Cross-sectional and longitudinal associations between serum vitamin D and continuous metabolic syndrome score among children and adolescents: roles of levels of inflammation in peripheral blood.

IF 3.9 2区 医学 Q2 NUTRITION & DIETETICS Nutrition & Metabolism Pub Date : 2025-01-17 DOI:10.1186/s12986-024-00893-x
Yanyan Li, Zhuang Ma, Yan Li, Ting Xiong, Ziyang Zhang, Bingxuan Kong, Wenlong Lu, Xiu Zhao, Rongfei Zheng, Yuhan Tang, Ping Yao, Zhe Su, Yuanjue Wu, Jingfan Xiong
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Abstract

Background: Serum vitamin D deficiency is intricately linked to metabolic disorders, however, evidence on its association with continuous metabolic risk in children and adolescents remains insufficient. This study aims to elucidate the relationship between serum vitamin D levels and continuous metabolic risk.

Methods: The cross-sectional analysis involved 4490 participants aged 6 ~ 18, and the longitudinal investigation included 1398 individuals aged 6 ~ 12 years. Serum 25(OH)D concentrations were quantified using liquid chromatography-mass spectrometry. Continuous Metabolic syndrome risk score (CMSRS), incorporating waist, blood pressure, blood lipid levels, and glucose metabolism as four components, utilizes age- and gender-specific Z scores to evaluate metabolic risk. Restricted cubic splines (RCS) were used to visualize dose-response relationships and generalized linear models (GLM) were used to estimate potential associations. Mediation analysis was used to evaluate the mediating role of levels of Neutrophil-to-lymphocyte ratio (NLR).

Results: The RCS indicated a negative linear association between serum 25(OH)D levels and CMSRS (P-overall = 0.0066, P-nonlinear = 0.1393). GLM revealed that compared to Q1, with the quartiles of serum 25(OH)D concentrations increase, the β value ranged from 0.028 (95% CI: - 0.093, 0.037) to 0.001(95%CI: - 0.067, 0.069), and then to -0.074 (95%CI: -0.146, -0.003, P for trend = 0.0659). For every 10 ng/mL increase in serum 25(OH)D concentration corresponded to the β value change -0.058 (95%CI: -0.098, -0.017). This association was more pronounced in younger or overweight/obese individuals. Furthermore, in the longitudinal study, as the baseline quartile of serum 25(OH)D concentration increased, the estimated change of subsequent CMSRS indicated a decreasing trend, ranging from -0.085 (95%CI: -0.203, 0.032) to -0.166 (95%CI: - 0.285, - 0.046), and then to - 0.174 (95%CI: - 0.296, -0.053, P for trend = 0.0031). The mediating proportion of levels of NLR was 7.2%.

Conclusions: Higher serum 25(OH)D concentration is significantly associated with reduced CMSRS in children and adolescents, and adequate serum vitamin D levels play a prominent role in preventing long-term metabolic disorders, partly meditating by inflammation in peripheral blood.

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儿童和青少年血清维生素D与持续代谢综合征评分之间的横断面和纵向关联:外周血炎症水平的作用
背景:血清维生素D缺乏与代谢紊乱有着错综复杂的联系,然而,关于其与儿童和青少年持续代谢风险之间关系的证据仍然不足。本研究旨在阐明血清维生素D水平与持续代谢风险之间的关系。方法:横断面分析纳入6 ~ 18岁4490人,纵向调查纳入6 ~ 12岁1398人。采用液相色谱-质谱法测定血清25(OH)D浓度。持续代谢综合征风险评分(CMSRS)将腰围、血压、血脂水平和葡萄糖代谢作为四个组成部分,利用年龄和性别特异性Z评分来评估代谢风险。限制三次样条(RCS)用于可视化剂量-反应关系,广义线性模型(GLM)用于估计潜在的关联。采用中介分析评价中性粒细胞与淋巴细胞比值(NLR)水平的中介作用。结果:RCS显示血清25(OH)D水平与CMSRS呈负线性相关(P-overall = 0.0066, P-nonlinear = 0.1393)。GLM显示,与Q1相比,随着血清25(OH)D浓度的增加,β值从0.028 (95%CI: - 0.093, 0.037)到0.001(95%CI: - 0.067, 0.069),再到-0.074 (95%CI: -0.146, -0.003, P为趋势= 0.0659)。血清25(OH)D浓度每增加10 ng/mL, β值变化对应于-0.058 (95%CI: -0.098, -0.017)。这种关联在年轻人或超重/肥胖人群中更为明显。此外,在纵向研究中,随着血清25(OH)D浓度基线四分位数的增加,随后CMSRS的估计变化呈下降趋势,范围从-0.085 (95%CI: -0.203, 0.032)到-0.166 (95%CI: - 0.285, - 0.046),再到- 0.174 (95%CI: - 0.296, -0.053, P为趋势= 0.0031)。NLR水平的中介比例为7.2%。结论:较高的血清25(OH)D浓度与儿童和青少年CMSRS降低显著相关,充足的血清维生素D水平在预防长期代谢性疾病中发挥重要作用,部分原因是外周血炎症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nutrition & Metabolism
Nutrition & Metabolism 医学-营养学
CiteScore
8.40
自引率
0.00%
发文量
78
审稿时长
4-8 weeks
期刊介绍: Nutrition & Metabolism publishes studies with a clear focus on nutrition and metabolism with applications ranging from nutrition needs, exercise physiology, clinical and population studies, as well as the underlying mechanisms in these aspects. The areas of interest for Nutrition & Metabolism encompass studies in molecular nutrition in the context of obesity, diabetes, lipedemias, metabolic syndrome and exercise physiology. Manuscripts related to molecular, cellular and human metabolism, nutrient sensing and nutrient–gene interactions are also in interest, as are submissions that have employed new and innovative strategies like metabolomics/lipidomics or other omic-based biomarkers to predict nutritional status and metabolic diseases. Key areas we wish to encourage submissions from include: -how diet and specific nutrients interact with genes, proteins or metabolites to influence metabolic phenotypes and disease outcomes; -the role of epigenetic factors and the microbiome in the pathogenesis of metabolic diseases and their influence on metabolic responses to diet and food components; -how diet and other environmental factors affect epigenetics and microbiota; the extent to which genetic and nongenetic factors modify personal metabolic responses to diet and food compositions and the mechanisms involved; -how specific biologic networks and nutrient sensing mechanisms attribute to metabolic variability.
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