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胆钙化醇治疗对单纯收缩期高血压老年患者的血压影响:VitDISH 随机对照试验。

Cholecalciferol treatment to reduce blood pressure in older patients with isolated systolic hypertension: the VitDISH randomized controlled trial.

出版信息

JAMA Intern Med. 2013 Oct 14;173(18):1672-9. doi: 10.1001/jamainternmed.2013.9043.

Abstract

IMPORTANCE

Observational data link low 25-hydroxyvitamin D levels to both prevalent blood pressure and incident hypertension. No clinical trial has yet examined the effect of vitamin D supplementation in isolated systolic hypertension, the most common pattern of hypertension in older people.

OBJECTIVE

To test whether high-dose, intermittent cholecalciferol supplementation lowers blood pressure in older patients with isolated systolic hypertension.

DESIGN

Parallel group, double-blind, placebo-controlled randomized trial.

SETTING

Primary care clinics and hospital clinics.

PARTICIPANTS

Patients 70 years and older with isolated systolic hypertension (supine systolic blood pressure >140 mm Hg and supine diastolic blood pressure <90 mm Hg) and baseline 25-hydroxyvitamin D levels less than 30 ng/mL were randomized into the trial from June 1, 2009, through May 31, 2011.

INTERVENTIONS

A total of 100,000 U of oral cholecalciferol or matching placebo every 3 months for 1 year.

MAIN OUTCOMES AND MEASURES

Difference in office blood pressure, 24-hour blood pressure, arterial stiffness, endothelial function, cholesterol level, insulin resistance, and b-type natriuretic peptide level during 12 months.

RESULTS

A total of 159 participants were randomized (mean age, 77 years). Mean baseline office systolic blood pressure was 163/78 mm Hg. Mean baseline 25-hydroxyvitamin D level was 18 ng/mL. 25-Hydroxyvitamin D levels increased in the treatment group compared with the placebo group (+8 ng/mL at 1 year, P < .001). No significant treatment effect was seen for mean (95% CI) office blood pressure (−1 [−6 to 4]/−2 [−4 to 1] mm Hg at 3 months and 1 [−2 to 4]/0 [−2 to 2] mm Hg overall treatment effect). No significant treatment effect was evident for any of the secondary outcomes (24-hour blood pressure, arterial stiffness, endothelial function, cholesterol level, glucose level, and walking distance). There was no excess of adverse events in the treatment group, and the total number of falls was nonsignificantly lower in the group receiving vitamin D (36 vs 46, P = .24).

CONCLUSIONS AND RELEVANCE

Vitamin D supplementation did not improve blood pressure or markers of vascular health in older patients with isolated systolic hypertension.

TRIAL REGISTRATION

isrctn.org Identifier: ISRCTN92186858.

摘要

重要性

观察性数据表明,25-羟维生素 D 水平较低与普遍的血压升高和高血压的发生有关。尚未有临床试验研究维生素 D 补充剂对老年人中最常见的单纯收缩期高血压的影响。

目的

检测大剂量、间歇性胆钙化醇补充剂是否能降低单纯收缩期高血压老年患者的血压。

设计

平行组、双盲、安慰剂对照随机试验。

地点

初级保健诊所和医院诊所。

参与者

2009 年 6 月 1 日至 2011 年 5 月 31 日,患有单纯收缩期高血压(仰卧位收缩压>140mmHg,仰卧位舒张压<90mmHg)和基线 25-羟维生素 D 水平<30ng/mL 的 70 岁及以上患者随机入组。

干预

口服胆钙化醇 100000U 或匹配的安慰剂,每 3 个月一次,共 1 年。

主要结局和测量指标

12 个月期间办公室血压、24 小时血压、动脉僵硬、内皮功能、胆固醇水平、胰岛素抵抗和 B 型利钠肽水平的差异。

结果

共 159 名参与者被随机分配(平均年龄 77 岁)。平均基线办公室收缩压为 163/78mmHg。平均基线 25-羟维生素 D 水平为 18ng/mL。与安慰剂组相比,治疗组 25-羟维生素 D 水平升高(1 年时升高 8ng/mL,P<.001)。在平均(95%CI)办公室血压方面,未见治疗效果显著(3 个月时为-1[-6 至 4]/-2[-4 至 1]mmHg,总体治疗效果为 1[-2 至 4]/0[-2 至 2]mmHg)。在任何次要结局方面,未见明显的治疗效果(24 小时血压、动脉僵硬、内皮功能、胆固醇水平、血糖水平和步行距离)。治疗组不良事件无增加,接受维生素 D 治疗组的总跌倒次数无显著降低(36 次比 46 次,P=0.24)。

结论和相关性

维生素 D 补充剂不能改善单纯收缩期高血压老年患者的血压或血管健康标志物。

试验注册

isrctn.org 标识符:ISRCTN92186858。

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