Can pharmacogenomics improve malaria drug policy?
Mary W Roederer a, Howard McLeod a & Jonathan J Juliano b
a. Institute of Pharmacogenomics and Individualized Therapy, Eshelman School of Pharmacy, University of North Carolina, 120 Mason Farm Road, Chapel Hill, NC, 27599-7361, United States of America (USA).
b. Center for Infectious Diseases, School of Medicine, University of North Carolina, Chapel Hill, USA.
Correspondence to Mary W Roederer (e-mail: email@example.com).
(Submitted: 15 February 2011 – Revised version received: 05 July 2011 – Accepted: 08 July 2011 – Published online: 01 September 2011.)
Bulletin of the World Health Organization 2011;89:838-845. doi: 10.2471/BLT.11.087320
Renewed efforts to control and eliminate malaria are making advances using the current generation of tools: long-lasting insecticide treated nets, artemisinin combination therapies (ACTs) and indoor residual spraying. Despite gains made by bednets and spraying, malaria control and elimination efforts will continue to rely heavily on chemotherapy and, in particular, ACTs.
Currently, the World Health Organization (WHO) endorses four ACT combinations for uncomplicated falciparum malaria in non-pregnant adults (Table 1).1 In 2001, WHO recommended the use of ACTs due to high efficacy rates and potential to reduce the development of resistance.2 By 2009, 88 countries, including every country in Africa, had officially adopted ACTs as first-line agents for uncomplicated malaria.2 Despite the official guidelines, only 14 countries report distributing enough ACTs to treat at least 50% of reported malaria cases in the public system, and only 5 countries reported distributing enough ACTs to treat all cases in 2008.3 Over the next 5–10 years, an increasing number of patients, including children and pregnant women, will be given ACT therapy.
Combination therapy, already in use for tuberculosis and HIV, is now recommended for malaria treatment to stem the tide of resistance and protect the widely available, highly efficacious class of drugs, the artemisinins. These combinations are based on the unlikely probability of a parasite becoming resistant simultaneously to two drugs with unrelated modes of action.4 With this in mind, the artemisinins are particularly good partner drugs for other antimalarials as they eliminate parasites rapidly from the blood and thereby limit the number of parasites exposed to the longer acting partner drug.
An example of host genetics
The success of drug therapy is dependent upon many contributing factors, including adherence to prescribed therapy, incorrect or suboptimal dosing, general health status and interactions with other drugs. Another crucial aspect of the lack of effectiveness (often due to low drug levels) and tolerability (often due to high drug levels) of chemotherapy is the way individuals metabolize the drug. Although the widespread use of modern antimalarials began in the 1940s, there was limited data about the absorption–distribution–metabolism–excretion parameters of antimalarials in humans until about 20 years ago.
The use of primaquine in the 1950s highlights the importance of pharmacogenetics for antimalarials, as severe reactions to the drug led to the discovery of glucose-6-phosphate dehydrogenase (G6PD) deficiency in 1956.5,6 The genetic variants among people with G6PD still confound our ability to develop effective antimalarials, illustrated by the withdrawal of the drug Lapdap® (chlorproguanil/dapsone) in 2008.7 This deficiency remains a cause for concern, as primaquine is used widely for terminal prophylaxis and to decrease transmission intensity by limiting reproduction of the malaria parasites.6
Certainly, scientists have investigated the contribution of parasite genetics, in particular relating to drug resistance. Several mutations in parasite drug target genes have been identified and associated with in vivo resistance to artemisinin partner drugs mefloquine, lumefantrine, amodiaquine and chlorproguanil.8–16 In addition to parasite genetics, host genetics can valuably inform national drug policy decisions for first-line antimalarials.
Selection of ACTs
New pharmacology data available for modern antimalarials has helped to identify the major metabolic pathways and to identify human genetic variations that affect the ability to metabolize these agents (Table 2). Beyond the case of G6PD, there remain numerous questions about the role that pharmacogenetics can play to predict adverse drug reactions to antimalarials. Clearly, point-of-care testing for genetic variants, such as those of the CYP2C8 gene, is far from a reality in the developing world. However, it is possible that pharmacogenetics could help inform drug formulary decisions on a regional or national scale.
