Wu Jie, Qiu Yong, Zhang Le, Sun Qiang, Qiu Xusheng, He Yongxiong
Department of Orthopaedic Surgery, Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, China.
Spine (Phila Pa 1976). 2006 May 1;31(10):1131-6. doi: 10.1097/01.brs.0000216603.91330.6f.
A case-control study is presented.
To investigate the association of estrogen receptor gene polymorphisms with adolescent idiopathic scoliosis (AIS) risk.
Previous studies have shown that genetic factors are important in the pathogenesis of idiopathic scoliosis. Only 1 publication suggested that XbaI site polymorphism was associated with curve severity of idiopathic scoliosis. However, to our knowledge, the relationship of estrogen receptor gene polymorphisms and the individual susceptibility to idiopathic scoliosis has not been studied.
This study included 202 patients with AIS and 174 healthy controls. Height, menarche status, curve pattern, Cobb angle, and Risser sign in female patients were recorded. There were 2 polymorphic loci, PvuII and XbaI locus, of estrogen receptor analyzed by restriction fragment length polymorphisms.
The frequency of XX genotype was significantly higher in patients than that in controls (P = 0.005). The X allele appeared to be overrepresented in patients compared with controls (P = 0.001). Furthermore, the frequencies of XX genotype in female patients whose height was > or = 160 cm and Cobb angle > or = 40 degrees were higher than those whose height was <160 cm and Cobb angle <40 degrees (P = 0.001 and P < 0.001, respectively).
The XbaI site polymorphism of estrogen receptor gene may be associated with a risk of AIS.
本研究为病例对照研究。
探讨雌激素受体基因多态性与青少年特发性脊柱侧凸(AIS)发病风险的相关性。
既往研究表明,遗传因素在特发性脊柱侧凸的发病机制中起重要作用。仅有1篇文献提示XbaI位点多态性与特发性脊柱侧凸的曲线严重程度相关。然而,据我们所知,雌激素受体基因多态性与特发性脊柱侧凸个体易感性的关系尚未得到研究。
本研究纳入202例AIS患者和174例健康对照。记录女性患者的身高、月经初潮状态、曲线类型、Cobb角和Risser征。通过限制性片段长度多态性分析雌激素受体的2个多态性位点,即PvuII和XbaI位点。
患者中XX基因型的频率显著高于对照组(P = 0.005)。与对照组相比,患者中X等位基因的比例似乎过高(P = 0.001)。此外,身高≥160 cm且Cobb角≥40°的女性患者中XX基因型的频率高于身高<160 cm且Cobb角<40°的患者(分别为P = 0.001和P < 0.001)。
雌激素受体基因的XbaI位点多态性可能与AIS发病风险相关。