The influence of depression and neuroinflammation on the progression of mild cognitive impairment to dementia: PET imaging of amyloid deposition and microglia activatio
- Conditions
- late onset depressionMild cognitive impairment1004225810012272
- Registration Number
- NL-OMON32861
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 48
• Informed consent
• Aged between 50-80 years
• Assigned by physician as competent to participate in the study
• Inclusion groups:
o Fulfilling the criteria for healthy volunteers
o Fulfilling the criteria for late onset depression
o Fulfilling the criteria for MCI
o Fulfilling the criteria for both late onset depression and MCI
• History of major psychiatric disorders such as schizophrenia and bipolar disorder and previous unipolar depression
• History of head trauma
• Ischemic cerebrovascular disease, determined by MRI
• Major medical illnesses such as coronary heart disease, diabetes and cancer
• Chronic inflammatory disease such as rheumatoid arthritis, osteoarthritis, chronic obstructive pulmonary disease, psoriasis, etc.
• Use of anti-inflammatory medication such as non-steroidal anti-inflammatory drugs (NSAID) and corticosteroids during a week before PET scan
• The use benzodiazepines a week before the PET scan
• The use of statins, acetylcholinesterase inhibitors, warfarin and digoxin
• History of substance abuse such as alcohol and nicotine (smoking) within the last 6 months
• Presence of dementia
• Any patients with MRI contradictions such as metal implantations and pacemakers
• Malnutrition (vitamin deficiency) or obesity (BMI > 30)
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Quantification of alterations of brain beta-amyloid and activated microglia on<br /><br>the progress of dementia in patients with mild cognitive impairment and late<br /><br>onset depression determined with PET.</p><br>
- Secondary Outcome Measures
Name Time Method <p>• Plasma pro-inflammatory proteins as well as brain derived neurotrophic factor.<br /><br>• Cognition.<br /><br>• Alterations in brain volume </p><br>