Association study of lipoprotein lipase Ser447Stop polymorphisms with acute ischemic stroke
Yumei Yang, Jiang Wu, DU Dan-hua, Feng Wang
Abstract
Yumei Yang, Jiang Wu, DU Dan-hua, Feng Wang
Abstract
Objective To investigate the genetic association between polymorphisms of Ser447Stop in lipoprotein lipase (LPL) gene and ischemic stroke. Methods A case-control study was performed in 563 acute ischemic stroke patients and 320 controls. LPL Ser447Stop genotypes in the subjects were detected by polymerase chain reaction and restriction fragment length polymorphism assay. The frequencies of the alleles in each group were statistically analyzed with Student t-test. Results No significant difference was found in the frequency of G allele of LPL Ser447Stop polymorphism between the case and the control. When subjects were divided into 2 subgroups of cerebral thrombosis infarction and lacunar infarction, the frequency of G allele was significantly higher in the cerebral thrombosis infarction group (9. 7% ) than that in the control (6. 6%, χ2= 3. 99,P = 0. 045 ), and an increased risk for thrombosis infarction was suggested in the G allele ( OR = 1. 510, 95% CI 1. 012--2. 261 ). Conclusion The G allele in polyim Ser447Stop in LPL may be associated with increased risk of cerebral thrombosis infarction. Key words: Brain infarction; Lipoprotein lipase; Polymorphism,single nucleotide
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Objective To investigate the genetic association between polymorphisms of Ser447Stop in lipoprotein lipase (LPL) gene and ischemic stroke. Methods A case-control study was performed in 563 acute ischemic stroke patients and 320 controls. LPL Ser447Stop genotypes in the subjects were detected by polymerase chain reaction and restriction fragment length polymorphism assay. The frequencies of the alleles in each group were statistically analyzed with Student t-test. Results No significant difference was found in the frequency of G allele of LPL Ser447Stop polymorphism between the case and the control. When subjects were divided into 2 subgroups of cerebral thrombosis infarction and lacunar infarction, the frequency of G allele was significantly higher in the cerebral thrombosis infarction group (9. 7% ) than that in the control (6. 6%, χ2= 3. 99,P = 0. 045 ), and an increased risk for thrombosis infarction was suggested in the G allele ( OR = 1. 510, 95% CI 1. 012--2. 261 ). Conclusion The G allele in polyim Ser447Stop in LPL may be associated with increased risk of cerebral thrombosis infarction. Key words: Brain infarction; Lipoprotein lipase; Polymorphism,single nucleotide
Key concepts: Internal medicine, Lipoprotein lipase, Medicine, Genotype, Allele, Cerebral infarction, Allele frequency, Thrombosis