尿酸
痴呆
内科学
逻辑回归
医学
肌酐
肥胖
病态的
阿尔茨海默病
认知障碍
小型精神状态检查
疾病
认知
精神科
作者
Qing Tian,Qing Dong,Zhumin Su,Yingying Liu,Lili Ma,Huimin Dong,Yiru Xu,Zhengkai Ma,Xiaohong Chen,Xiaomeng Ma
标识
DOI:10.1177/13872877251315011
摘要
Background Given the limited effective treatments for Alzheimer's disease (AD), obesity and serum uric acid (SUA) levels which are considered modifiable risk factors for dementia are of interest. However, research indicates conflicting results. Objective We aimed to further investigate the association of body weight (BW) and SUA with AD biomarkers and cognitive impairment. Methods Clinical data were collected from 139 adults (mean age 66.9 years) with chronic cognitive impairment. Cerebrospinal fluid (CSF) biomarkers and PET imaging were used to assess amyloid-β (A) and Tau (T) tangles load, classifying participants into AT profiles based on the results. The association of BW and SUA with AT profiles was evaluated using multivariable logistic regression, and their relationship with cognitive function (Mini-Mental State Examination (MMSE) scores) were analyzed using multivariable linear regression. Results Lower BW levels significantly influenced the presence of Aβ positive state (A+) (p = 0.007), while SUA levels did not (p = 0.263). Higher dementia proportion (p = 0.021), lighter BW (p = 0.019), and lower mean arterial pressure (MAP) levels (p = 0.025) were associated with AD pathological progress (A-T-→A+T-→A+T+), but SUA was not observed statistically significant. Among all participants regardless of Aβ state, high education levels (p < 0.001), high BW (p = 0.010), and high SUA (p=0.036) were associated with high MMSE scores, and high serum creatinine (p = 0.003) was associated with low MMSE scores. Conclusions Lower BW may accelerate AD pathology and cause cognitive impairment, while SUA is not linked to AD pathological progression but protects cognitive function.
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