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Brain Amyloid-β Peptide Is Associated with Pain Intensity and Cognitive Dysfunction in Osteoarthritic Patients
Chun-Hsien Wen1,2,3,4,5, Hong-Yo Kang1,6,7, Julie Y H Chan8
1Graduate Institute of Clinical Medical Sciences, Chang Gung University, Taoyuan 33302, Taiwan.
International Journal of Molecular Sciences
|December 17, 2024
Summary
Osteoarthritis (OA) is linked to cognitive decline, especially in patients with chronic pain. Alzheimer's disease (AD) biomarkers like Aβ40 and Aβ42 in cerebrospinal fluid may explain this connection.
Area of Science:
- Neuroscience
- Immunology
- Gerontology
Background:
- Osteoarthritis (OA) is a known risk factor for dementia.
- The underlying mechanisms linking OA to cognitive dysfunction are not fully understood.
- Inflammation and Alzheimer's disease (AD) biomarkers are implicated in cognitive decline.
Purpose of the Study:
- To investigate the associations between pro-inflammatory cytokines, AD biomarkers, pain intensity, and cognitive decline in knee OA patients.
- To explore the role of specific biomarkers in the OA-cognitive dysfunction relationship.
Main Methods:
- Prospective, observational study of 50 patients (26 OA, 24 controls).
- Assessed pain intensity (Visual Analogue Scale - VAS) and cognitive function (Cognitive Abilities Screening Instrument - CASI).
- Measured plasma and cerebrospinal fluid (CSF) levels of inflammatory molecules and AD biomarkers (Aβ40, Aβ42, tau) using multiplex immunoassay.
Main Results:
- OA patients showed poorer cognitive performance compared to controls.
- Higher VAS pain scores correlated negatively with CASI scores across multiple cognitive domains.
- In OA patients, VAS scores correlated positively with CSF fractalkine, Aβ40, and Aβ42.
- CSF Aβ40 and Aβ42 levels negatively correlated with attention and abstract thinking scores.
Conclusions:
- Knee OA is associated with impaired cognitive performance, particularly in patients experiencing chronic pain.
- Elevated levels of AD biomarkers (Aβ40, Aβ42) in CSF may partially mediate the relationship between OA, pain, and cognitive decline.
- Findings highlight the potential role of neuroinflammation and AD pathology in OA-related cognitive impairment.

