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

Author:

Nissen Frida Igland123,Esser Vivienne F C45,Bjørnerem Åshild1367ORCID,Hansen Ann Kristin12ORCID

Affiliation:

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

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

3. Department of Obstetrics and Gynecology, University Hospital of North Norway , Hansine Hansens veg 67, 9019 Tromsø, Norway

4. Centre for Epidemiology and Biostatistics , Melbourne School of Population and Global Health, , 207 Bouverie St, Carlton VIC 3053, Australia

5. University of Melbourne , Melbourne School of Population and Global Health, , 207 Bouverie St, Carlton VIC 3053, Australia

6. Norwegian Research Centre for Women’s Health , Oslo, , Sognsvannsveien 20, 0372 Oslo, Norway

7. University Hospital , Oslo, , Sognsvannsveien 20, 0372 Oslo, Norway

Abstract

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 (β) ranging from −.37 to .60, all p<.05). Using ICE FALCON, the cross-pair cross-trait associations attenuated toward zero after adjusting for the within-individual association (absolute values of β ranging from .05 to .31, all p<.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 (β ranging from −.23 to .34, all p<.001), and thinner trabeculae, higher trabecular number, lower trabecular separation, and higher trabecular vBMD (β ranging from −.31 to .39, all p<.05). Only cortical CSA attenuated toward zero after adjusting for the within-individual association between weight and bone microarchitecture (β = .042, p=.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.

Funder

Northern Norway Regional Health Authority

Australian Government Research Training Program

Centre of Research Excellence Grant

National Health & Medical Research Council

Publisher

Oxford University Press (OUP)

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3