■动脉粥样硬化性心血管疾病(ASCVD)对先天性心脏病(CHD)成人心血管死亡的影响尚不清楚。
■本研究的目的是确定成人冠心病患者ASCVD危险因素的患病率和预后意义。我们假设ASCVD危险因素与定义为心力衰竭住院的心血管事件相关,心脏移植,心血管死亡。
■这是一项在梅奥诊所(2003-2019)对冠心病成人进行的回顾性队列研究。排除有冠状动脉疾病(CAD)病史的患者。ASCVD危险因素定义为高血压,高脂血症,糖尿病,肥胖,吸烟,和早熟CAD家族史。
■有5,025例患者没有CAD病史。平均年龄为35(23-45)岁,男性为2,558人(51%)。在5025名患者中,2,382(47%)在基线时具有≥1个ASCVD危险因素,16%的患者在5年内出现了额外的ASCVD危险因素(新发ASCVD风险).基线ASCVD危险因素(风险比1.27,95%置信区间1.06-1.38)和随访期间新发ASCVD危险因素(风险比1.06,95%置信区间1.02-1.11)与心血管事件相关。
■ASCVD因子与成人冠心病患者心血管事件相关。由于改变ASCVD风险的干预措施已被证明可以降低普通人群的心血管死亡,预期此类干预措施也将改善CHD人群的临床结局是合乎逻辑的.
UNASSIGNED: The effect of atherosclerotic cardiovascular disease (ASCVD) on cardiovascular death in adults with congenital heart disease (CHD) is not well understood.
UNASSIGNED: The purpose of this study was to determine the prevalence and prognostic implications of ASCVD risk factors in adults with CHD. We hypothesized that ASCVD risk factors were associated with cardiovascular events defined as heart failure hospitalization, heart transplant, and cardiovascular death.
UNASSIGNED: This is a retrospective cohort study of adults with CHD at the Mayo Clinic (2003-2019). Patients with a history of coronary artery disease (CAD) were excluded. ASCVD risk factors were defined as hypertension, hyperlipidemia, diabetes, obesity, smoking, and family history of premature CAD.
UNASSIGNED: There were 5,025 patients without a prior history of CAD. The mean age was 35 (23-45) years, and 2,558 (51%) were males. Of 5,025 patients, 2,382 (47%) had ≥1 ASCVD risk factors at baseline, and 16% developed additional ASCVD risk factors within 5 years (new-onset ASCVD risk). ASCVD risk factors at baseline (hazard ratio 1.27, 95% confidence interval 1.06-1.38) and new-onset ASCVD risk factors during follow-up (hazard ratio 1.06, 95% confidence interval 1.02-1.11) were associated with cardiovascular events.
UNASSIGNED: ASCVD factors were associated with cardiovascular events in adults with CHD. Since interventions that modify ASCVD risk have been shown to decrease cardiovascular death in the general population, it is logical to expect that such interventions would also improve clinical outcomes in the CHD population.