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成年女性双胞胎对中身高、体重与胫骨远端微观结构及几何形状之间的因果关系。

Causal relationships between height and weight with distal tibia microarchitecture and geometry in adult female twin pairs.

作者信息

Nissen Frida Igland, Esser Vivienne F C, Bjørnerem Åshild, Hansen Ann Kristin

机构信息

Department of Clinical Medicine, UiT The Arctic University of Norway, Hansine Hansens veg 18, 9019 Tromsø, Norway.

Department of Orthopedic Surgery, University Hospital of North Norway, Hansine Hansens veg 67, 9019 Tromsø Norway.

出版信息

JBMR Plus. 2024 Jul 18;8(9):ziae095. doi: 10.1093/jbmrpl/ziae095. eCollection 2024 Sep.

Abstract

Higher stature and lower weight are associated with increased risk of fracture. However, the pathophysiology for the associations of height and weight with bone microarchitecture and geometry is unclear. We examined whether these associations were consistent with causation and/or with shared familial factors. In this cross-sectional study of 566 female twins aged 26-76 yr, a regression analysis for twin data, Inference about Causation by Examination of FAmilial CONfounding (ICE FALCON), was used for testing causation. The bone microarchitecture and geometry of the distal tibia was assessed using HR-pQCT and the StrAx1.0 software. Higher stature was associated with larger total bone cross-sectional area (CSA), lower total bone volumetric bone mineral density (vBMD), larger cortical CSA, thinner cortices, higher porosity of the total cortex, compact cortex, outer and inner transitional zone (TZ), lower cortical vBMD, and larger medullary CSA (regression coefficients () ranging from -.37 to .60, all <.05). Using ICE FALCON, the cross-pair cross-trait associations attenuated toward zero after adjusting for the within-individual association (absolute values of ranging from .05 to .31, all <.001). Higher weight was associated with higher total bone vBMD, larger cortical CSA and thicker cortices, lower porosity of the total cortex and inner TZ, and higher cortical vBMD ( ranging from -.23 to .34, all <.001), and thinner trabeculae, higher trabecular number, lower trabecular separation, and higher trabecular vBMD ( ranging from -.31 to .39, all <.05). Only cortical CSA attenuated toward zero after adjusting for the within-individual association between weight and bone microarchitecture (β = .042, =.046). Higher stature was associated with a weaker cortical, not trabecular bone traits, whereas higher weight was associated with stronger cortical and trabecular bone traits. The results were consistent with height having a causal effect on weaker cortical bone structure, whereas weight had a casual effect on the larger cortical CSA.

摘要

较高的身高和较低的体重与骨折风险增加相关。然而,身高和体重与骨微结构及几何形态之间关联的病理生理学尚不清楚。我们研究了这些关联是否与因果关系和/或共同的家族因素一致。在这项对566名年龄在26至76岁的女性双胞胎的横断面研究中,对双胞胎数据进行回归分析,即通过检查家族混杂因素推断因果关系(ICE FALCON)来检验因果关系。使用高分辨率外周定量CT(HR-pQCT)和StrAx1.0软件评估胫骨远端的骨微结构和几何形态。较高的身高与更大的总骨横截面积(CSA)、更低的总骨体积骨密度(vBMD)、更大的皮质CSA、更薄的皮质、总皮质、致密皮质、外层和内层过渡区(TZ)的更高孔隙率、更低的皮质vBMD以及更大的髓腔CSA相关(回归系数()范围为-.37至.60,均<.05)。使用ICE FALCON,在调整个体内关联后,跨对跨性状关联减弱至零(范围的绝对值为.05至.31,均<.001)。较高的体重与更高的总骨vBMD、更大的皮质CSA和更厚的皮质、总皮质和内层TZ的更低孔隙率以及更高的皮质vBMD相关(范围为-.23至.34,均<.001),以及更细的小梁、更高的小梁数量、更低的小梁间距和更高的小梁vBMD(范围为-.31至.39,均<.05)。在调整体重与骨微结构之间的个体内关联后,只有皮质CSA减弱至零(β = .042,P = .046)。较高的身高与较弱的皮质骨特征相关,而非小梁骨特征,而较高的体重与较强的皮质骨和小梁骨特征相关。结果表明身高对较弱的皮质骨结构有因果效应,而体重对更大的皮质CSA有因果效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d6f/11331039/3dd21a7efdeb/ziae095ga1.jpg

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