Role of TLR4 (C1196T) and CD14 (C-260T) Polymorphisms in Development of Ischemic Stroke, Its Subtypes and Hemorrhagic Stroke
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Date
2017
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Volume Title
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Springer New York LLC
Abstract
In the present study, we evaluated the association of TLR4 and CD14 polymorphisms, i.e. C1196T and C-260T, respectively, with ischemic stroke (n?=?700), its subtypes and hemorrhagic stroke (n?=?300) in a South Indian population from Telangana. The genotypes were determined using PCR?RFLP, and the strength of association between genotypes and stroke was determined by odds ratio with 95% confidence interval (CI) and chi-square analysis. The results revealed a lack of association for TLR4 variant with ischemic stroke and hemorrhagic stroke, although a significant association was observed with the subtypes extracranial large artery (p?=?0.008), other determined aetiology (p?=?0.03) and undetermined aetiology (p?=?0.01). Investigations on the variant of CD14 gene revealed negative association among ischemic stroke patients; however, a significant association was observed for hemorrhagic stroke following dominant and recessive genotypic model (p?=?0.05, p?=?0.02). Among ischemic stroke subtype, a significant association was observed with intracranial large artery, extracranial large artery, other determined aetiology and undetermined aetiology form of stroke (p?<?0.01). Further, analysis of the CD14 variant between the two major stroke types revealed a significant difference in genotype distribution following the co-dominant genotypic model (p?=?0.01). ? 2017, Springer Science+Business Media, LLC.
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Keywords
Cd14 Antigen, Toll Like Receptor 4, Adult Brain Hemorrhage, Brain Ischemia, Controlled Study, Female, Gene Frequency, Genetic Polymorphism, Genotype, Human, Major Clinical Study, Male, Polymerase Chain Reaction, Restriction Fragment Length Polymorphism, Telangana
Citation
Das, S., Kaul, S., Jyothy, A., & Munshi, A. (2017). Role of TLR4 (C1196T) and CD14 (C-260T) Polymorphisms in Development of Ischemic Stroke, Its Subtypes and Hemorrhagic Stroke. Journal of Molecular Neuroscience, 63(3-4), 300-307. doi: 10.1007/s12031-017-0979-9