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Inflammatory Biomarkers in AD: Implications for Diagnosis
1Department of Psychiatry, Korea University College of Medicine, Korea University Guro Hospital, Seoul, Korea.
Current Alzheimer Research
|December 28, 2020
Summary
Early diagnosis of Alzheimer's disease (AD) is crucial. This review explores inflammatory biomarkers in neuroimaging, CSF, and blood for improved AD diagnosis and patient selection for interventions.
Area of Science:
- Neuroscience
- Biomarker Discovery
- Dementia Research
Background:
- Alzheimer's disease (AD) is the leading cause of dementia, characterized by significant neuronal loss before diagnosis.
- Effective interventions are limited, highlighting the need for early and accurate diagnostic methods.
- Neuroinflammation plays a key role in AD pathogenesis, making inflammatory biomarkers promising diagnostic tools.
Purpose of the Study:
- To review the utility of inflammatory biomarkers for diagnosing Alzheimer's disease.
- To discuss biomarkers detectable via neuroimaging, cerebrospinal fluid (CSF), and peripheral blood.
- To suggest clinical implications and potential for improving patient stratification for early interventions.
Main Methods:
- Review of current literature on inflammatory biomarkers in AD diagnosis.
- Focus on neuroimaging ligands (e.g., TSPO), CSF markers (sTREM2, YKL-40, MCP-1), and peripheral blood markers.
- Analysis of the diagnostic potential and limitations of these biomarkers.
Main Results:
- Neuroimaging, CSF, and peripheral blood inflammatory biomarkers show potential for AD diagnosis.
- Specific biomarkers discussed include TSPO ligands, sTREM2, YKL-40, and MCP-1.
- Evidence suggests these markers can aid in identifying AD, though limitations exist.
Conclusions:
- Inflammatory biomarkers offer a promising avenue for the early diagnosis of Alzheimer's disease.
- Combining these biomarkers with conventional methods like genetic testing and amyloid imaging may enhance patient selection.
- Improved patient stratification can facilitate targeted and timely interventions for AD.
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