Key result
Higher TyG index is linked to ~6-fold higher odds of concurrent dyslipidemia and bone mass abnormalities.
Why the study?
Is the triglyceride-glucose (TyG) index associated with the comorbidity of bone mass abnormality and dyslipidemia?
Cross-Sectional (n=928)
Is the triglyceride-glucose (TyG) index associated with the comorbidity of bone mass abnormality and dyslipidemia?
Odds Ratio: 6.64 (95% CI 3.92–11.53)
p-value: p=<0.001
The TyG index is independently associated with the comorbidity of bone mass abnormality and dyslipidemia in a nonlinear J-shaped manner, suggesting its potential as a low-cost marker for risk stratification.
The triglyceride-glucose (TyG) index, a simple marker of insulin resistance, is widely used in metabolic research, but its association with comorbidity of bone mass abnormality and dyslipidemia remains unclear. This cross-sectional study included 928 participants. Bone mass abnormality and dyslipidemia were assessed according to standardized criteria. Multivariate logistic regression, restricted cubic spline (RCS) analysis, saturation effect analysis, receiver operating characteristic (ROC) curves, and the DeLong test were employed to evaluate the association between the TyG index and the comorbidity condition. After adjusting for confounding factors, the TyG index remained independently and significantly positively correlated with the comorbidity (OR = 6.64, 95% CI: 3.92–11.53, P < 0.001). RCS analysis revealed a nonlinear J-shaped association between the TyG index and the risk of comorbidity ( P for non-linearity<0.001), relatively lower-risk region. Saturation effect analysis suggested a possible threshold at TyG = 9.36. ROC analysis demonstrated that the TyG index had the highest observed AUC among the evaluated indices for the comorbidity (AUC = 0.732, 95% CI: 0.685–0.780) and the DeLong test confirmed that its AUC was significantly higher than that of the combined TyG-BMI index (AUC difference = 0.1703, P < 0.001). The TyG index is independently associated with comorbidity of bone mass abnormality and dyslipidemia in a nonlinear J-shaped manner. It demonstrated the highest observed AUC among the evaluated indices and may serve as a low-cost, readily available marker for population risk stratification; however, prospective validation is required before clinical screening use can be recommended, particularly in moderate-altitude populations with unique metabolic characteristics.
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Ma et al. (2026) conducted a cross-sectional in Comorbidity of bone mass abnormality and dyslipidemia (n=928). Triglyceride-glucose (TyG) index was evaluated on Comorbidity of bone mass abnormality and dyslipidemia (OR 6.64, 95% CI 3.92-11.53, p=<0.001). The triglyceride-glucose index was independently and significantly associated with the comorbidity of bone mass abnormality and dyslipidemia (OR 6.64; 95% CI 3.92-11.53; P<0.001).
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