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CSF biomarkers and medial temporal lobe atrophy predict dementia in mild cognitive impairment
F H Bouwman1, S N M Schoonenboom, W M van der Flier
1Department of Neurology, Alzheimer Centre, VU Medical Center, MB Amsterdam, The Netherlands. femke.bouwman@vumc.nl <femke.bouwman@vumc.nl>
Objective:
To study CSF biomarkers, beta-amyloid(1-42) (Abeta(1-42)) and tau, and medial temporal lobe atrophy (MTA) on MRI in their ability to predict dementia in patients with mild cognitive impairment (MCI).
Methods:
Fifty-nine MCI patients (49% male, mean age 69+/-8), follow-up 19 months, were included. Baseline CSF levels of Abeta(1-42), tau and MTA-score were dichotomized.
Results:
Thirty-three (56%) of the MCI patients progressed to dementia, 30 of which had Alzheimer's disease. Lower CSF Abeta(1-42) level, higher CSF-tau and higher MTA-scores at baseline were found in progressed patients. Cox proportional hazards models revealed that abnormal CSF Abeta(1-42), CSF tau and MTA were significantly associated with dementia at follow-up (hazard ratio (95% confidence interval): 4.0 (1.3-12.1), 5.9 (1.6-21.7) and 2.1 (1.0-4.6)). A fourfold higher risk was found for patients with both abnormal CSF biomarkers and MTA compared to patients with either test abnormal. Ninety-four percent of patients with both abnormalities converted to dementia.
Conclusions:
These findings suggest an added value of CSF to MRI in the diagnostic work up of patients presenting at a memory clinic.
Insights
Predicting dementia in mild cognitive impairment (MCI) patients is improved by combining cerebrospinal fluid (CSF) biomarkers, like beta-amyloid(1-42) and tau, with medial temporal lobe atrophy (MTA) MRI scans.
Area of Science:
- Neurology
- Biomarkers
- Neuroimaging
Background:
- Mild cognitive impairment (MCI) is a transitional stage between normal aging and dementia.
- Identifying individuals with MCI who will progress to dementia is crucial for timely intervention.
- Current diagnostic methods may lack sufficient predictive power for dementia conversion.
Purpose of the Study:
- To evaluate the predictive value of cerebrospinal fluid (CSF) biomarkers beta-amyloid(1-42) (Abeta(1-42)) and tau for dementia development in MCI patients.
- To assess the role of medial temporal lobe atrophy (MTA) on MRI in predicting dementia progression in MCI.
- To determine the combined predictive accuracy of CSF biomarkers and MTA for dementia conversion.
Main Methods:
- A cohort of 59 MCI patients (mean age 69±8 years) was followed for 19 months.
- Baseline CSF levels of Abeta(1-42) and tau, along with MTA scores from MRI, were dichotomized.
- Cox proportional hazards models were used to analyze the association between baseline measures and dementia conversion.
Main Results:
- 56% of MCI patients progressed to dementia, most commonly Alzheimer's disease.
- Lower CSF Abeta(1-42), higher CSF tau, and higher MTA scores were associated with dementia progression.
- Abnormal CSF Abeta(1-42), CSF tau, and MTA significantly predicted dementia (HRs: 4.0, 5.9, 2.1 respectively).
- Patients with both abnormal CSF biomarkers and MTA had a fourfold higher risk of dementia and 94% conversion rate.
Conclusions:
- CSF biomarkers (Abeta(1-42), tau) and MTA on MRI are significant predictors of dementia in MCI patients.
- Combining CSF biomarkers with MTA enhances the prediction of dementia conversion.
- These findings support the integrated use of CSF analysis and MRI in memory clinics for improved diagnostic workup.
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