Specific Cerebrospinal Fluid SerpinA1 Isoform Pattern in Alzheimer's Disease

被引:8
作者
Barba, Lorenzo [1 ,2 ,3 ]
Halbgebauer, Steffen [2 ]
Paoletti, Federico Paolini [3 ]
Bellomo, Giovanni [3 ]
Abu-Rumeileh, Samir [1 ]
Steinacker, Petra [1 ]
Massa, Federico [4 ]
Parnetti, Lucilla [3 ]
Otto, Markus [1 ,2 ]
机构
[1] Martin Luther Univ Halle Wittenberg, Dept Neurol, D-06120 Halle, Saale, Germany
[2] Ulm Univ Hosp, Dept Neurol, D-89081 Ulm, Germany
[3] Univ Perugia, Dept Med & Surg, Sect Neurol, I-06132 Perugia, Italy
[4] Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, I-16132 Genoa, Italy
关键词
serpinA1; cerebrospinal fluid; biomarker; CIEF immunoassay; Alzheimer's disease; MILD COGNITIVE IMPAIRMENT; CLINICAL DIAGNOSTIC-CRITERIA; ASSOCIATION WORKGROUPS; NATIONAL INSTITUTE; DEMENTIA; ALPHA-1-ANTITRYPSIN; RECOMMENDATIONS; GUIDELINES;
D O I
10.3390/ijms23136922
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SerpinA1 (alpha 1-antitrypsin) is a soluble glycoprotein, the cerebrospinal fluid (CSF) isoforms of which showed disease-specific changes in neurodegenerative disorders that are still unexplored in Alz-heimer's disease (AD). By means of capillary isoelectric focusing immunoassay, we investigated six serpinA1 isoforms in CSF samples of controls (n = 29), AD-MCI (n = 29), AD-dem (n = 26) and Lewy body disease (LBD, n = 59) patients and correlated the findings with CSF AD core biomarkers (A beta 42/40 ratio, p-tau, t-tau). Four CSF serpinA1 isoforms were differently expressed in AD patients compared to controls and LBD patients, especially isoforms 2 and 4. AD-specific changes were found since the MCI stage and significantly correlated with decreased A beta 42/40 (p < 0.05) and in-creased p-tau and t-tau levels in CSF (p < 0.001). Analysis of serpinA1 isoform provided good di-agnostic accuracy in discriminating AD patients versus controls (AUC = 0.80) and versus LBD patients (AUC = 0.92), with best results in patients in the dementia stage (AUC = 0.97). SerpinA1 isoform expression is altered in AD patients, suggesting a common, albeit disease-specific, in-volvement of serpinA1 in most neurodegenerative disorders.
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页数:12
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