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一项关于青少年血压轨迹与变异性及随后靶器官损害之间关联的队列研究

[A cohort study on the association between blood pressure trajectories and variability in adolescence and subsequent target organ damage].

作者信息

Guo T S, Sun Y, Wang D, Hu G L, Jia H, Du M F, Mu J J

机构信息

Department of Cardiology, First Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an710061, China.

出版信息

Zhonghua Xin Xue Guan Bing Za Zhi. 2025 Jan 24;53(1):28-36. doi: 10.3760/cma.j.cn112148-20241018-00627.

Abstract

To investigate the relationship between blood pressure trajectories and blood pressure variability with the risk of target organ damage in Chinese population from childhood to middle age. This study is a population-based, long-term follow-up cohort study. Participants who had their blood pressure measured at least 5 times in the Hanzhong Adolescent hypertension cohort from 1987 to 2023 were included in this study. Group-based trajectory modeling was used to identify different systolic and diastolic blood pressure trajectories, and the subjects were divided into low-increasing group, moderate-increasing group and high-increasing group according to blood pressure trajectories. Blood pressure variability was assessed using standard deviation (SD), variability independent of the mean (VIM), and average real variability (ARV). Target organ damage was evaluated during the final follow-up in 2023 (middle age). Logistic regression models were used to analyze the relationship between blood pressure trajectories and blood pressure variability with the risk of target organ damage. A total of 2 447 subjects were included, with a median age of 48 years, of whom 1 373 were male (56.1%). Based on systolic blood pressure, 868 were in the low-increasing group, 1 238 in the moderate-increasing group, and 341 in the high-increasing group. For diastolic blood pressure, the distribution was 894, 1 263 and 290, respectively. Compared with the low-increasing group of systolic blood pressure, the moderate-increasing group (arteriosclerosis: =4.14, 95% 2.96-5.79; proteinuria: =2.06, 95% 1.38-3.07; left ventricular hypertrophy: =1.68, 95% 1.00-2.82) and high-increasing group (arterial stiffness: =15.44, 95% 10.14-23.50; proteinuria: =5.80, 95% 3.63-9.29; left ventricular hypertrophy: =2.93, 95% 1.55-5.53) had a higher risk of target organ damage (all <0.005). The moderate-increasing group of diastolic blood pressure had a higher incidence of arterial stiffness (=3.72, 95% 2.69-5.12) and proteinuria (=1.67, 95% 1.15-2.42) than the low-increasing group (all <0.005), while the high-increasing group had a significantly higher risk of all type of target organ damage compared to the low-increasing group (arterial stiffness: =10.84, 95% 7.08-16.61; proteinuria: =3.72, 95% 2.31-5.99; left ventricular hypertrophy: =2.38, 95% 1.23-4.59; all <0.005). Additionally, higher systolic blood pressure variability was associated with an increased incidence of arterial stiffness (SD: R=2.25, 95% 1.96-2.57; VIM: =1.64, 95% 1.45-1.86; ARV: =1.70, 95% 1.50-1.93) and proteinuria (SD: =1.65, 95% 1.44-1.89; VIM: =1.41, 95% 1.22-1.63; ARV: =1.45, 95% 1.26-1.67; all <0.005). The results for diastolic blood pressure variability indicators were similar to those for systolic blood pressure. Early-life blood pressure trajectories are predictive of target organ damage risk in middle age. Higher blood pressure variability is related to an increased risk of arterial stiffness and proteinuria, but was less associated with left ventricular hypertrophy. Focusing on the risk of high blood pressure early in life can help prevent the occurrence of target organ damage in middle age.

摘要

旨在研究中国人群从童年到中年期间血压轨迹和血压变异性与靶器官损害风险之间的关系。本研究是一项基于人群的长期随访队列研究。本研究纳入了在1987年至2023年汉中青少年高血压队列中至少测量过5次血压的参与者。采用基于群组的轨迹模型来识别不同的收缩压和舒张压轨迹,并根据血压轨迹将受试者分为低增长组、中度增长组和高增长组。使用标准差(SD)、独立于均值的变异性(VIM)和平均实际变异性(ARV)来评估血压变异性。在2023年(中年)的最终随访期间评估靶器官损害。采用逻辑回归模型分析血压轨迹和血压变异性与靶器官损害风险之间的关系。共纳入2447名受试者,中位年龄为48岁,其中1373名男性(56.1%)。基于收缩压,低增长组有868人,中度增长组有1238人,高增长组有341人。舒张压方面,分布分别为894人、1263人和290人。与收缩压低增长组相比,中度增长组(动脉硬化:=4.14,95% 2.96 - 5.79;蛋白尿:=2.06,95% 1.38 - 3.07;左心室肥厚:=1.68,95% 1.00 - 2.82)和高增长组(动脉僵硬度:=15.44,95% 10.14 - 23.50;蛋白尿:=5.80,95% 3.63 - 9.29;左心室肥厚:=2.93,95% 1.55 - 5.53)发生靶器官损害的风险更高(均<0.005)。舒张压中度增长组的动脉僵硬度(=3.72,95% 2.69 - 5.12)和蛋白尿(=1.67,95% 1.15 - 2.42)发生率高于低增长组(均<0.005),而高增长组与低增长组相比,所有类型靶器官损害的风险均显著更高(动脉僵硬度:=10.84,95% 7.08 - 16.61;蛋白尿:=3.72,95% 2.31 - 5.99;左心室肥厚:=2.38,95% 1.23 - 4.59;均<0.005)。此外,较高的收缩压变异性与动脉僵硬度发生率增加相关(SD:R = 2.25,95% 1.96 - 2.57;VIM:=1.64,95% 1.45 - 1.86;ARV:=1.70,95% 1.50 - 1.93)和蛋白尿(SD:=1.65,95% 1.44 - 1.89;VIM:=1.41,95% 1.22 - 1.63;ARV:=1.45,95% 1.26 - 1.67;均<0.005)。舒张压变异性指标的结果与收缩压相似。生命早期的血压轨迹可预测中年时靶器官损害的风险。较高的血压变异性与动脉僵硬度和蛋白尿风险增加相关,但与左心室肥厚的相关性较小。关注生命早期的高血压风险有助于预防中年时靶器官损害的发生。

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