Bone parameters in T1D and T2D assessed by DXA and HR-pQCT-A cross-sectional study: The DIAFALL study

Nicklas Hojgaard-hessellund Rasmussen*, Jakob Dal, Annika Vestergaard Kvist, Joop P. van den Bergh, Morten Hasselstrom Jensen, Peter Vestergaard

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Introduction/aim: People with type 1 diabetes (T1D) , type 2 diabetes (T2D) have an increased risk of fractures due to skeletal fragility. We aimed to compare areal bone mineral density (aBMD), volumetric BMD (vBMD), cortical and trabecular measures , bone strength parameters in participants with diabetes vs. controls.Methods: In a cross-sectional study, we included adult participants with T1D (n = 111, MA = 52.9 years), T2D (n = 106, MA = 62.1 years) and controls (n = 328, MA = 57.7 years). The study comprised of DXA scans and HR-pQCT scans, biochemistry, handgrip strength (HGS), Timed Up and GO (TUG), vibration perception threshold (VPT), questionnaires, medical histories, alcohol use, and previous fractures. Group comparisons were performed after adjustment for sex, age, BMI, diabetes duration, HbA1c, alcohol, smoking, previous fractures, post-menopausal, HGS, TUG, and VPT.Results: We found decreased aBMD in participants with T1D at the femoral neck (p = 0.028), whereas T2D had significantly higher aBMD at peripheral sites (legs, arms, p < 0.01) vs. controls. In T1D we found higher vBMD (p < 0.001), cortical vBMD (p < 0.001), cortical area (p = 0.002) and thickness (p < 0.001), lower cortical porosity(p = 0.008), higher stiffness (p = 0.002) and failure load (p = 0.003) at radius and higher vBMD (p = 0.003), cortical vBMD(p < 0.001), bone stiffness (p = 0.023) and failure load(p = 0.044) at the tibia than controls. In T2D we found higher vBMD (p < 0.001), cortical vBMD (p < 0.001), trabecular vBMD (p < 0.001), cortical area (p < 0.001) and thickness (p < 0.001), trabecular number (p = 0.024), lower separation (p = 0.010), higher stiffness (p < 0.001) and failure load (p < 0.001) at the radius and higher total vBMD (p < 0.001), cortical vBMD (p < 0.011), trabecular vBMD (p = 0.001), cortical area (p = 0.002) and thickness (p = 0.021), lower trabecular separation (p = 0.039), higher stiffness (p < 0.001) and failure load (p = 0.034) at tibia compared with controls. Conclusion: aBMD measures were as expected lower in T1D and higher in T2D than controls. Favorable bone microarchitecture and strength parameters were seen at the tibia and radius for T1D and T2D.
Original languageEnglish
Article number116753
Number of pages10
JournalBone
Volume172
Issue number1
DOIs
Publication statusPublished - 1 Jul 2023

Keywords

  • Type 1 diabetes
  • Type 2 diabetes
  • DXA scan
  • HR-pQCT
  • Bone microarchitecture
  • QUANTITATIVE COMPUTED-TOMOGRAPHY
  • TYPE-2 DIABETES-MELLITUS
  • IN-VIVO ASSESSMENT
  • MINERAL DENSITY
  • POSTMENOPAUSAL WOMEN
  • HANDGRIP STRENGTH
  • DISTAL RADIUS
  • IMAGE QUALITY
  • FRACTURE RISK
  • MICROARCHITECTURE

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