Currently, national malaria control programmes select the most appropriate drugs for use in the respective country based upon costs, in vitro Plasmodium falciparum resistance patterns and the risk of adverse drug reactions. Very little attention has been paid to host genetics and their potential to affect major formulary decisions by decreasing toxicity, increasing efficacy and improving the time in the therapeutic range to combat resistance. This is especially important when ministries of health, national medicines review authorities or national malaria control programmes must choose between seemingly equal drugs without the aid of comprehensive local pharmacogenetic data (Fig. 1 and Fig. 2). Importantly, knowledge of genetic differences in populations could reduce costs by decreasing adverse events and increasing efficacy of drugs.
Fig. 1. World map showing frequencies of the CYP2C8*2 allele in different populations
Fig. 2. World map showing frequencies of the CYP2C8*3 allele in different populations
This paper looks at drugs commonly used as part of ACTs to treat uncomplicated falciparum malaria in adults and provides specific examples of how genetics may affect drug efficacy and toxicity at a population level. It does not serve as an exhaustive review of all relationships between host genetics and antimalarial drugs. Several high-quality comprehensive reviews have been done elsewhere.17,18 Table 3 lists the drugs and their potential relationships with various genes. This paper discusses ways to improve knowledge of genetic data in malaria-endemic regions and explores the issues that need to be addressed to make pharmacogenetic-guided drug policy a reality.
Table 3. Potential drug–gene relationships for first-line treatments of uncomplicated falciparum malaria in non-pregnant adults
Genetics to guide drug policy
The case of amodiaquine
The antimalarial amodiaquine is generally well tolerated, but its use in primarily Caucasian populations in the 1980s and 1990s was associated with high rates of agranulocytosis (1 in 2100 with a case fatality rate of 1 in 31 000) and hepatotoxicity (1 in 15 600).19–21 WHO removed amodiaquine from the Essential Medicines List due to the discovery of these toxicities, but it was added back on the list in the late 1990s as resistance to alternative drugs began to appear. Recent evidence points to frequent mild adverse events caused by amodiaquine. A trial in 15 subjects in Africa evaluating the pharmacokinetics of amodiaquine and the combination of amodiaquine and artesunate revealed the common adverse events of hepatotoxicity and leukopenia after just two doses given three weeks apart.22
People with mutant genotypes of CYP2C8, CYP1A1 and CYP1B1 have been found to have immunogenic adverse reactions to amodiaquine.23–28 Wide variations in the CYP2C8 genotype mean that individuals experience broad differences in the drug’s efficacy and toxicity. Evidence suggests that decreased function of the CYP2C8 enzyme impairs metabolism of the drug and can form a toxic metabolite that causes hepatotoxicity and agranulocytosis. Two more common CYP2C8 variants, CYP2C8*2 and *3, decrease the metabolizing ability of CYP2C8 as evidenced by reduced clearance of the anticancer drug paclitaxel and arachidonic acid, respectively.29,30 In fact, CYP2C8*3 displays no detectable metabolizing ability in vitro.30
In a study by Parikh et al., 275 subjects with malaria from Burkina Faso were evaluated for amodiaquine metabolism.30 The subjects with the CYP2C8*2 genotype (more common African variant) experienced more abdominal pain than subjects with the wild-type (i.e. the normal, non-mutated gene) (52% versus 30%; P < 0.01).30 Other adverse effects did not differ.30 However, as in many pharmacogenetic studies, this study used a rather small sample to evaluate rare toxicities and did not test for liver function change as a marker for hepatotoxicity or pharmacokinetic changes to test for drug concentrations or toxic intermediates. Studies in Burkina Faso and Ghana have not revealed a relationship between drug efficacy and CYP2C8 genotype.30,31
While the percentage of the population with an inactivating CYP2C8 genetic variant is not high in most malaria-endemic regions, the overall incidence of risk is significant due to the burden of disease. For example, Cavaco et al. estimated that the CYP2C8*2 and CYP2C8*3 genetic variants occur in 2.1% of the population in Zanzibar, United Republic of Tanzania: this translates into more than 30 000 patients per year at risk for severe drug reactions to amodiaquine (of a malaria patient population of ~1 000 000).32
