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联合利尿剂序贯肾单位阻断改善难治性高血压患者的舒张功能。

Sequential nephron blockade with combined diuretics improves diastolic function in patients with resistant hypertension.

机构信息

Centre d'Investigations Cliniques CIC1418, AP-HP, Hôpital Européen Georges Pompidou, Paris, France.

Paris Cardiovascular Research Center PARCC, INSERM, Université de Paris, Paris, France.

出版信息

ESC Heart Fail. 2020 Oct;7(5):2561-2571. doi: 10.1002/ehf2.12832. Epub 2020 Jun 29.

DOI:10.1002/ehf2.12832
PMID:32597565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7524081/
Abstract

AIMS

Hypertension is a major contributor to cardiac diastolic dysfunction. Different therapeutics strategies have been proposed to control blood pressure (BP), but their independent impact on cardiac function remains undetermined. In patients with resistant hypertension, we compared the changes in cardiac parameters between two strategies based on sequential nephron blockade (NBD) with a combination of diuretics or sequential renin-angiotensin system blockade (RASB).

METHODS AND RESULTS

After a 4-week period where all patients received Irbesartan 300 mg/day + hydrochlorothiazide 12.5 mg/day + amlodipine 5 mg/day, 140 resistant hypertension patients (54.8 ± 11.1 years, 76% men, mean duration with hypertension: 13.1 ± 10.5 years, no previous history of heart failure or current symptoms of congestive heart failure) were randomized 1:1 to the NBD regimen or to the RASB regimen at week 0 (W0, baseline). Treatment intensity was increased at week 4, 8, or 10 if home BP was ≥135/85 mmHg, by sequentially adding 25 mg spironolactone, 20-40 mg furosemide, and 5 mg amiloride (NBD group) or 5-10 mg ramipril and 5-10 mg bisoprolol (RASB group). No other antihypertensive drug was allowed during the study. BP, BNP levels, and echocardiographic parameters were assessed at weeks 0 and 12. The baseline characteristics, laboratory parameters, and plasma hormones (BNP, renin, and aldosterone) and cardiac echocardiographic parameters did not significantly differ between the NBD and the RASB groups. Over 12 weeks, BNP levels significantly decreased in NBD but increased in RASB (mean [CI 95%] change in log-transformed BNP levels: -43% [-67%; -23%] vs. +55% [46%; 62%] in NBD vs. RASB, respectively, P < 0.0001). Similarly, the proportion of patients presenting ≥2 echocardiographic criteria of diastolic dysfunction decreased between baseline and W12 from 31% to 3% in NBD but increased from 19% to 32% in RASB (P = 0.0048). As compared with RASB, NBD induced greater decrease in ambulatory systolic BP (P < 0.0001), pulse pressure (P < 0.0001), and systemic vascular resistance (P < 0.005). In multivariable linear regression analyses, NBD treatment was significantly associated with decreased BNP levels (adjusted ß: -46.41 ± 6.99, P < 0.0001) independent of age, gender, renal function, and changes in BPs or heart rate.

CONCLUSIONS

In patients with resistant hypertension, nephron blockade with a combination of diuretics significantly improves cardiac markers of diastolic dysfunction independently of BP lowering.

摘要

目的

高血压是导致心脏舒张功能障碍的主要原因。已经提出了不同的治疗策略来控制血压(BP),但它们对心脏功能的独立影响仍不确定。在耐药性高血压患者中,我们比较了基于顺行肾单位阻滞(NBD)的两种策略之间的心脏参数变化,一种是联合使用利尿剂,另一种是联合使用肾素-血管紧张素系统阻滞(RASB)。

方法和结果

在所有患者接受伊贝沙坦 300mg/天+氢氯噻嗪 12.5mg/天+氨氯地平 5mg/天 4 周后,140 例耐药性高血压患者(54.8±11.1 岁,76%为男性,高血压平均病程:13.1±10.5 年,无心力衰竭既往史或当前充血性心力衰竭症状)在第 0 周(W0,基线)按 1:1 随机分为 NBD 组或 RASB 组。如果家庭血压≥135/85mmHg,在第 4、8 或 10 周增加治疗强度,通过依次添加 25mg 螺内酯、20-40mg 呋塞米和 5mg 阿米洛利(NBD 组)或 5-10mg 雷米普利和 5-10mg 比索洛尔(RASB 组)。在研究期间不允许使用其他降压药物。在第 0 周和第 12 周评估血压(BP)、BNP 水平和超声心动图参数。NBD 和 RASB 组之间的基线特征、实验室参数和血浆激素(BNP、肾素和醛固酮)以及心脏超声心动图参数无显著差异。在 12 周内,NBD 组的 BNP 水平显著降低,而 RASB 组的 BNP 水平显著升高(log 转换 BNP 水平的平均[CI 95%]变化:-43%[-67%;-23%]vs. NBD 组与 RASB 组分别为+55%[46%;62%],P<0.0001)。同样,NBD 组从基线到 W12 时出现≥2 项舒张功能障碍超声心动图标准的患者比例从 31%降至 3%,而 RASB 组从 19%增至 32%(P=0.0048)。与 RASB 相比,NBD 可更大程度地降低动态收缩压(P<0.0001)、脉压(P<0.0001)和全身血管阻力(P<0.005)。多变量线性回归分析表明,NBD 治疗与 BNP 水平降低显著相关(调整后的β:-46.41±6.99,P<0.0001),与年龄、性别、肾功能以及血压或心率变化无关。

结论

在耐药性高血压患者中,联合使用利尿剂的肾单位阻滞可显著改善舒张功能障碍的心脏标志物,而与降压无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/7524081/26963a767ba8/EHF2-7-2561-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/7524081/e7dceacb0805/EHF2-7-2561-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/7524081/54664e2f475d/EHF2-7-2561-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/7524081/26963a767ba8/EHF2-7-2561-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/7524081/e7dceacb0805/EHF2-7-2561-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/7524081/54664e2f475d/EHF2-7-2561-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/7524081/26963a767ba8/EHF2-7-2561-g003.jpg

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