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The significance of biomarkers in the blood in the diagnosis and the course of Alzheimer*s disease

The significance of biomarkers in the blood in the diagnosis and the course of Alzheimer*s disease - Blood biomarkers for Alzheimer*s disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON34678
Enrollment
100
Registered
2010-10-22
Start date
2011-01-13
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimers disease

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patient inclusion criteria: - Patients with Alzheimer's disease - Mentally competent AD patient [Clinical Dementia Rating (CDR) scale 1] - The diagnosis of "probable Alzheimer's disease* should be made according to the NINCDS- ADRDA criteria. - Patients or carers should agree with the study (written informed consent is required form patients or their carers).;Inclusion criteria control group (healthy subjects in group A): - Men or women without cognitive or psychiatric disorders - Mini-Mental State Examination (MMSE) score >= 28

Exclusion criteria

Exclusion criteria: Patient exclusion criteria: - Mentally incompetent AD patient [Clinical Dementia Rating (CDR) scale 2 and 3] - Patients with infection or inflammatory disease less than 1 months ago. - Patients with active malignancy. - Patients with autoimmune disease (e.g. temporal arteritis, polymyalgia rheumatica). - Patients who use immune modulating drugs (e.g. Immunocyanin, interferon gamma, immunoglobulin). - Patients with renal dysfunction (MDRD

Design outcomes

Primary

MeasureTime frame
- Descriptives (gender, age, education level, demographics) - Biochemical biomarkers: neopterin, total amino acid spectrum, HVA, BDNF and S-100B - Comorbidity (CIRS-G) - Drug use - MMSE score, neuropsychological examination and MRI cerebrum - The Clinical Dementia Rating (CDR) scale - Evolution: intercurrent diseases

Secondary

MeasureTime frame
nvt

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)