Department of Echocardiography, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
The Key Laboratory of Remodeling-related Cardiovascular Diseases, Beijing Institute of Heart Lung and Blood Vessel Diseases, Beijing, China; Department of Atherosclerosis, Ministry of Education, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Am J Cardiol. 2021 Apr 15;145:58-63. doi: 10.1016/j.amjcard.2020.12.080. Epub 2021 Jan 14.
Patients with homozygous familial hypercholesterolemia (HoFH) have a high risk for premature death. Supravalvular aortic stenosis (SVAS) is a common and the feature lesion of the aortic root in HoFH. The relation between SVAS and the risk of premature death in patients with HoFH has not been fully investigated. The present study analysis included 97 HoFH patients with mean age of 14.7 (years) from the Genetic and Imaging of Familial Hypercholesterolemia in Han Nationality Study. During the median (±SD) follow-up 4.0 (±4.0) years, 40 (41.2%) participants had SVAS and 17 (17.5%) participants experienced death. The proportion of premature death in the non-SVAS and SVAS group was 7.0% and 32.5%, respectively. Compared with the non-SVAS group, SVAS group cumulative survival was lower in the HoFH (log-rank test, p <0.001). This result was further confirmed in the multivariable Cox regression models. After adjusting for age, sex, low density lipoprotein cholesterol (LDL_C)-year-score, lipid-lowering drugs, cardiovascular disease, and carotid artery plaque, SVAS was an independent risk factor of premature death in HoFH on the multivariate analysis (hazard ratio 4.45; 95% confidence interval, 1.10 to 18.12; p = 0.037). In conclusion, a significantly increased risk of premature death was observed in HoFH patients with SVAS. Our study emphasized the importance of careful and aggressive management in these patients when appropriate.
纯合子家族性高胆固醇血症(HoFH)患者有过早死亡的高风险。主动脉瓣上狭窄(SVAS)是 HoFH 患者主动脉根部的常见特征性病变。SVAS 与 HoFH 患者过早死亡风险之间的关系尚未得到充分研究。本研究分析了来自汉族遗传性高胆固醇血症基因与影像研究的 97 名 HoFH 患者,平均年龄为 14.7(岁)。在中位数(±SD)随访 4.0(±4.0)年期间,40(41.2%)名参与者患有 SVAS,17(17.5%)名参与者死亡。非 SVAS 和 SVAS 组的过早死亡率分别为 7.0%和 32.5%。与非 SVAS 组相比,HoFH 中 SVAS 组的累积生存率较低(对数秩检验,p<0.001)。多变量 Cox 回归模型进一步证实了这一结果。在校正年龄、性别、低密度脂蛋白胆固醇(LDL_C)-年评分、降脂药物、心血管疾病和颈动脉斑块后,SVAS 是 HoFH 患者过早死亡的独立危险因素(风险比 4.45;95%置信区间,1.10 至 18.12;p = 0.037)。总之,SVAS 的 HoFH 患者过早死亡的风险显著增加。我们的研究强调了在适当情况下对这些患者进行仔细和积极管理的重要性。