Functional promoter haplotypes of interleukin-18 condition susceptibility to severe malarial anemia and childhood mortality.
dc.contributor.author | T, Were, | |
dc.contributor.author | CW, Gichuki | |
dc.contributor.author | Ong'echa, JM | |
dc.contributor.author | Ouma, Collins | |
dc.contributor.author | Anyona, SB | |
dc.contributor.author | Kempaiah, P | |
dc.contributor.author | Raballah, E | |
dc.contributor.author | Davenpor, GC | |
dc.contributor.author | Konah, SN | |
dc.contributor.author | Vulule, JM | |
dc.contributor.author | Hittner, James B | |
dc.contributor.author | Perkins, DJ | |
dc.date.accessioned | 2018-01-24T13:21:34Z | |
dc.date.available | 2018-01-24T13:21:34Z | |
dc.date.issued | 2012 | |
dc.identifier.uri | https://repository.maseno.ac.ke/handle/123456789/249 | |
dc.description.abstract | Severe malarial anemia (SMA) is a leading cause of morbidity and mortality in children residing in regions where plasmodium falciparum transmission is holoendemic. Although largely unexplored in children with SMA, interleukin-18 (Il-1S) is important for regulating innate and acquired immunity in inflammatory and infectious diseases. As such, we selected two functional single-nucleotide polymorphisms (SNPS) in the Il-18 promoter (-137G-C [rs187238J and-607-CA [rs1946518J) whose haplotypes encompass significant genetic variation due to the presence of strong linkage disequilibrium among these variants. The relationship between the genotypes/haplotypes, SMA (hemoglobin [HbJ,< 5.0 g/dlJ, and longitudinal clinical outcomes were then investigated in Kenyan children (n= 719). Multivariate logistic regression analyses controlling for age, gender, sickle cell trait … | en_US |
dc.publisher | PubMed | en_US |
dc.title | Functional promoter haplotypes of interleukin-18 condition susceptibility to severe malarial anemia and childhood mortality. | en_US |
dc.type | Article | en_US |
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