Cerebrospinal Fluid Metals and the Association with Cerebral Small Vessel Disease.
Aged
Alzheimer Disease
/ cerebrospinal fluid
Amyloid beta-Peptides
/ cerebrospinal fluid
Apolipoprotein E2
/ genetics
Apolipoprotein E4
/ genetics
Cerebral Hemorrhage
/ cerebrospinal fluid
Cerebral Small Vessel Diseases
/ cerebrospinal fluid
Chromium
/ cerebrospinal fluid
Cognitive Dysfunction
/ cerebrospinal fluid
Copper
/ cerebrospinal fluid
Dementia, Vascular
/ cerebrospinal fluid
Diagnostic Self Evaluation
Female
Humans
Iron
/ cerebrospinal fluid
Magnetic Resonance Imaging
Male
Manganese
/ cerebrospinal fluid
Metals, Heavy
/ cerebrospinal fluid
Middle Aged
Nickel
/ cerebrospinal fluid
Peptide Fragments
/ cerebrospinal fluid
Phosphorylation
Zinc
/ cerebrospinal fluid
tau Proteins
/ cerebrospinal fluid
Alzheimer’s disease
cerebrospinal fluid
cognitive aging
dementia
magnetic resonance imaging
Journal
Journal of Alzheimer's disease : JAD
ISSN: 1875-8908
Titre abrégé: J Alzheimers Dis
Pays: Netherlands
ID NLM: 9814863
Informations de publication
Date de publication:
2020
2020
Historique:
pubmed:
27
10
2020
medline:
28
9
2021
entrez:
26
10
2020
Statut:
ppublish
Résumé
Brain metal homeostasis is essential for brain health, and deregulation can result in oxidative stress on the brain parenchyma. Our objective in this study was to focus on two hemorrhagic MRI manifestations of small vessel disease [cerebral microbleeds (CMBs) and cortical superficial siderosis (cSS)] and associations with cerebrospinal fluid (CSF) iron levels. In addition, we aimed to analyze CSF biomarkers for dementia and associations with CSF metal levels. This is a cross-sectional study of 196 patients who underwent memory clinic investigation, including brain MRI. CSF was collected and analyzed for metals, amyloid-β (Aβ) 42, total tau (T-tau), and phosphorylated tau (P-tau), and CSF/serum albumin ratios. Statistical analyses were performed using generalized linear models. No significant difference was found between CSF metal levels across diagnostic groups. Higher iron and copper levels were associated with higher CSF levels of Aβ42, T-tau, P-tau, and CSF/serum albumin ratios (p < 0.05). Zinc was associated with higher CSF/serum albumin ratios. There was no significant association between CMBs or cSS and CSF iron levels. An increase in CSF iron with the number of CMBs was seen in APOEɛ4 carriers. CSF iron levels are elevated with cerebral microbleeds in APOEɛ4 carriers, with no other association seen with hemorrhagic markers of small vessel disease. The association of elevated CSF iron and copper with tau could represent findings of increased neurodegeneration in these patients.
Sections du résumé
BACKGROUND
Brain metal homeostasis is essential for brain health, and deregulation can result in oxidative stress on the brain parenchyma.
OBJECTIVE
Our objective in this study was to focus on two hemorrhagic MRI manifestations of small vessel disease [cerebral microbleeds (CMBs) and cortical superficial siderosis (cSS)] and associations with cerebrospinal fluid (CSF) iron levels. In addition, we aimed to analyze CSF biomarkers for dementia and associations with CSF metal levels.
METHODS
This is a cross-sectional study of 196 patients who underwent memory clinic investigation, including brain MRI. CSF was collected and analyzed for metals, amyloid-β (Aβ) 42, total tau (T-tau), and phosphorylated tau (P-tau), and CSF/serum albumin ratios. Statistical analyses were performed using generalized linear models.
RESULTS
No significant difference was found between CSF metal levels across diagnostic groups. Higher iron and copper levels were associated with higher CSF levels of Aβ42, T-tau, P-tau, and CSF/serum albumin ratios (p < 0.05). Zinc was associated with higher CSF/serum albumin ratios. There was no significant association between CMBs or cSS and CSF iron levels. An increase in CSF iron with the number of CMBs was seen in APOEɛ4 carriers.
CONCLUSION
CSF iron levels are elevated with cerebral microbleeds in APOEɛ4 carriers, with no other association seen with hemorrhagic markers of small vessel disease. The association of elevated CSF iron and copper with tau could represent findings of increased neurodegeneration in these patients.
Identifiants
pubmed: 33104030
pii: JAD200656
doi: 10.3233/JAD-200656
doi:
Substances chimiques
Amyloid beta-Peptides
0
Apolipoprotein E2
0
Apolipoprotein E4
0
Metals, Heavy
0
Peptide Fragments
0
amyloid beta-protein (1-42)
0
tau Proteins
0
Chromium
0R0008Q3JB
Manganese
42Z2K6ZL8P
Copper
789U1901C5
Nickel
7OV03QG267
Iron
E1UOL152H7
Zinc
J41CSQ7QDS
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM