Biomarker Study for Alzheimer's Disease

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

115 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-02-28

Study Completion Date

2016-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The study aims to identify immune biomarkers in peripheral blood for identifying Alzheimer's disease (AD). Blood samples from subjects with AD will be compared to age-matched controls without cognitive symptoms, as well as healthy younger subjects.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Biomarker Study to Diagnose Alzheimer's Disease

NCT01874418

Alzheimer Disease Mild Cognitive Impairment

UNKNOWN NA

New Biomarker for Alzheimer's Disease Diagnostic

NCT01315639

Alzheimer's Disease Mild Cognitive Impairment

COMPLETED NA

Study on Biomarkers for Early Diagnosis of Alzheimer's Disease

NCT04575337

Alzheimer Disease

RECRUITING

Blood Biomarkers for Screening of Alzheimer's Disease

NCT06477484

Alzheimer's Disease Blood Biomarkers

RECRUITING

Central and Systemic Inflammation in Alzheimer's Disease

NCT01775696

Alzheimer's Disease

COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by the loss of cognitive brain functions and functional decline. One of the pathological features of this condition is the progressive deposition in the brain of amyloid beta-peptide (A-beta) (1). Once deposited in the brain, the peptide exerts a toxic effect by triggering a chronic inflammation that interferes initially with normal brain function and results eventually in neuronal death (2). It is currently postulated that at a certain threshold of A-beta accumulation compensatory mechanisms in the brain are no longer sufficient to cope with A-beta toxicity, and the clinical syndrome of AD develops. It is possible that A-beta may accumulate in the brain over a period of up to 10-15 years before clinical symptoms become significant. The question has been raised whether the accumulation of A-beta is possibly a normal process of aging, suggesting that all people may be susceptible to the disease if they live long enough - of note is that the prevalence of Alzheimer's disease rises to over 40% above the age of 85 years.

Among the many possible ageing-related factors involved in the development of AD, senescence of the immune system may significantly enhance changes in the brain and intensify the neurological decline in patients with this disease. A direct consequence of immunosenescence is the increased frequency of systemic infections and, in fact, many who die with AD have previously suffered from a severe infection. Since patients with AD have an ongoing chronic inflammatory response in the brain, associated with the activation of glial cells and a partially disrupted blood brain barrier, systemic inflammation may intensify this process in the brain and increase the overall neuronal damage.

In contrast to the damage caused by immune activation, A-beta vaccination studies have shown very promising effects in mouse models of the disease, particularly with regard to the clearance of amyloid plaques by A-beta antibodies (3). When tested in patients with AD, 6% of the vaccinated patients developed severe inflammatory reactions in the brain (4). Nonetheless, a cohort of patients showed improved cognitive tests where specific antibodies were induced (5). In a recent study we demonstrated that such brain inflammation may be due to increased levels of IFN-γ in the brain (6), possibly as a result of sub-clinical systemic infection and the specific immune responses observed in humans.

While the chronic inflammation progresses throughout the disease, the specific arm of the immune system, i.e., brain-specific lymphocytes, may also be stimulated to play a role. In contrast to previous assumptions, our findings in human subjects with AD demonstrate that a specific immune response to A-beta is indeed significantly induced in both elderly individuals and patients with AD as compared to middle-aged individuals (7). The nature and role of this immune response to A-beta in man is yet to be investigated, and may lead to the characterization of pathways associated with neuronal cell death, and result in new diagnostic modalities and immunotherapeutic approaches.

The purpose of this study is to determine whether peripheral markers possibly related to A-beta induced inflammation of the brain are increased in patients with clinical AD.

Method This is an observational pilot study comparing the level of inflammatory markers in the peripheral blood of patients with AD to that of age-matched and cognitively normal elderly individuals, as well as to healthy young controls.

Subjects will include males and females older than 60 years diagnosed as having clinical AD according to DSM-IV criteria. The control group will comprise cognitively normal community dwelling males and females older than 60 years. In addition, a group of healthy young male and female controls aged 20-30 years will serve as the reference group. The diagnosis of both older patients and controls will be determined independently by a multidisciplinary team of experts at the Memory Clinic of the Beersheva Mental Health Center.

All subjects and controls will be required to provide written informed consent for participation in the study. In the case of the patients with AD an independent psychiatrist will be required to confirm that the patient is capable of agreeing to participation in the study. In the case of patients with AD who have impaired judgment and are unable to consent to their participation, a legal guardian will be required to provide written informed consent.

Following the acquisition of demographic data, a single amount of 25 ml of blood will be drawn from all subjects. Blood will be drawn into two heparinized tubes of 10 ml each and one serological tube (with procoagulant) of five ml will be drawn for serum isolation. The heparinized tubes will be maintained at room temperature until lymphocytes are purified on the same day. Sera samples will be stored at 4°C. Blood will be drawn before midday to facilitate purification on the same day. Following peripheral blood mononuclear cell (PBMC) and sera isolation the following analysis will be performed:

1. Generation of AD-specific monoclonal antibodies. Since antibodies which bind the N-terminus portion of A-beta enhance its clearance from the brain and are now tested in a clinical trial, it is important to identify the naturally occurring specific monoclonal antibodies induced in patients with AD and determine whether they affect the course of the disease. Such specific antibodies also may have diagnostic and therapeutic properties. These specific human monoclonal antibodies will be isolated and produced in vitro by the hybridoma technique using a proprietary fusion partner cell line known as MFP-2. Briefly, PBMCs will be fused with MFP-2 and the resulting hybridomas will be screened for nonspecific Ig production and then for those immunoglobulins that are specific to A-beta using standard techniques of ELISA. Hybridomas that secrete specific human monoclonal antibodies will be serially subcloned for stabilization, expanded and grown in defined media for production of large quantities of monoclonal antibodies.
2. Analysis of T-cell subsets and serum-derived cytokines. Aging is associated with senecense of the immune system expressed by a decline in naïve T cells and an increase in memory and regulatory T cells. As a result cytokine homeostasis both in the periphery and in the brain is altered and may contribute to the pathogenesis of AD. Thus, analysis of T-cell subsets (naïve and memory CD4, CD8, and regulatory CD4CD25) using Fluorescence-activated cell sorting (FACS) and serum-derived cytokines by ELISA will be performed and correlated with the clinical score of the patients.

Statistical evaluation of differences in mean values between groups will be performed using the Student's-t test.