Impact of Adalimumab Therapy on Brachial Endothelial Function and Large Artery Stiffness in Patients With Rheumatoid Arthritis

Sponsor
Assistance Publique Hopitaux De Marseille (Other)
Overall Status
Completed
CT.gov ID
NCT01954381
Collaborator
(none)
60
1
2
45
1.3

Study Details

Study Description

Brief Summary

Rheumatoid arthritis (RA) is one of the most common inflammatory diseases in the general population and many cardiovascular diseases (valvular, myocardial, pericardial, coronary disease, stroke, heart failure etc.) have already been described in this disease. Large epidemiological studies have also demonstrated a higher degree of severity of atherosclerotic vascular disease in RA patients, to such a degree that several authors have highlighted the fact that, in the final analysis, the prognosis of RA is rather determined by the severity of atherosclerotic lesions.

By reducing RA-related systemic inflammation, it can therefore be hypothesized that 24 weeks of anti-TNF therapy would improve arterial endothelial function and large artery stiffness.

The proposed study will assess the effects of adalimumab therapy on these parameters. A group of 26 RA patients will be recruited from a rheumatologists association of the French PACA region (CONCERTO association). This study will be non invasive and will comprise:

  • in vivo study of endothelial function by measuring the post-ischaemic dilatation by 2D ultrasound;

  • study of large artery stiffness by pulse wave velocity determined by aplannation tonometry;

  • study of central pulse pressure;

  • evaluation of atherosclerosis-related parameters such as intima-media thickness.

The results obtained should provide a better understanding of the mechanisms involved in RA-related vascular disease and the effects of anti-TNF therapy.

In view of the high prevalence of RA, this study could potentially interest the medical community as a whole and could be largely diffused.

Condition or Disease Intervention/Treatment Phase
  • Device: transthoracic echocardiographic
  • Device: Doppler ultrasound.
  • Biological: blood samples
Phase 3

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Impact of Adalimumab Therapy on Brachial Endothelial Function and Large Artery Stiffness in Patients With Rheumatoid Arthritis
Study Start Date :
Oct 1, 2011
Actual Primary Completion Date :
Oct 1, 2014
Actual Study Completion Date :
Jul 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Other: control

Device: transthoracic echocardiographic

Device: Doppler ultrasound.

Biological: blood samples

Experimental: patient

Device: transthoracic echocardiographic

Device: Doppler ultrasound.

Biological: blood samples

Outcome Measures

Primary Outcome Measures

  1. evaluate the effects of 24 weeks of anti-TNF (adalimumab) therapy on [3 YEARS]

    - aortic stiffness by measuring carotid-femoral pulse wave velocity (CF-PWV)

  2. evaluate the effects of 24 weeks of anti-TNF (adalimumab) therapy on [3 YEARS]

    - central pulse pressure (aortic)

  3. evaluate the effects of 24 weeks of anti-TNF (adalimumab) therapy on [3 YEARS]

    - endothelial function by studying hyperaemia-induced vasodilation (FMD), reflecting the quality of endothelium-dependent vasorelaxation

Secondary Outcome Measures

  1. evaluate the resting blood pressure [3 YEARS]

  2. evaluate the systolic pressure index [3 YEARS]

  3. evaluate the structure of the carotid wall [3 YEARS]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients over the age of 18 years

  • Patients with RA according to ACR 1987 criteria

  • Indication for adalimumab therapy, according to guidelines:

  • moderately to severely active RA, when the response to disease-modifying anti-rheumatic drugs, including methotrexate, is inadequate,and,severe, active and active RA in adults not previously treated with methotrexate.

Exclusion Criteria:
  • Minors, pregnant women, not adequate contraception if female with childbearing potential, majors under guardianship, residents of social welfare or health care establishments, patients presenting an emergency situation, patients not covered by French social security, subjects deprived of their freedom and patients refusing to participate in the clinical research.

  • Absence of informed consent

  • Patients who have previously received anti-TNF therapy

  • Renal failure

  • History of demyelinising disease

  • Any unstable medical condition

  • Patients with recurrent serious infections

  • History of cardiovascular or cerebrovascular disease

  • History of cancer

  • Patients not having TB prophylaxis as per guidelines for latent TB, or patients non-treated active tuberculosis

  • Contraindication to adalimumab therapy:

  • Hypersensitivity to adalimumab or one of the excipients.

  • Active tuberculosis or other severe infections such as sepsis and opportunistic infections

  • Moderate to severe heart failure .

Contacts and Locations

Locations

Site City State Country Postal Code
1 Assistance Publique Hopitaux de Marseille Marseille France

Sponsors and Collaborators

  • Assistance Publique Hopitaux De Marseille

Investigators

  • Study Director: BERNARD BELAIGUES, Assistance Publique hôpitaux de Marseille

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique Hopitaux De Marseille
ClinicalTrials.gov Identifier:
NCT01954381
Other Study ID Numbers:
  • 2011-002883-26
  • 2011-15
First Posted:
Oct 1, 2013
Last Update Posted:
Jul 22, 2015
Last Verified:
Sep 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 22, 2015