Hongcun Sun, Jiandao Hu, Aijuan Qian, Wenbo Jiang
This study aimed to investigate the association between sedentary behavior and complex multimorbidity among American adults, verify the mediating role of the high-sensitivity C-reactive protein/high-density lipoprotein cholesterol (hs-CRP/HDL-C) ratio in this relationship, and provide a theoretical basis for the prevention and control of chronic diseases. A total of 8246 adults aged ≥20 years from the National Health and Nutrition Examination Survey 2015 to 2020 were enrolled as study participants. Sedentary time was collected via questionnaire surveys, while hs-CRP and HDL-C levels were obtained through laboratory tests. Complex multimorbidity (defined as the coexistence of ≥3 chronic diseases) was determined based on clinical diagnoses. Logistic regression analysis was used to examine the association between sedentary behavior and complex multimorbidity. A mediation effect model was applied to quantify the mediating effect of the hs-CRP/HDL-C ratio, and subgroup analyses were conducted to explore population heterogeneity. The prevalence of complex multimorbidity in the study population was 25.72%, with a mean daily sedentary time of 5.87 hours. After adjusting for potential confounding factors, each 1-hour increase in daily sedentary time was associated with a 3.46% higher risk of complex multimorbidity (odds ratio = 1.03, 95% confidence interval: 1.02-1.05, P < .001). Restricted cubic spline analysis revealed a linear association between sedentary time and complex multimorbidity. Mediation effect analysis indicated that the hs-CRP/HDL-C ratio exerted a partial mediating effect on the association, accounting for 5.17% of the total effect (95% confidence interval: 0.0001-0.0004, P < .001). Subgroup analyses demonstrated that this mediating effect was more pronounced in individuals aged 45 to 64 years and in males, with mediating proportions of 2.67% and 5.86%, respectively (both P < .05). Sedentary behavior may be positively associated with the risk of complex multimorbidity among American adults, and the hs-CRP/HDL-C ratio partially explain this association.