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Association between estrogen receptor gene polymorphisms and curve severity of idiopathic scoliosis.

机译:雌激素受体基因多态性与特发性脊柱侧弯的严重程度之间的关联。

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STUDY DESIGN: Analysis of the estrogen receptor gene of girls with idiopathic scoliosis. OBJECTIVES: To determine whether estrogen receptor gene polymorphisms correlate with curve severity of adolescent idiopathic scoliosis. SUMMARY OF BACKGROUND DATA: Studies suggest that idiopathic scoliosis is a familial condition and that curve progression is related to genetically determined factors, such as skeletal and sexual growth. METHODS: A total of 304 girls with idiopathic scoliosis were followed until growth maturation. Height, arm span, menarcheal age, and age at growth maturation were recorded, and curve severity was measured using Cobb's method. The estrogen receptor gene, which contains polymorphic PvuII and XbaI sites, was amplified from lymphocyte deoxyribonucleic acid by polymerase chain reaction. RESULTS: The mean maximum Cobb measurements for patients with genotypes XX and Xx were greater than for those with genotype xx (P = 0.002). The risk of curve progression, defined as progression of >5 degrees from initial evaluation, was higher with genotype Xx than with xx (P = 0.03). Patients with genotypes XX and Xx had a significantly higher risk for operative treatment than those with genotype xx (21.4%, 24.7% vs. 7.6%, P< 0.001). Growth examination around the time of the growth spurt revealed that the XbaI site polymorphism was also related to the age of growth maturation. The frequency of patients with growth maturation at >or=16 years was higher for genotypes XX and Xx than for genotype xx (33.3%, 29.9% vs. 16.8%, P= 0.013). CONCLUSION: Our results suggest that the XbaI site polymorphism is associated with curve severity. DNA analysis may predict curve progression.
机译:研究设计:特发性脊柱侧弯女孩的雌激素受体基因分析。目的:确定雌激素受体基因多态性是否与青少年特发性脊柱侧弯的严重程度相关。背景数据摘要:研究表明,特发性脊柱侧弯是家族性疾病,曲线的进展与遗传因素有关,例如骨骼和性生长。方法:总共304名患有特发性脊柱侧弯的女孩被随访至生长成熟。记录身高,臂展,月经初潮和生长成熟时的年龄,并使用Cobb方法测量曲线的严重程度。通过聚合酶链反应从淋巴细胞脱氧核糖核酸中扩增出含有多态性PvuII和XbaI位点的雌激素受体基因。结果:基因型为XX和Xx的患者的平均最大Cobb测量值大于基因型为xx的患者(P = 0.002)。基因型Xx的曲线进展风险定义为从初始评估开始进展> 5度,高于xx(P = 0.03)。基因型为XX和Xx的患者进行手术治疗的风险显着高于基因型为xx的患者(分别为21.4%,24.7%和7.6%,P <0.001)。生长突增期周围的生长检查表明,XbaI位点多态性也与生长成熟的年龄有关。 XX和Xx基因型在大于或等于16岁时的成长成熟患者的频率高于xx基因型(33.3%,29.9%和16.8%,P = 0.013)。结论:我们的结果表明XbaI位点多态性与曲线的严重程度有关。 DNA分析可以预测曲线的进展。

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