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Lack of Association of CYP2E1 and CYP1A1 Polymorphisms With Osteoporosis in Postmenauposal Women

机译:CYP2E1和CYP1A1基因多态性与骨质疏松症在月经后妇女中缺乏关联

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Osteoporosis is a metabolic bone disease affecting mostly elderly women. As metabolizing enzymes, the roles of few cytochromes have been studied in osteoporosis development. The aim of this study was to assess for the first time the association of CYP2E1 and CYP1A1 polymorphisms and osteoporosis in postmenopausal women. 112 postmenopausal women presenting osteoporosis and 93 age and sex matched healthy controls originating from north Iran were enrolled in this study. Rs2031920 and rs3813867 at CYP2E1 as well as rs4646421 and rs2198843 at CYP1A1 loci were studied in all subjects using polymerase chain reaction and restriction fragment length polymorphism analysis. Genotype analysis for rs2031920 showed that the CT genotype was present only in osteoporotic patients with a frequency of 4.17%. Similarly GC genotype at rs3813867 locus was present only in osteoporotic patients with a frequency of 3.13%. [G T] and [C C] haplotypes for rs3813867- rs2031920 were found with low frequencies only in osteoporotic patients. TT genotype at rs4646421 locus was higher in osteoporotic (8.05%) versus control subjects (3.22%), 14.28% of cases were homozygous for the C allele at rs2198843 locus which is higher than controls (11.84%). The [C G] haplotype for rs4646421- rs2198843 was predominant in cases (54.47%) and controls (58.6%). GT haplotype was rare in both groups. No significant differences in genotypes or haplotypes frequencies were observed among the osteoporotic and normal subjects. CYP1A1 and CYP2E1 loci are not associated to osteoporosis risk in the studied population.
机译:骨质疏松症是一种代谢性骨病,主要影响老年妇女。作为代谢酶,已经研究了几种细胞色素在骨质疏松症发展中的作用。这项研究的目的是第一次评估CYP2E1和CYP1A1基因多态性与绝经后妇女骨质疏松的关系。这项研究招募了112名出现骨质疏松症的绝经后妇女和93名年龄和性别相匹配的健康对照,这些健康对照来自伊朗北部。使用聚合酶链反应和限制性片段长度多态性分析研究了所有受试者中CYP2E1的Rs2031920和rs3813867以及CYP1A1基因座的rs4646421和rs2198843。 rs2031920的基因型分析表明,CT基因型仅存在于骨质疏松患者中,频率为4.17%。类似地,仅在骨质疏松患者中以rs3813867位点存在GC基因型,频率为3.13%。仅在骨质疏松患者中发现rs3813867-rs2031920的[G T]和[CC]单倍型。骨质疏松患者中rs4646421位点的TT基因型较高(8.05%),而对照对象(3.22%)更高,在rs2198843位点C等位基因纯合子的病例为14.28%,高于对照组(11.84%)。 rs4646421- rs2198843的[C G]单倍型在病例(54.47%)和对照(58.6%)中占主导地位。两组中GT单倍型很少见。在骨质疏松症患者和正常受试者之间未观察到基因型或单倍型频率的显着差异。 CYP1A1和CYP2E1基因座与所研究人群的骨质疏松风险无关。

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