Association of metabolic dysfunction-associated fatty liver disease with white matter hyperintensity and cognitive decline: A longitudinal cohort study.
Inha Jung, So Young Park, Da Young Lee, Hyun Joo Cho, Seung Ku Lee, Ji A Seo, Nan Hee Kim, Chol Shin, Ji Hee Yu
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引用次数: 0
Abstract
Aims: Metabolic dysfunction-associated fatty liver disease (MAFLD) has recently been proposed to describe the hepatic steatosis associated with metabolic abnormalities. Substantial evidence has shown that hepatic steatosis may be linked with cognitive impairment and dementia. This study aimed to clarify the association between MAFLD and brain structural and cognitive changes.
Materials and methods: We analysed data from 2155 participants with both baseline and 4-year follow-up brain magnetic resonance images and neuropsychological measures from the Ansan cohort of the Korean Genome Epidemiology Study. The presence of hepatic steatosis was defined as a liver attenuation index (LAI) value <5 Hounsfield units using computed tomography.
Results: Over a median follow-up of 4.1 years, MAFLD was associated with an increased risk of white matter hyperintensity (WMH) (RR 1.35; 95% CI 1.09-1.66, p = 0.006), but not with brain volume changes. When examined by individual components of MAFLD, the presence of hepatic steatosis was an independent factor associated with the risk of WMH regardless of metabolic derangements. Lower LAI values were linearly associated with greater executive function Z score decline (p = 0.007). This relationship was more evident in the non-obese group (body mass index <25 kg/m2, p for interaction = 0.003).
Conclusions: MAFLD was associated with an increased risk of WMH over 4.1 years in middle-aged adults. The hepatic steatosis itself was independently associated with an increased risk of WMH regardless of comorbid metabolic abnormalities. The degree of hepatic steatosis was associated with decreased executive function, especially in non-obese individuals.
期刊介绍:
Diabetes, Obesity and Metabolism is primarily a journal of clinical and experimental pharmacology and therapeutics covering the interrelated areas of diabetes, obesity and metabolism. The journal prioritises high-quality original research that reports on the effects of new or existing therapies, including dietary, exercise and lifestyle (non-pharmacological) interventions, in any aspect of metabolic and endocrine disease, either in humans or animal and cellular systems. ‘Metabolism’ may relate to lipids, bone and drug metabolism, or broader aspects of endocrine dysfunction. Preclinical pharmacology, pharmacokinetic studies, meta-analyses and those addressing drug safety and tolerability are also highly suitable for publication in this journal. Original research may be published as a main paper or as a research letter.