Key result
MASLD across all BMI phenotypes is linked to ~45% higher incidence of elevated arterial stiffness.
Why the study?
The association of metabolic dysfunction-associated steatotic liver disease (MASLD) with arterial stiffness across different body mass index (BMI) phenotypes remains uncertain.
Does metabolic dysfunction-associated steatotic liver disease across different BMI phenotypes increase arterial stiffness?
Cohort (n=39,541)
Does metabolic dysfunction-associated steatotic liver disease across different BMI phenotypes increase arterial stiffness?
Effect estimate: MD 58.80 to 92.68 cm/s (baseline baPWV); IRR 1.45 to 1.64 (incident elevated baPWV)
MASLD is associated with an unfavorable arterial stiffness profile and faster progression across all BMI categories, demonstrating that normal BMI does not preclude arterial stiffness risk in patients with MASLD.
Background and Aim Metabolic dysfunction-associated steatotic liver disease (MASLD) is associated with arterial stiffness, but whether this association differs across body mass index (BMI) phenotypes remains uncertain. We examined the associations of lean, overweight, and obese MASLD with baseline brachial-ankle pulse wave velocity (baPWV), annual baPWV progression, and incident elevated baPWV (≥ 1800 cm/s). Methods and Results Among Kailuan participants undergoing their first baPWV assessment during 2010–2019, 39 541 were included in the cross-sectional analysis, 21 205 in the progression analysis, and 18 310 in the incident elevated baPWV analysis. Multivariable linear regression was used for baseline baPWV and progression, and Poisson regression with follow-up time as an offset was used for incident elevated baPWV. Compared with participants without MASLD, all three MASLD phenotypes were associated with higher baseline baPWV, faster progression, and a higher incidence of elevated baPWV. Adjusted differences ranged from 58.80 to 92.68 cm/s for baseline baPWV and from 6.19 to 10.73 cm/s/year for progression, while incidence rate ratios ranged from 1.45 to 1.64. Significant heterogeneity across BMI categories was observed for baseline baPWV, with larger differences in lean MASLD, whereas no significant heterogeneity was observed for progression or incident elevated baPWV. Conclusions MASLD was associated with an adverse arterial stiffness profile across BMI phenotypes. Normal BMI did not preclude an unfavorable arterial stiffness profile in MASLD, and differences across BMI phenotypes varied by outcome.
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Fang et al. (2026) conducted a cohort in Metabolic dysfunction-associated steatotic liver disease (MASLD) (n=39,541). Lean, overweight, and obese metabolic dysfunction-associated steatotic liver disease (MASLD) vs. Participants without MASLD was evaluated on Baseline brachial-ankle pulse wave velocity (baPWV), annual baPWV progression, and incident elevated baPWV (≥ 1800 cm/s) (MD 58.80 to 92.68 cm/s (baseline baPWV); IRR 1.45 to 1.64 (incident elevated baPWV)). Metabolic dysfunction-associated steatotic liver disease across all BMI phenotypes was associated with higher baseline arterial stiffness and higher incidence of elevated baPWV (IRR 1.45 to 1.64).
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