Research Unit of Biomedicine and Internal Medicine University of Oulu Oulu Finland.
Biocenter Oulu University of Oulu Oulu Finland.
J Am Heart Assoc. 2024 Mar 5;13(5):e031824. doi: 10.1161/JAHA.123.031824. Epub 2024 Feb 23.
Regardless of progress in treatment of coronary artery disease (CAD), there is still a significant residual risk of death in patients with CAD, highlighting the need for additional risk stratification markers. Our previous study provided evidence for a novel blood pressure-regulating mechanism involving 4β-hydroxycholesterol (4βHC), an agonist for liver X receptors, as a hypotensive factor. The aim was to determine the role of 4βHC as a prognostic factor in CAD.
The ARTEMIS (Innovation to Reduce Cardiovascular Complications of Diabetes at the Intersection) cohort consists of 1946 patients with CAD. Men and women were analyzed separately in quartiles according to plasma 4βHC. Basic characteristics, medications, ECG, and echocardiography parameters as well as mortality rate were analyzed. At baseline, subjects with a beneficial cardiovascular profile, as assessed with traditional markers such as body mass index, exercise capacity, prevalence of diabetes, and use of antihypertensives, had the highest plasma 4βHC concentrations. However, in men, high plasma 4βHC was associated with all-cause death, cardiac death, and especially sudden cardiac death (SCD) in a median follow-up of 8.8 years. Univariate and comprehensively adjusted hazard ratios for SCD in the highest quartile were 3.76 (95% CI, 1.6-8.7; =0.002) and 4.18 (95% CI, 1.5-11.4; =0.005), respectively. In contrast, the association of cardiac death and SCD in women showed the lowest risk in the highest 4βHC quartile.
High plasma 4βHC concentration was associated with death and especially SCD in men, while an inverse association was detected in women. Our results suggest 4βHC as a novel sex-specific risk marker of cardiac death and especially SCD in chronic CAD.
clinicaltrials.gov. Identifier NCT01426685.
尽管在治疗冠状动脉疾病(CAD)方面取得了进展,但 CAD 患者的死亡仍存在显著的残余风险,这突出表明需要额外的风险分层标志物。我们之前的研究提供了证据表明,涉及到 4β-羟基胆固醇(4βHC)的新型血压调节机制是一种降压因子,4βHC 是肝脏 X 受体的激动剂。目的是确定 4βHC 作为 CAD 预后因素的作用。
ARTEMIS(创新以减少糖尿病心血管并发症在交叉口)队列包括 1946 例 CAD 患者。根据血浆 4βHC,男性和女性分别按四分位数进行分析。分析了基本特征、药物、心电图和超声心动图参数以及死亡率。在基线时,使用传统标志物(如体重指数、运动能力、糖尿病患病率和使用抗高血压药物)评估具有心血管有益特征的患者具有最高的血浆 4βHC 浓度。然而,在男性中,高血浆 4βHC 与全因死亡、心脏死亡,尤其是在中位随访 8.8 年后的心脏性猝死(SCD)相关。最高四分位数的 SCD 的单变量和综合调整后的危险比分别为 3.76(95%CI,1.6-8.7;=0.002)和 4.18(95%CI,1.5-11.4;=0.005)。相比之下,女性中 SCD 和心脏死亡的相关性显示最高四分位数的风险最低。
高血浆 4βHC 浓度与男性的死亡,尤其是 SCD 相关,而在女性中则检测到相反的关联。我们的结果表明,4βHC 是慢性 CAD 中心脏死亡和特别是 SCD 的新型性别特异性风险标志物。
clinicaltrials.gov。标识符 NCT01426685。