Liver X Receptor Agonist 4β‐Hydroxycholesterol as a Prognostic Factor in Coronary Artery Disease

• Published in: Journal of the American Heart Association Vol. 13; no. 5; p. e031824
• Main Authors: Rahunen, Roosa, Tulppo, Mikko, Rinne, Valtteri, Lepojärvi, Samuli, Perkiömäki, Juha S., Huikuri, Heikki V., Ukkola, Olavi, Junttila, Juhani, Hukkanen, Janne
• Format: Journal Article
• Language: English
• Published: England John Wiley and Sons Inc 05.03.2024; Wiley
• Subjects: 4β‐hydroxycholesterol; Coronary Artery Disease; Death; Death, Sudden, Cardiac - epidemiology; Female; Humans; Hydroxycholesterols; liver X receptor; Liver X Receptors; Male; Original Research; Prognosis; Risk Factors; sudden cardiac death; coronary artery disease; sudden cardiac death; 4β‐hydroxycholesterol; death; liver X receptor
• ISSN: 2047-9980; 2047-9980
• DOI: 10.1161/JAHA.123.031824

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.