In Ghana, with a total population of more than 25 million, 5 270 108 cases of malaria were documented in 2007. The majority of these cases were likely treated with artesunate plus amodiaquine, the first-line treatment of choice on the Ghanaian Essential Medicines List.33 Based on a 1.5% population incidence of low-metabolizing CYP2C8, almost 80 000 (79 052) of these malaria cases would have occurred in low metabolizers (Fig. 1 and Fig. 2). Collecting data on adverse drug reactions and their cost is the best way to evaluate amodiaquine-related adverse effects. Without pharmacovigilance and cost data to model the medical costs associated with potential adverse drug reactions among these low metabolizers, giving this drug combination to 79 000 low metabolizers each year wastes an estimated 0.57 United States dollars per treatment course (average cost per treatment ranges from US$ 0.57–0.88), a total of approximately US$ 45 000 a year.34
The known literature on CYP2C8 allele (gene) frequencies reveals a lack of data in malaria-endemic Africa but, in those African countries with data, there is a higher frequency than in American Caucasians (Fig. 1, Fig. 2 and Table 2). With the Ghana example showing a loss of more than US$ 45 000, the national control programme or national medicines review authority could choose an alternative from the three first-line antimalarial combinations to treat malaria.
The artemisinins as a group differ in the routes they take in the human body to convert to the major active metabolite, dihydroartemisinin (DHA). Artesunate undergoes rapid and extensive conversion via CYP2A6 and, to a lesser extent, CYP2B6 and CYP1A1 and CYP1A2.35 Almost 40 gene variants for CYP2A6 have been identified; at least 13 of these show decreased metabolizing function and five show no activity in vivo.36 The major antimalarial activity of artesunate is performed by DHA.37 People with poorly functioning CYP2A6 will have higher concentrations of artesunate and lower concentrations of DHA. This could reduce the drug’s antimalarial activity, kill fewer parasites and increase the potential for artesunate resistance.
Malaria endemicity is high in many areas of sub-Saharan Africa, such as Ghana. In contrast, in the Sabah region of Malaysia (which has the highest endemicity for malaria in this region) the burden of disease is considerably less than in Ghana. Almost two thirds of a Ghanaian population exhibited the wild-type genotype of CYP2A6 with more than 80% allele frequency of CYP2A6*1A.38 In contrast, a Malaysian population had an observed frequency for wild-type genotype of only 8% and an allele frequency for CYP2A6*1A of approximately 32%.39 With wild-type responsible for the majority of Ghanaian CYP2A6 activity, artesunate conversion to DHA and antimalarial activity are expected to be normal. In the Malaysian population with a low wild-type genotype frequency, CYP2A6 activity is decreased, the conversion to DHA decreased, and the antimalarial activity of artesunate may be compromised. Studies in other Asian populations also reveal a high frequency of non-wild-type alleles and an especially high frequency of the alleles that translate to no CYP2A6 activity (11.5–20.1% for Chinese, Japanese, Korean and Thai people)38
Resistance to artemisinin-based therapies is emerging in Thailand and approaches 10% in some areas.40 While not established, a potential contributor to artemisinin resistance in Thailand may be related to CYP2A6 activity (at least 14% frequency of the CYP2A6 alleles with no activity) and the inability to convert artesunate to DHA.41
Our understanding of the host factors contributing to the effectiveness of antimalarials is still in its infancy. As a community we need to determine ways to enhance our ability to study the pharmacokinetics and pharmacogenetics of antimalarials to help decrease the burden imposed by drug toxicity and to help protect their longevity. We can do this in three main ways: (i) integrating pharmacogenetic studies with the pharmacokinetic studies of antimalarials; (ii) increasing the generation of human genetic data and (iii) enhancing the infrastructure for pharmacogenetic research of antimalarial use in endemic countries.
