Associations of varicose veins with cerebrospinal fluid biomarkers of Alzheimer's disease pathologies in adults without dementia: the CABLE study

被引:0
作者
Liu, Min [1 ]
Ma, Li-Yun [2 ]
Li, Qiong-Yao [2 ]
Huang, Liang-Yu [2 ]
Hu, He-Ying [2 ]
Tan, Lan [1 ,2 ]
Hu, Hao [2 ]
机构
[1] Dalian Med Univ, Qingdao Municipal Hosp, Dept Neurol, Qingdao, Peoples R China
[2] Qingdao Univ, Qingdao Municipal Hosp, Dept Neurol, Qingdao, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; dementia; varicose veins; biomarkers; inflammation; AMYLOID-BETA; NEURODEGENERATION; DYSFUNCTION; PROGRESSION; MODEL; RISK;
D O I
10.3389/fnagi.2025.1502154
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background: Previous studies have found a correlation between varicose veins (VVs) and cognitive decline, and individuals with VVs have a higher prevalence of Alzheimer's disease (AD). However, the associations between VVs and the core pathologies of AD have not yet been investigated. The research was designed to analyze the relationships between VVs and cerebrospinal fluid (CSF) biomarkers of AD pathologies. Methods: We included 1,298 participants from the Chinese Alzheimer's Biomarker and LifestylE (CABLE) database without dementia. Multiple linear regression (MLR) model was applied to assess the relationships between the VVs and CSF AD biomarkers. Then, we conducted subgroup analyses according to age, gender, education levels and apolipoprotein E genotype epsilon 4 (APOE-epsilon 4) carrier status. Additionally, mediation effects were assessed using causal mediation analyses with 10,000 bootstrapped iterations. Results: In total subjects, VVs had negative correlations with CSF A beta(42) (beta = -0.157, p = 0.038) and CSF A beta(42)/A beta(40) ratio (beta = -0.272, p < 0.001), as well as positive correlations with CSF A beta(40) (beta = 0.170, p = 0.024), CSF p-tau (beta = 0.192, p = 0.008), CSF t-tau/A beta(42) ratio (beta = 0.190, p = 0.011), and CSF p-tau/A beta(42) ratio (beta = 0.248, p = 0.001), after adjusting for age, sex, education levels and APOE-epsilon 4 carrier status. Subgroup analyses demonstrated that the relations between VVs and CSF AD biomarkers were more significant in female, mid-life adults (40-65 years), less-educated individuals and APOE-epsilon 4 non-carriers. Moreover, CSF A beta(42)/A beta(40) ratio might be a partial mediator of the association between VVs and p-tau pathology. Conclusion: Our study found correlations between VVs and CSF AD biomarkers, suggesting that VVs may be a potential risk factor for the development of AD.
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页数:10
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