Evidence map›Paper›PMID 29909101›Full record

Observational studyJACC. Cardiovascular imaging2019

Lipoprotein Apheresis Acutely Reverses Coronary Microvascular Dysfunction in Patients With Severe Hypercholesterolemia.

Melinda D Wu, Federico Moccetti, Eran Brown, Brian P Davidson, Tamara Atkinson, J Todd Belcik, George Giraud, P Barton Duell, Sergio Fazio, Hagai Tavori and 2 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in JACC. Cardiovascular imaging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02388633 (Acute Microvascular Changes With LDL Apheresis), which is not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02388633 completednot on this map

Acute Microvascular Changes With LDL Apheresis

TypeobservationalSponsorOregon Health and Science UniversityRan2015 to 2018Enrolled8ConditionsHyperlipidemiaArmsPlasmapharesis
3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Oxidized phospholipids in cardiovascular disease.Nature reviews. Cardiology · 2024
    Review
  7. Article
  8. Influence of Atherosclerotic Risk Factors on the Effectiveness of Therapeutic Ultrasound Cavitation for Flow Augmentation.Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Contrast Ultrasound Assessment of Skeletal Muscle Recruitable Perfusion after Permanent Left Ventricular Assist Device Implantation: Implications for Functional Recovery.Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography · 2022
    Article
  15. Review
  16. Diagnosis and Treatment of Heterozygous Familial Hypercholesterolemia.Journal of the American Heart Association · 2019
    Review
  17. Review
  18. Microvascular Dysfunction and Clinical Outcomes.Circulation. Cardiovascular imaging · 2018
    Article
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Melinda D WuKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon; Doernbecher Children's Hospital, Oregon Health & Science University, Portland, Oregon.
Federico MoccettiKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Eran BrownKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Brian P DavidsonKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon; Portland Veterans Administration Hospital, Oregon Health & Science University, Portland, Oregon.
Tamara AtkinsonKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon; Portland Veterans Administration Hospital, Oregon Health & Science University, Portland, Oregon.
J Todd BelcikKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
George GiraudKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon; Portland Veterans Administration Hospital, Oregon Health & Science University, Portland, Oregon.
P Barton DuellKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Sergio FazioKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Hagai TavoriKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Sotirios TsimikasCardiovascular Division, University of California-San Diego, San Diego, California.
Jonathan R LindnerKnight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon; Oregon National Primate Research Center, Oregon Health & Science University, Portland, Oregon. Electronic address: linderj@ohsu.edu.

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
Project 4: APOB-specific CD4 and CD8 T cells exacerbate atherosclerosisP01HL136275 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Catherine C Hedrick · 2017 to 2026
$25.5M
Shear Regulation of MicroRNA Transportomes and Targetomes in Vascular HomeostasisR01HL106579 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHIEN, SHU, SHYY, JOHN YJ · 2011 to 2022
$8.3M
Targeted CEU Imaging of Atherosclerosis and AngiogenesisR01HL078610 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2004 to 2022
$6.8M
AIBP therapyR35HL135737 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MILLER, YURY · 2017 to 2023
$6.5M
Bioengineering a Chimeric Human LungR01HL120046 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SNOECK, HANS-WILLEM E, VUNJAK-NOVAKOVIC, GORDANA · 2013 to 2022
$6.1M
Augmentation of Tissue Perfusion with Ultrasound-mediated CavitationR01HL130046 · NHLBI · UNIVERSITY OF VIRGINIA · PI LINDNER, JONATHAN R · 2016 to 2023
$5.5M
Biomarkers of Inflammation and Vaso-occlusion in Sickle Cell DiseaseR01HL111969 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI FIELD, JOSHUA JEFFREY, LINDEN, JOEL M. · 2012 to 2016
$4.0M
Training in Translational Science and Cardiovascular MedicineT32HL094294 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI ALKAYED, NABIL J · 2009 to 2018
$3.5M
Local B-1 Regulation of AtherosclerosisR01HL136098 · NHLBI · UNIVERSITY OF VIRGINIA · PI MCNAMARA, COLEEN A · 2017 to 2020
$3.1M
Oxidation-specific nanoparticles for imaging atherosclerosisR01HL119828 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TSIMIKAS, SOTIRIOS · 2013 to 2017
$2.0M
Molecular and Genetic Epidemiology of Lp(a)-mediated Calcific Aortic Valve DiseaseR01HL128550 · NHLBI · MCGILL UNIVERSITY HEALTH CTR RES INST · PI THANASSOULIS, GEORGE · 2017 to 2020
$1.7M
NHLBI NIH HHS K08 HL133493NHLBI NIH HHS P01 HL136275NHLBI NIH HHS R01 HL078610NHLBI NIH HHS R01 HL106579NHLBI NIH HHS R01 HL111969NHLBI NIH HHS R01 HL119828NHLBI NIH HHS R01 HL120046NHLBI NIH HHS R01 HL128550NHLBI NIH HHS R01 HL130046NHLBI NIH HHS R01 HL136098NHLBI NIH HHS R35 HL135737NHLBI NIH HHS T32 HL094294NIH HHS P51 OD011092
6 · The paper itself