Much of the data concerning the pharmacogenetics of antimalarials is derived from small and under-powered studies conducted in a retrospective manner. In particular, we are lacking significant data for some ACT partner drugs, such as sulfadoxine-pyrimethamine and lumefantrine. A resurgent interest in the pharmacology and pharmacokinetics of antimalarials in the malaria drug resistance community has spurred the development of another potential new resource for gathering pharmacogenetic data. As part of the Worldwide Antimalarial Resistance Network, a module has been developed to improve the quality of antimalarial pharmacology data generated, to use the new information to define drug resistance and to inform optimal dosing schedules. The goal is to facilitate global cooperation between groups active in the antimalarial pharmacology field (available at: http://www.wwarn.org). Pharmacology researchers, especially pharmacokinetic researchers, of antimalarials should obtain informed consent from study participants to allow use of their samples for collaborative pharmacogenetic analysis, either prospectively or in future retrospective analyses.
Another potential resource for increasing our understanding of the pharmacogenetics of antimalarials are national control programmes, and the researchers and funding agencies associated with these programmes. During in vivo monitoring and efficacy studies carried out by these groups, samples obtained as dried blood spots are often collected and stored. The amount of DNA collected in these samples would not allow for assessment of a large number of genetic variations but it could allow for targeted testing of a small number that are vetted in strong pharmacogenetic studies. The key would be to encourage these groups to obtain consent from patients for retrospective human DNA testing. For example, considering the four first-line treatments, blood spots could provide a way to use pharmacogenetics to prioritize pharmacotherapy based on genetic differences within a defined population and to evaluate CYP2C8 genetics. Since amodiaquine requires CYP2C8 for metabolism to an active agent, national control programmes or the national medicines review authorities could use genotype frequencies in that population to determine the priority of a regimen containing amodiaquine.
Ethnic variability is known for its association with antimalarial metabolism, but genetic data are missing for much of the world’s population. An increasing number of resources and efforts has been put into place to help with gathering information about the genetic make-up of different ethnic groups. In malaria-endemic areas, there are no pharmacogenetics organizations, such as the National Institute of Genomic Medicine (INMEGEN) in Mexico, to evaluate population genetic differences. However, the ideas explored in the white paper, Harnessing genomic technologies towards improving health in Africa, detail the systematic process for improving the research infrastructure in Africa.42
There is a strong need for genetic research in Africa. The overarching needs are for infrastructure, education and training, disease-related research and a comprehensive and continued focus on ethical, legal and social issues. To address these needs the Human Health and Heredity in Africa Initiative aims to integrate pharmacogenetics in the selection of national formularies in Africa.
In the meantime, to address the gap in knowledge and need for resources to evaluate genetic differences in developing countries, the Pharmacogenetics for Every Nation Initiative (PGENI) plans to sample 500 people from every ethnic group that represents 10% or more of the population in 104 developing countries.25,43 To avoid any conflicts of interest, PGENI declines funding from any drug manufacturers. PGENI aims to start the development of basic genetic knowledge in traditionally underserved environments. With the generation of medication prioritization algorithms for diseases of global importance, PGENI produces country-specific, genetically-enhanced treatment algorithms for diseases such as malaria. Using known genetic information and the WHO recommended treatment for uncomplicated malaria, a prioritization algorithm includes entry points where pharmacogenetics may augment decision-making, such as for CYP2C8 and CYP2A6 polymorphism frequencies when evaluating the use of amodiaquine and artesunate, respectively. When considering local parasite resistance and drug costs, the pharmacogenetically-enhanced, medical decision-making algorithm becomes a practical mechanism for weighing the options for formulary inclusion or exclusion by national medicines review authorities or national control programmes.
