PMID- 31313754 OWN - NLM STAT- MEDLINE DCOM- 20200213 LR - 20200225 IS - 1643-3750 (Electronic) IS - 1234-1010 (Print) IS - 1234-1010 (Linking) VI - 25 DP - 2019 Jul 17 TI - Culprit Lesion Characteristics in Young Patients with Hyperhomocysteinemia. PG - 5306-5311 LID - 10.12659/MSM.914979 [doi] AB - BACKGROUND The relationships between culprit coronary plaque characteristics and hyperhomocysteinemia (HHcy) are not fully understood in young patients. In this study we investigated the relationship between culprit atherosclerotic plaque phenotype assessed by optical coherence tomography (OCT) and hyperhomocysteinemia (HHcy) in young patients. MATERIAL AND METHODS We investigated the OCT imaging and HHcy of 123 lesions in 123 young patients (/=15.5 micromol/l) and control group (70 cases, HHcy <15.5 micromol/l). RESULTS Compared with the control group, the HHcy group had a higher proportion of OCT-TCFA (p=0.03), OCT-vasa vasorum (p=0.013), and OCT-thrombus (p=0.012), and a larger lipid arc (p=0.002). HHcy (P=0.037) and metabolic syndrome (MetS) (P=0.016) remained independent predictors of TCFAs. HHcy (P=0.026) and smoking (P=0.005) remained independent determinants of thrombus. CONCLUSIONS HHcy and MetS are associated with TCFAs, and HHcy and smoking are associated with thrombus in young patients with coronary artery disease. FAU - Hou, Fang-Jie AU - Hou FJ AD - Department of Cardiology, 12th Ward, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart Lung and Blood Vessel Disease, Beijing Key Laboratory of Precision Medicine of Coronary Atherosclerotic Disease, Clinical Center for Coronary Heart Disease, Beijing, China (mainland). AD - Department of Cardiology, Qingdao Municipal Hospital, Qingdao, Shandong, China (mainland). FAU - Zhou, Yu-Jie AU - Zhou YJ AD - Department of Cardiology, 12th Ward, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart Lung and Blood Vessel Disease, Beijing Key Laboratory of Precision Medicine of Coronary Atherosclerotic Disease, Clinical Center for Coronary Heart Disease, Beijing, China (mainland). FAU - Ma, Xiao-Teng AU - Ma XT AD - Department of Cardiology, 12th Ward, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart Lung and Blood Vessel Disease, Beijing Key Laboratory of Precision Medicine of Coronary Atherosclerotic Disease, Clinical Center for Coronary Heart Disease, Beijing, China (mainland). FAU - He, Tao AU - He T AD - Department of Cardiology, Qingdao Municipal Hospital, Qingdao, Shandong, China (mainland). FAU - Yan, Rong-Qiang AU - Yan RQ AD - Department of Cardiology, Qingdao Municipal Hospital, Qingdao, Shandong, China (mainland). FAU - Geng, Qiang AU - Geng Q AD - Department of Cardiology, Qingdao Municipal Hospital, Qingdao, Shandong, China (mainland). FAU - Wang, Hai-Yang AU - Wang HY AD - Department of Cardiology, Qingdao Municipal Hospital, Qingdao, Shandong, China (mainland). FAU - Ma, Ying AU - Ma Y AD - Department of Cardiology, Qingdao Municipal Hospital, Qingdao, Shandong, China (mainland). FAU - Ren, Yong-Qiang AU - Ren YQ AD - Department of Cardiology, Qingdao Municipal Hospital, Qingdao, Shandong, China (mainland). FAU - Dong, Fu-Zong AU - Dong FZ AD - Department of Cardiology, Qingdao Municipal Hospital, Qingdao, Shandong, China (mainland). LA - eng PT - Journal Article DEP - 20190717 PL - United States TA - Med Sci Monit JT - Medical science monitor : international medical journal of experimental and clinical research JID - 9609063 SB - IM MH - Acute Coronary Syndrome/complications MH - Adult MH - China MH - Coronary Angiography/methods MH - Coronary Artery Disease/*complications/etiology MH - Coronary Vessels/pathology MH - Female MH - Humans MH - Hyperhomocysteinemia/complications/*physiopathology MH - Male MH - Overweight MH - Plaque, Atherosclerotic/metabolism/*pathology MH - Predictive Value of Tests MH - Retrospective Studies MH - Smoking MH - Tomography, Optical Coherence/methods PMC - PMC6659466 COIS- Conflicts of interest None. EDAT- 2019/07/18 06:00 MHDA- 2020/02/14 06:00 PMCR- 2019/07/17 CRDT- 2019/07/18 06:00 PHST- 2019/07/18 06:00 [entrez] PHST- 2019/07/18 06:00 [pubmed] PHST- 2020/02/14 06:00 [medline] PHST- 2019/07/17 00:00 [pmc-release] AID - 914979 [pii] AID - 10.12659/MSM.914979 [doi] PST - epublish SO - Med Sci Monit. 2019 Jul 17;25:5306-5311. doi: 10.12659/MSM.914979.