Zhang Jiajie, Jiang Hejun, Fu Guanghui, Wu Zou, Yao Yukai, Sun Jie
Department of Urology, National Children's Medical Center & Shanghai Children's Medical Center Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Front Nutr. 2024 Aug 23;11:1429123. doi: 10.3389/fnut.2024.1429123. eCollection 2024.
To examine the association of overweight/obesity and serum vitamin C (serum VC) with serum uric acid (SUA) and to assess causality using Mendelian randomization (MR).
4,772 participants from the National Health and Nutrition Examination Survey (NHANES), 2017-2018 were included in this study. Multivariate linear regression, variance inflation factor and quantile regression were used to analyze the relationships between overweight/obesity and serum VC and SUA levels. Secondly, Mendelian randomization (MR) was utilized to mitigate bias and prevent reverse causality in the observational study. Genetic variants associated with obesity ( = 13,848), vitamin C levels ( = 64,979) and serum uric acid levels ( = 343,836) were sourced from the most extensive genome-wide association studies (GWAS). The primary analytical method employed was inverse variance weighted (IVW).
Based on the observational study, BMI was positively associated with SUA (β = 0.06, 95% CI: 0.05 to 0.07, < 0.001) and serum VC was negatively associated with SUA (β = -0.14, 95% CI: -0.23 to -0.04, = 0.005). In individuals with overweight/obesity (BMI > =25), the negative effects of serum VC on SUA enhanced with increasing serum VC. High serum VC level (Q4 level, above 1.19 mg/dL) reduced SUA (β = -0.30, 95% CI: -0.47 to -0.14, < 0.001) in individuals with overweight/obesity compared to low serum VC level (Q1 level, below 0.54 mg/dL). IVW-MR analysis revealed a significant association between SUA levels and genetically elevated levels of VC (β = -0.03, 95% CI: -0.06 to -0.00, = 0.029) and obesity (β = 0.06, 95% CI: 0.04 to 0.07, < 0.001).
Cross-sectional observational analysis revealed that BMI exhibited a positive correlation with SUA levels and that serum VC was negatively correlated with SUA levels; moreover, moderate serum VC can reduce SUA, especially in individuals with overweight/obesity. There was evidence indicating a causal effect of VC and obesity on SUA. It highlights the importance of VC in the management of SUA levels, particularly in overweight/obese individuals. The findings might be helpful for the management of high SUA levels.
研究超重/肥胖及血清维生素C(血清VC)与血清尿酸(SUA)之间的关联,并使用孟德尔随机化(MR)方法评估因果关系。
本研究纳入了2017 - 2018年美国国家健康与营养检查调查(NHANES)中的4772名参与者。采用多元线性回归、方差膨胀因子和分位数回归分析超重/肥胖与血清VC及SUA水平之间的关系。其次,利用孟德尔随机化(MR)来减少观察性研究中的偏差并防止反向因果关系。与肥胖(n = 13848)、维生素C水平(n = 64979)和血清尿酸水平(n = 343836)相关的基因变异来自最广泛的全基因组关联研究(GWAS)。采用的主要分析方法是逆方差加权(IVW)。
基于观察性研究,BMI与SUA呈正相关(β = 0.06,95%CI:0.05至0.07,P < 0.001),血清VC与SUA呈负相关(β = -0.14,95%CI:-0.23至-0.04,P = 0.005)。在超重/肥胖个体(BMI≥25)中,血清VC对SUA的负面影响随血清VC水平升高而增强。与低血清VC水平(Q1水平,低于0.54mg/dL)相比,高血清VC水平(Q4水平,高于1.19mg/dL)可降低超重/肥胖个体的SUA(β = -0.30,95%CI:-0.47至-0.14,P < 0.001)。IVW - MR分析显示SUA水平与基因水平升高的VC(β = -0.03,95%CI:-0.06至-0.00,P = 0.029)和肥胖(β = 0.06,95%CI:0.04至0.07,P < 0.001)之间存在显著关联。
横断面观察性分析显示,BMI与SUA水平呈正相关,血清VC与SUA水平呈负相关;此外,中等血清VC水平可降低SUA,尤其是在超重/肥胖个体中。有证据表明VC和肥胖对SUA有因果效应。这突出了VC在管理SUA水平中的重要性,特别是在超重/肥胖个体中。这些发现可能有助于管理高SUA水平。