Serum DBI and biomarkers of neuroinflammation in Alzheimer's disease and delirium

被引:14
作者
Conti, Elisa [1 ,2 ]
Andreoni, Simona [1 ,2 ]
Tomaselli, Davide [1 ,2 ]
Storti, Benedetta [1 ,2 ,3 ]
Brovelli, Francesco [1 ,2 ,3 ]
Acampora, Roberto [1 ,2 ,3 ]
Da Re, Fulvio [1 ,2 ,3 ]
Appollonio, Ildebrando [1 ,2 ,3 ]
Ferrarese, Carlo [1 ,2 ,3 ]
Tremolizzo, Lucio [1 ,2 ,3 ]
机构
[1] Univ Milano Bicocca, Sch Med & Surg, Room 2043,Bldg U8,Via Cadore 48, I-20900 Monza, MB, Italy
[2] Univ Milano Bicocca, Milan Ctr Neurosci NeuroMI, Room 2043,Bldg U8,Via Cadore 48, I-20900 Monza, MB, Italy
[3] San Gerardo Hosp, Neurol Unit, Monza, Italy
关键词
Diazepam binding inhibitor; Alzheimer's disease; Delirium; Serum; Cytokines; Monocytes; DIAZEPAM-BINDING INHIBITOR; ANXIETY;
D O I
10.1007/s10072-020-04608-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Alzheimer's disease (AD) patients often express significant behavioral symptoms: for this reason, accessible related biomarkers could be very useful. Neuroinflammation is a key pathogenic process in both AD and delirium (DEL), a clinical condition with behavioral symptoms resembling those of AD. Methods A total ofn = 30 AD patients were recruited together withn = 30 DEL patients andn = 15 healthy controls (CTRL). Serum diazepam binding inhibitor (DBI), IL-17, IL-6, and TNF-alpha were assessed by ELISA. Results DBI serum levels were increased in AD patients with respect to CTRL (+ 81%), while DEL values were 70% higher than AD. IL-17 was increased in DEL with respect to CTRL (+ 146%), while AD showed dispersed values and failed to reach significant differences. On the other hand, IL-6 showed a more robust increase in DEL with respect to the other two groups (+ 185% and + 205% vs. CTRL and AD, respectively), and TNF-alpha failed to show any change. Conclusions DBI may be a very promising candidate for AD, perhaps marking psychomotor DEL-like symptoms, in view of developing future helping tool for practicing physicians. Furthermore, DBI rise in DEL offers novel cues for a better comprehension of the pathogenesis of this potentially fatal condition.
引用
收藏
页码:1003 / 1007
页数:5
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