Musculoskeletal Research Unit, Translational Health Sciences, Southmead Hospital, University of Bristol, Bristol BS10 5NB, United Kingdom.
Medical Research Council Integrative Epidemiology Unit, Population Health Sciences, University of Bristol, Bristol BS8 2BN, United Kingdom.
J Bone Miner Res. 2024 Apr 19;39(3):241-251. doi: 10.1093/jbmr/zjae002.
Femoral neck width (FNW) derived from DXA scans may provide a useful adjunct to hip fracture prediction. Therefore, we investigated whether FNW is related to hip fracture risk independently of femoral neck bone mineral density (FN-BMD), using a genetic approach. FNW was derived from points automatically placed on the proximal femur using hip DXA scans from 38 150 individuals (mean age 63.8 yr, 48.0% males) in UK Biobank (UKB). Genome-wide association study (GWAS) identified 71 independent genome-wide significant FNW SNPs, comprising genes involved in cartilage differentiation, hedgehog, skeletal development, in contrast to SNPs identified by FN-BMD GWAS which primarily comprised runx1/Wnt signaling genes (MAGMA gene set analyses). FNW and FN-BMD SNPs were used to generate genetic instruments for multivariable Mendelian randomization. Greater genetically determined FNW increased risk of all hip fractures (odds ratio [OR] 1.53; 95% CI, 1.29-1.82 per SD increase) and femoral neck fractures (OR 1.58;1.30-1.92), but not trochanteric or forearm fractures. In contrast, greater genetically determined FN-BMD decreased fracture risk at all 4 sites. FNW and FN-BMD SNPs were also used to generate genetic risk scores (GRSs), which were examined in relation to incident hip fracture in UKB (excluding the FNW GWAS population; n = 338 742, 3222 cases) using a Cox proportional hazards model. FNW GRS was associated with increased risk of all incident hip fractures (HR 1.08;1.05-1.12) and femoral neck fractures (hazard ratio [HR] 1.10;1.06-1.15), but not trochanteric fractures, whereas FN-BMD GRS was associated with reduced risk of all hip fracture types. We conclude that the underlying biology regulating FNW and FN-BMD differs, and that DXA-derived FNW is causally related to hip fractures independently of FN-BMD, adding information beyond FN-BMD for hip fracture prediction. Hence, FNW derived from DXA analyses or a FNW GRS may contribute clinically useful information beyond FN-BMD for hip fracture prediction.
股骨颈宽度(FNW)源自 DXA 扫描,可能为髋部骨折预测提供有用的补充。因此,我们采用遗传方法研究了 FNW 是否独立于股骨颈骨密度(FN-BMD)与髋部骨折风险相关。FNW 源自 UK Biobank(UKB)中 38150 名个体(平均年龄 63.8 岁,48.0%为男性)髋关节 DXA 扫描上自动放置的近端股骨点。全基因组关联研究(GWAS)确定了 71 个独立的全基因组显著 FNW SNPs,包括参与软骨分化、 hedgehog、骨骼发育的基因,而 FN-BMD GWAS 中确定的 SNPs 主要包括 runt1/Wnt 信号基因(MAGMA 基因集分析)。FNW 和 FN-BMD SNPs 用于生成多变量 Mendelian 随机化的遗传工具。更大程度上由遗传决定的 FNW 增加了所有髋部骨折(比值比 [OR] 1.53;95%CI,每增加 1 个标准差为 1.29-1.82)和股骨颈骨折(OR 1.58;1.30-1.92)的风险,但不增加转子间或前臂骨折的风险。相比之下,更大程度上由遗传决定的 FN-BMD 降低了所有 4 个部位的骨折风险。FNW 和 FN-BMD SNPs 也用于生成遗传风险评分(GRS),并使用 Cox 比例风险模型在 UKB 中(排除 FNW GWAS 人群;n=338742,3222 例)与新发髋部骨折相关进行了检查。FNW GRS 与所有新发髋部骨折(HR 1.08;1.05-1.12)和股骨颈骨折(风险比 [HR] 1.10;1.06-1.15)的风险增加相关,但不与转子间骨折相关,而 FN-BMD GRS 与所有髋部骨折类型的风险降低相关。我们的结论是,调节 FNW 和 FN-BMD 的潜在生物学机制不同,并且源自 DXA 的 FNW 与髋部骨折独立于 FN-BMD 相关,为髋部骨折预测提供了 FN-BMD 以外的信息。因此,源自 DXA 分析的 FNW 或 FNW GRS 可能为髋部骨折预测提供 FN-BMD 以外的临床有用信息。