gSOS多基因评分与儿童骨密度和骨折风险相关

IF 5.9 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Jonathan A Mitchell, Jonathan Bradfield, Shana E McCormack, Alessandra Chesi, Heidi J Kalkwarf, Joan M Lappe, Sharon E Oberfield, Dana L Duren, John A Shepherd, Kurt D Hankenson, Andrea Kelly, Hakon Hakonarson, Struan F A Grant, Babette S Zemel
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引用次数: 0

摘要

多基因风险评分遗传定量超声声速(gSOS)是在欧洲血统的成年人中使用机器学习算法开发的,并与成人骨折几率降低有关。我们的目的是确定gSOS是否与儿童骨骼健康有关。我们对两项儿童观察性研究进行了评估:(1)有遗传数据的儿童骨密度研究(BMDCS) (N = 1727);(2)在费城儿童医院进行研究的具有遗传数据的儿童(CHOP; N = 10 301)。遗传变异用于计算gSOS和遗传祖先。对于BMDCS,自我报告青春期阶段、膳食钙、体力活动和骨折积累(无骨折或≥1骨折),测量身高和体重并计算BMI。采用双能x线骨密度仪测定腰椎、髋部、桡骨和全身的骨矿物质密度(aBMD),并用z分数表示。CHOP研究将遗传数据与电子健康记录(EHR)中的骨折记录配对。gSOS与7个骨骼部位较高的aBMD z评分相关[例如,gSOS升高1 SD与腰椎aBMD z评分升高0.17 (95% CI: 0.10-0.24)相关]。这些关联在男性和女性、年龄、青春期阶段和生活方式因素中都是一致的,在欧洲遗传血统的儿童中最为一致。gSOS每增加1个标准差,BMDCS自我报告骨折的可能性降低24% (OR = 0.76, 95% CI: 0.66, 0.88), CHOP EHR记录骨折的可能性降低12% (OR = 0.88, 95% CI: 0.82, 0.95)。没有发现性别或遗传血统的差异。在两个独立的儿科样本中,gSOS评分越高,多个骨骼部位的aBMD越高,骨折几率越低。这种基因工具可能具有临床应用价值,有助于提高早期骨骼健康,并在整个生命周期中防止骨折。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The gSOS Polygenic Score is Associated with Bone Density and Fracture Risk in Childhood.

The polygenic risk score genetic quantitative ultrasound speed of sound (gSOS) was developed using machine learning algorithms in adults of European ancestry and associates with reduced odds of fracture in adults. We aimed to determine if gSOS was associated with bone health in children. Two observational studies of children were evaluated: (1) children enrolled in the Bone Mineral Density in Childhood Study (BMDCS) with genetic data (N = 1727); and (2) children with genetic data for research at the Children's Hospital of Philadelphia (CHOP; N = 10 301). Genetic variants were used to calculate gSOS and genetic ancestry. For the BMDCS, puberty stage, dietary calcium, physical activity and fracture accumulation (none or ≥ 1 fracture) were self-reported, height and weight were measured and BMI calculated. Areal bone mineral density (aBMD) of the lumbar spine, hip, radius, and whole body were assessed by dual energy X-ray absorptiometry and expressed as Z-scores. The CHOP study paired genetic data with documentation of fracture in the electronic health record (EHR). gSOS associated with higher aBMD Z-scores across 7 skeletal sites [eg, a 1 SD increase in gSOS associated with 0.17 (95% CI: 0.10-0.24) higher lumbar spine aBMD Z-score]. These associations were consistent for males and females, age, puberty stage, and lifestyle factors, and most consistent among children of European genetic ancestry. A 1 SD increase in gSOS associated with 24% reduced likelihood of self-reported fracture in the BMDCS (OR = 0.76, 95% CI: 0.66, 0.88) and a 12% reduced likelihood of a recorded fracture in the CHOP EHR (OR = 0.88; 95% CI: 0.82, 0.95). No sex or genetic ancestry differences were found. A higher gSOS score associated with higher aBMD at multiple skeletal sites and reduced odds of fracture in two independent pediatric samples. This genetic tool may have clinical utility to help enhance bone health in early life and protect against fracture across the lifespan.

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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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