A Pilot Study of Inflammatory Markers in Alzheimer's Disease

Alzheimer's Disease Clinical Trial

Official title:

A Pilot Study Comparing Inflammatory Biomarkers in Blood and CSF in Patients With Alzheimer's Disease and Age-Matched Controls

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00715858
• Other study ID #: R07-63
• Status: Recruiting
• Phase: Phase 3
• First received: July 11, 2008
• Last updated: February 3, 2009
• Start date: May 2008
• Est. completion date: October 2009

Study information

• Verified date: February 2009
• Source: McMaster University
• Contact: D. William Molloy, MB
• Phone: 905-777-3837
• Email: wmolloy[@]stpetes.ca
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to examine the cerebrospinal fluid (CSF) of patients with Alzheimer's disease for biomarkers of inflammation and their response to the antibiotics doxycycline and rifampin. The results of this preliminary analysis will be used in defining the direction of further research.

Description:

Doxycycline and rifampicin are two antibiotics which may be useful in the treatment of Alzheimer's disease (AD). Besides their antimicrobial effects they may also decrease specific contributors to AD pathology including: 1. amyloid beta, 2. inflammatory mediators,

3. proteolytic enzymes, and 4. metal ions. Evidence indicates an inflammatory response in AD. This includes complement activation, elevated C-reactive protein (CRP), elevated pro-inflammatory cytokines (including IL-1-beta, IL-6, TNF-α, TGF-β, S100-β), chemokine alterations (IL-8, MIP-1-alpha, MIP-1-beta, MCP-1), and microglial activation. In our previous study of AD patients treated with combined doxycycline and rifampicin versus placebo, we demonstrated that antibiotic treatment significantly delayed progression of clinical impairment. Treatment also reduced blood CRP levels suggesting an anti-inflammatory role of these antibiotics. In this study we suggest analysis of biomarkers including both pro and anti-inflammatory cytokines TNF-alpha, IL-1beta, IL-4, IL-10,the chemokine MCP-1 and other inflammatory markers in both the cerebrospinal fluid (CSF) and blood from AD patients and age-matched controls.

AD patients are participants in a 12 month randomized clinical trial of doxycyline and rifampin or placebo (DARAD) for treatment of AD. Each patient is asked if they wish to contribute a sample of CSF and blood at baseline and at 12 months when treatment is completed. About half the patients are consenting to this. Since consent is given to the lumbar puncture before the double-blinded DARAD treatment is initiated, we expect the distribution of samples collected to be random among the four treatment groups. We will compare CSF biomarker levels among the four treatment groups. Ten age-matched healthy controls are also being asked to contribute CSF and blood samples for comparison. The controls are not participants in the DARAD trial.

We feel that this is an important pilot study to determine whether there are any differences in blood or CSF concentrations of commonly studied cytokines between AD patients and normal controls. As such, this study could contribute to the search for a diagnostic biomarker. Also, it could provide a solid foundation for future studies aimed at elucidating the effects of antibiotics on various biomarkers in the blood and CSF of AD patients. From this, we may be able to correlate previous findings that antibiotics delay progression of clinical outcome in AD with changes in blood or CSF biomarker levels.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 21
• Est. completion date: October 2009
• Est. primary completion date: August 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 50 Years and older

Eligibility

Inclusion Criteria:

• Giving informed consent to lumbar puncture

• Participation in the DARAD clinical trial which requires the following:

• diagnosis of probable Alzheimer's disease

• SMMSE 14-26 inclusive

• community-dwelling

• age 50 or greater

• caregiver to monitor study medication and report on ADLs, behaviour, etc.

• adequate English literacy to complete neuropsychological testing

• generally stable level of health

Exclusion Criteria:

• Contraindication to lumbar puncture

• DARAD exclusion criteria as follows:

• dementia due to other neurodegenerative diseases

• cognitive impairment due to head trauma, etc.

• stroke or significant cerebrovascular disease

• clinically significant cardiac disease such as recent MI, uncontrolled hypertension

• taking other anti-dementia treatments or investigational drugs

• allergy to doxycycline or rifampin

• significant psychiatric conditions like depression

• cancer

Study Design

Allocation: Non-Randomized, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Alzheimer Disease
• Alzheimer's Disease

Intervention

Drug:
• doxycycline
capsule, 100 mg, b.i.d., 12 months
• rifampin
capsule, 300 mg, od, 12 months
• placebo
placebo matched to rifampin; placebo matched to doxycycline

Locations

Country	Name	City	State
Canada	St.Peter's Hospital	Hamilton	Ontario

Sponsors (2)

Lead Sponsor	Collaborator
McMaster University	The Physicians' Services Incorporated Foundation

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Loeb MB, Molloy DW, Smieja M, Standish T, Goldsmith CH, Mahony J, Smith S, Borrie M, Decoteau E, Davidson W, McDougall A, Gnarpe J, O'DONNell M, Chernesky M. A randomized, controlled trial of doxycycline and rifampin for patients with Alzheimer's disease. J Am Geriatr Soc. 2004 Mar;52(3):381-7. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	IL-1beta		baseline and 12 months	No
Primary	TNF-alpha		baseline and 12 months	No
Primary	MCP-1		baseline and 12 months	No
Primary	IL-4		baseline and 12 month	No
Primary	IL-10		baseline and 12 months	No
Secondary	Other inflammatory markers.		Baseline and 12 month	No

External Links

•   DARAD Study clinical trial registration on ISRCTN15039674. Details provided.