成人血清 5'- 磷酸吡哆醛水平与全因死亡率、心血管死亡率和心血管疾病之间的关系:一项基于人群的队列研究。

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Chronic Disease Pub Date : 2024-10-18 eCollection Date: 2024-01-01 DOI:10.1177/20406223241290411
Chao Xuan, Ru-Hua Liu, Cong Zhao, Jing Li, Ting-Ting Zhou, Qing-Wu Tian, Guo-Wei He
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引用次数: 0

摘要

背景:5'- 磷酸吡哆醛(PLP)与心血管疾病(CVD)之间的关系仍是一个讨论话题:本研究旨在探讨血清PLP水平与美国人口全因死亡率、心血管死亡率和心血管疾病风险之间的关系:设计:基于人群的队列研究:本研究分析了美国国家健康与营养调查(National Health and Nutrition Examination Survey)的数据。使用加权 Cox 比例危险回归模型计算调整后的危险比 (HR) 及其相应的 95% 置信区间 (CI),以评估与全因死亡率和心血管死亡率相关的风险。加权二元逻辑回归用于评估血清 PLP 水平与心血管疾病风险之间的关系。使用多变量调整限制性立方样条对非线性关联进行了评估:在平均 11.36 年的随访期间,共有 2546 例全因死亡病例和 867 例心血管疾病死亡病例。在完全调整模型中,与血清PLP水平升高相关的全因死亡率调整HRs(95% CI)分别为0.83(0.74-0.93)、0.71(0.63-0.80)和0.64(0.56-0.74),与四分位数间范围相对应。同样,血清 PLP 水平每增加四分位数,心血管死亡率分别降低 0.78(0.62-0.97)、0.63(0.49-0.81)和 0.62(0.50-0.77)。血清 PLP 水平越高,心血管疾病风险越低(几率比:0.87,95% CI:0.79-0.96)。血清PLP水平与全因死亡率、心血管死亡率和心血管疾病风险呈非线性关系:本研究结果证明,血清 PLP 是美国成年人降低全因死亡率、心血管死亡率和心血管疾病风险的保护因素,两者之间存在剂量反应关系。
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Association between serum pyridoxal 5'-phosphate levels and all-cause, cardiovascular mortality, and cardiovascular disease in adults: a population-based cohort study.

Background: The association between pyridoxal 5'-phosphate (PLP) and cardiovascular disease (CVD) remains a topic of discussion.

Objectives: This study aimed to explore the relationship between serum PLP levels and the incidence of all-cause mortality, cardiovascular mortality, and the risk of CVD among the US population.

Design: A population-based cohort study.

Methods: This study analyzed data from the National Health and Nutrition Examination Survey. Adjusted hazard ratios (HRs) and their corresponding 95% confidence intervals (CIs) were calculated using weighted Cox proportional hazards regression models to assess the risk associated with all-cause and cardiovascular mortality. Weighted binary logistic regression was utilized to assess the relationship between serum PLP levels and the risk of CVD. Nonlinear associations were evaluated using multivariable-adjusted restricted cubic splines.

Results: There were 2546 cases of all-cause mortality and 867 cases of cardiovascular mortality over a mean follow-up of 11.36 years. In the fully adjusted model, the adjusted HRs with 95% CIs for all-cause mortality associated with increases in serum PLP levels corresponding to the interquartile ranges were 0.83 (0.74-0.93), 0.71 (0.63-0.80), and 0.64 (0.56-0.74), respectively. Similarly, cardiovascular mortality decreased by 0.78 (0.62-0.97), 0.63 (0.49-0.81), and 0.62 (0.50-0.77) with each quartile increase in serum PLP levels. Higher serum PLP levels confer protection against CVD risk (odds ratio: 0.87, 95% CI: 0.79-0.96). Serum PLP levels showed nonlinear relationships with risk of all-cause mortality, cardiovascular mortality, and CVD.

Conclusion: The results of this study provide evidence that serum PLP serves as a protective factor against all-cause mortality, cardiovascular mortality, and CVD in US adults, with dose-response relationships.

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来源期刊
Therapeutic Advances in Chronic Disease
Therapeutic Advances in Chronic Disease Medicine-Medicine (miscellaneous)
CiteScore
6.20
自引率
0.00%
发文量
108
审稿时长
12 weeks
期刊介绍: Therapeutic Advances in Chronic Disease publishes the highest quality peer-reviewed research, reviews and scholarly comment in the drug treatment of all chronic diseases. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers involved in the medical treatment of chronic disease, providing a forum in print and online for publishing the highest quality articles in this area.
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