{"title":"脑脊液心脏脂肪酸结合蛋白作为阿尔茨海默病神经退行性变的预测性生物标志物","authors":"Lu Pan, Ya-Nan Ou, Lin Tan, L. Tan, Jin-Tai Yu","doi":"10.26599/BSA.2021.9050003","DOIUrl":null,"url":null,"abstract":"Objective This study aims to investigate whether the heart fatty acid‐binding protein (HFABP) in the cerebrospinal fluid (CSF) was a potential predictive biomarker for Alzheimer’s disease (AD). Methods We evaluated the associations of CSF HFABP levels with core biomarkers, cognition, and brain structure in a sample population (n = 302) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. Multiple linear regression and mixed‐effects models were employed in the analyses. AD progression was assessed using the Kaplan–Meier survival analysis. Results CSF HFABP was higher in patients with mild cognitive impairment and AD than the normal controls (p < 0.001) and was particularly higher in those with amyloid‐β (Aβ) pathologic features. CSF HFABP was associated with higher baseline CSF t‐tau (p < 0.001), CSF p‐tau (p < 0.001), and CSF t‐tau/Aβ42 and CSF p‐tau/Aβ42 (p < 0.01). Moreover, CSF HFABP was found to play predictive roles in hippocampal atrophy (p < 0.01), cognitive decline (p < 0.05), and the risk of AD (p < 0.001). Conclusion Our findings suggest that CSF HFABP can be a predictive biomarker of AD.","PeriodicalId":67062,"journal":{"name":"Brain Science Advances","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Cerebrospinal fluid heart fatty acid‐binding protein as a predictive biomarker of neurodegeneration in Alzheimer’s disease\",\"authors\":\"Lu Pan, Ya-Nan Ou, Lin Tan, L. Tan, Jin-Tai Yu\",\"doi\":\"10.26599/BSA.2021.9050003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective This study aims to investigate whether the heart fatty acid‐binding protein (HFABP) in the cerebrospinal fluid (CSF) was a potential predictive biomarker for Alzheimer’s disease (AD). Methods We evaluated the associations of CSF HFABP levels with core biomarkers, cognition, and brain structure in a sample population (n = 302) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. Multiple linear regression and mixed‐effects models were employed in the analyses. AD progression was assessed using the Kaplan–Meier survival analysis. Results CSF HFABP was higher in patients with mild cognitive impairment and AD than the normal controls (p < 0.001) and was particularly higher in those with amyloid‐β (Aβ) pathologic features. CSF HFABP was associated with higher baseline CSF t‐tau (p < 0.001), CSF p‐tau (p < 0.001), and CSF t‐tau/Aβ42 and CSF p‐tau/Aβ42 (p < 0.01). Moreover, CSF HFABP was found to play predictive roles in hippocampal atrophy (p < 0.01), cognitive decline (p < 0.05), and the risk of AD (p < 0.001). Conclusion Our findings suggest that CSF HFABP can be a predictive biomarker of AD.\",\"PeriodicalId\":67062,\"journal\":{\"name\":\"Brain Science Advances\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain Science Advances\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.26599/BSA.2021.9050003\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Science Advances","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.26599/BSA.2021.9050003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
目的本研究旨在探讨脑脊液(CSF)中心脏脂肪酸结合蛋白(HFABP)是否是阿尔茨海默病(AD)的潜在预测生物标志物。研究人员从阿尔茨海默病神经影像学倡议(ADNI)数据库中提取样本人群(n = 302),评估脑脊液HFABP水平与核心生物标志物、认知和大脑结构的关系。分析采用多元线性回归和混合效应模型。使用Kaplan-Meier生存分析评估AD进展。结果轻度认知障碍和AD患者脑脊液HFABP高于正常对照组(p < 0.001),特别是具有淀粉样蛋白β (Aβ)病理特征的患者脑脊液HFABP较高。脑脊液HFABP与较高的基线脑脊液t - tau (p < 0.001)、脑脊液p - tau (p < 0.001)、脑脊液t - tau/ a - β42和脑脊液p - tau/ a - β42相关(p < 0.01)。此外,脑脊液HFABP在海马萎缩(p < 0.01)、认知能力下降(p < 0.05)和AD风险(p < 0.001)中具有预测作用。结论脑脊液HFABP可作为阿尔茨海默病的一种预测性生物标志物。
Cerebrospinal fluid heart fatty acid‐binding protein as a predictive biomarker of neurodegeneration in Alzheimer’s disease
Objective This study aims to investigate whether the heart fatty acid‐binding protein (HFABP) in the cerebrospinal fluid (CSF) was a potential predictive biomarker for Alzheimer’s disease (AD). Methods We evaluated the associations of CSF HFABP levels with core biomarkers, cognition, and brain structure in a sample population (n = 302) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. Multiple linear regression and mixed‐effects models were employed in the analyses. AD progression was assessed using the Kaplan–Meier survival analysis. Results CSF HFABP was higher in patients with mild cognitive impairment and AD than the normal controls (p < 0.001) and was particularly higher in those with amyloid‐β (Aβ) pathologic features. CSF HFABP was associated with higher baseline CSF t‐tau (p < 0.001), CSF p‐tau (p < 0.001), and CSF t‐tau/Aβ42 and CSF p‐tau/Aβ42 (p < 0.01). Moreover, CSF HFABP was found to play predictive roles in hippocampal atrophy (p < 0.01), cognitive decline (p < 0.05), and the risk of AD (p < 0.001). Conclusion Our findings suggest that CSF HFABP can be a predictive biomarker of AD.