Fan Wenxiao, Yang Shuping, Wei Yiran, Tian Minle, Liu Qianying, Li Xiaomeng, Ding Jiahao, Li Xuewei, Mao Ming, Han Xiaolei, Du Yifeng, Qiu Chengxuan, Dong Yi, Wang Yongxiang
Key Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Ministry of Education, Department of Neurology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, People's Republic of China.
Shandong Institute of Brain Science and Brain-inspired Research, Medical Science and Technology Innovation Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, People's Republic of China.
Diabetes Obes Metab. 2025 Jun;27(6):3419-3430. doi: 10.1111/dom.16362. Epub 2025 Apr 2.
Emerging evidence has linked metabolic dysfunction-associated steatotic liver disease (MASLD) with accelerated cognitive decline and dementia. We aimed to investigate the associations of MASLD with volumes of total brain tissue and subcortical grey matter, and white matter microstructures in the UK Biobank.
This cross-sectional study included 29,195 individuals (aged 45-82 years) from the UK Biobank who undertook a magnetic resonance imaging (MRI) sub-study between 2014 and 2022. The brain MRI covers three modalities (T1, T2 FLAIR, and diffusion). Volumes of grey matter, subcortical grey matter structures, and regional cortex were derived from T1-weighted images. Fractional anisotropy (FA) and mean diffusivity (MD) were derived from diffusion tensor imaging (DTI) to assess global and tract-specific microstructure. MASLD was defined as the MRI-derived proton density fat fraction (MRI-PDFF) ≥5% and the presence of at least one cardiometabolic criterion. Data were analysed using multiple linear regression models.
MASLD was significantly associated with smaller volumes of total grey matter and subcortical grey matter (p < 0.05) and reduced Alzheimer's disease (AD)-signature cortical thickness (multivariable-adjusted β = -0.04; 95% confidence interval [CI]: -0.07, -0.01). Having MASLD was associated with higher total white matter hyperintensity (WMH) volume (multivariable-adjusted β = 0.12; 95% CI: 0.10, 0.15). For white matter microstructure, MASLD was associated with increased global FA (multivariable-adjusted β = 0.05; 95% CI: 0.03, 0.08) and reduced global MD (multivariable-adjusted β = -0.04; 95% CI: -0.07, -0.01).
Brain morphology associated with MASLD is characterized by smaller subcortical grey matter volume and higher coherence but lower magnitudes of white matter microstructure.
新出现的证据表明,代谢功能障碍相关脂肪性肝病(MASLD)与认知能力加速下降和痴呆症有关。我们旨在研究在英国生物银行中,MASLD与全脑组织体积、皮质下灰质体积以及白质微结构之间的关联。
这项横断面研究纳入了英国生物银行中29195名年龄在45至82岁之间的个体,这些个体在2014年至2022年间进行了磁共振成像(MRI)子研究。脑部MRI涵盖三种模式(T1、T2 FLAIR和弥散)。灰质、皮质下灰质结构和区域皮质的体积由T1加权图像得出。分数各向异性(FA)和平均扩散率(MD)由弥散张量成像(DTI)得出,以评估整体和特定纤维束的微结构。MASLD被定义为MRI衍生的质子密度脂肪分数(MRI-PDFF)≥5%且存在至少一项心血管代谢标准。数据使用多元线性回归模型进行分析。
MASLD与总灰质和皮质下灰质体积较小显著相关(p<0.05),且与阿尔茨海默病(AD)特征性皮质厚度降低相关(多变量调整β=-0.04;95%置信区间[CI]:-0.07,-0.01)。患有MASLD与更高的总白质高信号(WMH)体积相关(多变量调整β=0.12;95%CI:0.10,0.15)。对于白质微结构,MASLD与整体FA增加(多变量调整β=0.05;95%CI:0.03,0.08)和整体MD降低(多变量调整β=-0.04;95%CI:-0.07,-0.01)相关。
与MASLD相关的脑形态学特征是皮质下灰质体积较小,白质微结构的连贯性较高但强度较低。