共 50 条
Coronary Artery Disease and Major Adverse Cardiovascular Events in People With Hepatic Steatosis at Low Atherosclerotic Cardiovascular Disease Risk
被引:1
|作者:
Karady, Julia
[1
,2
]
Mayrhofer, Thomas
[1
,3
]
Foldyna, Borek
[1
]
Lu, Michael T.
[1
]
Meyersohn, Nandini
[1
]
Hoffmann, Udo
[1
,4
]
Balogon, Oluwafemi
[5
]
Pagidipati, Neha
[6
]
Shah, Svati
[6
,7
]
Douglas, Pamela S.
[6
]
Ferencik, Maros
[8
]
Corey, Kathleen
[5
]
机构:
[1] Harvard Med Sch, Massachusetts Gen Hosp, Cardiovasc Imaging Res Ctr, Boston, MA USA
[2] Semmelweis Univ, Heart & Vasc Ctr, Budapest, Hungary
[3] Stralsund Univ Appl Sci, Sch Business Studies, Stralsund, Germany
[4] Cleerly Inc, Denver, CO USA
[5] Harvard Med Sch, Massachusetts Gen Hosp, Div Gastroenterol, Boston, MA 02115 USA
[6] Duke Univ, Sch Med, Duke Clin Res Inst, Durham, NC USA
[7] Duke Univ, Duke Mol Physiol Inst, Durham, NC USA
[8] Oregon Hlth & Sci Univ, Knight Cardiovasc Inst, Portland, OR USA
关键词:
cardiovascular risk;
coronary artery disease;
coronary CT imaging;
hepatic steatosis;
major adverse cardiovascular events;
FATTY LIVER-DISEASE;
UNITED-STATES;
CHEST-PAIN;
PREVALENCE;
ADULTS;
NAFLD;
D O I:
10.1111/apt.18415
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Background: Hepatic steatosis (HS) and 10-year atherosclerotic cardiovascular disease (ASCVD) risk >= 7.5% are associated with increased risk for cardiovascular events. Aim: To assess underlying coronary artery disease (CAD) and major adverse cardiovascular event (MACE) among those with and without HS at different ASCVD risk. Methods: We evaluated stable chest pain patients receiving coronary computed tomography (CT) in the PROMISE trial. HS and CAD endpoints were defined on coronary CT. MACE was defined as unstable angina, non-fatal myocardial infarction, and all-cause death. Multivariable Cox regression, adjusting for CAD characteristics, assessed the association of HS with MACE for ASCVD < 7.5%. Results: One thousand two hundred and four of 3702 (32.5%) patients were at ASCVD < 7.5% and 20.3% (244/1204) of them had HS. Individuals with HS were younger (54.3 +/- 5.2 vs. 55.8 +/- 5.2; p < 0.001), more often males (40.2% [98/244] vs. 27.1% [260/960]; p < 0.001), had more risk factors/person (2.06 +/- 0.89 vs. 1.93 +/- 0.91; p = 0.047). CAD characteristics were similar between HS vs. non-HS patients at ASCVD < 7.5% and ASCVD >= 7.5% (all p > 0.05). Patients with HS had greater MACE rate compared to non-HS patients (ASCVD < 7.5%: 3.75%[9/244] vs. 1.5% [14/960]; p = 0.027 and ASCVD >= 7.5%: 4.7% [33/696] vs. 3.1% [56/1802]; p = 0.043). In patients without HS, MACE rate was higher in the ASCVD >= 7.5% vs. < 7.5% (3.1% [56/1802] vs. 1.5% [14/960]; p = 0.011). In patients with HS, MACE rates were not significantly different between ASCVD >= 7.5% vs. < 7.5% (4.7% [33/696] vs. 3.7% [9/244]; p = 0.484). In ASCVD < 7.5%, HS predicted MACE (aHR:2.34, 95%CI:1.01-5.43; p = 0.048), independent of CAD characteristics. Conclusions: Individuals with HS at ASCVD < 7.5% risk had similar CAD characteristics as patients without HS at < 7.5% ASCVD risk, yet experienced comparable MACE rates as those at ASCVD >= 7.5%.
引用
收藏
页码:558 / 569
页数:12
相关论文