Relationship between metabolic dysfunction-associated steatotic liver disease and cardiovascular mortality risk in individuals with CKM stages 0-2: Mediating roles of inflammation and insulin resistance.
Jul 2026· Diabetes Research and Clinical Practice· Vol 239, pp.
113411
· 0 citations· 55 references
Medicine
TL;DR
The results support the potential value of integrating MASLD screening into early CKM syndrome risk stratification and management and support the potential value of integrating insulin resistance and inflammation in early CKM syndrome risk stratification and management.
Abstract
Objective
To examine the association of metabolic dysfunction-associated steatotic liver disease (MASLD) with cardiovascular disease (CVD) mortality in adults with cardiovascular-kidney-metabolic (CKM) syndrome and to explore the possible roles of insulin resistance and inflammation.
Methods
We analyzed 2009-2018 NHANES data including 10,061 adults with CKM staging (8340 at stages 0-2). MASLD was defined by the United States Fatty Liver Index (USFLI). We used restricted cubic spline models, Kaplan-Meier analysis, multivariable Cox regression, sensitivity analyses and mediation analysis to test the dose-response relationship, survival disparities and mediating effects.
Results
MASLD prevalence rose with CKM stage progression. In CKM stages 0-2, USFLI scores linearly correlated with CVD mortality risk (P < 0.001). Participants with MASLD had poorer survival and a higher hazard of CVD mortality than those without MASLD (HR = 4.03, 95 % CI 1.55-10.48). Insulin resistance and inflammation partially mediated the observed association.
Conclusions
In early CKM syndrome, MASLD was associated with higher CVD mortality risk. Insulin resistance and inflammation may partly explain this association. These results support the potential value of integrating MASLD screening into early CKM syndrome risk stratification and management.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent condition closely linked to cardiovascular diseases and type 2 diabetes. Although the triglyceride-glucose (TyG) index is widely acknowledged as an indicator of insulin resistance, its standalone prognostic value for mortality in MASLD re...
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Metabolic dysfunction-associated steatotic liver disease (MASLD) is being increasingly recognized as a systemic cardiometabolic disorder rather than a liver-limited condition. However, the combined association of insulin resistance, systemic inflammation, and depressive symptoms with mortality remains unclear. Therefor...
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BACKGROUND
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a growing public health challenge, highlighting the need for accessible markers of metabolic liver disease risk. Serum uric acid (SUA) has been linked to metabolic dysfunction, but its association with MASLD across the full clinical spectrum...
Hafiz M. Ahmed, Umm E. Aimen· Metabolic Syndrome and Relat...· 0 citations
Composite indices integrating insulin resistance and adiposity may improve mortality risk stratification in metabolic dysfunction-associated steatotic liver disease (MASLD). We evaluated eight triglyceride-glucose (TyG)-related indices in 6,159 U.S. adults with MASLD from the 1999–2018 National Health and Nutrition E...
Kai Zhang, Na-Ni Long, Long-Hao Zhang et al.· Scientific Reports· 0 citations
TyG and TyG-WHtR showed positive associations with CVD in patients with MASLD, with a remarkable threshold effect observed for TyG, which are simple auxiliary markers to screen high-risk subgroups during population epidemiological surveys.
Song-Shan Li, Shu-Ling Rong, Bin Yang et al.· Therapeutic Advances in Endo...· 0 citations
MASLD significantly increases the risk of cardiovascular events and all-cause mortality (ACM). The impact of the C-reactive protein-triglyceride-glucose index (CTI) and its derivatives on mortality in the MASLD population remains unclear. This study aimed to investigate their associations with mortality in the MA...
Guang-Jie Tu, Hang Zhai, Jun-Ming Xu et al.· BMC Cardiovascular Disorders· 0 citations
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