Key result
Metabolic dysfunction-associated steatotic liver disease was independently associated with a 2.05-fold increased risk of major adverse cardiovascular and cerebrovascular events in patients with acute coronary syndrome.
Why the study?
The relationship between MASLD and OCT-defined coronary plaque vulnerability in ACS patients, and whether plaque vulnerability mediates the link between MASLD and MACCE, remained unclear.
Does the presence of MASLD increase the risk of MACCE and coronary plaque vulnerability in patients with ACS?
Observational (n=820)
No
Does the presence of MASLD increase the risk of MACCE and coronary plaque vulnerability in patients with ACS?
In patients with ACS, MASLD is associated with increased coronary plaque vulnerability and serves as an independent risk factor for MACCE, partially mediated by plaque vulnerability.
Answers are grounded in this paper and cite their sources.
MASLD may flag higher OCT plaque vulnerability in ACS; leaves open whether it mediates MACCE or warrants targeted intervention.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is increasingly recognized as a risk factor for cardiovascular events. However, MASLD’s relationship with optical coherence tomography (OCT)-defined coronary plaque vulnerability in patients with acute coronary syndrome (ACS) remains unclear. Moreover, the mediating role of plaque vulnerability in the association between MASLD and major adverse cardiovascular and cerebrovascular events (MACCE) has rarely been investigated. Therefore, this study used OCT to examine the association between MASLD and coronary plaque vulnerability in ACS patients, to assess the impact of MASLD on MACCE, and to explore whether plaque vulnerability mediates this relationship. A total of 820 patients with ACS were enrolled in this study. All patients underwent OCT-guided percutaneous coronary intervention (PCI) and completed abdominal ultrasound (US) or non-contrast computed tomography (CT) examinations. Patients meeting the diagnostic criteria for MASLD were categorized into the MASLD group, while those who did not were assigned to the non-MASLD group. The MASLD group had a significantly higher prevalence of multivessel disease, more complex coronary artery disease on OCT, and higher detection rates of lipid-rich plaques, cholesterol crystals, and thin-cap fibroatheroma (TCFA). Multivariate analysis confirmed that MASLD was independently associated with these vulnerable plaque features and served as an independent risk factor for major adverse cardiovascular and cerebrovascular events (MACCE) (adjusted hazard ratio [aHR] = 2.05, 95% confidence interval [CI]: 1.34–3.14, P < 0.001). Notably, plaque vulnerability, as represented by cholesterol crystals and TCFA, partially mediated the association between MASLD and MACCE, with mediation proportions of 9.90% and 23.70%, respectively. In patients with ACS, MASLD is associated with more complex coronary artery disease and increased plaque vulnerability assessed by OCT. Furthermore, MASLD is an independent risk factor for MACCE, and this association is partially mediated by plaque vulnerability.
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Xu et al. (2026) conducted an observational in Acute coronary syndrome (n=820). Metabolic dysfunction-associated steatotic liver disease (MASLD) vs. Non-MASLD was evaluated on Major adverse cardiovascular and cerebrovascular events (MACCE) (aHR 2.05, 95% CI 1.34-3.14, p=<0.001). Metabolic dysfunction-associated steatotic liver disease was independently associated with a 2.05-fold increased risk of major adverse cardiovascular and cerebrovascular events in patients with acute coronary syndrome.
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