Department of Cardiology, State Key Laboratory of Cardiovascular Disease, Fu Wai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences, Peking Union Medical College, BeiLiShi Road 167, Beijing, 100037, China.
Sci Rep. 2018 Jun 11;8(1):8861. doi: 10.1038/s41598-018-27248-w.
Familial hypercholesterolemia (FH) is one of the most common causes of premature myocardial infarction (MI). However, The patterns of FH remained unrecognized in clinical care, especially in very young patients (VYPs, ≤35 years) with MI. The present study enrolled a total of 1,093 VYPs (≤35 years) presenting a first MI. Clinical diagnosis of FH was made using Dutch Lipid Clinic Network criteria. Coronary severity was assessed by Gensini score (GS). Patients were followed for a median of 40-months with cardiac death, stroke, MI, post-discharge revascularization or unstable angina as primary endpoints. The detected rates of definite/probable FH were 6.5%. The prevalence reached up to 10.3% in patients ≤25 years. The FH had similar levels of comorbidities but was younger, more likely to be very high risk (VHR) and had higher GS (p < 0.05) than unlikely FH. Notably, the FH on prior lipid-lowering medication presented a lower GS compared to those untreated. Differences in event rates were similar in FH as unlikely FH (11.8% vs. 8.1%, adjusted hazard ratio 1.35 [0.64-2.86], p = 0.434) but patients on treatment improved outcome (6.5% vs. 10.5%, adjusted hazard ratio 0.35[0.13-0.95], p = 0.039). The early identification and treatment might be critical to reduce cardiovascular risk in VYPs with MI.
家族性高胆固醇血症(FH)是导致早发性心肌梗死(MI)的最常见原因之一。然而,FH 的模式在临床治疗中仍未被识别,尤其是在患有 MI 的非常年轻患者(VYPs,≤35 岁)中。本研究共纳入了 1093 名首次 MI 的 VYPs(≤35 岁)。FH 的临床诊断采用荷兰脂质诊所网络标准进行。通过 Gensini 评分(GS)评估冠状动脉严重程度。患者中位随访 40 个月,主要终点为心脏性死亡、中风、MI、出院后血运重建或不稳定型心绞痛。明确/可能 FH 的检出率为 6.5%。≤25 岁的患者患病率高达 10.3%。FH 患者具有相似的合并症,但年龄更小,更有可能是极高风险(VHR),GS 更高(p<0.05),而不太可能是 FH。值得注意的是,与未接受治疗的患者相比,正在接受降脂药物治疗的 FH 患者的 GS 较低。FH 和不太可能 FH 的事件发生率差异相似(11.8%比 8.1%,调整后的危险比 1.35[0.64-2.86],p=0.434),但接受治疗的患者改善了预后(6.5%比 10.5%,调整后的危险比 0.35[0.13-0.95],p=0.039)。早期识别和治疗对于降低 VYPs 中 MI 的心血管风险可能至关重要。