Is There a Causal Relationship between Physical Activity and Bone Microarchitecture? A Study of Adult Female Twin Pairs

Author:

Nissen Frida Igland123ORCID,Esser Vivienne F. C.4,Bui Minh4,Li Shuai4567,Hopper John L.4,Bjørnerem Åshild138ORCID,Hansen Ann Kristin12

Affiliation:

1. Department of Clinical Medicine UiT The Arctic University of Norway Tromsø Norway

2. Department of Orthopedic Surgery University Hospital of North Norway Tromsø Norway

3. Department of Obstetrics and Gynecology University Hospital of North Norway Tromsø Norway

4. Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health University of Melbourne Melbourne VIC Australia

5. Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care University of Cambridge Cambridge UK

6. Precision Medicine, School of Clinical Sciences at Monash Health Monash University Melbourne VIC Australia

7. Murdoch Children's Research Institute, Royal Children's Hospital Melbourne VIC Australia

8. Norwegian Research Center for Women's Health, Oslo University Hospital Oslo Norway

Abstract

ABSTRACTThe reasons for the association between physical activity (PA) and bone microarchitecture traits are unclear. We examined whether these associations were consistent with causation and/or with shared familial factors using a cross‐sectional study of 47 dizygotic and 93 monozygotic female twin pairs aged 31–77 years. Images of the nondominant distal tibia were obtained using high‐resolutionperipheral quantitative computed tomography. The bone microarchitecture was assessed using StrAx1.0 software. Based on a self‐completed questionnaire, a PA index was calculated as a weighted sum of weekly hours of light (walking, light gardening), moderate (social tennis, golf, hiking), and vigorous activity (competitive active sports) = light + 2 * moderate + 3 * vigorous. We applied Inference about Causation through Examination of FAmiliaL CONfounding (ICE FALCON) to test whether cross‐pair cross‐trait associations changed after adjustment for within‐individual associations. Within‐individual distal tibia cortical cross‐sectional area (CSA) and cortical thickness were positively associated with PA (regression coefficients [β] = 0.20 and 0.22), while the porosity of the inner transitional zone was negatively associated with PA (β = −0.17), all p < 0.05. Trabecular volumetric bone mineral density (vBMD) and trabecular thickness were positively associated with PA (β = 0.13 and 0.14), and medullary CSA was negatively associated with PA (β = −0.22), all p ≤ 0.01. Cross‐pair cross‐trait associations of cortical thickness, cortical CSA, and medullary CSA with PA attenuated after adjustment for the within‐individual association (p = 0.048, p = 0.062, and p = 0.028 for changes). In conclusion, increasing PA was associated with thicker cortices, larger cortical area, lower porosity of the inner transitional zone, thicker trabeculae, and smaller medullary cavities. The attenuation of cross‐pair cross‐trait associations after accounting for the within‐individual associations was consistent with PA having a causal effect on the improved cortical and trabecular microarchitecture of adult females, in addition to shared familial factors. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Publisher

Oxford University Press (OUP)

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

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