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Association of oxidized ApoB and oxidized ApoA-I with high-risk coronary plaque features in cardiovascular disease.
Sorokin, Alexander V; Hong, Christin G; Aponte, Angel M; Florida, Elizabeth M; Tang, Jingrong; Patel, Nidhi; Baranova, Irina N; Li, Haiou; Parel, Philip M; Chen, Vicky; Wilson, Sierra R; Ongstad, Emily L; Collén, Anna; Playford, Martin P; Eggerman, Thomas L; Chen, Marcus Y; Kotani, Kazuhiko; Bocharov, Alexander V; Remaley, Alan T.
Afiliação
  • Sorokin AV; Section of Inflammation and Cardiometabolic Diseases, Cardiovascular Branch.
  • Hong CG; Section of Inflammation and Cardiometabolic Diseases, Cardiovascular Branch.
  • Aponte AM; Proteomics Core, and.
  • Florida EM; Section of Inflammation and Cardiometabolic Diseases, Cardiovascular Branch.
  • Tang J; Section of Lipoprotein Metabolism, Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, Maryland, USA.
  • Patel N; Section of Inflammation and Cardiometabolic Diseases, Cardiovascular Branch.
  • Baranova IN; Department of Laboratory Medicine, Clinical Center, NIH, Bethesda, Maryland, USA.
  • Li H; Section of Inflammation and Cardiometabolic Diseases, Cardiovascular Branch.
  • Parel PM; Section of Inflammation and Cardiometabolic Diseases, Cardiovascular Branch.
  • Chen V; Bioinformatics/Integrated Data Sciences Section, Research Technology Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.
  • Wilson SR; Section of Lipoprotein Metabolism, Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, Maryland, USA.
  • Ongstad EL; Bioscience Cardiovascular, Research and Early Development, and.
  • Collén A; Projects, Research and Early Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, Maryland, USA.
  • Playford MP; Section of Inflammation and Cardiometabolic Diseases, Cardiovascular Branch.
  • Eggerman TL; Department of Laboratory Medicine, Clinical Center, NIH, Bethesda, Maryland, USA.
  • Chen MY; Section of Inflammation and Cardiometabolic Diseases, Cardiovascular Branch.
  • Kotani K; Division of Community and Family Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
  • Bocharov AV; Department of Laboratory Medicine, Clinical Center, NIH, Bethesda, Maryland, USA.
  • Remaley AT; Section of Lipoprotein Metabolism, Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, NIH, Bethesda, Maryland, USA.
JCI Insight ; 8(20)2023 Oct 23.
Article em En | MEDLINE | ID: mdl-37698922
ABSTRACT

BACKGROUND:

Oxidized apolipoprotein B (oxLDL) and oxidized ApoA-I (oxHDL) are proatherogenic. Their prognostic value for assessing high-risk plaques by coronary computed tomography angiography (CCTA) is missing.

METHODS:

In a prospective, observational study, 306 participants with cardiovascular disease (CVD) had extensive lipoprotein profiling. Proteomics analysis was performed on isolated oxHDL, and atherosclerotic plaque assessment was accomplished by quantitative CCTA.

RESULTS:

Patients were predominantly White, overweight men (58.5%) on statin therapy (43.5%). Increase in LDL-C, ApoB, small dense LDL-C (P < 0.001 for all), triglycerides (P = 0.03), and lower HDL function were observed in the high oxLDL group. High oxLDL associated with necrotic burden (NB; ß = 0.20; P < 0.0001) and fibrofatty burden (FFB; ß = 0.15; P = 0.001) after multivariate adjustment. Low oxHDL had a significant reverse association with these plaque characteristics. Plasma oxHDL levels better predicted NB and FFB after adjustment (OR, 2.22; 95% CI, 1.27-3.88, and OR, 2.80; 95% CI, 1.71-4.58) compared with oxLDL and HDL-C. Interestingly, oxHDL associated with fibrous burden (FB) change over 3.3 years (ß = 0.535; P = 0.033) when compared with oxLDL. Combined Met136 mono-oxidation and Trp132 dioxidation of HDL showed evident association with coronary artery calcium score (r = 0.786; P < 0.001) and FB (r = 0.539; P = 0.012) in high oxHDL, whereas Met136 mono-oxidation significantly associated with vulnerable plaque in low oxHDL.

CONCLUSION:

Our findings suggest that the investigated oxidized lipids are associated with high-risk coronary plaque features and progression over time in patients with CVD. CLINICALTRIALS gov NCT01621594.

FUNDING:

National Heart, Lung, and Blood Institute at the NIH Intramural Research Program.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Placa Aterosclerótica Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: JCI Insight Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Placa Aterosclerótica Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: JCI Insight Ano de publicação: 2023 Tipo de documento: Article