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无痴呆症老年人的多重疾病负担与阿尔茨海默病病理之间的关联:CABLE研究

Associations between multimorbidity burden and Alzheimer's pathology in older adults without dementia: the CABLE study.

作者信息

Aerqin Qiaolifan, Chen Xiao-Tong, Ou Ya-Nan, Ma Ya-Hui, Zhang Ya-Ru, Hu He-Ying, Tan Lan, Yu Jin-Tai

机构信息

Department of Neurology and Institute of Neurology, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai, China.

Department of Rheumatology and Immunology, The First Hospital of China Medical University, Shenyang, China.

出版信息

Neurobiol Aging. 2024 Feb;134:1-8. doi: 10.1016/j.neurobiolaging.2023.09.014. Epub 2023 Sep 27.

Abstract

Studies have shown that multimorbidity may be associated with the Alzheimer's disease (AD) stages, but it has not been fully characterized in patients without dementia. A total of 1402 Han Chinese older adults without dementia from Chinese Alzheimer's Biomarker and LifestylE (CABLE) study were included and grouped according to their multimorbidity patterns, defined by the number of chronic disorders and cluster analysis. Multivariable linear regression models were used to detect the associations with AD-related cerebrospinal fluid (CSF) biomarkers. Multimorbidity and severe multimorbidity (≥4 chronic conditions) were significantly associated with CSF amyloid and tau levels (p < 0.05). Metabolic patterns were significantly associated with higher levels of CSF Aβ40 (β = 0.159, p = 0.036) and tau (P-tau: β = 0.132, p = 0.035; T-tau: β = 0.126, p = 0.035). The above associations were only significant in the cognitively normal (CN) group. Multimorbidity was associated with brain AD pathology before any symptomatic evidence of cognitive impairment. Identifying such high-risk groups might allow tailored interventions for AD prevention.

摘要

研究表明,多种疾病并存可能与阿尔茨海默病(AD)的阶段有关,但在无痴呆症患者中尚未得到充分描述。纳入了来自中国阿尔茨海默病生物标志物与生活方式(CABLE)研究的1402名无痴呆症的汉族老年人,并根据其多种疾病并存模式进行分组,多种疾病并存模式由慢性疾病数量和聚类分析定义。使用多变量线性回归模型来检测与AD相关脑脊液(CSF)生物标志物的关联。多种疾病并存和严重多种疾病并存(≥4种慢性疾病)与CSF淀粉样蛋白和tau水平显著相关(p<0.05)。代谢模式与较高水平的CSF Aβ40(β=0.159,p=0.036)和tau显著相关(磷酸化tau蛋白:β=0.132,p=0.035;总tau蛋白:β=0.126,p=0.035)。上述关联仅在认知正常(CN)组中显著。在出现任何认知障碍症状证据之前,多种疾病并存就与脑AD病理相关。识别此类高危人群可能有助于为AD预防制定针对性干预措施。

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