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超重个体中可溶性转铁蛋白受体浓度与心血管疾病风险的倒U型关联:一项横断面研究。

Inverted U-Shaped Association of Soluble Transferrin Receptor Concentrations with Risks of Cardiovascular Diseases in Overweight Individuals: A Cross-Sectional Study.

作者信息

Hu Xiao, Xu Jing, Gu Yang

机构信息

Department of Cardiology, The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, 223300 Huaian, Jiangsu, China.

Department of Respiratory and Critical Care Medicine, The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, 223300 Huaian, Jiangsu, China.

出版信息

Rev Cardiovasc Med. 2024 Dec 16;25(12):439. doi: 10.31083/j.rcm2512439. eCollection 2024 Dec.

Abstract

BACKGROUND

Iron metabolism may play a role in cardiovascular disease (CVD) pathogenesis. The association between iron metabolism and CVD has yet to be fully investigated. This study evaluated whether iron metabolism was associated with CVD risk and whether the body mass index (BMI) of US adults varied the association.

METHODS

A cross-sectional study was performed using the National Health and Nutrition Examination Survey (NHANES), conducted from 2017 to 2018. Generalized additive models (GAMs) and multivariable logistic regression were adopted to analyze the association between iron metabolism (serum iron (SI), serum ferritin (SF), transferrin saturation (TSAT), and soluble transferrin receptor (sTfR)) and CVD risk. Further, stratified analysis was conducted to identify patients with high CVD risk.

RESULTS

Participants with CVD tended to have significantly increased levels of sTfR ( < 0.001) and decreased levels of TSAT ( < 0.001) and SI ( < 0.001). After adjusting for confounding factors, sTfR levels had a significant positive association with CVD risk (Q1 as reference, Q4 odds ratio (OR) 2.1, 95% CI 1.54-2.87, < 0.001). Notably, the association between sTfR and CVD risk differed in the BMI subgroup ( for interaction < 0.05). We identified an inverted U-shaped relationship between sTfR and the CVD risk in the group of overweight individuals (non-linear < 0.001). When the sTfR level was below the turning point (sTfR = 5.35 mg/L), a per unit increase in the sTfR level was correlated with a 78% greater adjusted OR of CVD risk (OR, 1.78 [1.44, 2.19]).

CONCLUSIONS

Increased sTfR levels were non-linearly related to the CVD risk in the overweight population.

摘要

背景

铁代谢可能在心血管疾病(CVD)发病机制中起作用。铁代谢与CVD之间的关联尚未得到充分研究。本研究评估了铁代谢是否与CVD风险相关,以及美国成年人的体重指数(BMI)是否会改变这种关联。

方法

使用2017年至2018年进行的美国国家健康与营养检查调查(NHANES)进行了一项横断面研究。采用广义相加模型(GAMs)和多变量逻辑回归分析铁代谢(血清铁(SI)、血清铁蛋白(SF)、转铁蛋白饱和度(TSAT)和可溶性转铁蛋白受体(sTfR))与CVD风险之间的关联。此外,进行分层分析以识别CVD高风险患者。

结果

患有CVD的参与者的sTfR水平往往显著升高(<0.001),TSAT水平(<0.001)和SI水平(<0.001)降低。在调整混杂因素后,sTfR水平与CVD风险呈显著正相关(以Q1为参照,Q4的优势比(OR)为2.1,95%置信区间为1.54-2.87,<0.001)。值得注意的是,sTfR与CVD风险之间的关联在BMI亚组中有所不同(交互作用P<0.05)。我们在超重个体组中发现sTfR与CVD风险之间呈倒U形关系(非线性P<0.001)。当sTfR水平低于转折点(sTfR = 5.35 mg/L)时,sTfR水平每单位增加与CVD风险的校正OR增加78%相关(OR,1.78 [1.44,2.19])。

结论

超重人群中sTfR水平升高与CVD风险呈非线性相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eba1/11683708/1ae1b1ed60eb/2153-8174-25-12-439-g1.jpg

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