Tranah Gregory J, Taylor Brent C, Lui Li-Yung, Zmuda Joseph M, Cauley Jane A, Ensrud Kristine E, Hillier Teresa A, Hochberg Marc C, Li Jia, Rhees Brian K, Erlich Henry A, Sternlicht Mark D, Peltz Gary, Cummings Steven R
CPMC Research Institute, San Francisco, CA 94120, USA.
Calcif Tissue Int. 2008 Sep;83(3):155-66. doi: 10.1007/s00223-008-9165-y. Epub 2008 Sep 12.
Candidate osteoporosis gene variants were examined for associations with fracture risk and bone mineral density (BMD). A total of 9,704 white women were recruited at four U.S. clinical centers and enrolled into the Study of Osteoporotic Fractures, a longitudinal cohort study. Genotyping of 31 polymorphisms from 18 candidate osteoporosis genes was performed in 6,752 women. Incident radiographic fractures were identified at the third and eighth examinations compared with the baseline examination. BMD was measured at the total hip by dual-energy X-ray absorptiometry. Analyses were adjusted for age, clinic site, and self-reported ethnicity. During a mean follow-up of 14.5 years, a total of 849 hip, 658 vertebral, and 2,496 nonhip/nonvertebral fractures occurred in 6,752 women. Women carrying the ALOX15_G48924T T/T genotype had a higher rate of hip fracture (hazard ratio [HR] = 1.33;95% confidence interval [95% CI] = 1.00-1.77) compared with the G/G genotype. Compared with those carrying the PRL_T228C T/T genotype, women with either the C/C (HR = 0.80; 95% CI = 0.67-0.95) or C/T (HR = 0.81; 95% CI = 0.68-0.97) genotype had a lower rate of nonvertebral/nonhip fractures. Women carrying the BMP2_A125611G G/G genotype had a higher rate of vertebral fracture (odds ratio [OR] = 1.51; 95% CI = 1.03-2.23) compared with the A/A genotype. Women with the ESR1_C1335G G/G genotype had a higher rate of vertebral fracture (OR = 1.64; 95% CI = 1.07-2.50) compared with the C/C genotype. Compared with those with the MMP2_C595T C/C genotype, women with the C/T (OR = 0.79; 95% CI = 0.65-0.96) or T/T (OR = 0.44; 95% CI = 0.27-0.72) genotype had a lower rate of vertebral fracture. In conclusion, polymorphisms in several candidate genes were associated with hip, vertebral, and nonhip/nonvertebral fractures but not with total hip BMD in this large population based cohort study.
对候选骨质疏松症基因变异体与骨折风险和骨密度(BMD)的关联进行了研究。在美国的四个临床中心招募了总共9704名白人女性,并将她们纳入骨质疏松性骨折研究,这是一项纵向队列研究。对6752名女性进行了来自18个候选骨质疏松症基因的31个多态性的基因分型。在第三次和第八次检查时与基线检查相比确定了新发的影像学骨折。通过双能X线吸收法测量全髋部的骨密度。分析对年龄、临床地点和自我报告的种族进行了校正。在平均14.5年的随访期间,6752名女性中总共发生了849例髋部骨折、658例椎体骨折和2496例非髋部/非椎体骨折。携带ALOX15_G48924T T/T基因型的女性与G/G基因型相比,髋部骨折发生率更高(风险比[HR]=1.33;95%置信区间[95%CI]=1.00-1.77)。与携带PRL_T228C T/T基因型的女性相比,C/C(HR=0.80;95%CI=0.67-0.95)或C/T(HR=0.81;95%CI=0.68-0.97)基因型的女性非椎体/非髋部骨折发生率较低。携带BMP2_A125611G G/G基因型的女性与A/A基因型相比,椎体骨折发生率更高(优势比[OR]=1.51;95%CI=1.03-2.23)。ESR1_C1335G G/G基因型的女性与C/C基因型相比,椎体骨折发生率更高(OR=1.64;95%CI=1.07-2.50)。与MMP2_C595T C/C基因型的女性相比,C/T(OR=0.79;95%CI=0.65-0.96)或T/T(OR=0.44;95%CI=0.27-0.72)基因型的女性椎体骨折发生率较低。总之,在这项基于大人群的队列研究中,几个候选基因的多态性与髋部、椎体和非髋部/非椎体骨折相关,但与全髋部骨密度无关。