We are analyzing https://link.springer.com/article/10.1186/1476-511x-13-34.

Title:
Association of liver X receptor α (LXRα) gene polymorphism and coronary heart disease, serum lipids and glucose levels | Lipids in Health and Disease
Description:
Background To explore the relationship between the liver X receptor α gene (LXRα) rsl2221497 polymorphism and the susceptibility of coronary heart disease (CHD) and serum lipids and glucose levels. Methods The single fluorescently labeled probes technique was used to detect the genotype of rsl2221497 in LXRα gene in 240 CHD patients and 250 healthy control subjects. The difference of genotype distribution between the two groups was analyzed using of Chi-square test. The serum lipids and glucose levels between the different genotypes were also compared. Results The risk of CHD in carriers with (AA + GA) genotype was 1.76 times as that in the GG genotype carriers (OR = 1.76, 95% CI: 1.18-2.87, P <0.05), and the risk of CHD in carriers with A allele increased 0.88 times compared to that in G allele carriers (OR = 1.88, 95% CI:1.21-3.43, P <0.01). Logistic regression analysis showed that after adjusting for other confounding factors, A allele was an independent risk for CHD. However, there were no differences in serum lipids and glucose levels between each genotype. Conclusions The rsl2221497 polymorphism in LXRα gene was associated with susceptibility of CHD in Han population.
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Keywords {🔍}

chd, article, pubmed, gene, google, scholar, study, disease, liver, risk, receptor, cas, lxrα, allele, genotype, lipids, serum, group, polymorphism, cholesterol, coronary, control, history, analysis, glucose, levels, carriers, genetic, association, heart, zhang, factors, population, diabetes, lipid, lxr, table, data, access, han, macrophages, blood, expression, information, open, patients, subjects, logistic, regression, independent,

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Schema {🗺️}

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         headline:Association of liver X receptor α (LXRα) gene polymorphism and coronary heart disease, serum lipids and glucose levels
         description:To explore the relationship between the liver X receptor α gene (LXRα) rsl2221497 polymorphism and the susceptibility of coronary heart disease (CHD) and serum lipids and glucose levels. The single fluorescently labeled probes technique was used to detect the genotype of rsl2221497 in LXRα gene in 240 CHD patients and 250 healthy control subjects. The difference of genotype distribution between the two groups was analyzed using of Chi-square test. The serum lipids and glucose levels between the different genotypes were also compared. The risk of CHD in carriers with (AA + GA) genotype was 1.76 times as that in the GG genotype carriers (OR = 1.76, 95% CI: 1.18-2.87, P <0.05), and the risk of CHD in carriers with A allele increased 0.88 times compared to that in G allele carriers (OR = 1.88, 95% CI:1.21-3.43, P <0.01). Logistic regression analysis showed that after adjusting for other confounding factors, A allele was an independent risk for CHD. However, there were no differences in serum lipids and glucose levels between each genotype. The rsl2221497 polymorphism in LXRα gene was associated with susceptibility of CHD in Han population.
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            Lipidology
            Medical Biochemistry
            Clinical Nutrition
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      headline:Association of liver X receptor α (LXRα) gene polymorphism and coronary heart disease, serum lipids and glucose levels
      description:To explore the relationship between the liver X receptor α gene (LXRα) rsl2221497 polymorphism and the susceptibility of coronary heart disease (CHD) and serum lipids and glucose levels. The single fluorescently labeled probes technique was used to detect the genotype of rsl2221497 in LXRα gene in 240 CHD patients and 250 healthy control subjects. The difference of genotype distribution between the two groups was analyzed using of Chi-square test. The serum lipids and glucose levels between the different genotypes were also compared. The risk of CHD in carriers with (AA + GA) genotype was 1.76 times as that in the GG genotype carriers (OR = 1.76, 95% CI: 1.18-2.87, P <0.05), and the risk of CHD in carriers with A allele increased 0.88 times compared to that in G allele carriers (OR = 1.88, 95% CI:1.21-3.43, P <0.01). Logistic regression analysis showed that after adjusting for other confounding factors, A allele was an independent risk for CHD. However, there were no differences in serum lipids and glucose levels between each genotype. The rsl2221497 polymorphism in LXRα gene was associated with susceptibility of CHD in Han population.
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      dateModified:2014-02-17T00:00:00Z
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         Gene
         Coronary heart disease
         Polymorphism
         Lipidology
         Medical Biochemistry
         Clinical Nutrition
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