TABLE 5.
Humans | Animals | Human evidence for: | |||||
---|---|---|---|---|---|---|---|
Marker | Human evidence | References | Evidence of causal effects in animal models | Refs | Risk markers | Disease markers | Outcome markers |
Biofluid Based | |||||||
Inflammatory | |||||||
• AGP | ↑ CSF | 145 | |||||
• CHI3L1/YKL-40 | ↑ Blood | 146 | X | X | |||
• Complement factor C3 | ↑ Blood, CSF | 147 | |||||
• CCL2 | ↑ Blood | 148 | X | ||||
• CRP | ↑ Blood, CSF | 149–151 | X | X | |||
• FGF-21, FGF-23 | ↑ Blood | 152 | X | ||||
• Gal-3BP | ↑ Blood | 153 | |||||
• IGF-1 | ↓ Blood | 148,154 | X | ||||
• IL-1β | ↑ Blood, CSF | 155 | Causal in multiple models | X | |||
• IL-1RA | ↑ Blood, CSF | 156,160 | Protective in some models | ||||
• IL-2 | ↑ Blood | 157 | X | ||||
• IL-6 | ↑ Blood, CSF | 156–162 | X | X | |||
• sIL-6R | ↑ Blood, CSF | 163 | |||||
• IL-8 | ↑ Blood, CSF | 162 | X | ||||
• IL-12 | ↑ CSF | 164 | |||||
• MCP-1 | ↑ Blood | 165 | X | ||||
• Natural killer (NK) cells | ↑ Blood | 166 | |||||
• Syndecan-1 | ↑ Blood | 167 | X | ||||
• TNF-α | ↑ Blood, CSF | 168 | Causal in some models | X | X | ||
Neurodegeneration or neuronal injury | |||||||
• Aβ | ↑ CSF | 169,170 | |||||
• GFAP | ↑ Blood, CSF | 170–173 | X | ||||
• Neurogranin | ↑ Blood | 174 | X | ||||
• Neutrophil:Lymphocyte ratio | ↑ Blood | 175,176 | X | X | |||
• NSE | ↑ Blood | 173,177,178 | X | ||||
• NfL | ↑ Blood | 170,171,179 | X | ||||
• P-tau | ↑ CSF | 180 | X | ||||
• PAI-1 | ↑ Blood | 161 | |||||
• S100β | ↑ Blood, CSF | 162,178,181 | X | ||||
• T-tau | ↑ Blood, CSF | 170,180,182 | X | ||||
• UCHL1 | ↓ Blood | 183 | X | ||||
Biochemical: | |||||||
• AChE | ↓ Blood, CSF | 168,183,184 | X | X | |||
• Adrenaline | ↓ CSF | 176 | X | ||||
• Anticholinergic activity | ↑ Blood, CSF | 185 | Disruption of relevantfunctions by cholinergic antagonists | ||||
• BuChE | ↓ Blood, CSF | 186,187 | X | ||||
• Dopamine | ↓ CSF | 187 | X | ||||
• FA5 | ↑ CSF | 188 | |||||
• Troponin | ↑ Blood | 175 | X | ||||
Neurophysiological | |||||||
• EEG—oscillatory dynamics | Relative power increase in slow frequencies and decrease in fast frequencies | 87,89–102,189–192 | ↑ slow wave activity | 107 | X | ||
—↑ θ | |||||||
—↑ δ | |||||||
—↓ β | |||||||
—↓ α | |||||||
And loss of high-frequency activity, especially in posterior brain regions | X | ||||||
Altered α/θ, α/(θ+δ) or (α+β)/(θ+δ) ratio | 94,101,192 | X | |||||
Reduced peak frequency | 101 | X | |||||
High preoperative alpha power | 95 | X | X | ||||
• EEG—connectivity | ↓ α band connectivity (possible marker for disturbed consciousness) and loss of directionality | 94,102,103,191,192 | ↓ α band connectivity | 107 | X | ||
↑ θ band connectivity (possible marker for attention/memory deficits) | 94,192 | X | |||||
↓ β band connectivity (possible marker for instability of cognitive processes) | 192 | x | |||||
↑ δ band connectivity directed to frontal regions | 191,192 | X | |||||
Disturbance in default mode (DMN), salience (SN), and executive control (ECN) networks | 192 | X | |||||
Decrease in frontal-occipitoparietal connectivity | 95 | X | |||||
• SSEP/BAEP | ↑ Short- and long-latency sensory evoked potentials (SEP) | 113 | X | ||||
Local field potentials (LFPs), Single neuron activity | ↓ Hippocampal θ frequency; ↓θ frequency and amplitude in medial prefrontal cortex; ↑ short-term δ frequency | 118 | |||||
Imaging | |||||||
• Structural (MRI, DTI-MRI) | |||||||
↑ Ventricular size (as a vulnerability marker) | 193 | X | |||||
New ischemic lesions, ↑ white matter hyperdensity/disruption | 194–198 | X | X | X | |||
↓ Gray matter volume | 196 | X | |||||
↓ Brain volume | 199 | X | |||||
• Functional (fMRI) | |||||||
↓ Connectivity strength (in aging and dementia) | 103 | X | |||||
↓ Efficiency and local clustering | 103 | X | |||||
Imbalanced connectivity in default mode network (DMN) and disrupted connectivity between DMN and dorsolateral prefrontal cortex (executive network) | 74,200 | X | |||||
Excessive striatum-salience network (anterior cingulate cortex and insula) connectivity | 200 | X | |||||
Disconnection of mesencephalic tegmentum, ventral tegmental area, and nucleus basalis with striatum/thalamus | 74,200 | LPS-induced T-maze deficits reversed by peripheral glucose | X | X | |||
• Functional (PET, SPECT) | |||||||
↓ Whole-brain glucose consumption, especially in posterior cingulate cortex | 200 | 59 | |||||
↓ Blood flow ratios in frontal and parietal cortex | 201 | ↓ glucose consumption in neocortex | X |
Abbreviations: AChE, acetylcholinesterase; AGP, alpha-1-Acid glycoprotein; BuChE, butyryl cholinesterase; CRP, C-reactive protein; CSF, cerebrospinal fluid; FA5, coagulation factor V; GFAP, glial fibrillary acidic protein; IGF, insulin-like growth factor; IL, interleukin; CHI3L1/YKL-40, chitinase 3-like protein 1; fMRI, functional magenetic resonance imaging; Gal-3BP, galectin-3 binding protein; LPS, lipopolysaccharide; NfL, neurofilament light chain; MCP-1, monocyte chemoattractant protein-1; NSE, neuron-specific enolase; PAI-1, plasminogen activating inhibitor-1; R, receptor; PET, positron emission tomography; RA, receptor agonist; s, soluble; S100β, S100 calcium binding B; UCHL1, ubiquitin carboxyl-terminal-esterase-L1.