:167–170.
    1. Diawara A, Drake LS, Suswillo RR, Kihara J, Bundy DA, et al. Assays to detect B tubulin Codon 200 polymorphism in Trichuris trichiura and Ascaris lumbricoides. PLoS Negl Trop Dis. 2009;3:e397.
    1. Marti H, Haji HJ, Savioli L, Chwaya HM, Mgeni AF, et al. A comparative trial of a single-dose ivermectin versus three days of albendazole for treatment of Strongyloides stercoralis and other soil-transmitted helminth infections in children. Am J Trop Med Hyg. 1996;55:477–481.
    1. Hoagland KE, Schad GA. Necator americanus and Ancylostoma duodenale: life history parameters and epidemiological implications of two sympatric hookworms of human. Exp Parasitol. 1978;44:36–49.
    1. El-Masry NA, Trabolsi B, Bassily S, Farid Z. Albendazole in the treatment of Ancylostoma duodenale and Ascaris lumbricoides infections. Trans R Soc Trop Med Hyg. 1983;77:160–161.
    1. Sacko M, De Clercq D, Behnke JM, Gilbert FS, Dorny P, et al. Comparison of the efficacy of mebendazole, albendazole and pyrantel in treatment of human hookworm infections in the southern region of Mali, West Africa. Trans R Soc Trop Med Hyg. 1999;93:195–203.
    1. World Health Organization. CCTA/WHO African conference on ancylostomiasis, Brazzaville 22–29 August 1961. Technical Report Series No. 225 1961
    1. McKellar QA, Scott EW. The benzimidazole anthelmintic agents. A review. J Vet Pharmacol Ther. 1990;13:223–247.
    1. Dayan AD. Albendazole, mebendazole and praziquantel. Review of non-clinical toxicity and pharmacokinetics. Acta Trop. 2003;86:141–159.
    1. Sanchez SF, Alvarez LI, Lanusse CE. Nutritional condition affects the disposition kinetics of albendazole in cattle. Xenobiotica. 1996;25:307–320.
    1. Kopp SR, Coleman GT, McCarthy JS, Kotze AC. Application of in vitro anthelmintic sensitivity assays to canine parasitology: detecting resistance to pyrantel in Ancylostoma caninum. Vet Parasitol. 2008;152:284–293.
    1. Kotze AC, Kopp SR. The potential impact of density dependent fecundity on the use of the fecal egg count reduction test for detecting drug resistance in human hookworms. PLoS Negl Trop Dis. 2009;2:e297.
    1. World Health Organization. Report of the WHO informal consultation on monitoring of drug efficacy in the control of schistosomiasis and intestinal nematodes. 1999. WHO/CDS/CPC/SIP/99.1, World Health Organization, Geneva.

Source: PubMed

3
Se inscrever