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维生素 D 治疗与慢性肾脏病患者的心脏结构和功能:PRIMO 随机对照试验。

Vitamin D therapy and cardiac structure and function in patients with chronic kidney disease: the PRIMO randomized controlled trial.

机构信息

Division of Nephrology, Massachusetts General Hospital, 55 Fruit St, Boston, MA 02114, USA.

出版信息

JAMA. 2012 Feb 15;307(7):674-84. doi: 10.1001/jama.2012.120.

Abstract

CONTEXT

Vitamin D is associated with decreased cardiovascular-related morbidity and mortality, possibly by modifying cardiac structure and function, yet firm evidence for either remains lacking.

OBJECTIVE

To determine the effects of an active vitamin D compound, paricalcitol, on left ventricular mass over 48 weeks in patients with an estimated glomerular filtration rate of 15 to 60 mL/min/1.73 m(2).

DESIGN, SETTING, AND PARTICIPANTS: Multinational, double-blind, randomized placebo-controlled trial among 227 patients with chronic kidney disease, mild to moderate left ventricular hypertrophy, and preserved left ventricular ejection fraction, conducted in 11 countries from July 2008 through September 2010.

INTERVENTION

Participants were randomly assigned to receive oral paricalcitol, 2 μg/d (n =115), or matching placebo (n = 112).

MAIN OUTCOME MEASURES

Change in left ventricular mass index over 48 weeks by cardiovascular magnetic resonance imaging. Secondary end points included echocardiographic changes in left ventricular diastolic function.

RESULTS

Treatment with paricalcitol reduced parathyroid hormone levels within 4 weeks and maintained levels within the normal range throughout the study duration. At 48 weeks, the change in left ventricular mass index did not differ between treatment groups (paricalcitol group, 0.34 g/m(2.7) [95% CI, -0.14 to 0.83 g/m(2.7)] vs placebo group, -0.07 g/m(2.7) [95% CI, -0.55 to 0.42 g/m(2.7)]). Doppler measures of diastolic function including peak early diastolic lateral mitral annular tissue velocity (paricalcitol group, -0.01 cm/s [95% CI, -0.63 to 0.60 cm/s] vs placebo group, -0.30 cm/s [95% CI, -0.93 to 0.34 cm/s]) also did not differ. Episodes of hypercalcemia were more frequent in the paricalcitol group compared with the placebo group.

CONCLUSION

Forty-eight week therapy with paricalcitol did not alter left ventricular mass index or improve certain measures of diastolic dysfunction in patients with chronic kidney disease.

TRIAL REGISTRATION

clinicaltrials.gov Identifier: NCT00497146.

摘要

背景

维生素 D 与降低心血管相关发病率和死亡率有关,可能是通过改变心脏结构和功能来实现的,但仍缺乏确凿的证据。

目的

在肾小球滤过率估计值为 15 至 60ml/min/1.73m²的患者中,确定活性维生素 D 化合物帕立骨化醇对 48 周时左心室质量的影响。

设计、地点和参与者:这是一项多国、双盲、随机安慰剂对照试验,在 11 个国家进行,共纳入 227 例慢性肾脏病、轻度至中度左心室肥厚和左心室射血分数正常的患者,试验于 2008 年 7 月至 2010 年 9 月进行。

干预措施

参与者随机分为口服帕立骨化醇 2μg/d(n=115)或匹配安慰剂(n=112)组。

主要终点

48 周时通过心血管磁共振成像评估左心室质量指数的变化。次要终点包括超声心动图检查左心室舒张功能的变化。

结果

帕立骨化醇治疗在 4 周内降低甲状旁腺激素水平,并在整个研究期间将其维持在正常范围内。48 周时,治疗组间左心室质量指数的变化无差异(帕立骨化醇组为 0.34g/m²[95%CI,-0.14 至 0.83g/m²],安慰剂组为-0.07g/m²[95%CI,-0.55 至 0.42g/m²])。包括舒张早期外侧二尖瓣环组织速度峰值在内的多普勒舒张功能测量(帕立骨化醇组为-0.01cm/s[95%CI,-0.63 至 0.60cm/s],安慰剂组为-0.30cm/s[95%CI,-0.93 至 0.34cm/s])也无差异。与安慰剂组相比,帕立骨化醇组更常发生高钙血症。

结论

慢性肾脏病患者应用帕立骨化醇治疗 48 周并未改变左心室质量指数或改善某些舒张功能指标。

试验注册

clinicaltrials.gov 标识符:NCT00497146。

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