From the Johns Hopkins University, Baltimore, MD (C.C.N., H.T.M., H.D.V., Q.N.A., J.A.C.L.).
Department of Family Medicine and Community Health, Duke University, NC (Y.Y., A.J.V.).
Hypertension. 2020 Aug;76(2):404-409. doi: 10.1161/HYPERTENSIONAHA.120.15394. Epub 2020 Jun 29.
Recent evidence links long-term (visit-to-visit) blood pressure (BP) variability to the risk of cardiovascular disease, independent of mean BP levels. Potential associations between long-term BP variability and cardiovascular disease risk may be reflected in early life course alterations in coronary artery calcium (CAC) and carotid intima-media thickness. We evaluated 2482 CARDIA study (Coronary Artery Risk Development in Young Adults) participants (mean [SD] age at the year 20 exam [2005-2006] was 45.4 [3.6] years, 43.2% men, and 41.3% black). We included participants with BP assessments across 20-years (year 0, 2, 5, 7, 10, 15, 20 exams) and carotid intima-media thickness and CAC data at the year 20 exam. BP variability was assessed using variability independent of the mean and SD. Adjusted multivariable linear or logistic regression models (as appropriate) were used to assess associations between long-term BP variability measures and carotid intima-media thickness. and CAC (ln [CAC+1] and prevalent CAC). Long-term systolic BP variability independent of the mean (per 1 SD) was positively associated with carotid intima-media thickness (β=10 μm, SE=3, =0.002). Similarly, long-term diastolic BP variability independent of the mean was associated with carotid intima-media thickness (β=10 μm, SE (3), =0.001). Long-term BP variability was not associated with either ln [CAC+1] or prevalent CAC. Long-term systolic and diastolic BP variability across early adulthood was positively associated with modest adverse midlife alterations in carotid intima-media thickness but not to CAC. Our findings provide further insights into pathophysiologic mechanisms that link long-term BP variability to cardiovascular disease.
近期证据表明,血压(BP)变异性与心血管疾病风险相关,独立于平均 BP 水平。长期 BP 变异性与心血管疾病风险之间的潜在关联可能反映在冠状动脉钙(CAC)和颈动脉内膜中层厚度的早期生命过程改变中。我们评估了 2482 名 CARDIA 研究(年轻人冠状动脉风险发展)参与者(20 检查时的平均[标准差]年龄[2005-2006]为 45.4[3.6]岁,43.2%为男性,41.3%为黑人)。我们纳入了在 20 年内进行 BP 评估(0 年、2 年、5 年、7 年、10 年、15 年和 20 年检查)且在 20 年检查时具有颈动脉内膜中层厚度和 CAC 数据的参与者。使用独立于均值和标准差的变异性评估 BP 变异性。使用适当的多变量线性或逻辑回归模型(视情况而定)评估长期 BP 变异性测量与颈动脉内膜中层厚度之间的关联。和 CAC(ln[CAC+1]和已发生 CAC)。长期收缩压变异性独立于均值(每 1 标准差)与颈动脉内膜中层厚度呈正相关(β=10 μm,SE=3,=0.002)。同样,长期舒张压变异性独立于均值与颈动脉内膜中层厚度相关(β=10 μm,SE(3),=0.001)。长期 BP 变异性与 ln[CAC+1]或已发生 CAC 无关。整个成年早期的长期收缩压和舒张压变异性与适度的中年颈动脉内膜中层厚度改变呈正相关,但与 CAC 无关。我们的研究结果为长期 BP 变异性与心血管疾病相关的病理生理机制提供了进一步的见解。