ArticleIrish journal of medical science2026
The association between the estimated small dense low-density lipoprotein cholesterol and multimorbidity: a national longitudinal study.
Article in Irish journal of medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
objectiveTo investigate the relationship between E-sdLDL-C and the risk of multimorbidity and to explore whether E-sdLDL-C is a stronger predictor of multimorbidity than the traditional lipid profiles.
methodsThis study included 10,763 participants in the cross-sectional analysis and 7,321 in the longitudinal analysis from the China Health and Retirement Longitudinal Study, all of whom were aged over 45 years. E-sdLDL-C was calculated using the formula: E-sdLDL-C (mg/dL) = LDL-C -(1.43 × LDL-C -(0.14 × (ln (TG) × LDL-C)) - 8.99). Multimorbidity was defined as the coexistence of at least two chronic diseases. Logistic regression and Cox proportional hazards models were used to evaluate the cross-sectional and longitudinal relationships between E-sdLDL-C and traditional lipid profiles and multimorbidity, respectively. Additionally, cumulative E-sdLDL-C (CumE-sdLDL-C) exposure was analyzed to assess its long-term impact on multimorbidity development.
resultsCompared to individuals with lower E-sdLDL-C levels, those with higher E-sdLDL-C levels had a significantly increased risk of multimorbidity in both cross-sectional (odds ratio [OR] 1.223, 95% confidence interval [CI] 1.095-1.366) and cohort analyses (hazard ratio [HR] 1.278, 95% CI 1.163-1.404). Discordantly high E‑sdLDL‑C had a higher risk of multimorbidity in discordance analyses with triglycerides (HR 1.251, 95% CI 1.094-1.429) as compared with the respective concordantly low groups. Furthermore, higher CumE-sdLDL-C exposure was associated with an increased risk of incident multimorbidity (HR 1.335, 95% CI 1.098-1.623).
conclusionsElevated E-sdLDL-C levels were associated with an increased risk of multimorbidity in middle‑aged and older adults, both at baseline and over time.
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