Countries such as the United Kingdom of Great Britain and Northern Ireland and the United States of America have made tremendous investments in research towards genomic medicine. However, in parts of the world where national health expenditures are as low as US$ 30 a day, the investment in genomic research has been extremely low.44 Importantly however, some malaria-endemic countries, such as India, South Africa and Thailand, have begun to invest in large-scale studies of human genomic variation.45,46 In addition, smaller projects, such as the DNA data bank in the Gambia and a biobank and pharmacogenetics database in Harare, Zimbabwe, are emerging and may be able to provide valuable data to inform national control programmes and medicines review authorities.47,48
Make it practical
While research is necessary to develop an objective strategy, individualized antimalarial therapy based on genetics will not be practical in most endemic countries for decades. However, that should not prevent the application of pharmacogenetic knowledge in public policy decisions. Just as regional sampling of a small number of malaria (or HIV or tuberculosis) isolates is used for sensitivity predictions for the infecting agents, we can use regional data from the population as part of the selection of therapy. The hope is that international cooperation through agencies such as PGENI, the Public Population Project in Genomics and the Genome-based Research and Population Health International Network, will help to build infrastructure in endemic countries and provide the training necessary to support a sustained skilled human resource. Enhancing the research infrastructure in developing countries should improve the capability for future genetic research and support continued efforts to address the gaps in knowledge of host genetics. By encouraging collaboration with the malaria control programmes and parasitologists, as well as with the national medicines review authorities, the stakeholders in genomic research will grow substantially and sustainably. Any use of human samples will require an informed consent that allows future use in research, including genetic research. As the pharmacogenetic markers with significant impact on drug response and/or toxicity are vetted, using the malaria control programme samples in malaria-endemic countries provides a good first step to expanding the potential to impact global drug use through improved efficacy and decreased drug toxicity. This should help to populate a map of pharmacogenetic data to guide national formulary decision-making by using existing samples, data and processes.
To accomplish the considerable goal of developing pharmacogenetically-informed drug policies, there is a need for strong collaboration between parasitologists studying parasite resistance, public health officials from control programmes and researchers identifying genetic causes of differences in drug toxicity and efficacy. The African Medicines Regulatory Harmonization Initiative will provide a regional regulatory process and may allow improvements not only at the national but also at the regional level.49 These collaborations, in conjunction with others investigating new drug entities, may help to affect the delivery of care to real patients in malaria-endemic regions. The work to create collaborations and to develop systems that allow for sampling large populations to establish a map of genetic differences will not be easy, but it is certainly worthwhile to include pharmacogenetic information when considering the data and defining the limited number of drugs that will be available to a population.
Jonathan J Juliano was supported by award number KL2RR025746 from the National Center for Research Resources, National Institutes of Health, USA. This work is part of the Pharmacogenetics for Every Nation Initiative. Mary W Roederer and Howard McLeod complete research with PGENI.
- Guidelines for the treatment of malaria. Geneva: World Health Organization; 2006. Available from: http://whqlibdoc.who.int/publications/2006/9241546948_eng_full.pdf [accessed 23 August 2011].
- Lin JT, Juliano JJ, Wongsrichanalai C. Drug-resistant malaria: the era of ACT. Curr Infect Dis Rep 2010; 12: 165-73 doi: 10.1007/s11908-010-0099-y pmid: 21308525.
- World malaria report 2009. Geneva: World Health Organization; 2009. Available from: http://whqlibdoc.who.int/publications/2009/9789241563901_eng.pdf [accessed 23 August 2011].
- Yeung S, Pongtavornpinyo W, Hastings IM, Mills AJ, White NJ. Antimalarial drug resistance, artemisinin-based combination therapy, and the contribution of modeling to elucidating policy choices. Am J Trop Med Hyg 2004; 71: 179-86 pmid: 15331836.
- Carson PE, Flanagan CL, Ickes CE, Alving AS. Enzymatic deficiency in primaquine-sensitive erythrocytes. Science 1956; 124: 484-5 doi: 10.1126/science.124.3220.484-a pmid: 13360274.
- Luzzatto L. The rise and fall of the antimalarial Lapdap: a lesson in pharmacogenetics. Lancet 2010; 376: 739-41 doi: 10.1016/S0140-6736(10)60396-0 pmid: 20599264.
- Update on GSK’s malaria treatments: Dacart and Lapdap. [media release]. 29 February 2008. Brentford: GlaxoSmithKline;2008. Available from: http://www.gsk.com/media/pressreleases/2008/2008_pressrelease_0014.htm. [accessed 23 August 2011].
- Basco LK, Ringwald P. Analysis of the key pfcrt point mutation and in vitro and in vivo response to chloroquine in Yaounde, Cameroon. J Infect Dis 2001; 183: 1828-31 doi: 10.1086/320726 pmid: 11372041.
