Wu Qing, Xiao Xiangxue, Xu Yingke
Nevada Institute of Personalized Medicine, University of Nevada, Las Vegas, NV 89154, USA.
Department of Environmental and Occupational Health, School of Public Health, University of Nevada Las Vegas, NV 89154, USA.
J Clin Med. 2020 Feb 12;9(2):499. doi: 10.3390/jcm9020499.
Whether the bone mineral density (BMD) T-score performs differently in osteoporosis classification in women of different genetic profiling and race background remains unclear.
The genomic data in the Women's Health Initiative study was analyzed (n = 2417). The polygenic score (PGS) was calculated from 63 BMD-associated single nucleotide polymorphisms (SNPs) for each participant. The World Health Organization's (WHO) definition of osteoporosis (BMD T-score ≤-2.5) was used to estimate the cumulative incidence of fracture.
T-score classification significantly underestimated the risk of major osteoporotic fracture (MOF) in the WHI study. An enormous underestimation was observed in African American women (POR: 0.52, 95% CI: 0.30-0.83) and in women with low PGS (predicted/observed ratio [POR]: 0.43, 95% CI: 0.28-0.64). Compared to Caucasian women, African American, African Indian, and Hispanic women respectively had a 59%, 41%, and 55% lower hazard of MOF after the T-score was adjusted for. The results were similar when used for any fractures.
Our study suggested the BMD T-score performance varies significantly by race in postmenopausal women.
在不同基因特征和种族背景的女性中,骨密度(BMD)T评分在骨质疏松症分类中的表现是否不同仍不清楚。
分析了妇女健康倡议研究中的基因组数据(n = 2417)。为每位参与者从63个与骨密度相关的单核苷酸多态性(SNP)计算多基因评分(PGS)。采用世界卫生组织(WHO)对骨质疏松症的定义(BMD T评分≤-2.5)来估计骨折的累积发生率。
在妇女健康倡议研究中,T评分分类显著低估了主要骨质疏松性骨折(MOF)的风险。在非裔美国女性(POR:0.52,95%CI:0.30 - 0.83)和低PGS女性(预测/观察比值[POR]:0.43,95%CI:0.28 - 0.64)中观察到了巨大的低估。在调整T评分后,与白人女性相比,非裔美国、非洲印第安和西班牙裔女性发生MOF的风险分别降低了59%、41%和55%。用于任何骨折时结果相似。
我们的研究表明,绝经后女性中BMD T评分的表现因种族而异。