英国一项研究表明,N端脑利钠肽前体(NT-proBNP)可改善心血管疾病风险评估,并可帮助评估特定降压方案的疗效。该研究12月9日在线发表于《高血压》(Hypertension)杂志。 研究简介 研究者进行了三个假设:(1)NT-proBNP可预测高血压患者的心血管疾病事件;(2)NT-proBNP与血压变异性有关;(3)NT-proBNP预测可从抗高血压治疗中获益; 研究者从英属斯堪的那维亚心脏终点试验(Anglo-Scandinavian Cardiac Outcomes Trial,ASCOT)研究中随机抽取一个子集。共纳入6549例无冠心病病史的高危患者,随机给予基于阿替洛尔或氨氯地平的降压治疗。在5.5年随访期间,共出现485例心血管疾病,将485例患者与1367例对照者相匹配。在基线和试验6个月时测量NT-proBNP。 研究结果: (1)NT-proBNP可在已确定预测因素基础上改善心血管疾病风险预测,净重分类改善为22.3%(P<0.0001)。 (2)收缩压SD每升高1 mmHg,基线NT-proBNP水平升高2%(P<0.0001)。 (3)然而,NT-proBNP预测心血管疾病风险独立于血压变异(OR 1.24,95% CI1.06-1.45,P=0.007)。 (4)6个月时,基于阿替洛尔的治疗使NT-proBNP升高69.6%(P<0.0001)。相比之下,基于氨氯地平的治疗使NT-proBNP降低36.5%(P<0.0001)。调整混杂因素后,与6个月时NT-proBNP不低于中位值(61 pg/mL)的氨氯地平组患者相比,NT-proBNP低于中位值者心血管疾病风险降低(OR 0.58,95% CI 0.37-0.91)。 结论:NT-proBNP可帮助改善心血管疾病风险评估,并帮助评估特定的降压方案疗效。进一步的相关研究非常必要。 原文阅读:The Value of N-Terminal Pro-B-Type Natriuretic Peptide in Determining Antihypertensive Benefit: Observations From the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT).
Abstract
We investigated 3 hypotheses: (1) N-terminal pro-B-type natriuretic peptide (NT-proBNP) predicts cardiovascular disease events in patients with hypertension, (2) NT-proBNP is associated with blood pressure variability, and (3) NT-proBNP predicts benefit from antihypertensive regimens. The Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT) randomized a subset of 6549 patients at risk with no history of coronary heart disease to either atenolol-based or amlodipine-based blood pressure-lowering treatment. During 5.5 years of follow-up, 485 cardiovascular disease cases accrued and were matched with 1367 controls. Baseline and 6-month in-trial NT-proBNP were measured. The results show that NT-proBNP improves cardiovascular disease risk prediction beyond established predictors, continuous net reclassification improvement of 22.3% (P<0.0001). Furthermore, a 1-mm Hg increase in the SD of systolic blood pressure was associated with 2% higher baseline NT-proBNP in a multivariable regression analysis (P<0.0001). However, NT-proBNP predicted cardiovascular disease risk independently of blood pressure variation (odds ratio per SD increase in log NT-proBNP 1.24; 95% confidence interval, 1.06-1.45; P=0.007). Atenolol-based treatment led to a 69.6% increase in NT-proBNP at 6 months (P<0.0001). In contrast, amlodipine-based treatment reduced NT-proBNP by 36.5% (P<0.0001). Amlodipine recipients who achieved a 6-month NT-proBNP below the median (61 pg/mL) were at lower risk of cardiovascular disease when compared with those who did not (odds ratio, 0.58; 95% confidence interval, 0.37-0.91) after adjustment for confounders inclusive of baseline NT-proBNP and achieved blood pressure. If confirmed, these novel results suggest that NT-proBNP, as well as aiding cardiovascular disease risk assessment, may also help assess the efficacy of specific antihypertensive regimens. Further relevant studies seem warranted.
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