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Published on: November 10, 2008
Cerebrospinal Fluid sTREM2 in Alzheimer's Disease Is Associated with Both Amyloid and Tau Pathologies but not with
Tao-Ran Li1, Di-Yang Lyu2, Feng-Qi Liu1,3
1Department of Neurology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.
Background:
Cerebrospinal fluid (CSF) soluble triggering receptor expressed on myeloid cells 2 (sTREM2) is considered a biomarker of microglial activation. The relationships between CSF sTREM2 levels and Alzheimer's disease (AD) CSF core biomarkers, cognitive status, and neurodegeneration remain unclear.
Objective:
To assess the association between CSF sTREM2 levels and AD progression and other AD hallmarks.
Methods:
Using the Alzheimer's Disease Neuroimaging Initiative database, we investigated 1,035 participants, including 310 cognitively normal controls, 527 patients with mild cognitive impairment, and 198 patients with dementia. They were grouped according to CSF pathology (A/T profile) severity. CSF sTREM2 levels were compared between the groups, and linear regression analysis was performed to evaluate the factors affecting sTREM2 levels. The predictive effectiveness of sTREM2 levels was tested, and the correlation with other indicators was explored. The increase rate was assessed using linear mixed-effects models.
Results:
Higher CSF sTREM2 levels were associated with older age as well as higher CSF p-tau or t-tau and amyloid-β levels (all p < 0.001), but not with cognitive status. sTREM2 levels were not correlated with the baseline or longitudinal scale and neuroimaging result changes, and could not predict clinical conversion, but were correlated with multiple non-amyloid-β and non-tau CSF cytokines related to inflammation and neurodegeneration (p < 0.0001). The increased sTREM2 expression rate did not change among groups.
Conclusion:
CSF sTREM2 levels were jointly determined by age, amyloid-β, and tau pathologies, leading to complex AD cognitive continuum changes. Although sTREM2 levels could not predict cognitive deterioration and neurodegeneration, they could reflect the microglial state as a non-specific biomarker.
Insights
Cerebrospinal fluid soluble triggering receptor expressed on myeloid cells 2 (sTREM2) reflects microglial activation but does not predict Alzheimer's disease progression. sTREM2 levels are influenced by age and core Alzheimer's biomarkers, not cognitive decline.
Area of Science:
- Neuroscience
- Biomarker Discovery
- Alzheimer's Disease Research
Background:
- Soluble triggering receptor expressed on myeloid cells 2 (sTREM2) in cerebrospinal fluid (CSF) is a marker of microglial activation.
- The relationship between CSF sTREM2, Alzheimer's disease (AD) biomarkers, cognition, and neurodegeneration is not fully understood.
Purpose of the Study:
- To investigate the association between CSF sTREM2 levels and AD progression.
- To determine the relationship between CSF sTREM2 and other AD hallmarks, including core biomarkers and neurodegeneration.
Main Methods:
- Analysis of 1,035 participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database, categorized by cognitive status and CSF pathology.
- Utilized linear regression and mixed-effects models to assess factors affecting sTREM2 levels, its predictive power, and longitudinal changes.
Main Results:
- Higher CSF sTREM2 levels correlated with older age and increased levels of CSF p-tau, t-tau, and amyloid-β.
- sTREM2 levels did not correlate with cognitive status, neurodegeneration markers, or predict clinical conversion.
- CSF sTREM2 levels were associated with inflammatory cytokines but not specific to amyloid-β or tau pathologies.
Conclusions:
- CSF sTREM2 levels are influenced by age, amyloid-β, and tau pathologies, reflecting complex changes in the AD continuum.
- While not a predictor of cognitive decline or neurodegeneration, sTREM2 serves as a non-specific biomarker of microglial activity in AD.
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