- Berens N, Schwoebel B, Jordan S, Vanisaveth V, Phetsouvanh R, Christophel EM, et al., et al. Plasmodium falciparum: correlation of in vivo resistance to chloroquine and antifolates with genetic polymorphisms in isolates from the south of Lao PDR. Trop Med Int Health 2003; 8: 775-82 doi: 10.1046/j.1365-3156.2003.01099.x pmid: 12950663.
- Happi TC, Thomas SM, Gbotosho GO, Falade CO, Akinboye DO, Gerena L, et al., et al. Point mutations in the pfcrt and pfmdr-1 genes of Plasmodium falciparum and clinical response to chloroquine, among malaria patients from Nigeria. Ann Trop Med Parasitol 2003; 97: 439-51 doi: 10.1179/000349803235002489 pmid: 12930607.
- Maguire JD, Susanti AI, Kristin , Sismadi P, Fryauff DJ, Baird JK. The T76 mutation in the pfcrt gene of Plasmodium falciparum and clinical chloroquine resistance phenotypes in Papua, Indonesia. Ann Trop Med Parasitol 2001; 95: 559-72 doi: 10.1080/00034980120092516 pmid: 11672462.
- Nelson AL, Purfield A, McDaniel P, Uthaimongkol N, Buathong N, Sriwichai S, et al., et al. pfmdr1 genotyping and in vivo mefloquine resistance on the Thai-Myanmar border. Am J Trop Med Hyg 2005; 72: 586-92 pmid: 15891133.
- Ochong EO, van den Broek IV, Keus K, Nzila A. Short report: association between chloroquine and amodiaquine resistance and allelic variation in the Plasmodium falciparum multiple drug resistance 1 gene and the chloroquine resistance transporter gene in isolates from the upper Nile in southern Sudan. Am J Trop Med Hyg 2003; 69: 184-7 pmid: 13677373.
- Omar SA, Adagu IS, Warhurst DC. Can pretreatment screening for dhps and dhfr point mutations in Plasmodium falciparum infections be used to predict sulfadoxine-pyrimethamine treatment failure? Trans R Soc Trop Med Hyg 2001; 95: 315-9 doi: 10.1016/S0035-9203(01)90250-0 pmid: 11491006.
- Pillai DR, Labbe AC, Vanisaveth V, Hongvangthong B, Pomphida S, Inkathone S, et al., et al. Plasmodium falciparum malaria in Laos: chloroquine treatment outcome and predictive value of molecular markers. J Infect Dis 2001; 183: 789-95 doi: 10.1086/318836 pmid: 11181156.
- Price RN, Uhlemann AC, Brockman A, McGready R, Ashley E, Phaipun L, et al., et al. Mefloquine resistance in Plasmodium falciparum and increased pfmdr1 gene copy number. Lancet 2004; 364: 438-47 doi: 10.1016/S0140-6736(04)16767-6 pmid: 15288742.
- Kerb R, Fux R, Morike K, Kremsner PG, Gil JP, Gleiter CH, et al., et al. Pharmacogenetics of antimalarial drugs: effect on metabolism and transport. Lancet Infect Dis 2009; 9: 760-74 doi: 10.1016/S1473-3099(09)70320-2 pmid: 19926036.
- Mehlotra RK, Henry-Halldin CN, Zimmerman PA. Application of pharmacogenomics to malaria: a holistic approach for successful chemotherapy. Pharmacogenomics 2009; 10: 435-49 doi: 10.2217/146224126.96.36.1995 pmid: 19290792.
- Hatton CS, Peto TE, Bunch C, Pasvol G, Russell SJ, Singer CR, et al., et al. Frequency of severe neutropenia associated with amodiaquine prophylaxis against malaria. Lancet 1986; 327: 411-4 doi: 10.1016/S0140-6736(86)92371-8 pmid: 2868340.
- Phillips-Howard PA, West LJ. Serious adverse drug reactions to pyrimethamine-sulphadoxine, pyrimethamine-dapsone and to amodiaquine in Britain. J R Soc Med 1990; 83: 82-5 pmid: 2138674.
- Raymond JM, Dumas F, Baldit C, Couzigou P, Beraud C, Amouretti M. Fatal acute hepatitis due to amodiaquine. J Clin Gastroenterol 1989; 11: 602-3 doi: 10.1097/00004836-198910000-00034 pmid: 2794450.
