Kjeldsen Sverre E, Berge Eivind, Bangalore Sripal, Messerli Franz H, Mancia Giuseppe, Holzhauer Björn, Hua Tsushung A, Zappe Dion, Zanchetti Alberto, Weber Michael A, Julius Stevo
a University of Oslo, Ullevaal Hospital , Oslo , Norway.
b University of Michigan Medical Center , Ann Arbor , MI , USA.
Blood Press. 2016;25(2):83-92. doi: 10.3109/08037051.2015.1106750. Epub 2015 Oct 29.
Previous studies have debated the notion that low blood pressure (BP) during treatment, particularly diastolic (DBP), is associated with increased risk of cardiovascular disease. We evaluated the impact of low BP on cardiovascular outcomes in a high-risk population of 15,244 hypertensive patients, almost half of whom had a history of coronary artery disease (CAD). In the prospective Valsartan Antihypertensive Long-term Use Evaluation (VALUE) trial, patients were randomized to valsartan or amlodipine regimens and followed for 4.2 years (mean) with no difference in the primary cardiovascular endpoint. A Cox proportional hazards model was used to evaluate the relationship between average on-treatment BP and clinical outcomes. The relationship between BP and cardiovascular events was adjusted for age, gender and body mass index, and baseline qualifying risk factors and diseases (smoking, high total cholesterol, diabetes mellitus, proteinuria, CAD, previous stroke and left ventricular hypertrophy). DBP ≥ 90 mmHg, compared with < 90 mmHg, was associated with increased incidence of the primary cardiovascular endpoint (all cardiac events); however, DBP < 70 mmHg, compared with ≥ 70 mmHg, was not associated with increased incidence after covariate adjustment (no J-shaped curve). Similar results were observed for death, myocardial infarction (MI), heart failure and stroke, considered separately. Nadir for MI was at DBP of 76 mmHg and for stroke 60 mmHg. The ratio of MI to stroke increased with lower DBP. In CAD patients the MI to stroke ratio was more pronounced than in patients without CAD but there was no significant J-curve in either group. Systolic BP ≥ 150 but not < 130 mmHg, compared with 130-149 mmHg, similarly was associated with increased risk for primary outcome. In conclusion, patients in BP strata ≥ 150/90 mmHg, but not patients in BP strata < 130/70 mmHg, were at increased risk for adverse outcomes in this hypertensive, high-risk population. Although benefit in preventing MI in relation to preventing stroke levels off for the lowest BPs, these data provide no support for a J-curve in the treatment of high-risk hypertensive patients . The increase in the ratio of MI to stroke with lower DBP indicates target organ heterogeneity in that the optimal on-treatment DBP for cerebroprotection is below that for cardioprotection.
既往研究对治疗期间低血压(BP),尤其是舒张压(DBP)与心血管疾病风险增加相关这一观点存在争议。我们评估了低血压对15244例高危高血压患者心血管结局的影响,其中近一半患者有冠状动脉疾病(CAD)病史。在缬沙坦抗高血压长期应用评估(VALUE)前瞻性试验中,患者被随机分配至缬沙坦或氨氯地平治疗方案,并随访4.2年(平均),主要心血管终点无差异。采用Cox比例风险模型评估治疗期间平均血压与临床结局之间的关系。血压与心血管事件之间的关系根据年龄、性别、体重指数以及基线合格风险因素和疾病(吸烟、高总胆固醇、糖尿病、蛋白尿、CAD、既往中风和左心室肥厚)进行了调整。与舒张压<90mmHg相比,舒张压≥90mmHg与主要心血管终点(所有心脏事件)的发生率增加相关;然而,经协变量调整后,与舒张压≥70mmHg相比,舒张压<70mmHg与发生率增加无关(无J形曲线)。分别考虑死亡、心肌梗死(MI)、心力衰竭和中风时,观察到类似结果。MI的最低点是舒张压76mmHg,中风是60mmHg。MI与中风的比例随舒张压降低而增加。在CAD患者中,MI与中风的比例比无CAD患者更明显,但两组均无显著的J形曲线。与130 - 149mmHg相比,收缩压≥150mmHg而非<130mmHg同样与主要结局风险增加相关。总之,在这一高血压高危人群中,血压≥150/90mmHg的患者不良结局风险增加,而血压<130/70mmHg的患者则不然。尽管在预防MI方面相对于预防中风的益处对于最低血压水平趋于平稳,但这些数据不支持在治疗高危高血压患者时存在J形曲线。随着舒张压降低MI与中风比例增加表明靶器官存在异质性,即脑保护的最佳治疗舒张压低于心脏保护的最佳治疗舒张压。