Blood‐brain barrier breakdown, neuroinflammation, and cognitive decline in older adults

脑脊液 认知功能衰退 血脑屏障 痴呆 内科学 医学 神经炎症 炎症 免疫学 病理 疾病 中枢神经系统
作者
Gene L. Bowman,Loı̈c Dayon,Richard Kirkland,Jérôme Wojcik,Gwendoline Peyratout,India C. Severin,Hugues Henry,Aikaterini Oikonomidi,Eugenia Migliavacca,Michael Bacher,Julius Popp
出处
期刊:Alzheimers & Dementia [Wiley]
卷期号:14 (12): 1640-1650 被引量:258
标识
DOI:10.1016/j.jalz.2018.06.2857
摘要

Abstract Introduction Blood‐brain barrier (BBB) breakdown is observed in older versus younger adults and in late‐onset Alzheimer's disease versus age‐matched controls, but its causes and consequences in aging are unclear. We tested the hypothesis that BBB breakdown is associated with cognitive decline and inflammation in nondemented elders. Methods Cerebrospinal fluid and serum inflammatory markers were measured using sandwich immunoassays in 120 subjects. Least Absolute Shrinkage and Selection Operator‐logistic regression selected cerebrospinal fluid and serum signatures that best classified BBB impairment defined by the cerebrospinal fluid albumin index ≥9. Linear regression examined changes in Clinical Dementia Rating sum of boxes as a function of BBB integrity at baseline. Results Mean age was 70 years, mean Mini–Mental State Examination was 27, and BBB impairment was recorded in 13.5%. BBB breakdown was associated with cognitive decline ( P = .015). Cerebrospinal fluid intercellular adhesion molecule‐1, vascular endothelial growth factor, interleukin‐8, serum amyloid A, macrophage derived chemokine, and gender generated an area under the curve of 0.95 for BBB impairment, and serum IL‐16, VEGF‐D, IL‐15, and other variables generated an AUC of 0.92 for BBB impairment. Discussion BBB breakdown is associated with more rapid cognitive decline. Inflammatory mechanisms, including cell adhesion, neutrophil migration, lipid metabolism, and angiogenesis may be implicated.
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