Remnant cholesterol: an independent, dose-dependent risk factor for hyperuricemia in a normolipidemic chinese population

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Authors: Huali Xiong, Fengxun Ma
Cited by: 1
References: 59

Abstract

Backgroud: The association between remnant cholesterol (RC) and hyperuricemia (HUA) remains unclear in the general population with entirely normal lipid profiles and no prior lipid-lowering therapy. This study aimed to investigate the association between RC and HUA in a normolipidemic Chinese population. Method: We recruited 2,171 participants aged 30-79 years from Rongchang, Chongqing Municipality, southwest China, as part of the China Multi-Ethnic Cohort Study. Logistic regression, restricted cubic spline (RCS), and mediation analyses were applied to evaluate the association between RC and HUA. Furthermore, subgroup and sensitivity analyses were conducted to assess the consistency of the findings. Results: >0.05), with no evidence of a threshold. These findings remained robust in sensitivity analyses that excluded participants with hypertension, diabetes, overweight/obesity or central obesity. Subgroup analyses revealed consistent RC-HUA associations across strata of age, sex, smoking status, drinking status, hypertension status, diabetes status, overweight/obesity status, central obesity status, DASH score. Mediation analyses revealed a potential mediation effect between RC and uric acid(UA), indicating that IR may mediated 39.91% of the total association between RC and UA. Conclusion: Remnant cholesterol emerges as a fully independent, dose-dependent, and readily modifiable determinant of incident hyperuricemia in Chinese adults, which can serve as an ideal candidate for inclusion in routine metabolic panels and presenting as a hypothesis for future longitudinal research.

Fields of Study & Subjects

Gout Hyperuricemia Uric Acid Thyroid Disorders and Treatments Diet Metabolism and Disease

Publication details

Journal / source
Frontiers in Endocrinology
Publisher
Frontiers Media SA
Volume
16
Pages
1718817–1718817
Publication date
12 January 2026
Language
EN