Xuan Chao, Liu Ru-Hua, Zhao Cong, Li Jing, Zhou Ting-Ting, Tian Qing-Wu, He Guo-Wei
Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, No. 1677, Wutai Mountain Road, Qingdao 266500, China.
Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, China.
Ther Adv Chronic Dis. 2024 Oct 18;15:20406223241290411. doi: 10.1177/20406223241290411. eCollection 2024.
The association between pyridoxal 5'-phosphate (PLP) and cardiovascular disease (CVD) remains a topic of discussion.
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.
A population-based cohort study.
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.
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.
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.
5'-磷酸吡哆醛(PLP)与心血管疾病(CVD)之间的关联仍是一个讨论话题。
本研究旨在探讨美国人群血清PLP水平与全因死亡率、心血管死亡率及CVD风险之间的关系。
一项基于人群的队列研究。
本研究分析了来自美国国家健康与营养检查调查的数据。使用加权Cox比例风险回归模型计算调整后的风险比(HRs)及其相应的95%置信区间(CIs),以评估与全因和心血管死亡率相关的风险。采用加权二元逻辑回归评估血清PLP水平与CVD风险之间的关系。使用多变量调整的受限立方样条评估非线性关联。
在平均11.36年的随访期内,有2546例全因死亡病例和867例心血管死亡病例。在完全调整模型中,血清PLP水平对应于四分位间距增加时,与全因死亡率相关的调整后HRs及95% CIs分别为0.83(0.74 - 0.93)、0.71(0.63 - 0.80)和0.64(0.56 - 0.74)。同样,随着血清PLP水平每增加一个四分位,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)。较高的血清PLP水平可降低CVD风险(优势比:0.87,95% CI:0.79 - 0.96)。血清PLP水平与全因死亡率、心血管死亡率及CVD风险呈非线性关系。
本研究结果提供了证据,表明血清PLP是美国成年人全因死亡率、心血管死亡率及CVD的保护因素,且存在剂量反应关系。