Specific Cerebrospinal Fluid SerpinA1 Isoform Pattern in Alzheimer's Disease.
Alzheimer Disease
/ cerebrospinal fluid
Amyloid beta-Peptides
/ cerebrospinal fluid
Biomarkers
/ cerebrospinal fluid
Humans
Lewy Body Disease
/ cerebrospinal fluid
Neurodegenerative Diseases
Peptide Fragments
/ cerebrospinal fluid
Protein Isoforms
alpha 1-Antitrypsin
/ cerebrospinal fluid
tau Proteins
/ cerebrospinal fluid
Alzheimer’s disease
CIEF immunoassay
biomarker
cerebrospinal fluid
serpinA1
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
22 Jun 2022
22 Jun 2022
Historique:
received:
25
05
2022
revised:
16
06
2022
accepted:
20
06
2022
entrez:
9
7
2022
pubmed:
10
7
2022
medline:
14
7
2022
Statut:
epublish
Résumé
SerpinA1 (α1-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 (Aβ42/40 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 Aβ42/40 (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.
Identifiants
pubmed: 35805926
pii: ijms23136922
doi: 10.3390/ijms23136922
pmc: PMC9266332
pii:
doi:
Substances chimiques
Amyloid beta-Peptides
0
Biomarkers
0
Peptide Fragments
0
Protein Isoforms
0
SERPINA1 protein, human
0
alpha 1-Antitrypsin
0
tau Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : EU Joint Programme-Neurodegenerative Diseases networks Genfi-Prox
ID : 01ED2008A
Organisme : German Federal Ministry of Education and Research
ID : FTLDc 01GI1007A
Organisme : EU (Moodmarker) program
ID : 01EW2008
Organisme : German Research Foundation/DFG
ID : SFB1279
Organisme : Foundation of the State Baden-Württemberg
ID : D.3830
Organisme : Boehringer Ingelheim Ulm University BioCenter
ID : D.5009
Organisme : Thierry Latran Foundation
ID : D.2468
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