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Bone Abstracts (2026) 8 OC1.1 | DOI: 10.1530/obabs.08.OC1.1

OP2026 Oral Communications Oral Communications 1: Research 1 (7 abstracts)

Trabecular bone score version 4 reduces abdominal adiposity bias compared with version 3 across type 2 diabetes status: a cross-sectional study

Claire Mennan , Diane Powell , Tracey Roberts , Julie Cole , Shu Ho & Chadi Rakieh


The Robert Jones & Agnes Hunt Orthopaedic Hospital NHS Foundation Trust, Oswestry, United Kingdom


Background: Type 2 Diabetes Mellitus (T2DM) presents a "bone paradox" where high bone mineral density (BMD) masks skeletal fragility. Trabecular bone score (TBS) assesses microarchitecture, but legacy algorithms (v3) are confounded by abdominal adiposity. This study evaluates whether TBS v4, with enhanced soft-tissue compensation, improves fracture risk assessment across T2DM status.

Methods: Logistic regression predicted major osteoporotic fractures (MOF) in patients over 50. We compared TBS v3 and v4, adjusting for age, sex, and waist-to-height ratio (WHtR). Full models integrated lumbar spine (LS) BMD and T2DM status. Predictive performance was quantified using area under the ROC curve (AUC).

Results: Despite higher BMD values at the lumbar spine and hip (P 0.001, Table 1), T2DM patients had double the hip fracture prevalence (17.1% vs 8.6%, P 0.001). In models using TBSv3, WHtR was significantly associated with fracture (P 0.029), indicating residual confounding by abdominal adiposity. This association disappeared when TBSv4 was used (P 0.239), suggesting improved soft-tissue correction. In the full model including BMD and T2DM, TBSv4 remained an independent predictor of fracture (Or 0.742, P 0.002). Adding TBSv4 to BMD modestly increased AUC from 0.646 to 0.655, although this did not reach statistical significance (P 0.192).

Table 1. Clinical characteristics by T2DM status
VariableT2DM (n158)No T2DM (n1041)p
BMI (kg/m²)30.2726.870.001
WHtR0.6370.5770.001
FN T-score–1.531.900.001
LS T-score–0.261.340.001
Hip fracture (%)17.18.60.001
Table 2. WHtR and TBS in fracture-prediction models
Model Variable OR (95% CI) p
v3 WHtR 0.118 (0.018–0.801) 0.029
TBSv3 0.668 (0.570–0.783) <0.001
v4 WHtR 0.412 (0.094–1.803) 0.239
TBSv4 0.674 (0.586–0.775) <0.001
Full TBSv4 0.742 (0.615–0.896) 0.002
LS BMD 0.829 (0.678–1.012) 0.066
T2DM 1.441 (0.961–2.160) 0.077

Conclusions: TBS v4 eliminates the abdominal adiposity bias (WHtR) seen in v3. In T2DM, where BMD is often falsely elevated, TBS v4 provides a robust, independent predictor of fracture. While overall AUC improvement was not statistically significant, the removal of soft-tissue interference makes TBS v4 more clinically reliable for metabolic bone assessment.

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