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A Pilot Study of Inflammatory Markers in Alzheimer's Disease

Primary Purpose

Alzheimer's Disease

Status
Unknown status
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
doxycycline
rifampin
placebo
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer's Disease focused on measuring Alzheimer's disease, dementia, inflammation, cytokine, biomarker, cerebrospinal fluid, serum, doxycycline, rifampin

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • St.Peter's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Active Comparator

Active Comparator

Active Comparator

Placebo Comparator

No Intervention

Arm Label

1 AD doxycycline + rifampin

2 AD doxycycline

3 AD rifampin

4 AD placebo

5 Control

Arm Description

Participants with AD allocated to doxycycline 100 mg bid od and rifampin 300 mg od for 12 months

Participants with AD allocated to rifampin 300 mg od od and placebo matched to doxycycline bid for 12 months

Participants with AD allocated to placebo matched to doxycycline and placebo matched to rifampin for 12 months

Age-matched cognitively healthy participants (untreated)

Outcomes

Primary Outcome Measures

IL-1beta
TNF-alpha
MCP-1
IL-4
IL-10

Secondary Outcome Measures

Other inflammatory markers.

Full Information

First Posted
July 11, 2008
Last Updated
February 3, 2009
Sponsor
McMaster University
Collaborators
The Physicians' Services Incorporated Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00715858
Brief Title
A Pilot Study of Inflammatory Markers in Alzheimer's Disease
Official Title
A Pilot Study Comparing Inflammatory Biomarkers in Blood and CSF in Patients With Alzheimer's Disease and Age-Matched Controls
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Unknown status
Study Start Date
May 2008 (undefined)
Primary Completion Date
August 2009 (Anticipated)
Study Completion Date
October 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
McMaster University
Collaborators
The Physicians' Services Incorporated Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer's Disease
Keywords
Alzheimer's disease, dementia, inflammation, cytokine, biomarker, cerebrospinal fluid, serum, doxycycline, rifampin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Non-Randomized
Enrollment
21 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1 AD doxycycline + rifampin
Arm Type
Active Comparator
Arm Description
Participants with AD allocated to doxycycline 100 mg bid od and rifampin 300 mg od for 12 months
Arm Title
2 AD doxycycline
Arm Type
Active Comparator
Arm Title
3 AD rifampin
Arm Type
Active Comparator
Arm Description
Participants with AD allocated to rifampin 300 mg od od and placebo matched to doxycycline bid for 12 months
Arm Title
4 AD placebo
Arm Type
Placebo Comparator
Arm Description
Participants with AD allocated to placebo matched to doxycycline and placebo matched to rifampin for 12 months
Arm Title
5 Control
Arm Type
No Intervention
Arm Description
Age-matched cognitively healthy participants (untreated)
Intervention Type
Drug
Intervention Name(s)
doxycycline
Other Intervention Name(s)
Apo-doxy
Intervention Description
capsule, 100 mg, b.i.d., 12 months
Intervention Type
Drug
Intervention Name(s)
rifampin
Other Intervention Name(s)
rifampicin, Rofact, Rifadin
Intervention Description
capsule, 300 mg, od, 12 months
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo matched to rifampin; placebo matched to doxycycline
Primary Outcome Measure Information:
Title
IL-1beta
Time Frame
baseline and 12 months
Title
TNF-alpha
Time Frame
baseline and 12 months
Title
MCP-1
Time Frame
baseline and 12 months
Title
IL-4
Time Frame
baseline and 12 month
Title
IL-10
Time Frame
baseline and 12 months
Secondary Outcome Measure Information:
Title
Other inflammatory markers.
Time Frame
Baseline and 12 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
D. William Molloy, MB
Phone
905-777-3837
Ext
12440
Email
wmolloy@stpetes.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Timothy I Standish, MA
Phone
905-777-3837
Ext
12442
Email
tstandish@stpetes.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
D.William Molloy, MB, MRCPI, FRCPC
Organizational Affiliation
McMaster University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Brandon M Kucher, PhD, MD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Shucui Jiang, MD,PhD
Organizational Affiliation
McMaster University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Michel P Rathbone, MB, PhD
Organizational Affiliation
McMaster University
Official's Role
Study Director
Facility Information:
Facility Name
St.Peter's Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8M1W9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
D. William Molloy, MB

12. IPD Sharing Statement

Citations:
PubMed Identifier
14962152
Citation
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. doi: 10.1111/j.1532-5415.2004.52109.x.
Results Reference
background
Links:
URL
http://www.controlled-trials.com/
Description
DARAD Study clinical trial registration on ISRCTN15039674. Details provided.

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A Pilot Study of Inflammatory Markers in Alzheimer's Disease

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