- Orrell C, Little F, Smith P, Folb P, Taylor W, Olliaro P, et al., et al. Pharmacokinetics and tolerability of artesunate and amodiaquine alone and in combination in healthy volunteers. Eur J Clin Pharmacol 2008; 64: 683-90 doi: 10.1007/s00228-007-0452-8 pmid: 18415093.
- Kerb R, Fux R, Morike K, Kremsner PG, Gil JP, Gleiter CH, et al., et al. Pharmacogenetics of antimalarial drugs: effect on metabolism and transport. Lancet Infect Dis 2009; 9: 760-74 doi: 10.1016/S1473-3099(09)70320-2 pmid: 19926036.
- Li XQ, Bjorkman A, Andersson TB, Ridderstrom M, Masimirembwa CM. Amodiaquine clearance and its metabolism to N-desethylamodiaquine is mediated by CYP2C8: a new high affinity and turnover enzyme-specific probe substrate. J Pharmacol Exp Ther 2002; 300: 399-407 doi: 10.1124/jpet.300.2.399 pmid: 11805197.
- Roederer MW. Cytochrome P450 enzymes and genotype-guided drug therapy. Curr Opin Mol Ther 2009; 11: 632-40 pmid: 20072940.
- Clarke JB, Maggs JL, Kitteringham NR, Park BK. Immunogenicity of amodiaquine in the rat. Int Arch Allergy Appl Immunol 1990; 91: 335-42 doi: 10.1159/000235138 pmid: 2210868.
- Harrison AC, Kitteringham NR, Clarke JB, Park BK. The mechanism of bioactivation and antigen formation of amodiaquine in the rat. Biochem Pharmacol 1992; 43: 1421-30 doi: 10.1016/0006-2952(92)90198-R pmid: 1567466.
- Jewell H, Maggs JL, Harrison AC, O'Neill PM, Ruscoe JE, Park BK. Role of hepatic metabolism in the bioactivation and detoxication of amodiaquine. Xenobiotica 1995; 25: 199-217 doi: 10.3109/00498259509061845 pmid: 7618347.
- Dai D, Zeldin DC, Blaisdell JA, Chanas B, Coulter SJ, Ghanayem BI, et al., et al. Polymorphisms in human CYP2C8 decrease metabolism of the anticancer drug paclitaxel and arachidonic acid. Pharmacogenetics 2001; 11: 597-607 doi: 10.1097/00008571-200110000-00006 pmid: 11668219.
- Parikh S, Ouedraogo JB, Goldstein JA, Rosenthal PJ, Kroetz DL. Amodiaquine metabolism is impaired by common polymorphisms in CYP2C8: implications for malaria treatment in Africa. Clin Pharmacol Ther 2007; 82: 197-203 doi: 10.1038/sj.clpt.6100122 pmid: 17361129.
- Adjei GO, Kristensen K, Goka BQ, Hoegberg LC, Alifrangis M, Rodrigues OP, et al., et al. Effect of concomitant artesunate administration and cytochrome P4502C8 polymorphisms on the pharmacokinetics of amodiaquine in Ghanaian children with uncomplicated malaria. Antimicrob Agents Chemother 2008; 52: 4400-6 doi: 10.1128/AAC.00673-07 pmid: 18779360.
- Cavaco I, Strömberg-Nörklit J, Kaneko A, Msellem MI, Dahoma M, Ribeiro VL, et al., et al. CYP2C8 polymorphism frequencies among malaria patients in Zanzibar. Eur J Clin Pharmacol 2005; 61: 15-8 doi: 10.1007/s00228-004-0871-8 pmid: 15785959.
- The health sector in Ghana: facts and figures, 2008. Accra: Ghana Health Service; 2008. Available from: http://www.ghanahealthservice.org/includes/upload/publications/Facts%20and%20Figures%202008.pdf [accessed 23 August 2011].
- Drug prices for artesunate/amodiaquine. International Drug Price Indicator Guide. Cambridge: Management Sciences for Health; 2009. Available from: http://erc.msh.org [accessed 23 August 2011].
