Lipoprotein Subclasses Associated With High‐Risk Coronary Atherosclerotic Plaque: Insights From the PROMISE Clinical Trial

Author:

McGarrah Robert W.12ORCID,Ferencik Maros3ORCID,Giamberardino Stephanie N.2ORCID,Hoffmann Udo4ORCID,Foldyna Borek4ORCID,Karady Julia45ORCID,Ginsburg Geoffrey S.6ORCID,Kraus William E.12ORCID,Douglas Pamela S.17ORCID,Shah Svati H.127ORCID

Affiliation:

1. Division of Cardiology, Department of Medicine Duke University School of Medicine Durham NC

2. Duke Molecular Physiology Institute Duke University School of Medicine Durham NC

3. Knight Cardiovascular Institute Oregon Health and Science University Portland OR

4. Cardiovascular Imaging Research Center Harvard Medical School–Massachusetts General Hospital Boston MA

5. MTA‐SE Cardiovascular Imaging Research Group, Heart and Vascular Center Semmelweis University Budapest Hungary

6. Duke Center for Applied Genomics & Precision Medicine Duke University School of Medicine Durham NC

7. Duke Clinical Research Institute Duke University School of Medicine Durham NC

Abstract

BACKGROUND More than half of major adverse cardiovascular events (MACE) occur in the absence of obstructive coronary artery disease and are often attributed to the rupture of high‐risk coronary atherosclerotic plaque (HRP). Blood‐based biomarkers that associate with imaging‐defined HRP and predict MACE are lacking. METHODS AND RESULTS Nuclear magnetic resonance–based lipoprotein particle profiling was performed in the biomarker substudy of the PROMISE (Prospective Multicenter Imaging Study for Evaluation of Chest Pain) trial (N=4019) in participants who had stable symptoms suspicious for coronary artery disease. Principal components analysis was used to reduce the number of correlated lipoproteins into uncorrelated lipoprotein factors. The association of lipoprotein factors and individual lipoproteins of significantly associated factors with core laboratory determined coronary computed tomographic angiography features of HRP was determined using logistic regression models. The association of HRP‐associated lipoproteins with MACE was assessed in the PROMISE trial and validated in an independent coronary angiography biorepository (CATHGEN [Catheterization Genetics]) using Cox proportional hazards models. Lipoprotein factors composed of high‐density lipoprotein (HDL) subclasses were associated with HRP. In these factors, large HDL (odds ratio [OR], 0.70 [95% CI, 0.56–0.85]; P <0.001) and medium HDL (OR, 0.84 [95% CI, 0.72–0.98]; P =0.028) and HDL size (OR, 0.82 [95% CI, 0.69–0.96]; P =0.018) were associated with HRP in multivariable models. Medium HDL was associated with MACE in PROMISE (hazard ratio [HR], 0.76 [95% CI, 0.63–0.92]; P =0.004), which was validated in the CATHGEN biorepository (HR, 0.91 [95% CI, 0.88–0.94]; P <0.001). CONCLUSIONS Large and medium HDL subclasses and HDL size inversely associate with HRP features, and medium HDL subclasses inversely associate with MACE in PROMISE trial participants. These findings may aid in the risk stratification of individuals with chest pain and provide insight into the pathobiology of HRP. REGISTRATION URL: https://clinicaltrials.gov ; Unique identifier: NCT01174550

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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