Plaque Regression and Endothelial Progenitor Cell Mobilization With Intensive Lipid Elimination Regimen (PREMIER).


Journal

Circulation. Cardiovascular interventions
ISSN: 1941-7632
Titre abrégé: Circ Cardiovasc Interv
Pays: United States
ID NLM: 101499602

Informations de publication

Date de publication:
08 2020
Historique:
entrez: 15 8 2020
pubmed: 15 8 2020
medline: 22 6 2021
Statut: ppublish

Résumé

Low-density lipoproteins (LDLs) are removed by extracorporeal filtration during LDL apheresis. It is mainly used in familial hyperlipidemia. The PREMIER trial (Plaque Regression and Progenitor Cell Mobilization With Intensive Lipid Elimination Regimen) evaluated LDL apheresis in nonfamilial hyperlipidemia acute coronary syndrome patients treated with percutaneous coronary intervention. We randomized 160 acute coronary syndrome patients at 4 Veterans Affairs centers within 72 hours of percutaneous coronary intervention to intensive lipid-lowering therapy (ILLT) comprising single LDL apheresis and statins versus standard medical therapy (SMT) with no LDL apheresis and statin therapy alone. Trial objectives constituted primary safety and primary efficacy end points and endothelial progenitor cell colony-forming unit mobilization in peripheral blood. Mean LDL reduction at discharge was 53% in ILLT and 17% in SMT groups ( PREMIER is the first randomized clinical trial to demonstrate safety and a trend for early coronary plaque regression with LDL apheresis in nonfamilial hyperlipidemia acute coronary syndrome patients treated with percutaneous coronary intervention. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT01004406 and NCT02347098.

Sections du résumé

BACKGROUND
Low-density lipoproteins (LDLs) are removed by extracorporeal filtration during LDL apheresis. It is mainly used in familial hyperlipidemia. The PREMIER trial (Plaque Regression and Progenitor Cell Mobilization With Intensive Lipid Elimination Regimen) evaluated LDL apheresis in nonfamilial hyperlipidemia acute coronary syndrome patients treated with percutaneous coronary intervention.
METHODS
We randomized 160 acute coronary syndrome patients at 4 Veterans Affairs centers within 72 hours of percutaneous coronary intervention to intensive lipid-lowering therapy (ILLT) comprising single LDL apheresis and statins versus standard medical therapy (SMT) with no LDL apheresis and statin therapy alone. Trial objectives constituted primary safety and primary efficacy end points and endothelial progenitor cell colony-forming unit mobilization in peripheral blood.
RESULTS
Mean LDL reduction at discharge was 53% in ILLT and 17% in SMT groups (
CONCLUSIONS
PREMIER is the first randomized clinical trial to demonstrate safety and a trend for early coronary plaque regression with LDL apheresis in nonfamilial hyperlipidemia acute coronary syndrome patients treated with percutaneous coronary intervention. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT01004406 and NCT02347098.

Identifiants

pubmed: 32791950
doi: 10.1161/CIRCINTERVENTIONS.119.008933
doi:

Substances chimiques

Biomarkers 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Lipoproteins, LDL 0

Banques de données

ClinicalTrials.gov
['NCT01004406', 'NCT02347098']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e008933

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

Auteurs

Subhash Banerjee (S)

Veterans Affairs North Texas Health Care System, Dallas (S.B., J.L.H.).
University of Texas Southwestern Medical Center, Dallas (S.B., J.L.H., A.B., P.K.).

Ping Luo (P)

Cooperative Studies Program Coordinating Center, Edward Hines, Jr Veterans Affairs Hospital, Hines, IL (P.L., D.J.R., D.L., Y.W.).

Domenic J Reda (DJ)

Cooperative Studies Program Coordinating Center, Edward Hines, Jr Veterans Affairs Hospital, Hines, IL (P.L., D.J.R., D.L., Y.W.).

Faisal Latif (F)

Oklahoma City Veterans Affairs Medical Center (F.L.).
University of Oklahoma Health Sciences Center (F.L., M.A.-F.).

Jeffrey L Hastings (JL)

Veterans Affairs North Texas Health Care System, Dallas (S.B., J.L.H.).
University of Texas Southwestern Medical Center, Dallas (S.B., J.L.H., A.B., P.K.).

Ehrin J Armstrong (EJ)

Rocky Mountain Regional Veterans Affairs Medical Center, Aurora, CO (E.J.A.).

Jayant Bagai (J)

Veterans Affairs Tennessee Valley Health Care System, Nashville (J.B.).

Mazen Abu-Fadel (M)

University of Oklahoma Health Sciences Center (F.L., M.A.-F.).

Amutharani Baskar (A)

University of Texas Southwestern Medical Center, Dallas (S.B., J.L.H., A.B., P.K.).

Preeti Kamath (P)

University of Texas Southwestern Medical Center, Dallas (S.B., J.L.H., A.B., P.K.).

Daniel Lippe (D)

Cooperative Studies Program Coordinating Center, Edward Hines, Jr Veterans Affairs Hospital, Hines, IL (P.L., D.J.R., D.L., Y.W.).

Yongliang Wei (Y)

Cooperative Studies Program Coordinating Center, Edward Hines, Jr Veterans Affairs Hospital, Hines, IL (P.L., D.J.R., D.L., Y.W.).

Alexandra Scrymgeour (A)

Cooperative Studies Program Clinical Research Pharmacy Coordinating Center, Albuquerque, NM (A.S.).

Theresa C Gleason (TC)

Department of Veterans Affairs, Office of Research and Development, Washington, DC (T.C.G.).

Emmanouil S Brilakis (ES)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, MN (E.S.B.).

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Classifications MeSH