Key result
Stable-Middle TyG trajectory linked to slower annual eGFR decline vs Stable-Low in high-risk adults.
Why the study?
The association between longitudinal triglyceride-glucose index trajectories and annual eGFR decline in a high cardiovascular-risk Chinese population was unknown, particularly across sexes.
Does an intermediate or high stable TyG trajectory improve annual eGFR change in a high cardiovascular-risk Chinese cohort compared to a low stable trajectory?
Cohort (n=4,814)
Does an intermediate or high stable TyG trajectory improve annual eGFR change in a high cardiovascular-risk Chinese cohort compared to a low stable trajectory?
Mean Difference: 0.94 (95% CI 0.34–1.53)
p-value: p=0.002
In a high cardiovascular-risk cohort, an intermediate stable TyG trajectory was associated with slower short-term eGFR decline than a low stable trajectory, suggesting a non-monotonic relationship where lower TyG is not strictly better.
Intermediate stable TyG trajectory was associated with slower eGFR decline; challenges lower-is-better assumption but leaves open causal effects.
This study aimed to identify longitudinal triglyceride-glucose (TyG) index trajectories and evaluate their association with annual estimated glomerular filtration rate (eGFR) change in a high cardiovascular-risk Chinese cohort, with sex-stratified analyses. A prospective cohort analysis was conducted using data from the China PEACE Million Persons Project. The primary longitudinal analysis included 4814 participants (2233 men and 2581 women) contributing 9378 observations. TyG index trajectories were identified using finite mixture modeling. Linear mixed-effects models after multiple imputation with 20 imputed datasets were used to assess associations between trajectory groups and annual eGFR change, adjusting for demographics, blood pressure, body mass index, and baseline medication use. Three short-term stable TyG trajectories were identified: Stable-Low, Stable-Middle, and Stable-High. In the m = 20 multiple-imputation analysis, the Stable-Middle trajectory was associated with slower annual eGFR decline compared with the Stable-Low trajectory in the overall cohort (beta for group × time = 0.94; 95% CI 0.34–1.53; P = 0.002), in men (beta = 1.01; 95% CI 0.17–1.85; P = 0.019), and in women (beta = 0.87; 95% CI 0.03–1.71; P = 0.043). The Stable-High trajectory was not significantly different from the Stable-Low trajectory in either sex. In this high cardiovascular-risk cohort, an intermediate stable TyG trajectory was associated with slower short-term eGFR decline than a low stable trajectory, with broadly similar direction in both sexes. These findings support cautious trajectory-based interpretation of TyG rather than a simple lower-is-better assumption, but the short follow-up and modest trajectory separation require longer-term validation.
No takes yet. Share an insight, caveat, or question.
Mi et al. (2026) conducted a cohort in High cardiovascular risk (n=4,814). Triglyceride-glucose (TyG) index trajectories vs. Stable-Low trajectory was evaluated on Annual rate of change in estimated glomerular filtration rate (eGFR) (beta 0.94, 95% CI 0.34 to 1.53, p=0.002). A Stable-Middle triglyceride-glucose index trajectory was associated with a slower annual eGFR decline compared with a Stable-Low trajectory (beta 0.94) in adults at high cardiovascular risk.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: