Transition from LDL apheresis to evolocumab in heterozygous FH is equally effective in lowering LDL, without lowering HDL cholesterol

被引:14
作者
Lappegard, Knut Tore [1 ,2 ]
Enebakk, Terje [3 ]
Thunhaug, Hilde [3 ]
Hovland, Anders [1 ,2 ]
机构
[1] Nordland Hosp, Div Internal Med, Coronary Care Unit, Bodo, Norway
[2] Univ Tromso, Inst Clin Med, Tromso, Norway
[3] Nordland Hosp, Div Internal Med, Dialysis Unit, Bodo, Norway
关键词
Familial hypercholesterolemia; LDL-apheresis; PCSK9; inhibitors; FAMILIAL HYPERCHOLESTEROLEMIA; LIPOPROTEIN(A) CONCENTRATIONS; CARDIOVASCULAR EVENTS; REDUCING LIPIDS; EFFICACY; SAFETY; PCSK9; MANAGEMENT; INHIBITORS; STATEMENT;
D O I
10.1016/j.atherosclerosis.2016.06.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aims: LDL apheresis is effective in reducing low-density lipoprotein (LDL) cholesterol (LDL-C) and clinical endpoints, however, the treatment is invasive and time consuming. In the present study, we explored lipid profiles and quality of life in patients with heterozygous familial hypercholesterolemia (FH) when altering the treatment regimen from weekly LDL apheresis to bi-weekly evolocumab treatment. Methods: Three patients with FH and coronary artery disease, established in LDL apheresis for 135 +/- 13(SD) months, participated. The patients were examined with blood sampling before and after LDL apheresis (week 0), and before evolocumab administration (week 1-7), quality of life was assessed (week 1, 3, 7). Results: The historically highest, untreated LDL-C was 10.3 +/- 0.8 mmol/L, during weekly LDL apheresis, 5.5 +/- 0.9 mmol/L pre-apheresis and 1.2 +/- 0.2 mmol/L post-apheresis (p = 0.02). One week after apheresis, LDL-C was 6.1 +/- 0.7 mmol/L, after three (bi-weekly) injections of evolocumab, LDL-C was 5.0 +/- 0.7 (p < 0.001). High-density lipoprotein cholesterol (HDL-C) was reduced from 1.0 +/- 0.2 mmol/L pre- to 0.5 +/- 0.1 mmol/L post-apheresis (p = 0.03), it increased after apheresis and remained constant during evolocumab treatment. Lipoprotein(a) (Lp(a)) decreased from 484 +/- 76 mg/L pre- to 142 +/- 15 mg/L post-apheresis (p = 0.02), but increased during evolocumab treatment, with a small increase from week one to week seven (p < 0.01). There was a non-significant trend towards an increase in perceived health status (week 0; 57 +/- 21, week three; 65 +/- 9 and week seven; 77 +/- 10). Conclusions: In the current study, we demonstrate reductions in LDL-C, HDL-C, triglycerides and Lp(a) during apheresis. Switching from LDL apheresis to evolocumab maintained the LDL-lowering effect but did not decrease HDL levels. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:119 / 123
页数:5
相关论文
共 33 条
[1]   Lipoprotein(a) Levels in Familial Hypercholesterolemia An Important Predictor of Cardiovascular Disease Independent of the Type of LDL Receptor Mutation [J].
Alonso, Rodrigo .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2014, 63 (19) :1983-1989
[2]   Targeting PCSK9 for therapeutic gains: Have we addressed all the concerns? [J].
Banerjee, Yajnavalka ;
Santos, Raul D. ;
Al-Rasadi, Khalid ;
Rizzo, Manfredi .
ATHEROSCLEROSIS, 2016, 248 :62-75
[3]   A proprotein convertase subtilisin/kexin type 9 neutralizing antibody reduces serum cholesterol in mice and nonhuman primates [J].
Chan, Joyce C. Y. ;
Piper, Derek E. ;
Cao, Qiong ;
Liu, Dongming ;
King, Chadwick ;
Wang, Wei ;
Tang, Jie ;
Liu, Qiang ;
Higbee, Jared ;
Xia, Zhen ;
Di, Yongmei ;
Shetterly, Susan ;
Arimura, Ziva ;
Salomonis, Heather ;
Romanow, William G. ;
Thibault, Stephen T. ;
Zhang, Richard ;
Cao, Ping ;
Yang, Xiao-Ping ;
Yu, Timothy ;
Lu, Mei ;
Retter, Marc W. ;
Kwon, Gayle ;
Henne, Kirk ;
Pan, Oscar ;
Tsai, Mei-Mei ;
Fuchslocher, Bryna ;
Yang, Evelyn ;
Zhou, Lei ;
Lee, Ki Jeong ;
Daris, Mark ;
Sheng, Jackie ;
Wang, Yan ;
Shen, Wenyan D. ;
Yeh, Wen-Chen ;
Emery, Maurice ;
Walker, Nigel P. C. ;
Shan, Bei ;
Schwarz, Margrit ;
Jackson, Simon M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (24) :9820-9825
[4]   The Agenda for Familial Hypercholesterolemia A Scientific Statement From the American Heart Association [J].
Gidding, Samuel S. ;
Champagne, Mary Ann ;
de Ferranti, Sarah D. ;
Defesche, Joep ;
Ito, Matthew K. ;
Knowles, Joshua W. ;
McCrindle, Brian ;
Raal, Frederick ;
Rader, Daniel ;
Santos, Raul D. ;
Lopes-Virella, Maria ;
Watts, Gerald F. ;
Wierzbicki, Anthony S. .
CIRCULATION, 2015, 132 (22) :2167-2192
[5]   Reverse cholesterol transport in familial hypercholesterolemia [J].
Guerin, Maryse .
CURRENT OPINION IN LIPIDOLOGY, 2012, 23 (04) :377-385
[6]   Lipoprotein(a) metabolism: Potential sites for therapeutic targets [J].
Hoover-Plow, Jane ;
Huang, Menggui .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2013, 62 (04) :479-491
[7]   Three different LDL apheresis columns efficiently and equally reduce lipoprotein(a) concentrations in patients with familial hypercholesterolemia and small apolipoprotein(a) particles [J].
Hovland, Anders ;
Marcovina, Santica ;
Hardersen, Randolf ;
Enebakk, Terje ;
Mollnes, Tom Eirik ;
Lappegard, Knut Tore .
TRANSFUSION AND APHERESIS SCIENCE, 2012, 46 (01) :73-76
[8]  
Hovland A, 2010, J PANCREAS, V11, P467
[9]   Different Inflammatory Responses Induced by Three LDL-Lowering Apheresis Columns [J].
Hovland, Anders ;
Hardersen, Randolf ;
Sexton, Joe ;
Mollnes, Tom Eirik ;
Lappegard, Knut Tore .
JOURNAL OF CLINICAL APHERESIS, 2009, 24 (06) :247-253
[10]   Longitudinal cohort study on the effectiveness of lipid apheresis treatment to reduce high lipoprotein(a) levels and prevent major adverse coronary events [J].
Jaeger, Beate R. ;
Richter, Yvonne ;
Nagel, Dorothea ;
Heigl, Franz ;
Vogt, Anja ;
Roeseler, Eberhard ;
Parhofer, Klaus ;
Ramlow, Wolfgang ;
Koch, Michael ;
Utermann, Gerd ;
Labarrere, Carlos A. ;
Seidel, Dietrich .
NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE, 2009, 6 (03) :229-239