- Li XQ, Björkman A, Andersson TB, Gustafsson LL, Masimirembwa CM. Identification of human cytochrome P(450)s that metabolise anti-parasitic drugs and predictions of in vivo drug hepatic clearance from in vitro data. Eur J Clin Pharmacol 2003; 59: 429-42 doi: 10.1007/s00228-003-0636-9 pmid: 12920490.
- Di YM, Chow VD, Yang LP, Zhou SF. Structure, function, regulation and polymorphism of human cytochrome P450 2A6. Curr Drug Metab 2009; 10: 754-80 doi: 10.2174/138920009789895507 pmid: 19702528.
- Ilett KF, Ethell BT, Maggs JL, Davis TM, Batty KT, Burchell B, et al., et al. Glucuronidation of dihydroartemisinin in vivo and by human liver microsomes and expressed UDP-glucuronosyltransferases. Drug Metab Dispos 2002; 30: 1005-12 doi: 10.1124/dmd.30.9.1005 pmid: 12167566.
- Gyamfi MA, Fujieda M, Kiyotani K, Yamazaki H, Kamataki T. High prevalence of cytochrome P450 2A6*1A alleles in a black African population of Ghana. Eur J Clin Pharmacol 2005; 60: 855-7 doi: 10.1007/s00228-004-0854-9 pmid: 15660270.
- Yusof W, Gan SH. High prevalence of CYP2A6*4 and CYP2A6*9 alleles detected among a Malaysian population. Clin Chim Acta 2009; 403: 105-9 doi: 10.1016/j.cca.2009.01.032 pmid: 19361454.
- White NJ. Qinghaosu (artemisinin): the price of success. Science 2008; 320: 330-4 doi: 10.1126/science.1155165 pmid: 18420924.
- Noedl H, Socheat D, Satimai W. Artemisinin-resistant malaria in Asia. N Engl J Med 2009; 361: 540-1 doi: 10.1056/NEJMc0900231 pmid: 19641219.
- Harnessing genomic technologies towards improving health in Africa. Bethesda: Human Heredity and Health in Africa Initiative; 2011. Available from: http://www.h3africa.org/whitepaper.cfm [accessed 23 August 2011].
- Marsh S, Van Booven DJ, McLeod HL. Global pharmacogenetics: giving the genome to the masses. Pharmacogenomics 2006; 7: 625-31 doi: 10.2217/146224188.8.131.525 pmid: 16753009.
- Hardy BJ, Seguin B, Goodsaid F, Jimenez-Sanchez G, Singer PA, Daar AS. The next steps for genomic medicine: challenges and opportunities for the developing world. Nat Rev Genet 2008; 9: S23-7 doi: 10.1038/nrg2444 pmid: 18802418.
- Hardy BJ, Seguin B, Singer PA, Mukerji M, Brahmachari SK, Daar AS. From diversity to delivery: the case of the Indian Genome Variation initiative. Nat Rev Genet 2008; 9: S9-14 doi: 10.1038/nrg2440 pmid: 18802420.
- Hardy BJ, Seguin B, Ramesar R, Singer PA, Daar AS. South Africa: from species cradle to genomic applications. Nat Rev Genet 2008; 9: S19-23 doi: 10.1038/nrg2441 pmid: 18802417.
- Sirugo G, Schim van der Loeff M, Sam O, Nyan O, Pinder M, Hill AV, et al., et al. A national DNA bank in The Gambia, West Africa, and genomic research in developing countries. Nat Genet 2004; 36: 785-6 doi: 10.1038/ng0804-785 pmid: 15284842.
- Matimba A, Oluka MN, Ebeshi BU, Sayi J, Bolaji OO, Guantai AN, et al., et al. Establishment of a biobank and pharmacogenetics database of African populations. Eur J Hum Genet 2008; 16: 780-3 doi: 10.1038/ejhg.2008.49 pmid: 18382479.
- Ndomondo-Sigonda M, Ambali A. The african medicines regulatory harmonization initiative: rationale and benefits. Clin Pharmacol Ther 2011; 89: 176-8 doi: 10.1038/clpt.2010.299 pmid: 21252936.