痴呆
医学
优势比
内科学
逻辑回归
索引(排版)
血管性痴呆
体质指数
置信区间
可能性
疾病
炎症
肿瘤坏死因子α
免疫学
脂蛋白
风险因素
阿尔茨海默病
趋化因子
血脂谱
血脂
全身炎症
单核细胞
疾病严重程度
老年学
甘油三酯
肿瘤科
白细胞介素6
内分泌学
C反应蛋白
胃肠病学
范畴变量
作者
Yun Liu,Zhifeng Shang,Jianjun Wang,Tingting Hou,Cuicui Liu,Yajun Liang,L. Cong,Yongxiang Wang,Na Tian,Yifeng Du,C. Qiu
标识
DOI:10.1177/13872877261427765
摘要
BackgroundThe lipid accumulation product (LAP) index, a sex-specific indicator of abdominal lipid accumulation, has emerged as a predictor for cardiometabolic disease. However, its association with dementia has been rarely explored in population-based studies.ObjectiveWe sought to investigate the associations of LAP index with all-cause dementia, Alzheimer's disease (AD), and vascular dementia (VaD) as well as with serum inflammatory cytokines among rural-dwelling older adults in China.MethodsThis cross-sectional study included 5670 participants (age ≥ 60 years), with data available in 1851 individuals on serum inflammatory cytokines (interleukin-6, tumor necrosis factor-α, and monocyte chemoattractant protein-1). Dementia and subtypes were diagnosed following the international criteria. The LAP index was calculated as [waist circumference (cm)-65] × triglycerides (mmol/L) for men and [waist circumference (cm)-58] × triglycerides (mmol/L) for women. Data were analyzed using multiple logistic and linear regression models.ResultsOf the 5670 participants, dementia was diagnosed in 305 persons (194 with AD and 100 with VaD). As a continuous variable, the LAP index was associated with multivariable-adjusted odds ratios of 1.28 (95% confidence interval: 1.01-1.61) for all-cause dementia, 1.40 (1.05-1.86) for AD, and 1.12 (0.75-1.66) for VaD. As a categorical variable, the highest (versus lowest) quintile of LAP index was associated with multivariable-adjusted odds ratios of 1.91 (1.17-3.12) for dementia, 2.18 (1.19-3.99) for AD, and 1.88 (0.78-4.53) for VaD. A higher LAP index was significantly correlated with serum inflammatory cytokines (p < 0.05).ConclusionsHigh LAP index is linked with dementia and AD in older adults and chronic systemic inflammation might represent a plausible biological pathway.
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