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[Correlation study between the levels of serum MCP-1,SAA and cognitive function in patients with COPD-OSAHS]
1Department of Respiratory, North China University of Science and Technology Affiliated Hospital,Tangshan,063000, China.
Patients with overlap syndrome (OS) experience cognitive impairment linked to higher levels of monocyte chemoattractant protein-1 (MCP-1) and serum amyloid A (SAA). These inflammatory markers correlate with reduced cognitive function in OS patients.
Area of Science:
- Medical Research
- Biomarkers
- Neurology
Background:
- Chronic obstructive pulmonary disease (COPD) and obstructive sleep apnea hypopnea syndrome (OSAHS) are common conditions.
- Overlap syndrome (OS) combines both COPD and OSAHS, potentially leading to complex health issues.
- Cognitive impairment is a growing concern in patients with respiratory disorders.
Purpose of the Study:
- To investigate the relationship between serum monocyte chemoattractant protein-1 (MCP-1) and serum amyloid A (SAA) levels and cognitive function in patients with OS.
- To compare cognitive function and inflammatory markers between patients with OS and those with COPD alone.
- To determine if MCP-1 and SAA are associated with cognitive decline in OS.
Main Methods:
- Sixty patients with OS and 33 patients with COPD were enrolled.
- Serum levels of MCP-1 and SAA were measured in all participants.
- Cognitive function was assessed using the Montreal Cognitive Assessment (MoCA) scale.
Main Results:
- OS patients exhibited significantly higher serum levels of MCP-1 and SAA compared to COPD patients.
- The OS group demonstrated significantly lower Montreal scale scores, indicating cognitive impairment.
- A significant negative correlation was observed between Montreal scale scores and serum levels of MCP-1 and SAA in OS patients.
Conclusions:
- Patients with OS show significant cognitive impairment compared to COPD patients.
- OSAHS may be an independent risk factor for cognitive impairment.
- MCP-1 and SAA levels are negatively associated with cognitive function in OS patients, suggesting their role in cognitive impairment pathogenesis.
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