Retinal Neuro-vascular Coupling in Patients With Neurodegenerative Disease

This is an interventional basic science trial for Mild Cognitive Impairment Read More

Inclusion Criteria:

Inclusion criteria for healthy subjects

• Men and women aged over 50 years
• Non-smokers
• Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant
• Normal ophthalmic findings, ametropia < 6 Dpt

Inclusion criteria for patients with AD:

• Men and women aged over 50 years
• Normal ophthalmic findings, ametropia < 6 Dpt.

• Confirmed diagnosis of probable AD of mild to moderate degree defined as:

  1. Diagnosis of probable Alzheimer's disease based on the NINCDS/ADRDA criteria
  2. Assessing the severity of Alzheimer's disease of mild to moderate degree by the Mini Mental State Examination (MMSE). AD of mild to moderate degree has been confirmed if the MMSE score is in the range of 20 to 26 inclusive
• Hachinski Ischemia Scale is used to try and distinguish AD from multi-infarct dementia. A score of ≤ 4 suggests AD Informed consent capability
• Adequate visual and auditory acuity to allow neuropsychological testing and participation in the ocular blood flow measurements
• A potential participant has to be on stable doses of all medications he/she is taking because of consisting illnesses according to medical history (except AD therapy itself which will be recorded separately) for at least 30 days prior inclusion, if considered relevant by the investigator.

Inclusion criteria for patients with mild cognitive impairment:

• Men and women aged over 50 years
• Normal ophthalmic findings, ametropia < 6 Dpt.

• Diagnosis of probable mild cognitive impairment (MCI) defined as:

  1. memory complaint, corroborated by an informant
  2. abnormal memory function, documented by delayed recall of one paragraph from the Logical Memory II subtest of the Wechsler Memory Scale-Revised (cutoff scores: ≤8 for ≥16 years of education; ≤4 for 8 to 15 years of education; and ≤2 for 0 to 7 years of education [the maximum number of paragraph items possible to correctly recall is 25])
  3. normal general cognitive function, as determined by a clinician's judgment based on a structured interview with the patient and an informant (Clinical Dementia Rating [CDR]) and a Mini-Mental State Examination (MMSE) score greater than 26
  4. no or minimal impairment in activities of daily living (ADLs), as determined by a clinical interview with the patient and informant
  5. not sufficiently impaired, cognitively and functionally, to meet the NINCDS/ADRDA criteria, as judged by an experienced AD research clinician
• Hachinski Ischemia Scale is used to try and distinguish MCI from multi-infarct dementia. A score of ≤ 4 suggests MCI Informed consent capability
• Adequate visual and auditory acuity to allow neuropsychological testing and participation in the ocular blood flow measurements
• A potential participant has to be on stable doses of all medications he/she is taking because of consisting illnesses according to medical for at least 30 days prior inclusion, if considered relevant by the investigator.

Exclusion Criteria for patients:

• Presence or history of a severe medical condition other than cognitive impairment as judged by the clinical investigator
• Untreated Arterial hypertension
• History or family history of epilepsy
• Presence of any abnormalities preventing reliable measurements in the study eye as judged by the investigator
• Best corrected visual acuity < 0.5 Snellen
• Ametropia greater than 6 Dpt
• pregnancy or planned pregnancy
• Major psychiatric disorder (e.g. schizophrenia), if considered relevant by the investigator
• Significant neurological disease other than AD or MCI, if considered relevant by the investigator
• Alcoholism or substance abuse

Exclusion criteria for healthy volunteers:

• Presence or history of a severe medical condition as judged by the clinical investigator
• Untreated Arterial hypertension
• History or family history of epilepsy
• Presence of any abnormalities preventing reliable measurements in the study eye as judged by the investigator
• Family history of AD
• Best corrected visual acuity < 0.5 Snellen
• Ametropia 6 Dpt
• Pregnancy or planned pregnancy