Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2004-7-1
pubmed:abstractText
Mutations in the dihydrofolate reductase gene (dhfr) of Plasmodium falciparum have been proposed as molecular markers for the surveillance of sulfadoxine-pyrimethamine (SP)-resistant malaria, but such proposals have not been validated. At 7 Ugandan sites in 1999, we determined the population-based prevalence of infections with mutations and the mutant allele frequency of dhfr codons 108, 51, and 59 using a random sample of infected individuals aged 1-45 years. Sulfadoxine-pyrimethamine treatment failure was independently estimated by in vivo tests in 327 children aged 6-59 months with clinical malaria. The prevalence of infections with the single point mutations and the dhfr codons 108 and 51 mutant allele frequency were not correlated to SP treatment failure. However, the dhfr codon 59 mutant allele frequency was positively correlated to SP treatment failure (r = 0.72, P = 0.06). The ratio of the infections with the mutant to wild genotype (M/W) and that of the mutant to wild allele (MA/WA) had the same values. Both dhfr codon 59 M/W and MA/WA ratio were significantly and positively correlated to SP treatment failure (r = 0.73, P = 0.05). Moreover, the prevalence of infections with only 2 mutations (Asn-108 plus Ile-51) was significantly and inversely correlated to the prevalence of infections with 3 mutations (Asn-108 plus Ile-51 plus Arg-59) (r = 0.92, P = 0.004), suggesting the stepwise accumulation of the dhfr mutations is Asn-108 Ile-51 Arg-59 and further supporting the idea of using the dhfr codon 59 M/W ratio as a molecular index for the prediction of SP treatment failure. Atthe population level, the dhfr codon 59 M/W ratio is a simple and stable index for the estimation of SP treatment failure.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0035-9203
pubmed:author
pubmed:issnType
Print
pubmed:volume
97
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
338-42
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15228255-Adolescent, pubmed-meshheading:15228255-Adult, pubmed-meshheading:15228255-Animals, pubmed-meshheading:15228255-Antimalarials, pubmed-meshheading:15228255-Child, pubmed-meshheading:15228255-Child, Preschool, pubmed-meshheading:15228255-Drug Combinations, pubmed-meshheading:15228255-Drug Resistance, pubmed-meshheading:15228255-Gene Frequency, pubmed-meshheading:15228255-Genes, Protozoan, pubmed-meshheading:15228255-Genetic Markers, pubmed-meshheading:15228255-Humans, pubmed-meshheading:15228255-Infant, pubmed-meshheading:15228255-Malaria, Falciparum, pubmed-meshheading:15228255-Middle Aged, pubmed-meshheading:15228255-Plasmodium falciparum, pubmed-meshheading:15228255-Point Mutation, pubmed-meshheading:15228255-Prevalence, pubmed-meshheading:15228255-Pyrimethamine, pubmed-meshheading:15228255-Sulfadoxine, pubmed-meshheading:15228255-Tetrahydrofolate Dehydrogenase, pubmed-meshheading:15228255-Treatment Failure, pubmed-meshheading:15228255-Uganda
pubmed:articleTitle
Population-based validation of dihydrofolate reductase gene mutations for the prediction of sulfadoxine-pyrimethamine resistance in Uganda.
pubmed:affiliation
Ministry of Health, Kampala, Uganda. atalisuna@itg.be
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Validation Studies