One year follow-up of patients with reduced left ventricular ejection fraction (LVEF) on lipoprotein apheresis

4区 医学 Q1 Medicine Atherosclerosis. Supplements Pub Date : 2019-12-01 DOI:10.1016/j.atherosclerosissup.2019.08.039
Georgiana-Aura Giurgea , Elodie Karkutli , Susanne Granegger , Robert Berent , Kurt Derfler , Helmut Sinzinger
{"title":"One year follow-up of patients with reduced left ventricular ejection fraction (LVEF) on lipoprotein apheresis","authors":"Georgiana-Aura Giurgea ,&nbsp;Elodie Karkutli ,&nbsp;Susanne Granegger ,&nbsp;Robert Berent ,&nbsp;Kurt Derfler ,&nbsp;Helmut Sinzinger","doi":"10.1016/j.atherosclerosissup.2019.08.039","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p><span>Left ventricular ejection fraction (LVEF) is a valuable measure to assess left ventricular </span>systolic function<span>. 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.</span></p><p>Patients involved in a regular LP-apheresis program are supposed to undergo a number of follow-up investigations among them myocardial scintigraphy<span> and LVEF, measured by radionuclide ventriculography.</span></p></div><div><h3>Methods</h3><p><span>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<span> 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) &lt; 30 mg/dl. As part of the usual follow-up monitoring, LVEF was determined by means of radionuclide ventriculography after application of 550 MBq </span></span><sup>99m</sup> Tc-pertechnetate.</p></div><div><h3>Results</h3><p>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 &lt; 0.001) and B: 41.9±8.4 → 46.5±6.3 %; p &lt; 0.001). The relative rise was nearly identical (group A 9.6%, in group B 9.7%).</p></div><div><h3>Conclusions</h3><p>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.</p></div>","PeriodicalId":8592,"journal":{"name":"Atherosclerosis. Supplements","volume":"40 ","pages":"Pages 44-48"},"PeriodicalIF":0.0000,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.atherosclerosissup.2019.08.039","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atherosclerosis. Supplements","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1567568819300625","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 2

Abstract

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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
左室射血分数(LVEF)降低患者脂蛋白采血1年随访。
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。
求助全文
约1分钟内获得全文 去求助
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.
期刊最新文献
Historical and pathological overview of Castleman disease. Clinical outcomes in pediatric hydrocephalus patients treated with endoscopic third ventriculostomy and choroid plexus cauterization: a systematic review and meta-analysis. Smoker characteristics and trends in tobacco smoking in Rakai, Uganda, 2010-2018. A Potential Nutritional Indicator Predictable for Stroke-Related Sarcopenia. CORRIGENDUM: Outcomes of Dilated Cardiomyopathy in Japanese Children - A Retrospective Cohort Study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1