| Literature DB >> 31367899 |
Kazuhiro Dan1, Hector M Garcia-Garcia2, Omar Yacob1, Kayode O Kuku1, Paul Kolm1, Nikunj Shah3, Martin R Bennett4, Nick Curzen5,6, Ron Waksman1, Michael Mahmoudi5,6.
Abstract
Deoxyribonucleic acid (DNA) damage and repair signaling cascades are related to the development of atherosclerosis. Pathological studies have demonstrated that healed coronary plaque rupture (HCPR) contributes to plaque progression and predisposes to sudden ischemic cardiac death. The objective of this study is to investigate the relationship between HCPR detected by optical coherence tomography (OCT) and DNA ligase. Forty-two patients with both OCT and DNA ligase were prospectively enrolled. The population included patients with stable angina pectoris (SA) and non-ST-elevation myocardial infarction (NSTEMI). It was found that the prevalence of HCPR was greater in subjects with higher DNA ligase activity (correlation coefficient 0.36, p = 0.019). The presence of HCPR in patients with NSTEMI was greater than in patients with SA per OCT analysis; however, there was no statistical difference in this limited population (22.53% versus 12.83%, respectively, p = 0.116). DNA repair activity by DNA ligase was associated with HCPR in advanced coronary artery plaque by OCT.Entities:
Keywords: DNA repair; Healed coronary plaque rupture; Optical coherence tomography
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Year: 2019 PMID: 31367899 DOI: 10.1007/s12265-019-09904-2
Source DB: PubMed Journal: J Cardiovasc Transl Res ISSN: 1937-5387 Impact factor: 4.132