自童年开始的超长期就诊血压变化与中年血管老化的关系:一项为期 30 年的前瞻性队列研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-11-01 Epub Date: 2024-09-12 DOI:10.1097/HJH.0000000000003819
Guan-Ji Wu, Ai-Ma Si, Yang Wang, Chao Chu, Ming-Fei Du, Dan Wang, Hao Jia, Gui-Lin Hu, Ze-Jiaxin Niu, Xi Zhang, Yue Sun, Ming-Ke Chang, Teng Zhang, Zi-Yue Man, Xia Wang, Jie Ren, Fang-Yao Chen, Jian-Jun Mu
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引用次数: 0

摘要

目的:根据动脉结构和功能特性评估的血管老化是心血管预后的独立预测因素。本研究旨在探讨儿童期至中年期超长期血压变化与中年期血管老化的关系:方法:利用汉中青少年高血压研究的纵向队列数据,对 2065 名 6-18 岁的参与者进行了登记,并在 30 年内进行了 7 次随访。超长期血压变异性(BPV)定义为 30 年(7 次随访)内血压的标准差(SD)和平均实际变异性(ARV)。血管老化包括动脉僵化、颈动脉肥厚和颈动脉斑块:结果:在对人口统计学变量、临床特征和 30 年平均血压进行调整后,自童年起较高的 SDSBP、ARVSBP、SDDBP 和 ARVDBP 与中年动脉僵化显著相关。此外,较高的 SDDBP 和 ARVDBP 与中年时颈动脉肥厚和颈动脉斑块的存在也有显著关联。当我们使用从童年到中年的累积血压暴露而非平均血压作为调整因素时,结果与之相似。此外,我们还发现,儿童期至青少年期的长期血压值与颈动脉斑块的存在有显著关联,而青年期至成年期的长期血压值则与动脉僵化有关:结论:儿童期至成年期较高的血压值与中年期血管老化有关,而与平均血压或累积血压暴露无关。因此,从幼年开始的长期血压变异值可作为晚年心血管疾病(CVDs)的预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations of ultra long-term visit-to-visit blood pressure variability, since childhood with vascular aging in midlife: a 30-year prospective cohort study.

Objective: Vascular aging, as assessed by structural and functional arterial properties, is an independent predictor of cardiovascular outcomes. In this study, we aimed to investigate the associations of ultra long-term blood pressure (BP) variability from childhood to midlife with vascular aging in midlife.

Methods: Using data from the longitudinal cohort of Hanzhong Adolescent Hypertension Study, 2065 participants aged 6-18 years were enrolled and followed up with seven visits over 30 years. Ultra long-term BP variability (BPV) was defined as the standard deviation (SD) and average real variability (ARV) of BP over 30 years (seven visits). Vascular aging included arterial stiffness, carotid hypertrophy, and carotid plaque.

Results: After adjusting for demographic variables, clinical characteristics and mean BP over 30 years, higher SD SBP , ARV SBP , SD DBP and ARV DBP since childhood were significantly associated with arterial stiffness in midlife. Additionally, higher SD DBP and ARV DBP were significantly associated with carotid hypertrophy and the presence of carotid plaque in midlife. When we used cumulative exposure to BP from childhood to midlife instead of mean BP as adjustment factors, results were similar. Furthermore, we found a significant association between long-term BPV from childhood to adolescence and the presence of carotid plaque, whereas long-term BPV from youth to adulthood is associated with arterial stiffness.

Conclusion: Higher BPV from childhood to adulthood was associated with vascular aging in midlife independently of mean BP or cumulative BP exposure. Therefore, long-term BPV from an early age may serve as a predictor of cardiovascular diseases (CVDs) in later life.

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CiteScore
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