左室射血分数(LVEF)降低患者脂蛋白采血1年随访。

4区 医学 Q1 Medicine
Georgiana-Aura Giurgea , Elodie Karkutli , Susanne Granegger , Robert Berent , Kurt Derfler , Helmut Sinzinger
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引用次数: 2

摘要

背景:左心室射血分数(LVEF)是评价左心室收缩功能的重要指标。他汀类药物降脂治疗已被证明在治疗6个月后对LVEF有影响。据报道,高剂量的他汀类药物比常规的更有效,甚至亲脂化合物和亲水化合物之间也存在差异。常规脂蛋白分离(LP-apheresis)对LVEF的影响以前很少被研究。参与常规lp分离计划的患者应进行一系列随访检查,其中包括心肌显像和LVEF,通过放射性核素心室造影测量。方法我们对18例患者在开始前和持续一年后进行了检查。13例患者(男11例,女2例,平均年龄58.3 ± 5.3岁,A组)接受稳定不变的他汀类药物治疗超过一年(阿托伐他汀40 mg,辛伐他汀40 mg,瑞舒伐他汀20 mg±依折替米贝),另外5例患者(男3例,女2例,平均年龄57.1 ± 4.6岁,B组)对他汀类药物不耐受,服用微粉非诺贝特±吸收抑制剂(胆胺)。所有患者Lp(a) < 30 mg/dl。作为常规随访监测的一部分,应用550 MBq 99m高锝酸盐后,通过放射性核素脑室造影测定LVEF。结果a组随访LVEF平均为48.7周,B组平均为51.2周。除a组1例患者(LVEF 46.8%, lp采血开始后为45.2%)外,a组12例患者(92%)和B组所有患者LVEF均显著升高(a: 42.7±8.1 → 46.5±7.5% (p < 0.001),B: 41.9±8.4 → 46.5±6.3%;p & lt; 0.001)。相对上升幅度几乎相同(A组9.6%,B组9.7%)。结论长期规律的低脂单采治疗可显著提高LVEF,与目前他汀类药物治疗无关。这意味着降低致动脉粥样硬化脂蛋白的作用是潜在的机制。一项前瞻性研究应阐明lp分离诱导LVEF改善的相对程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
One year follow-up of patients with reduced left ventricular ejection fraction (LVEF) on lipoprotein apheresis

Background

Left ventricular ejection fraction (LVEF) is a valuable measure to assess left ventricular systolic function. Lipid lowering therapy by statins has been shown to have an impact on LVEF already after a 6 months treatment. Higher doses of statins have been claimed to be more effective as compared to a conventional one and even a difference between lipophilic and hydrophilic compounds has been reported. The effect of regular lipoprotein-apheresis (LP-apheresis) on LVEF was previously poorly examined.

Patients involved in a regular LP-apheresis program are supposed to undergo a number of follow-up investigations among them myocardial scintigraphy and LVEF, measured by radionuclide ventriculography.

Methods

We examined 18 patients before initiation and after one year of ongoing LP-apheresis. 13 patients (11 males, 2 females, mean age 58.3 ± 5.3 years, groups A) were since more than a year on stable, unchanged statin treatment (atorvastatin 40 mg, simvastatin 40 mg, rosuvastatin 20 mg±ezetimibe), the other 5 patients (3 males, 2 females, mean age 57.1 ± 4.6 years, group B) were intolerant to statins being on micronized fenofibrate±resorption inhibitors (cholestyramine). All patients had a Lp(a) < 30 mg/dl. As part of the usual follow-up monitoring, LVEF was determined by means of radionuclide ventriculography after application of 550 MBq 99m Tc-pertechnetate.

Results

The follow-up LVEF was checked at a mean of 48.7 weeks in group A and 51.2 weeks in group B. Except in 1 patient (LVEF 46.8% before vs. 45.2% after LP-apheresis initiation) in group A we noted a significant increase in LVEF in 12 patients of group A (92%) and in all patients of group B. Mean LVEF increased significantly in both groups (A: 42.7±8.1 → 46.5±7.5% (p < 0.001) and B: 41.9±8.4 → 46.5±6.3 %; p < 0.001). The relative rise was nearly identical (group A 9.6%, in group B 9.7%).

Conclusions

Our findings indicate that regular long-term LP-apheresis treatment apparently increases LVEF, independently on current statin treatment. This implies a role of lowering of atherogenic lipoproteins as underlying mechanism. A prospective study should clarify the relative extent of LVEF improvement induced by LP-apheresis.

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来源期刊
Atherosclerosis. Supplements
Atherosclerosis. Supplements 医学-外周血管病
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Atherosclerosis brings together, from all sources, papers concerned with investigation on atherosclerosis, its risk factors and clinical manifestations.
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