Abstract

objectivesThis study evaluated whether lipoprotein apheresis produces immediate changes in resting perfusion in subjects with severe hypercholesterolemia, and whether there is a difference in the response between peripheral and coronary microcirculations.

backgroundLipoprotein apheresis is used in patients with severe hypercholesterolemia to reduce plasma levels of low-density lipoprotein cholesterol.

methodsQuantitative contrast-enhanced ultrasound perfusion imaging of the myocardium at rest and skeletal muscle at rest and during calibrated contractile exercise was performed before and immediately after lipoprotein apheresis in 8 subjects with severe hypercholesterolemia, 7 of whom had a diagnosis of familial hypercholesterolemia. Myocardial perfusion imaging was also performed in 14 normal control subjects. Changes in myocardial work and left ventricular function were assessed by echocardiography. Ex vivo ovine coronary and femoral artery ring tension assays were assessed in the presence of pre- and post-apheresis plasma.

resultsApheresis acutely decreased low-density lipoprotein cholesterol (234.9 ± 103.2 mg/dl vs. 67.1 ± 49.5 mg/dl; p < 0.01) and oxidized phospholipid on apolipoprotein B-100 (60.2 ± 55.2 nmol/l vs. 47.0 ± 24.5 nmol/l; p = 0.01), and acutely increased resting myocardial perfusion (55.1 [95% confidence interval: 77.2 to 73.1] IU/s vs. 135 [95% confidence interval: 81.2 to 189.6] IU/s; p = 0.01), without changes in myocardial work. Myocardial longitudinal strain improved in those subjects with reduced pre-apheresis function. Skeletal muscle perfusion at rest and during contractile exercise was unchanged by apheresis. Acetylcholine-mediated dilation of ex vivo ovine coronary but not femoral arteries was impaired in pre-apheresis plasma and was completely reversed in post-apheresis plasma.

conclusionsLipoprotein apheresis produces an immediate improvement in coronary microvascular function, which increases myocardial perfusion and normalizes endothelial-dependent vasodilation. These changes are not observed in the periphery. (Acute Microvascular Changes With LDL Apheresis; NCT02388633).

Indexed as

Blood Component RemovalCoronary CirculationMicrocirculationAgedAnimalsBiomarkersCase-Control StudiesCholesterol, LDLCoronary DiseaseDown-RegulationFemaleHumansHypercholesterolemiaMaleMiddle AgedMuscle, SkeletalBiomarkersCholesterol, LDLapheresiscontrast ultrasoundfamilial hypercholesterolemiamyocardial contrast echocardiography

Identifiers

PMID29909101
PMCPMC6458098

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.