A recent MRI study published in Liver International reveals a strong connection between metabolic dysfunction-associated steatotic liver disease (MASLD) and accelerated brain aging, irrespective of age or apolipoprotein E4 (APOE ɛ4) carrier status. The study analyzed data from over 26,000 participants, including individuals with various subtypes of MASLD, such as those with increased alcohol intake (MetALD).
The findings show that people with MASLD/related liver disease exhibited a brain age 1.07 years older than their chronological age, compared to just 0.19 years for those without MASLD. Particularly, those with MetALD had a brain age 1.87 years older. This association remained even after accounting for factors like age and APOE ɛ4 carrier status.
Notably, MetALD, which is linked to heavy alcohol consumption, showed the most significant brain aging effect. Excessive alcohol intake has been linked to brain atrophy and neuron loss, further compounding brain aging. The study also suggests that addressing low-grade systemic inflammation could help mitigate the accelerated brain aging associated with MASLD, with roughly 13.5% of the MASLD-brain aging link potentially preventable through this intervention.
Key Findings:
- MASLD and Brain Aging: Individuals with MASLD, including MetALD, experience significant brain aging, even in middle-aged adults and those without the APOE ɛ4 allele.
- MetALD’s Impact: MetALD shows the greatest brain aging effect, highlighting alcohol’s damaging role in accelerating brain aging.
- Inflammation as a Target: Addressing low-grade inflammation could prevent up to 13.5% of the MASLD-related brain aging, offering a potential intervention for brain health.
This study emphasizes the importance of early intervention and management of MASLD in reducing the risk of accelerated brain aging, underscoring the critical role of proactive care in promoting long-term brain and liver health.
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