Identification of Biomarkers Sensitive to Disease Progression in Patients With Mild Cognitive Impairment

Qualissima

Status

Completed

Conditions

MILD COGNITIVE IMPAIRMENT

Treatments

Procedure: Lumbar puncture

Study type

Interventional

Funder types

Other

Identifiers

NCT01425957

2011-A00985-36 (Other Identifier)

WP5P001

Details and patient eligibility

About

THE STUDY WILL BE A TWO-PART RESEARCH

PART A and PART A extended:

To implement a "common" MRI acquisition protocol in multiple centers across Europe (Pharma-COG partners).
Apply the common MRI protocol on phantoms and human subjects to characterize, compare and minimize test-retest variability across the MR sites of WP5 for all the quantitative metrics that will be later assessed on patients.

PART B: By collecting clinical, biochemical, neuroimaging, neuropsychological and neurophysiological data in Mild Cognitive Impairment patient, we aim to:

To develop a biomarker MATRIX (made of a combination of biological secondary endpoints) which is more sensitive than the changes observed in the loss of hippocampal volume (primary endpoint) and correlate with the neuropsychological progression and conversion (clinical secondary endpoints).
To develop a biomarker MATRIX (made of a combination of biological secondary endpoints) at baseline which is more predictive of the loss of hippocampal volume (primary endpoint) and neuropsychological progression (clinical secondary endpoint) in MCI patients.
To harmonize the biomarker MATRIX collection and qualify multiple centres across Europe

Enrollment

229 patients

Sex

All

Ages

50 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

PART A:

Participants will be (i) healthy volunteers (between 50 and 80 years old) and/or (ii) subjects (between 50 and 80 years old), who will perform a 3T-MRI for reasons such as migraine, headache, auditory or visual symptoms, paresthesias, and whose scan will be negative (see exclusion criteria below). Such subjects will be selected and asked to perform additional sequences according to the part A study protocol.

PART B:

Specific inclusion criteria:

Written Informed Consent to participate in a up to 3 year imaging study
Male and female aged between 55-90 years
Memory complaint by patient or partner that is verified by a physician. (Memory complains expressed by the patients or their informant that the examiner considers to be relevant and exceed those expected for a patient of their age. The patient may or may not have symptoms of deficiency in other cognitive areas.)
Abnormal memory functions documented by scoring 1 SD below the age-adjusted mean on the Logical Memory II subscale, (Delayed Paragraph Recall) from the Wechsler Memory Scale.
General cognition and functional performance sufficiently preserved such that a diagnosis of Alzheimer's disease cannot be made by the site physician at the time of the screening visit.
Mini-Mental State Exam score between 24 and 30 (inclusive)
Clinical Dementia Rating = 0.5. Memory Box score must be at least 0.5.
Amnestic Mild Cognitive Impairment (MCI) (pure amnestic or multidomain)
Geriatric Depression Scale less than 6
Hachinski Modified Ischemic scale< to 4
Patient is untreated or under a permitted medication (Cholinesterase inhibitors and memantine, before the enrolment and newly prescriptions during the study, are permitted for aMCI patients.)
At least 5 grades education
Must speak (language) fluently
Have a study partner with 10+ hr/wk contact (can be in person and telephone), accompanies to visits
Willing and able to comply with the requirements of the study, as judged by the investigator

Exclusion criteria

PART A:
1. Ischaemic lesions already detected in a previous scan
2. Head injury with loss of consciousness > 24 hours
3. Current substance abuse
4. Current therapy with steroids or current chemotherapy
5. Loss of weight > 5 kg in the last 6 months
6. Systemic disease with frequent involvement of the CNS (lupus, HIV, rheumatoid arthritis)
7. CNS disease diagnosed by a specialist or in treatment (such as epilepsy, ictus)
8. Cerebral metastasis or CNS primary tumour still benign (except for pituitary microadenoma)
9. Suspected multiple sclerosis + MRI evidence of white matter lesions
10. Suspected recent stroke + MRI evidence of infarct
11. Aneurysm > 10 mm and arteriovenous malformations (except for venous angioma)
12. Dysgenesia of central nervous system
PART B:
1. Visual and auditory acuity inadequate for neuropsychological testing
2. Enrolment in other trials or studies not compatible with study objectives (in particular, those with experimental drugs)
3. History of significant neurological or psychiatric illnesses or presence of other diseases precluding enrolment.
4. Use of forbidden medications
5. Ferromagnetic implants and devices not eligible for MRI scanning. Brain malformation or other conditions that may complicate lumbar puncture
6. Excluded Medication: Antidepressants with anti-cholinergic properties and within 4 weeks of the screening: Regular use of narcotic analgesics (>2 doses per week), Use of neuroleptics with anti-cholinergic properties (e.g., chlorpromazine, thioridazine), Chronic use of other medications with significant central nervous system anticholinergic activity (e.g., diphenhydramine), Use of Anti-Parkinsonian medications (including Sinemet, amantadine, bromocriptine, pergolide, selegiline), Participation in any other investigational drug study (individuals may not participate in any drug study while participating in this protocol). Diuretic drugs should not be started or discontinued within 4 weeks prior to screening (Any change in diuretic medication during the study should be reported).