Risk Factors for Bone Microarchitecture Impairments in Older Men With Type 2 Diabetes—The MrOS Study - Report - MDSpire

Risk Factors for Bone Microarchitecture Impairments in Older Men With Type 2 Diabetes—The MrOS Study

  • By

  • Malak Faraj

  • Ann V Schwartz

  • Andrew J Burghardt

  • Dennis Black

  • Eric Orwoll

  • Elsa S Strotmeyer

  • Eric Vittinghoff

  • Marta Fogolari

  • Silvia Angeletti

  • Giuseppe Banfi

  • Giovanni Lombardi

  • Gina Woods

  • Li-Yung Lui

  • Mary Bouxsein

  • Nicola Napoli

  • July 12, 2024

  • 0 min

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Risk Factors for Bone Microarchitecture Deficits in Elderly Men with Type 2 Diabetes

Overview

In older men, type 2 diabetes mellitus (T2DM) is associated with smaller bone size and cortical deficits, which may contribute to increased skeletal fragility. Longer diabetes duration and insulin use correlate with specific impairments in bone microarchitecture and strength, increasing fracture risk.

Background

Fragility fractures pose a significant health burden, with increased risk and mortality observed in patients with T2DM. Despite normal or elevated areal bone mineral density in T2DM, bone fragility is paradoxically increased, suggesting microarchitectural deficits. High-resolution peripheral quantitative computed tomography (HR-pQCT) allows detailed assessment of bone microarchitecture, but data in older men with T2DM remain limited. Understanding diabetes-related factors influencing bone quality is critical for fracture prevention.

Data Highlights

ParameterComparison (T2DM vs Non-T2DM)P-value
Total cross-sectional area (distal tibia)Smaller in T2DM0.028
Total cross-sectional area (diaphyseal tibia)Smaller in T2DM0.025
Cortical area (distal tibia)Smaller in T2DM0.009
Cortical area (diaphyseal tibia)Smaller in T2DM0.023
Cortical porosity (T2DM duration ≥10 years)Higher vs <10 years durationSignificant
Trabecular thickness (distal radius, T2DM duration ≥10 years)Higher vs <10 years durationSignificant
Cortical area and thickness (insulin use)Lower at distal radius and diaphyseal tibiaSignificant
Failure load (insulin use)Lower at all 3 scan sitesSignificant

Key Findings

  • Older men with T2DM have significantly smaller total cross-sectional and cortical areas at the distal and diaphyseal tibia compared to non-diabetic men.
  • Trabecular bone indices and cortical porosity do not differ significantly between T2DM and non-T2DM groups overall.
  • Among men with T2DM, diabetes duration ≥10 years is associated with increased cortical porosity and greater trabecular thickness at the distal radius.
  • Insulin use in T2DM men correlates with reduced cortical area and thickness and decreased failure load, indicating compromised bone strength.
  • Lower cortical area, thickness, bone mineral density, and failure load at distal sites are linked to higher risk of incident nonvertebral fractures in T2DM men.

Clinical Implications

Clinicians should recognize that older men with T2DM may have smaller bone size and cortical deficits contributing to fracture risk despite normal bone density measurements. Longer diabetes duration and insulin therapy are important factors associated with bone microarchitectural deterioration and reduced bone strength. These findings highlight the need for targeted fracture risk assessment and prevention strategies in this population.

Conclusion

In elderly men, T2DM is associated with specific deficits in bone size and cortical microarchitecture that likely contribute to increased skeletal fragility. Diabetes duration and insulin use further exacerbate these bone quality impairments, underscoring the importance of comprehensive bone health evaluation in this group.

References

  1. MrOS Study Group 2024 -- Identifying Risk Factors for Bone Microarchitecture Deficiencies in Elderly Males with Type 2 Diabetes

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